Monday, January 21, 2013

Bridging the gap in HIV-AIDS treatment in private hospitals

Focus is on free HIV-AIDS testing, and care for pregnant HIV-positive women. PPP programme makes testing easily accessible for persons reluctant to visit ICTC centre.

While government and non-government agencies are keen on pulling out all stops to ensure that children are no longer born with HIV-AIDS infection, lack of information pertaining to patients seeking treatment in private hospitals stands in the way, believe authorities concerned. Roping in more hospitals and doctors in private health sector can strengthen public-private partnership.

While more than one lakh persons across the State are taking anti-retroviral (ART) treatment in government hospitals, there are an undisclosed number seeking care in private hospitals, clinics, and nursing homes.
Various meetings held in the district have issued a call to private hospitals to share this information as not only does this help in arriving at absolute figures, but also ensures that treatment is standardised and uniform for all patients in the State.
300 private hospitals
The Public Private Partnership (PPP) Programme initiated by Tamil Nadu State AIDS Control Society (TANSACS) is being strengthened by including more private hospitals and nursing homes under the programme, according to A.Sathishkumar, coordinator, SAATHI, an NGO that acts as a technical advisor for TANSACS. While the programme kicked off in 2009 with 76 hospitals in the State, the number has risen only to 100 in 2012. But things are set to change with 300 hospitals to be included by March this year, says Mr.Sathiskumar. The PPP encompasses Integrated Counselling and Testing Centre (ICTC) and Prevention of Parent to Child Transmission of HIV Centre (PPTCT) services in private hospitals.
In simple terms, the programme hopes to plug gaps in HIV-AIDS treatment in the private sector by providing free HIV-AIDS testing, and care for pregnant HIV-positive women.
Among the four common methods of transmission of HIV, mother to foetus transmission is one.
The importance of screening all pregnant women for HIV-AIDS on their first visit to the gynaecologist is what the agency advocates to all doctors in the private sector. Women who test positive after voluntary testing in private hospitals will be linked to the Prevention of Parent to Child Transmission Programme to ensure HIV virus is not transmitted to infants.
Ante-natal care
“The main focus of the programme is to track women receiving ante-natal care,” says Selvakumar, district supervisor, District AIDS Prevention and Control Unit. “While we keep track of those in primary health care centres and government hospitals, there is no information on children born to HIV-positive mothers in private healthcare sector.” Public-private partnership also enables providing free triple drug ARV ART to all HIV-positive pregnant women which in turn would ensure that infection is not transmitted to infants.
The PPP programme also makes testing easily accessible for persons who are reluctant to visit an ICTC centre. Free testing kits are provided by TANSACS to hospitals enrolled in the programme. If a person tests positive in the preliminary test, he or she is referred to ICTC centres for confirmatory tests. “The partnership will help us track persons reporting to private hospitals and ensure they continue treatment,” says Mr.Sathishkumar.
“When a private hospital enters the PPP programme, they can coordinate with doctors at government hospitals to ensure that patients they refer have turned up for testing or treatment.” SAATHI will be engaged in the sensitisation of private hospitals and practitioners, which it has been doing in 800 hospitals across four States. Recently, a similar programme was organised by TRIOGS and IMA for city doctors here. - Copyright by - THE HINDU NEWSPAPER  - 22 nd January 2013

Friday, October 19, 2012

THE PROBLEMS OF CHILD LABOUR IN TAMIL NADU


Child labour rampant in Erode, say rights activists

They blame Labour Department for prevailing state of affairs
The rescue of 38 children from the clutches of child labour in the last two days in Erode town has come as a shock to the people of Erode.
Despite tall claims of abolishing child labour by the Labour Department, two units of a yarn processing mills were found to employ children, all from the economically backward areas of Dharmapuri, Krishnagiri, Tiruvannamalai, Salem and Vilupuram districts.
The two units functioned within urban limits. It was also alleged that the mills forced these children and 100 others into bonded labour as well.
“All the children belonged to poor families and brought to Erode by agents through false promises,” a senior revenue official, who was among the rescue team, said.
The children, deprived of education and other basic human rights, claimed that they were forced to work in inhuman conditions for long hours for meagre daily wages. A majority of them claimed that they were not allowed to visit their home for the past several months.
And most of the children were scared to talk and did not understand why it was wrong to work.
Some of the children said their parents received an advance payment, which was why they were sent to work.
The officials in the Department of Labour had taken steps to send the rescued children and other labourers to their native places and launched a detailed probe.
A case was also registered against the management of the unit for employing the children.
Meanwhile, child rights activists here blamed the Department of Labour for their failure to monitor the industrial units properly and curb the menace.
“Lack of monitoring was the primary reason that encouraged industrial units to employ children. There were a number of units that exploited children through cheap labour,” pointed out S.C. Nataraj of Sudar, a non-governmental organisation.
The officials, however, claimed that the acute staff shortage in the department hampered the activities aimed at curbing the menace of child labour.
“The office of the Inspector of Factories has just two staff members. It was very difficult to monitor hundreds of factories in the district with the current staff strength,” a senior official said on condition of anonymity.
61 more rescued
Revenue officials in another major drive rescued 61 more bonded labourers – including 17 children aged below 14 years – on Tuesday.
They were employed in another unit of the private yarn processing mill in Karungalpalayam near Erode from where 77 bonded labourers were rescued by a team of officials led by Mayor Mallika Paramasivam on Monday.
Revenue officials said the bonded labourers who were rescued on Tuesday were employed in the unit’s factory in Solar near Erode Town.
They were taken on a tour to Manarampalayam temple on the banks of River Cauvery and to a picnic spot near the temple on Tuesday.
The mill authorities were alerted by the raid on Monday and planned to take them to this spot before dropping them in their native towns.
Revenue Inspector Bhuvaneswaran and Village Administrative Officer Sasikala who were there on regular inspection spotted the labourers.

Haryana Congress leader says most rapes were “consensual”


Under fire for spiralling rape cases, the Haryana Congress has found itself in a middle of another row with a local party leader stating that 90 per cent rapes were “consensual” only to retract the comments later.
Haryana Pradesh Congress Committee member and Congress Hisar district spokesman Dharambir Goyat told reporters in Hisar last night that “90 per cent of rape cases are (a case of) consensual sex between the girl and boy.”
He was asked about the rising rape incidents in Haryana in the past one month for which the state government has been facing criticism from opposition Indian National Lok Dal, Haryana Janhit Congress and BJP for the “worsening” law and order situation.
Mr. Goyat said, “The girl gets into an affair with a boy and she goes with him without knowing that he is of criminal mindset. It’s not the state government which is responsible for rapes, in fact in most of the cases its consensual sex.”
“In 90 per cent cases, the girls and women initially accompany boys on their own and are later trapped in gangrape by criminals,” Mr. Goyat said, noting that Uttar Pradesh reported the highest number of rapes.
“In Haryana all the rapists have been sent to jail. The rapist has no caste or creed. In Hisar district in one year alone among the 38 rape cases, 19 were against minors and 19 against women,” he said, adding in many cases Dalit boys were involved in rape cases against Dalit girls.
However after his statement led to an outcry, Mr. Goyat said his remarks were “twisted and misinterpreted.”
He also stated that had not spoken on behalf of the party and they were his personal views.

Friday, August 5, 2011

STILL BIRTHS IN INDIA current issues

 
 
                                                    STILL BIRTHS IN INDIA
According to the recent research data revealed during the launch of British Medical Journal Lancet, on an average six lakh stillbirths take place in India every year.
According to World Health Organization, stillbirth is a birth weight of at least 1000 gm or a gestational age of at least 28 weeks (third trimester stillbirth).Of the 2.7 crore babies born in India, there are 22 stillbirths per 1000 births. Many doctors believe that the lack of obstetric care to the pregnant women is one of the prime causes of stillbirths.
Nigeria and Pakistan have the highest stillbirth rates of 42 and 46 per 1000 births respectively whereas Finland and Singapore have 2 per 1000 births.

Tuesday, July 26, 2011

WORKING MOTHER

The Working Mother
With inputs from Dr. Sushma Mehrotra, psychologist

Democratic notions
 
The tide is beginning to turn in the world social order. Traditional family roles are changing as democratic notions creep into the social system. Earlier, it was assumed to be written in stone that the man was the provider in the family and the woman the homemaker. In India, while a majority of the women may still be fighting against the old order, some have definitely seen the light at the end of the tunnel. And it is not just because women are beginning to realize that there is a world outside their kitchen windows. Women are also turning out in large numbers in the work force due to economic necessity. 
But as in the case of every social change, there is a lag between actions and attitudes. While people may be willing to accept the idea of career women, they are not willing to excuse them from their duties as career moms. The attitude towards working women seems to be that while people have no objection to availing of their talents and abilities outside the home, women are not allowed to compromise on home life. And if they do, they should be made to feel the error of their ways. In the first place, the term 'working mother' is a misnomer as mothers are working round the clock even if they don't go to an office. Being a working mother is not the easiest job in the world. Some women are good at it, some don't have a choice, some choose a middle path and some don't even try it. The point is that it is the women who should have the right to exercise the option to work or not to work, assuming that they have one. And if they do elect to pursue a career, it is important that their families be supportive. 
 
Making the decision
Mothers who have a choice whether to work or not to work have to consider many things before they take the decision. First of all, they need to be clear about their priorities. Does the baby and family come first or is a career and financial security of greater importance? They also have to decide whether they would be happy having servants or other family members look after their children. They need to realize that by taking the decision to work, they will probably miss out on all the major milestones of their babies' lives. Mothers need to remember that a job can be very demanding not only in terms of time, but also energy. Women spread themselves really thin trying to juggle work life and home life. They will have to consider the stress factor of the job because it is not easy to cope with the pressures of a high-stress job and the demands of a baby. Women should also discuss their decision to work or not with their spouses because they will need their support. It may help to find a job that has flexi-hours. It will make it easier for mothers to be able to stay home on days when there is no other caretaker for the baby or to leave early if there is an emergency. 
Sushmita Roy gave up a lucrative career as a management consultant with a multinational and started her own web design firm so that she could work from home. She says, "After Tara was born, I decided that I couldn't go back to working at a job with such long and erratic hours. I didn't want to miss out on any special moments in my daughter's life.  But at the same time, I didn't want to be a full-time mother because I really enjoyed working. Working from home was the only option."
Some women have no choice. Veena Marathe had to start working because she and her husband realized that his salary would not be enough to live on once the baby arrived. Veena started working as a receptionist when her baby was one year old. She says. "I felt terrible leaving my baby at such a young age, but I had no choice. It's not easy being a working mother. I come home tired from work and I have to look after the baby and cook and clean. I get so irritated with my husband and I have even begun to resent the baby's demands and I know it's because I'm so tired. To make things worse, I don't like my job. I'm just doing it for the money. " 
Suhasini Mehta dreams of becoming a partner in the law firm she works for. She says, "My job is high-stress and I have to work long hours, but I am determined to make it to the top. I live with my in-laws and both they and my husband are very supportive. I know that my in-laws will take good care of my daughter so I can work with a clear conscience."
 
When to return to work
Mothers often worry that their babies will forget them once they return to work. But they need not fear because babies recognize their mother's voices right from birth and are not going to forget even if their mothers are away for the whole day. The question then is when is the best time to go back to work? According to Dr. Sushma Mehrotra, "Ideally a working mother should only return to work when her baby is at least one year old. Otherwise, there is a danger that the baby may develop separation anxiety." Experts feel that mothers should wait till they have bonded with the baby and feel confident in their new role as mothers. For women who don't have a choice, it really depends on the amount of maternity leave they can wangle. 
 
Spending quality time
According to Dr. Mehrotra, it is not the quantity of time mothers spend with their children but the quality that matters. "A working mother who spends one hour of quality time every day with her child will probably establish a better bond with her child than one who is home nagging the child all the time." 
In Dr. Mehrotra's view, "Working mothers definitely have less time to spend with their children than the mothers who are at home. But it's not that a housewife is a better mother than a working mother. Even if the working mother is pressed for time, as long as she spends quality time with her child it is enough. Sometimes mothers are around the house the whole day but they don't even look at their children. They provide them with food and other facilities, but their involvement with the child is minimum. They think their presence is enough. But that is not true. It is quality time and the way you interact with your children that makes the difference." 
"For instance, if a working mother takes the trouble to find out what her child has been doing the whole day and accepts the child's reply, she will probably have a better bond with her child. On the other hand, a child may feel rejected if a mother who has been home the whole day has not bothered to see what her child is up to. It really depends on the kind of communication and bonding that mothers have with their children. Mothers must talk to their children, they must interact with them and must accept their children." 
Quality time does not imply that the mother must cram a hundred activities in the little free time that she has to spend with her child. It is enough to just spend time together doing routine things like eating together or just cuddling each other. Mothers should talk to their children telling them about their day and asking about theirs. Given the fact that time is of the essence, mothers need to prioritize household chores and only do those that are absolutely essential on a daily basis. Mothers should try to tune out distractions like the television, radio and telephone calls when they are spending some special time with their babies. Quality time should not be restricted to the mother and baby alone. Mothers shouldn't forget the fathers and should make it a point to involve them in quality time activities. 
 
The disadvantages
In the long run, in a situation where both parents are working and not spending enough time with their children, it can have an adverse effect on the child's development. Dr. Mehrotra feels, "Children may feel neglected and seek stimulation outside the house. Servants can look after a child's basic needs, but they cannot be responsible for the child's intellectual, social and emotional development."
In her experience, Dr. Mehrotra has found that very often, mothers who have to go back to work are not happy leaving their child at such a young age. They feel guilty and anxious and their anxiety is transmitted to the child. The mother will phone home ten times a day to find out what is happening and try to give instructions over the phone. This can make the whole family develop neurotic tendencies. "When a mother is anxious, she makes everybody anxious." 
"Often working mothers succumb to children's demands very easily because they feel guilty. They feel that they can compensate for their absence by giving their children money. But a child's needs are not material. Children want warmth and emotional security," says Dr. Mehrotra. 
Probably the best thing for women to do if they want to work is to either work part-time or to get a job that has flexi-hours or to work freelance. However, in cases where mothers have no family at home to leave their children with, a good creche may be an option to consider. Ideally, a person running a creche will be educated and experienced with children and definitely a better option than leaving children to their own devices or with servants. But mothers must be very careful about checking the credentials of the person running the creche and speak to parents of other children in the creche before they take a decision to send their child to one. 

Friday, January 7, 2011

PROBLEMS OF SLUMDWELLERS

93 million slumdwellers by next year

NEW DELHI: Despite the country's robust economic growth, around 93.06 million people will live in slums in cities by next year, an increase of around 23% since 2001 forced by a lack of space and means.

According to an expert committee set up to estimate "reliable" urban slum population, there has been a growth of 17.8 million across the country in the last decade.

Defending the increase in slum population figures, minister for housing and urban poverty alleviation Kumari Selja said this trend is on expected lines due to a spurt in urbanisation. However, she assured that the percentage would come down, with the efforts of UPA-II towards slum development and rehabilitation.

The committee, headed by Pranab Sen, principal adviser to the Planning Commission and former chief statistician, pointed out that the projected slum population in 2011 would be go up to 93.06 million from 75.26 million that was estimated in 2001 as per the new methodology. The 2001 Census figures peg the slum population at 52.4 million.

By next year, 31.63 lakh people will be living in slums in Delhi as compared to 23.18 lakh in 2001, going by the panel's methodology.

Among the states, Maharastra tops the chart with around 1.815 crore will be living in slums in 2011, followed by Uttar Pradesh (1.087 crore), Tamil Nadu (86.44 lakh), West Bengal (85.46 lakh) and Andhra Pradesh (81.88 lakh).

The ministry appointed the committee to come out with reliable slum data to ensure better implementation of Rajiv Awas Yojana (RAY) that aims to eradicate slums in India.

Selja said there was "paucity of correct data earlier" as small towns were left out, and the new definition put forth by the committee would serve as a guideline for Slum Census 2011 and state governments.

A major reason for the total slum population being underreported was due to the fact that the Census 2001 took into account only notified slums in 1,764 towns across the country.

Officials attributed the rise in slum figures to wider definition of slum and expanding the coverage as the committee has factored in all 5,161 towns, including 3,799 statutory towns, and has also modified the definition of slum as followed by the Registrar General of India (RGI), which conducts the Census.

Selja said the target of achieving a slum-free India in five years, as outlined by President Pratibha Patil, was not unachievable if states cooperate fully.

Admitting that urban population is growing and there are many challenges to realise the goal, the minister said, "UPA government has committed itself to RAY and money should not be a constraint".

The committee recommended to adopt a normative definition based on appropriate indicators and checklists for the purpose of identification of slum areas and enumeration of population of area with 20-25 households, having slum-like characteristics in an enumeration block in Census 2011.

All clusters of 20-25 or more households having no roofs or non-concrete roofs, and not having any facility of drinking water, toilets or drainage will be considered as slums. Earlier, the cluster size for identification of slums was 60 households.

The panel has suggested that for the purpose of policy formulation -- for Slum Census 2011 -- it is absolutely essential to "count the slum population even in cities having less than 20,000 population".

The committee has recommended that Registrar General of India, which is conducting the 2011 survey, should share layout maps with the ministry as an aid for slum surveys.

Tuesday, January 4, 2011

PROBLEMS OF CHILDREN LIVING WITH HIV/AIDS IN MANIPUR


The Untouchables: Children living with HIV, AIDS in Manipur
Wednesday December 01, 2010 07:10:02 PM, Kamini Kumari, IANS
Imphal: Growing up in a conflict zone, children living with HIV in the northeastern state of Manipur are deprived of more than their childhood.

Eleven-year-old Tina, who is HIV-positive, contracted measles and had to be taken to the far-off Imphal General Hospital. After initial treatment and medication was administered, the doctors referred her to an isolation ward of a neighbouring hospital.

When Tina and her mother arrived at the hospital, they found the isolation ward had been converted into staff quarters. So Tina returned home though her weakened condition demanded hospitalisation.

Consequently, she could not access the anti-retroviral therapy (ART) course either. She now lives in the shadow of death, without access to the only medication that promises survival.

According to the World Health Organisation, ART consists of the use of at least three anti-retroviral (ARV) drugs to maximally suppress the HIV virus and stop the progression of HIV disease.

Huge reductions have been seen in rates of death and suffering when use is made of a potent anti-retroviral regimen. The ongoing conflict within the state often leads to curfews and restrictions on movement, in turn cutting off access to ART.

Frequent shutdowns and blockades called by different actors add seriously to the problem. For HIV-positive children, it results in sporadic supply of medication to the hospitals and healthcare centres.

"Only two of the state-specified seven hospitals that offer ART are regularly stocked with the necessary medication," says Dipankar Majumder, director, development support, Child Rights and You (CRY).

"The hospital in Imphal gets overcrowded because people from all across the state come to it in the search of treatment."

CRY's Ashim Ghosh, who also works in the region, adds: "Patients have to travel for up to 40 km, in a place where public transport is non-existent, to access the central hospital. Even then, care is not guaranteed."

Staff absenteeism, especially in remote districts, is common, due to the frequent outbursts of violence. This means that even when people from remote areas manage to make the expensive trip to the city to get their monthly stock of ART medicines, they cannot always get a health check-up at the same time.

"The importance of a stable education environment as a nurturing setting in which children can be taught about HIV/AIDS is underrated. Schools can be, and often are, a place for peer-to-peer learning, myth-breaking and monitoring the spread of the disease in key populations at higher risk within the local community," says Majumder.

Lack of access to healthcare and education are not the only struggles in the lives of Manipur's HIV-positive children. Efforts to change people's existing perceptions of the disease remain woefully unaddressed.

The stigma attached to HIV and AIDS is still widely prevalent across all sectors of the Manipuri community.

There is little evidence pointing towards concentrated efforts by the government to address the issue of children living with HIV.

CRY partner CCRP (Coalition on Children's Right to Protection) works extensively to influence policies to benefit children in Manipur. It says that there is no adequate provision for shelter, education and food to deal with the emerging issues.

Key figures of the number of children living with HIV in India are not officially published. HIV-positive children don't even feature as a category in the Manipur AIDS Control Society (MACS) 2007 Sentinel Surveillance report on the rate of HIV prevalence among various categories of population.

Even though Manipur was the first state in the country to have its own policy statement on AIDS, it has yet to develop a comprehensive plan to provide support and protection to children, both infected and affected by the AIDS epidemic.

"The situation of children living with HIV and AIDS cannot be separated from the other challenges that children in general are coping with in the region," says Yogita Verma Saigal, director, CRY.
(Kamini Kumari can be contacted at kamini.k@ians.in)

Hidden Burden of Alcoholic Parents

Hidden Burden of Alcoholic Parents

At the start of Children of Alcoholics Week, victims talk about their shame, loneliness and guilt with nowhere to turn for help
When Mary Smith pulled the car off the road to answer her mobile and hear the news of her father’s death, she felt just “a calm relief”.
“Really, I had lost my dad many years before. His mind had gone at least four years before,” said Smith (not her real name). “Sometimes I think about what we went through and I can’t quite believe that we got through it. There were a lot of bad times.”
Her father was an alcoholic who drank himself to death. All the help his young daughters and his wife tried to get him, from detox programmes, to rehab, to psychiatric sessions, had failed. “He chose to drink, and he chose that over us. It took me a long, long time to accept he had a disease, but my anger had gone before he died.” Smith, now 27, spent her late teenage years trying to protect her younger sisters, support her mother and get help for her father. There was little time for her to enjoy her youth.
“I did take the brunt of it. No one should have to beg their mother to get a divorce, or their father to stop drinking and choose them over alcohol.”
Smith and her three sisters are among the 3.6 million people in Britain who have had their childhoods scarred by the drinking of one or both of their parents. The latest research suggest that almost one million children in Britain are today living with an alcoholic parent, but campaigners say the true number is far higher, obscured behind the front doors of a society where drinking is so much the norm that even social workers don’t take it seriously.
“If a social worker goes to a home where a parent is smoking heroin or cannabis, action is taken straight away,” said Don Shenker, chief executive of Alcohol Concern. “But if alcohol is being taken, they won’t even bother recording it. We are finding a lot of problems with alcohol abuse not being included in case notes.”
He said that far too much policy consideration was given to drugs users, while the far bigger picture, the problem of families living with alcohol addiction, was being overlooked.
“It’s the forgotten issue, but it’s actually on a far greater scale than drug addiction,” said Shenker, who is calling for better training for social workers to recognise alcohol-related issues. “The support services are not there, certainly not working with the families. Even where alcohol dependency is being treated, no one is saying to these people, ‘And do you have children? And how is your drinking impacting on them?’
“It’s just not talked about… The kids don’t want to talk about it because they will feel guilty, the parents who are drinking [feel they] have something to hide, and society doesn’t really want to come out against alcohol. So there’s this mismatch where families at risk through drugs get strategies, but those at risk through alcoholism do not.”
But there is now a growing support community for children living with alcoholic parents, set up and run mostly by people who have been through the experience themselves.
This week marks the second Children of Alcoholics Week, run by the National Association for Children of Alcoholics (Nacoa), to raise awareness of the difficulties faced by millions who are, or were, parented by alcoholics. The charity saw the number of calls to its helpline double to 38,000 during a 12-month period over 2007 and 2008, and believes the hidden issue is blighting many more young lives than previously thought.
The campaign is backed by celebrities including Lauren Booth, Calum Best, Virginia Ironside and Geraldine James, all themselves children of alcoholics.
“As children, we were never allowed to talk openly about our mother’s drinking,” said actress James, who said she desperately wished there had been help. “I remember my brother being slapped very hard when he asked my father if she was drunk – ‘Never use that word in this house again.’
“I grew up feeling ashamed, frightened, lost, guilty and lonely; feeling unconfident, unsafe, unlistened to, unprotected, unloved, unlovable; feeling there was no one there, inside or out. But there was literally no one to turn to.”
It is a sentiment shared by Emma Spiegler, 26, a Nacoa trustee who started Children of Addicted Parents in 2006 after realising that children living in shame and guilt would find it easier to use online forums where they could have anonymity. Her own family was “pulled apart” by her mother’s drinking.
“There was nothing out there at all, and I know how lonely and isolating it can be. It’s all about loyalty and the guilt and the shame, it’s just so massively ­hidden.
“Mum was a social drinker from when I was about four upwards. She was in rehab when I was 10. But she drank at night, so it wasn’t until I was about 13 and starting to stay up later that I realised, and realised it wasn’t normal, the wine bottles lying around and her falling asleep downstairs. Unlike a lot of people, my mum wasn’t a violent drunk or aggressive, just emotional, so she would cry and get very vulnerable and say, ‘I’ve been a bad mother and I’ve messed every­thing up’, and I’d have to comfort and emotionally reassure her.
“I was a very angry child, really unhappy, and she was too involved in her relationship with the bottle to ever be there. I didn’t tell anyone and I don’t know why. I saw my dad at weekends, my parents were divorced, but I never talked to him about it. I think children just don’t. I lived my life for my mum.”
Spiegler’s mother has now been sober for four years: “I don’t think she really realises what happened.”
Statistics back the damage that drinking does inside Britain’s families. Growing up in an alcoholic household was inextricably linked to abuse, with 55% of domestic violence incidents happening in alcoholic homes and drink being a factor in 90% of child abuse cases. The NSPCC reports that one in four cases of neglect reported to them involves a parent who drinks.
A study by the Priory Clinic group in 2006 found that children who grow up with alcoholic parents bear emotional, behavioural and mental scars and their early lives were characterised by chaos, trauma, confusion and shame and, quite often, sexual and physical abuse. Studies have also shown that a third of daughters of alcoholics experienced physical abuse and a fifth sexual abuse – up to four times higher than in non-alcoholic homes.
The report said that children reacted in one of three ways: they became withdrawn, went into denial or used the experience to benefit themselves by becoming stronger. They also struggled to develop strong personal relationships. The report added: “Their feelings about themselves are the opposite of the serene image they present – they generally feel insecure, inadequate, dull, unsuccessful, vulnerable and anxious.”
Dr Michael Bristow, an addictions expert at the Priory, said: “There is a widespread misconception that addiction is all about the addict, that it is solely the addict who suffers. The reality? Alcoholism affects the adult alcoholic’s entire family, particularly the children.”
Partly because of their genes, children of alcoholics are four times more likely to become alcoholics than the one in 20 average in the population that currently have the condition, and 50% will end up marrying an alcoholic.
Natalie McArdle, 26, is a new mother with a three-month-old son. After nine months of not drinking and missing the odd glass of wine, she is grateful that after having her baby the desire to have a drink has gone: “I am quite like my dad in temperament. And I am the kind of person who can’t have one glass of wine when I could have the bottle, so I am very aware and very conscious.
“From the age of about 11 my life was about walking on eggshells. My dad always drank at home, alcoholism is an antisocial thing. You don’t really understand until you start going to friends’ houses that not all dads are like that, obliterated by drink and argumentative. Christmas Day was an utter nightmare because he’d get drunk first thing, then go to bed, then get up again and drink more. You’d dread hearing the sound of him upstairs getting out of bed.
“My dad finally left when I was 16 and didn’t come back, and for us it was the best thing in the world. Most kids are devastated when a parent leaves, but we were just so happy. We could breathe in our own home again.”
But McArdle is still in contact with her father and helps with his care at a nursing home, where he is suffering from early onset dementia because of his drinking.
“At the end of the day he is still my dad and I love him more now than then, even though I get very frustrated that he can’t tell me why he did it to us. He can’t feed himself or go to the toilet and certainly can’t explain himself to me, and funnily enough he is back to being very aggressive because of dementia, so I’m a little bit afraid of him still.
“My mum comes with me to visit him sometimes and she is very good. I don’t blame her for not leaving him as she loves my dad and always thought it might just be his last drink. But it never was.”
What the late Mo Mowlam, who was patron of Nacoa and whose father was an alcoholic, called the “hidden suffering” of UK families is getting worse as excessive drinking becomes more of an issue.
“If this could happen to me and my family, how many other families must be suffering in silence?” said Mary.

 

Thursday, December 2, 2010

PROBLEMS OF TODAY's YOUTH

Today's youth: anxious, depressed, anti-social

The mental health of teenagers has sharply declined in the last 25 years and the chances that 15-year-olds will have behavioural problems such as lying, stealing and being disobedient, have more than doubled.
The rate of emotional problems such as anxiety and depression has increased by 70% among adolescents, according to the biggest time trend study conducted in Britain.
Boys are more likely to exhibit behavioural problems and girls are more likely to suffer emotional problems. The rate is higher for emotional problems, now running at one in five of 15-year-old girls. The study found no increase in aggressive behaviour, such as fighting and bullying, and no increase in rates of hyperactivity.
The study looked at three generations of 15-year-olds, in 1974, 1986 and 1999. Behavioural problems increased over the whole period, while emotional problems were stable until 1986 and have subsequently shot up. The increases cannot be explained by the rise in divorce and single parenthood, argues the team of researchers, because they found comparable increases in all types of families, although there is a higher rate of adolescent mental health problems in single-parent families.
Nor can growing inequality over the 25 years explain the rise in problem teenagers because rates of increase were comparable in all social classes. There was no difference between white and ethnic minority teenagers.
The research found that the rising rate of 15-year-olds with behavioural problems correlated to their increased chances of experiencing a range of poor outcomes as adults, such as homelessness, being sacked, dependency on benefits and poor mental and physical health. This indicated that the rise in problems cannot be attributed to a greater likelihood to report them.
The deterioration of adolescents' mental health in Britain is in contrast to the findings of research in the US which showed that a comparable decline tailed off in the 90s, while in Holland, there was no decline at all.
The study, Time Trends in Adolescent Mental Health, to be published in the Journal of Child Psychology and Psychiatry in November, is the first to provide evidence in support of the increasing concern from parents and teachers about the welfare of teenagers.
The research conducted by a team from the Institute of Psychiatry, King's College London, and the University of Manchester, provides specific evidence for Britain which is in line with the World Health Organisation's warning last year that the fastest-growing mental health problem in the world, and particularly in the developed world, was among adolescents. "We are doing something peculiarly unhelpful for adolescent mental health in Britain," said Sharon Witherspoon, deputy director of the Nuffield Foundation which funded the research. "This is not a trend which is being driven by a small number of kids who are getting worse. It is not a small tail pulling down the average but a more widespread malaise."
"The route people take to adulthood has become much more difficult with the pressure on for qualifications," said John Coleman, director of the Trust for the Study of Adolescence. "When young people are faced with all these choices, they say they have to 'make it up as they go along'."
The study was not focused on the most serious cases such as suicide and self-harm where other recent studies have shown significant increases, but the more general experience of adolescents which is less likely to reach the point of needing professional intervention.
The findings are likely to fuel debates about how we are raising our children and whether they reflect parenting in early years or are linked to Britain's secondary education system with its emphasis on academic achievement, and poor record of out of school activities.
A recent survey showed that discipline in secondary schools comes ahead of funding as parents' greatest concern.
Next month, the Tomlinson report into 14-19 year-old education and training - commissioned by the Department for Education and Skills - is due to be published; a green paper on youth services is also expected this autumn.
The study did not look into possible causes, which are to be the subject of further research.
Also subject to further research is whether there has been a comparable rise in emotional and behavioural disorders among younger age groups or whether this is a specific problem in adolescence.

 

WORLD AIDS DAY 2010 THEME

Started on 1st December 1988, World AIDS Day is about raising money, increasing awareness, fighting prejudice and improving education. The World AIDS Day theme for 2010 is 'Universal Access and Human Rights'. World AIDS Day is important for reminding people that HIV has not gone away, and that there are many things still to be done.


According to UNAIDS estimates, there are now 33.3 million people living with HIV, including 2.5 million children. During 2009 some 2.6 million people became newly infected with the virus and an estimated 1.8 million people died from AIDS.
The vast majority of people with HIV and AIDS live in lower- and middle-income countries. But HIV today is a threat to men, women and children on all continents around the world.

World AIDS Day theme: Universal Access and Human Rights

The theme for World AIDS Day 2010 is 'Universal Access and Human Rights'. Global leaders have pledged to work towards universal access to HIV and AIDS treatment, prevention and care, recognizing these as fundamental human rights. Valuable progress has been made in increasing access to HIV and AIDS services, yet greater commitment is needed around the world if the goal of universal access is to be achieved. Millions of people continue to be infected with HIV every year. In low- and middle-income countries, less than half of those in need of antiretroviral therapy are receiving it, and too many do not have access to adequate care services.
The protection of human rights is fundamental to combating the global HIV and AIDS epidemic. Violations against human rights fuel the spread of HIV, putting marginalised groups, such as injecting drug users and sex workers, at a higher risk of HIV infection. By promoting individual human rights, new infections can be prevented and people who have HIV can live free from discrimination.
World AIDS Day provides an opportunity for all of us - individuals, communities and political leaders - to take action and ensure that human rights are protected and global targets for HIV/AIDS prevention, treatment and care are met.

In recent years, considerable energy and money have been spent trying to achieve universal access to treatment for HIV and AIDS. This is part of a wider objective to provide universal access to treatment, care and prevention by 2010. Most countries aspiring to expand treatment access have set themselves a goal of providing antiretroviral treatment to around 80% of those in need.

History of the targets

At the beginning of the 21st century, very few people in the developing world had access to HIV treatment.  This was in large part because of the very high prices of antiretroviral drugs (ARVs) and the international patents that stopped them from being manufactured at cheaper prices. However, in 2001 drug manufacturers in developing countries began to produce generic drugs under special terms in international trade law. In sub-Saharan Africa, countries including Kenya and South Africa passed bills that made it legal for them to purchase generic drugs from abroad. The vast reduction in price made possible by the manufacturing of generic drugs meant expansion of treatment on a global scale was possible.
In 2003, the World Health Organisation (WHO) launched the ambitious target of reaching 3 million people in low and middle-income countries with ARVs by 2005. It was not intended as a final objective, but as a stepping stone to universal access. Though the target was not attained until 2007, it was seen by some as succeeding in a number of ways. Treatment was vastly expanded with coverage tripling from 400,000 people in December 2003 to 1.3 million in December 2005. This included an eight-fold increase in sub-Saharan Africa.
Considering the relative success of the 3 by 5 target, the international community set another target in 2005 that aimed for universal access to HIV treatment, prevention and care by 2010.  However, by the time of the WHO’s 2008 universal access report, the heads of UNAIDS, UNICEF and the WHO conceded that most countries would not meet the 2010 targets of 80% of those in need receiving treatment.
The 2010 target is also part of Millennium Development Goal 6 which includes the goal of halting and beginning to reverse the spread of HIV/AIDS by 2015.

 Understanding antiretroviral therapy coverage

From 2006 to 2010, an extra three million people in low and middle-income countries were put on treatment for HIV. Access to treatment has greatly expanded, rising by a third from 2008-2009. However, the number of people in need of treatment has also increased due to a 2010 change in WHO guidelines, which recommends starting treatment at an earlier stage. This means that of the 33.3 million people living with HIV worldwide, the number of people in need of treatment has risen from 10 million to 14.6 million. Under the previous guidelines HIV treatment coverage would have increased from 42% in 2008 to 52% in 2009. However, according to the new guidelines, treatment coverage in low and middle-income countries is 36%.

Regional antiretroviral therapy coverage

Region (lower- and middle-income countries) Antiretroviral therapy coverage Estimated number of people receiving antiretroviral therapy Estimated number of people needing antiretroviral therapy
Sub-Saharan Africa 37% 3,911,000 10,600,000

Eastern and Southern Africa 41% 3,203,000 7,700,000

Western and Central Africa 25% 709,000 2,900,000
Latin America and the Caribbean 50% 478,000 950,000

Latin America 51% 425,000 840,000

The Caribbean 48% 52,400 110,000
East, South and South-East Asia 31% 739,000 2,400,000
Europe and Central Asia 19% 114,000 610,000
North Africa and the Middle East 11% 12,000 100,000
Total 36% 5,254,000 14,600,00

 

In sub-Saharan Africa, which accounts for 72 percent of antiretroviral therapy need in low and middle-income countries, treatment coverage increased by 10 percent from 2008-2009. However, coverage within this region varies widely; in the most highly affected areas of Eastern and Southern Africa, coverage is higher (41%) than in West and Central Africa (25%).
Eight low-and middle-income countries (Botswana, Cambodia, Croatia, Cuba, Guyana, Oman, Romania and Rwanda) had achieved universal access to treatment by December 2009. Under the previous WHO guidelines, 9 other countries, including Swaziland and Zambia, would have achieved universal access.

Achieving universal access to treatment

Universal access is broadly defined. It does not necessarily mean 100% coverage of all services but can be seen as a desire to move to a high level of access for the most effective interventions that are "equitable, accessible, affordable, comprehensive and sustainable over the long-term". Ninety nine countries have set their own 2010 universal treatment access targets with most countries aiming for 80% treatment coverage.
Scaling-up the number of people on treatment involves great challenges including the need for:
 * widespread awareness of the value of testing and subsequent treatment
* life-long commitment to antiretroviral drugs (ARVs) and supporting patients to adhere to a daily regimen
* adequate health infrastructure including health staff
 * supply chains of effective drugs

Counselling, testing and treatment awareness levels

Before people can be treated they need to know they are infected. This requires not only HIV testing facilities but also widespread knowledge of the importance of testing and where it can be done. People may be more inclined to test if they are aware of the benefits of antiretroviral therapy and know they could be treated if they test positive. Confronting stigma and denial are absolutely necessary as these are often "the two factors that often determine whether a person seeks an HIV test or not".5 Testing and treatment services also need to reach marginalised and difficult-to-reach groups, such as men who have sex with men and sex workers.
“Universal access means more than ensuring that those who need treatment or prevention services receive them. It implies an extra effort to reach those who are marginalized, criminalized or disenfranchised.”Secretary-General Ban Ki-moon6
The number of HIV testing and counselling facilities has increased in recent years. In 2009, there were 107,000 health facilities in low and middle income countries that provided HIV testing and counselling, compared to 78,000 in 2009.

When HIV treatment should begin

In more economically developed countries, generally the threshold for treatment is a CD4 count that has dropped below 350 cells per cubic millimetre (mm3) of blood, which is what has been recommended by WHO for all countries since 2010. In less developed countries governments decide whether to follow old guidelines, which recommend treatment starts at 200 cells/mm3, or follow the WHO 2010 guidelines. The stage of infection at which people are eligible to begin taking ARVs provides some context to the percentage of people regarded as in ‘need’ of treatment. Someone with a CD4 count of 300 in the United Kingdom, for example, would be considered in need of treatment, whereas someone with a similarly advanced infection in a less developed country which is not following the latest WHO guidelines, may not be regarded as needing treatment. The levels of investment and resources that are necessary to obtain a certain level of access to treatment are therefore very much linked to a country’s definition of need.
Treatment centre, 
Botswana 
Treatment centre, Botswana Deferring treatment until infection has progressed may seem a cheaper option for funders of treatment programmes, but some say that initiating treatment earlier is cost-effective in the long run. This is because the costs of a deferred treatment approach are ‘substantially increased’ by intensive clinical care, having to make more likely switches to expensive second-line treatment, an increased infection rate, and the loss of patients’ economic productivity. However, despite the potential cost savings, treating patients earlier will inevitably require greater initial spending on antiretroviral drugs.
As of October 2010, 45 countries had adopted the new guidelines, including China, Kenya, Lesotho, Malawi, Tanzania, Zambia and Zimbabwe and some countries in Eastern Europe such as Romania and Ukraine. However, adopting the new guidelines has at least doubled the number of people in need of treatment in these countries and therefore makes universal access a more challenging target to reach.

Patient retention

Deciding when, how and who initiates treatment is one set of issues that need to be considered when establishing and maintaining HIV treatment programmes. However, keeping people on treatment programmes – patient retention – should be considered as important a factor as boosting the numbers of people beginning treatment.
“High rates of attrition from treatment programs thus poses a serious challenge to program implementers and constitute an inefficient use of scarce treatment resources.”Sydney Rosen, Center for International Health and Development, Boston University.

Patients who do not start treatment or who do not continue with treatment are often classified as “lost to follow-up”. This could be for a range of possible reasons including simply stopping or interrupting treatment, death, or finding alternative sources of ARVs. The nature of loss to follow-up is that very often a patient’s eventual whereabouts or outcome is unknown, even if efforts are made to trace such patients.
In a review of studies examining patient retention in antiretroviral therapy programmes in Africa, just 60% of patients remained with their programme after two years. The remainder were lost to follow-up or had died. Another study examining data on 5,491 patients beginning antiretroviral therapy in 15 treatment programmes in Africa, South America and Asia, found 21% of patients became lost within six months, including 4% who were not seen since receiving their first prescription of ARVs. Globally, it is estimated that almost 20 percent of patients are not retained on antiretroviral therapy after 12 months, while for children, 25 percent are lost after 12 months.

Some studies suggest that patient retention actually suffers as a result of the drive to boost patient initiation. The research across three continents found the proportion of patients who were lost to follow-up was greater in 2003-2004 than in 2000 or earlier. This, it was suggested, was due to difficulties following-up the growing patient numbers:
“Early patient losses were increasingly common when programmes were scaled up and were associated with a fee for service and advanced immunodeficiency at baseline.”
The delay between eligibility for antiretroviral treatment and actually starting treatment is also an issue of concern according to studies in South Africa, Malawi and Uganda. When patients test HIV positive, they may not all be ready to take ARV drugs yet but many of those who are eligible do not start treatment on time. Substantial numbers have also shown to be lost before they should start taking treatment.

Why do people stop treatment?

A variety of factors influence why individuals discontinue their treatment. Cost has a major impact on patient retention and mortality levels.16 Similarly, associated costs such as transportation or “opportunity costs” such as having to forgo a day’s pay are other more structural factors. Adverse side effects of ARVs may cause someone to stop taking them, as could successful therapy if it leads people to become complacent.
Social, cultural and psychological influences should also be considered. Perceptions of disease severity, susceptibility and the benefits or disadvantages of staying on treatment are key in determining clinical attendance. Believing that God or alternative medicine can cure AIDS can also influence treatment patterns. Similarly, misconceptions about ARVs can alter patients’ motivation to stick with them.
“Those medicines were so confusing. Sometimes you hear that if you use those medicines you will die. So it used to confuse people so much…we used to fear it so much that it means if you take these medicines you may die.”ART patient, Tanzania
Nutritional support is vital too as a lack of adequate food security could determine whether people remain on treatment. Some medications can only be taken on a full stomach while some ARV side effects are reduced by having adequate nutrition.

Keeping people on treatment

Sticking to a treatment regimen for life that involves taking daily medication, with potential side effects, presents many challenges that must be overcome if patients are to successfully remain on treatment. If drug resistance occurs through failure to adhere to ARVs, far more expensive second-line therapy, may be necessary.
Having supportive family and community environments, as well as strong networks of people living with HIV are key to promoting adherence to ARV treatment. This could come in the form of very practical assistance such as transport to a clinic or help with other activities. Patients may require emotional support to continue their treatment both from their family and HIV-positive peers. The success of other people on ARVs can encourage patients to continue with their therapy. One study in Kenya has also shown that the use of mobile phones texts by nurses to check on patients is effective in improving adherence. One reason why the patients involved were 'highly satisfied' by the service and wanted it to continue was because they felt "like someone cares." Community involvement is particularly important for reaching high-risk groups such as sex workers, men who have sex with men or injecting drug users. These groups are more likely to be criminalised and either find it difficult or are unwilling to access public services. However, they are more likely to trust fellow members, or 'peers', of their group.
“…other patients who used to hide themselves have seen their fellows who come to these services are getting relief so they now turn up too.”ART clinic staff member, Tanzania.
South African 
woman with her daily medication  
South African woman with her daily medication
There is also a risk that people may experience unplanned treatment interruptions - where a person may have to stop their treatment for reasons beyond their control. Floods in Mozambique, the unstable political and economic situation in Zimbabwe, and the 2007 and 2010 public sector strikes in South Africa, are all situations where people taking ARVs may have had difficulty in accessing their medication.
“AIDS poses a challenge for health systems that is fundamentally different from all of the other health problems ever faced. Transforming a deadly disease into a manageable chronic one turns millions of people into chronic patients, in need of life-long regular follow-up. This implies that present efforts and commitments will have to be continuously increased for many years to come.”Wim Van Damme, Institute of Tropical Medicine, Belgium

The effect of universal treatment on prevention

Apart from the effects of treatment on quality of life and productivity, HIV treatment is also a possible preventative measure. This is because a higher level of HIV in the blood, or viral load, increases the risk of HIV transmission and antiretroviral therapy reduces the levels of HIV in the blood. A number of studies have shown that reducing the viral load in a population in turn reduces new infections and it is already known that antiretroviral therapy can drastically reduce the risk of HIV transmission from mother-to-child. The feasibility of rolling out large-scale treatment programmes, that would immediately treat people on diagnosis of HIV on a global scale, is unlikely however due to the costs and ethical considerations involved (drug resistance, side effects of drugs and need for patient consent).
Therefore, increased treatment coverage is not a substitute for other preventative measures that have been proven to work in reducing new HIV infections. Yet,  one result of the drive to rapidly boost treatment figures may be a reduced focus on other areas of HIV and AIDS work. Even in 2006, it was believed energy and resources were being redirected from prevention towards treatment:
“In Africa many grass roots organizations and NGOs…traditionally involved in community mobilization and prevention, have shifted their focus to treatment support activities” Wim Van Damme, Institute of Tropical Medicine, Belgium.
This raises questions about the approach of boosting the numbers on treatment  at the expense of prevention programmes designed to reduce new HIV infections in the long term. The effects of the economic crisis and reduced external funding are expected to impact prevention programmes the most, as their effects are harder to measure. Prevention programmes such as HIV/AIDS education in schools, condom distribution, counselling and testing, and targeted prevention programmes for high risk groups like sex workers and men who have sex with men must therefore be expanded alongside treatment programmes.
“The implications of HIV prevention failures are clear: unless we act now, treatment queues will get longer and longer and it will become more and more difficult to get anywhere near universal access to antiretroviral therapy.”former head of UNAIDS, Peter Piot.

Resources needed to achieve universal access

Trained staff

Many health staff are required at various stages of treatment programmes. However, countries with higher HIV prevalence tend to have lower health staff-to-patient ratios compared with more developed countries. Malawi, for example, has just one doctor per 50,000 people compared to the United States with one per 390 people. On average, there are 15 times the number of doctors and 8 times the number of nurses in Europe compared to Africa. The World Health Organization estimates that the global shortage of trained health care staff exceeds four million.
There are several reasons for this, one of which is AIDS itself. In Botswana, for example, 17% of the health-care workforce died due to AIDS between 1999 and 2005.
Nurses on an HIV 
ward, Uganda 
Nurses on an HIV ward, Uganda Migration of health staff from poorer to wealthier countries has also damaged the health infrastructure of countries ravaged by AIDS. It has even been suggested that the widespread recruitment of African health workers by more developed countries should be viewed as an ‘international crime’.

One proposal for tackling HIV with diminished staff capacity is to train or permit lesser-qualified health workers to perform tasks which they were previously unqualified to do. This is known as ‘task-shifting’. Allowing nurses to perform some of the tasks of doctors, and community workers the roles of nurses, for example, could facilitate access to ART and improve adherence and management of therapy. It is argued that quality of care would not be compromised and that it could be more cost-effective than the present division of labour.
However, as a study in Uganda has shown, a transfer of tasks is not always accompanied by appropriate training.
Task-shifting has existed in Zambia since 2004, and was implemented in South Africa in May 2010.

Reliable supply chains

Ensuring there are no interruptions in treatment requires a guaranteed supply of antiretroviral drugs from the factories where they are produced, to the treatment centres in perhaps remote areas of a country. Laboratory supplies, testing kits and information also needs to pass along the supply chain.
In order to be cost-effective, accurate forecasting of the necessary quantity of drugs is needed. Over-purchasing of ARVs can put strains on money and storage space, and may lead to wasting of drugs with limited shelf-life.

Under-estimating may lead to stockouts and the need to purchase costlier emergency supplies. One report found stockouts were ‘commonplace’ in China, India, Uganda, Russia and Zimbabwe. It was conservatively estimated that 30 people were dying daily in Free State, South Africa, after ARVs ran out towards the end of the 2009 financial year. Such events not only adversely affect those who desperately need to begin treatment but also patients who are on treatment already and who may develop drug resistance.
The transportation phase of the supply chain requires delivery tracking and needs to account for potential customs barriers. Special refrigerated containers may also be needed. In unstable regions theft of the drugs may be a concern and armed escorts and decoy trucks are known to protect expensive deliveries.
Intermediate storage of the medication – such as in large regional warehouses – needs to be safe and secure and be able to efficiently process orders and distribute ARVs to health facilities. Similarly, local facilities should be able to safely and securely store medication at controlled temperatures.
All of these requirements mean that the costs involved in distributing the drugs are higher than the antiretroviral drugs themselves. World Health Organization's Director of HIV/AIDS, Gottfried Hirnschall, points out:
"About 20 to 30 percent of the costs related to treatment are drug-related costs, and the other 70 to 80 percent are systems and delivery costs...We need to shift the conversation towards asking how we can use resources that we have more efficiently and effectively."
The massive international logistical exercise involved in creating a reliable supply chain for thousands of vital deliveries has meant the consortium that operates PEPFAR’s supply chain, the Supply Chain Management System, was the organisation that received the most money from PEPFAR in 2007.

Effective drugs and equipment

It goes without saying that HIV treatment programmes need a steady supply of drugs. However, the quality and type of drugs that are available will also have an impact on the effectiveness of the programme. The majority of treatment regimens in most developing countries use a drug called stavudine, or d4T, which has severe side effects that have led to its discontinued use in richer countries. Such side effects may dissuade patients from taking their medication, whereas better quality, though often more expensive, ARVs may encourage people to continue treatment and could require fewer costly treatment switches.
The most common regimen is d4T + 3TC (lamivudine) + nevirapine, with 59% of patients in low and middle-income countries taking this particular first-line combination. However, the phase out of d4T and replacement with less toxic regime combinations has already started in 33 countries, including Lesotho, Kenya and Uganda.
Other medical supplies besides antiretroviral drugs are also required. In developed countries, HIV positive patients on antiretroviral therapy undertake routine tests to monitor treatment efficacy and toxic effects. These tests require expensive equipment, electricity and trained technicians, and so are often unavailable in less economically developed countries.
A short video about the DART trial in Africa
A major study in Uganda and Zimbabwe looked at whether the availability of these tests had a significant impact on the long-term clinical outcomes of HIV-infected patients receiving antiretroviral therapy. Conclusions drawn from the DART trial suggest that first-line antiretroviral therapy can be delivered safely without these routine tests. However, routine monitoring tests appear to be slightly more beneficial when switching to second-line therapy.
Although more research is needed in this area, the findings suggest there will be a greater public health benefit if money is channelled into providing more people with antiretroviral drugs than providing those already receiving treatment with routine laboratory monitoring.

Cost of HIV treatment

It was estimated in 2009 that to achieve universal access targets an investment of 7 billion was required for treatment and care out of the $25 billion total needed to achieve all targets in low and middle-income countries.  However,  only $15.9 billion was made available in 2009. The Global Fund, which provides antiretroviral treatment to 2.5 million people worldwide, received $11.3 billion in 2010 out of the $20 billion it calculated it needed over a three year period. Funding from the US government, mainly through PEPFAR, was also flat-lined from 2009-2010 for the first time since its creation in 2003. That year the PEPFAR budget for antiretroviral treatment was also reduced and funds for ARV drugs fell by 17%.
In a global economic downturn, the prospect of greater funding for AIDS seems unlikely. UNAIDS reported in 2009 that “the crisis, together with the increasing demand for treatment, will have a serious negative impact on antiretroviral treatment in the long run.”
One fifth (all in sub-Saharan Africa) said they had already felt the impact of the crisis on their treatment programmes by 2009. Moreover, the percentage of countries where antiretroviral treatment programmes were adversely affected by reduced external funding rose from 11% to 21% from July 2008 to July 2009. Treatment expansion will be difficult in countries with a high HIV prevalence but low government spending on HIV/AIDS (such as Uganda, Zambia and Tanzania), as they are heavily reliant on foreign funding.
Eastern Europe and Central Asia are seen as particularly vulnerable to the effects of reduced external funding and the economic crisis. Already less than a fifth of people in need of treatment in the region are receiving it but drug stock-outs are common and government health expenditure on AIDS treatment programmes has fallen sharply, according to UNAIDS country coordinators. In September 2010, the arrests of activists in Moscow protesting against ARV drug stock outs in hospitals highlighted the grave lack of access to HIV treatment in Russia.

Achieving universal access to HIV and AIDS prevention, treatment and care

Significant progress has been made in getting millions of people on treatment. Over 3 million life years were gained from 2002-2008, including 2 million in sub-Saharan Africa, thanks to antiretroviral therapy. Treatment expansion led to a ten-fold increase in the number of people on treatment in low and middle-income countries by the end of 2008 (around 4 million) compared with 2003 (around 400,000) when the ‘3 by 5’ target was set. Although the ‘3 by 5’ and universal access target were not met on time, it is likely that they have played a major part in progressing treatment levels far beyond what would have been achieved otherwise.
AVERT's Universal Access video
Ensuring that people start treatment early and that access and adherence to treatment is as straightforward as possible is vital to the overall aim of achieving universal access to HIV/AIDS prevention, treatment and care. Huge and sustainable investments on the part of governments, multinational organisations and citizens are needed to realise these aims; investment in better health infrastructure, medical research, and in the most effective drug treatments available.
In 2010, UNAIDS outlined a comprehensive approach to HIV treatment designed to cut deaths from AIDS by ten million by 2025. ‘Treatment 2.0’ emphasises the role that improved access to treatment can play in stemming the epidemic, by reducing mortality from AIDS but also by cutting new infections.



 


 


 


 


Saturday, November 27, 2010

Urbanisation in India faster than rest of the world

Urbanisation in India faster than rest of the world

The urbanisation of India is taking place at a faster rate than in the rest of the world. By 2030, 40.76 per cent of India’s population will be living in urban areas compared to about 28.4 per cent now. So says the United Nations’ ‘State of the World Population 2007’ report, which was released on Tuesday.
But at the same time, the report adds, metropolitan cities like Mumbai and Kolkata have a far greater number of people moving out than coming in. It also says that a few cities will be the size doomsayers had predicted in the 1970s. Mega cities are still dominant but they have not grown to the size once projected and have consistently declined in most world regions, the report says.
Releasing the report in India, Urban Development Minister Jaipal Reddy said urbanisation was a sign of liberalisation but the condition of slum-dwellers was even worse than that of the poor in villages.
According to the report, over 90 per cent of slum-dwellers live in developing countries with China and India accounting for 37 per cent of them. About 56 per cent of the urban population lives in slum conditions. The report also says that in countries like India, Pakistan and Bangladesh, the literacy rate of women living in slums is as low as 52 per cent.
For countries like India, the report says, getting ready for the aging population is another big challenge. In Chennai, it says, total fertility rate has fallen to below replacement levels. The city has closed down 10 maternity clinics and reopened them as geriatric units.
Nesim Tumkaya, United National Population Fund representative in India, said that by next year, half of the world’s population would be living in urban areas. But in most regions, the rate of urbanisation is showing a decline except in growing economies like India.
The population of towns and cities in developing countries like India is set to double in the space of a generation, while the urban population in the developed world is expected to grow relatively lower, the report says.
In comparison to the urban population growth rate, the world’s rural population is expected to decrease by some 28 million between 2005 and 2030.


Psychiatric Problems of AIDS Inpatients at the New YorkHospital:


GENERAL Psychiatric Problems of AIDS Inpatients at the New YorkHospital: Preliminary Report
SAMUEL W. PERRY, MD
SUSAN TROSS, PhD

Dr. Perry is associate of professor of psychiatry at Cornell University Medical College and associate director of consultationliaison  psychiatry at the New York Hospital, New York City. Dr. Tross is a psychology fellow at the Memorial Sloan-Kettering Cancer Center and instructor of psychology in psychiatry at Cornell
University Medical College. John Falkenberg, R.N., helped record the data. 

This work was supported by the National Institute of General  Medical Science's grant No. GM 26145 to the New York Hospital  Burn Center. Tearsheet requests to Samuel W. Perry, MD, 525 East 68th St.,
New York, N.Y. 10021.
Synopsis ....................................

A retrospective review of the charts of52 patients with  acquired immune deficiency syndrome (AIDS) in the New York Hospital was conducted to determine  the prevalence of recorded psychiatric complications and the use of
psychiatric consultation. Neuropsychiatric complications were found to be pervasive clinical features in AIDS patients hospitalized during acute illness. Mood disturbance was identified in an overwhelming majority of the patients (82.7 percent), and signs of organic mental syndrome (DSM III) were
noted in 65.4 percent; references to neuropsychiatric complications appeared in every patient's chart.


Neurological complications were seldom explicitly diagnosed or treated. Psychiatric consultation was requested for 10 patients (19.2 percent) because of management problems, for diagnostic assessment, or by selfreferral.
Only one patient was given a psychiatric diagnosis at discharge. The results suggest that the neuropsychiatric complications of AIDS are underdiagnosed
during acute medical illness and that psychiatric consultation is underutilized.
AIDS patients have a heightened risk of psychological problems. Contributing factors may include the threat to life, severe physical debilitation, central nervous system involvement, fear of contagion, disclosure of homosexuality
or drug abuse, and guilt associated with sexual transmission. SINCE THE FIRST REPORrED CASES IN 1981 (1), acquired immune deficiency syndrome (AIDS) has been identified as a public health emergency. As ofDecember 12, 1983,
a total of 2,952 cases had been reported to the Centers for Disease Control (CDC), and 1,225 of these patients (42 percent) had died (2). Among high-risk groups, the mean number of cases was doubling every 6 months, but
may now be increasing at a lower rate. These groups are homosexual or bisexual men, especially those with multiple sexual partners-71 percent of the cases (1,3-5);  intravenous drug users-17 percent (6); and hemophilia
A patients treated with Factor VIII-1 percent (7). The  Public Health Service regards recent Haitian immigrants  (less than 7 percent) as a high-risk group. However, there has been controversy about this categorization (8,9).
The current definition of AIDS used in CDC's surveillance  activities requires the presence of a disease at  least moderately indicative of defective cell-mediated immunity in a person who has no known underlying cause for such a defect or any other reason for diminished resistance to disease (10). Diseases that are indicative of AIDS include Pneumocystis carinii pneumonia
(PCP) with or without other opportunistic infections, 51 percent of the cases; Kaposi's sarcoma (KS) with or without opportunistic infection, 26 percent; other opportunistic infections alone, 15 percent; or KS and PCP with or without other opportunistic infection, 8 percent (2). Although the cause of AIDS is not known, a major current theory favors exposure to an unidentified viral agent to which the immunosuppressed individual is more vulnerable (11-15). The treatment of opportunistic infections has included trimethoprim-sulfamethoxazole,
ketoconazole, acyclovir, and pentamidine. Treatment for KS has included recombinant leukocyte A interferon, radiotherapy to the skin, and systemic chemotherapy (doxorubicin, vinblastine, bleomycin). These treatments
for opportunistic infections or KS may provide transient relief of symptoms, but there is no evidence that they improve the overall survival rate (16).
The psychiatric aspects of AIDS await systematic documentation. Although writers in the media (17,18), psychotherapists (19,20), and authors in medical journals  200 Public Health Reports (21-23) have suggested that emotional reactions to the illness can be quite pronounced, these observations have
often been based on impressions and not on scientific data. This problem has been compounded by a lack of specificity in published reports and a failure to distinguish different kinds of psychiatric complications during different phases of the illness.
These psychiatric complications may include (a) adjustment
reactions at time of confirmed diagnosis (for
example, numbness, shock, and denial); (b) adjustment
reactions during progression of the illness (for example,
depression, self-imposed or peer-inflicted isolation, and
guilt about sexual or drug-related behavior; (c) intense
emotional reactions in members of high-risk groups with
no evidence of the disease (for example, anxiety about
contracting AIDS, somatic preoccupation, convictions of
discrimination, forced attempts to change sexual preference,
and anger at the perceived insensitivity and impotence
of the medical establishment); and (d) exaggerated
emotional reactions in individuals who are not members
of high-risk groups (for example, homophobia or unreasonable
fears of contagion).
In addition to these emotional reactions, organic
symptoms arising from AIDS itself or from its therapy
may present psychiatric complications. Fatigue and
weight loss may signal the prodromal phase of AIDS and
may mimic major depression. A "flu-like" complex of
lethargy, fever, and depressed mood has been associated
with recombinant leukocyte A interferon (24). Central
nervous system diseases, especially encephalitis (25) and
primary lymphoma (26), frequently produce cognitive
deficits, mood disturbance, vegetative signs, personality
change, and impulsive behavior that mimic psychogenic
disorders.
Methods
To provide effective care, physicians must be able to
anticipate the frequency, nature, and severity of neuropsychiatric
problems in the AIDS population and recommend
useful psychological interventions. We reviewed
the medical charts of all adults meeting CDC criteria for
AIDS (10) who were admitted to the New York Hospital,
New York City, between September 1, 1981, and September
1, 1983.
We reviewed the notes of physicians, nurses, social
workers, and medical students, and we recorded neuropsychiatric
symptoms and adjustment problems on the
basis of face validity. When a psychiatric consultation
had been requested, the reasons for consultation, diagnostic
impression and recommendations for treatment
were noted. The senior author (S.W.P.) interviewed the
psychiatrists, physicians, and other personnel familiar
with the patients to obtain more detailed information
about the nature and resolution of the presenting problem.
All references to adjustment problems and psychiatric
symptoms were noted. In addition to this review, we
explored the implications of the detection and management
of psychological problems of AIDS patients.
Results
During the 2-year period, 83 adult patients with AIDS
were admitted to the New York Hospital. Complete medical
records were available for 52 of these patients (62.6
percent).
Table 1 lists relevant. sociodemographic and medical
characteristics of the population studied. The majority of
patients were middle-class homosexual men in their 30s,
a small portion of whom also infrequently used intravenous
drugs. Only two patients (including the woman)
denied belonging to any high-risk group. Opportunistic
infection (primarily PCP, mucosal candidiasis, and disseminated
cytomegalovirus) occurred in 43 patients
(82.7 percent) and was regarded as the most critical
medical problem. A large portion of the study population
was terminally ill: at least 19 patients (36.5 percent) died
during hospitalization or within 6 weeks after discharge.
Psychiatric diagnosis detected by chart review are
summarized in table 2. Thirty-one patients (59.6 percent)
met criteria in the Diagnostic and Statistical Manual
of Mental Disorders, third edition (DSM IIl) for one
or more psychiatric diagnoses (27). The most common
DSM III diagnosis was organic mental syndrome (OMS)
with or without a major depression, which was present in
21 patients (40.4 percent). Major depression was present
in nine patients (17.3 percent). However, only the patient
Table 1. Sociodemographic and medical characteristics of 52
hospitalized AIDS patients'
Charactenstic Number Percent
Sex:
Male ............... .............. 51 98.1
Female ............. ............. 1 1.9
Risk group:
Homosexual-bisexual .............. 41 78.8
Homosexual-intravenous drug user .. 5 9.6
Haitian immigrant .......... ....... 3 5.8
Intravenous drug user ........ ..... 1 1.9
Undetermined .................... 2 3.8
Primary medical illness:
Opportunistic infection ........ ..... 3771.2
Kaposi's sarcoma .......... ....... 9 17.3
Both opportunistic infection and
Kaposi's sarcoma ......... ...... 6 11.5
Mortality:
Dunng hospitalization ........ ...... 11 21.2
Known following discharge ......... 8 15.4
1 Mean age: 36 ± 2.1 years (range: 20-69).
March-April 1984, Vol. 99, No. 2 201
Table 2. DSM III and presumptive diagnoses of 52 hospitalized
AIDS patients
Diagnoses Number Percent
Mood disturbance:
DSM IlIl major depression .......... 9 17.3
Presumptive depression ...... ...... 34 65.4
Total ......................... 43 82.7
Organic mental syndrome:
DSM III delirium .......... ........ 15 28.8
DSM IlIl dementia ......... ........ 6 11.5
Presumptive organic mental
syndrome ...................... 13 25.0
Total ......................... 34 65.4
Other diagnoses:
Substance abuse disorder ......... 6 11.5
Schizophrenia .................... 1 1.9
with chronic undifferentiated schizophrenia actually received
a psychiatric diagnosis at discharge.
References to neuropsychiatric complications-such
as being depressed, anxious, lethargic, or withdrawnappeared
in the charts of all 52 patients. These references
indicated neuropsychiatric problems in some patients
whose medical records did not supply sufficient information
to make a DSM III diagnosis. In addition to 21
diagnoses of DSM III delirium or dementia, a presumptive
diagnosis of OMS was strongly suggested for
13 patients (for example, repeated nurses' notes stating
that the patient was "confused" or "disoriented"). Nine
patients met DSM III criteria for major depression; mood
disturbance was strongly suggested in 34 other patients
but the recorded information was not sufficient to distinguish
a primary affective disorder from a normal grief
response or a mood impairment secondary to neurological
or systemic disease. Five patients had suicidal
ideation (9.6 percent), but only one patient was considered
a suicidal risk (1.9 percent). Forty-three patients
(82.7 percent) were noted to have an aberrant lifestyle
(for example, antisocial behavior or chaotic interpersonal
relationships), but no record provided sufficient detail to
meet DSM III criteria for a personality disorder.
Management problems were encountered in seven patients
(13.5 percent). Three of these patients left the
hospital against medical advice; one was subsequently
readmitted and another was followed as an outpatient.
Two patients refused to comply with medication or a
diagnostic procedure; a few days later, both of these
developed a delirium and died. Two patients were considered
belligerent or abusive to staff when their demands
for more narcotic analgesics were not met.
Psychiatric consultation was requested for 10 patients
(19.2 percent) because of the management problems described
previously, for diagnostic assessment, or by selfreferral.
The six management problems occurred when
patients refused procedures, had explosive episodes on
the ward, or signed out against medical advice; two
patients in this group left abruptly before consultation.
(The number of patients actually seen by a psychiatrist
therefore differs from the number of requests for consultation.)
In the two patients seen for diagnostic assessment,
the psychiatrist was asked to help distinguish
organic from psychogenic pathology. Two consultations
were performed at the patients' initiative because of "depression."
Case vignettes. The following case vignettes illustrate
the three major reasons for psychiatric consultation:
1. Management problems. Mr. A., a 30-year-old
homosexual musician, had been hospitalized for several
weeks because of gastrointestinal infections and renal
failure. Psychiatric consultation was sought after a nurse
observed that he was not taking his prescribed medicine.
During the first two interviews, the psychiatrist was not
certain whether noncompliance stemmed from hopelessness
or from a chronic tendency to be manipulative
and passive-aggressive. During the third interview, the
consultant observed how the patient fluctuated between
hypervigilance and indifference and how he avoided formal
testing of cognitive functions. The psychiatrist suspected
that a mild OMS was exaggerating personality
problems; she therefore recommended that the staff appreciate
the patient's confusion and that a neurological
evaluation be made. The patient immediately responded
to less complicated explanations and began taking his
medications; he had a grand mal seizure 4 days later and
soon died from encephalitis.
2. Diagnostic assessment. Mr. B., a 49-year-old married
bisexual executive, was referred for psychiatric consultation
18 months after AIDS was first diagnosed
(PCP). During the early stages of his illness-both because
of an unrecognized mild OMS and because of
depression causing him to drink alcohol-he had driven
his successful business to financial collapse and destroyed
his family life. By the time of his second hospitalization
for disseminated cytomegalovirus, he had lost
70 pounds, was going blind, and was living a marginal
existence in his elderly mother's apartment.
The manifest reason for psychiatric referral was to
determine the role depression was playing in a man with
a now well-documented case of dementing encephalitis.
After the first interview, the consultant suspected a latent
reason for the referral because at that point the diagnostic
distinctions between psychogenic and organic causes appeared
academic: Mr. B. was so cachectic and debilitated
202 Public Health Reports
he could not lift his head from the pillow and could not
maintain the most superficial conversation before drifting
back to sleep. He was not oriented to time or place,
could not name any President, and had neither immediate
nor short-term recall.
Recognizing that the patient was terminally ill, the
psychiatrist directed his efforts toward the referring staff
members who were depressed themselves. A liaison staff
conference enabled them to work through the discouragement
and hopelessness they felt watching AIDS
patients die despite heroic efforts.
3. Self-referral. Mr. C., a 39-year-old homosexual
artist, requested a psychiatric consultation during his
second admission for PCP and KS. During the interview,
though weak and sickly, he was able to maintain his
flamboyant style and poignantly convey his fears of
"walking alone towards death." Geographically and
emotionally distant from his relatives, he had relied on
support from friends and a homosexual self-help group
since his first admission, but he now wanted an "insider"
who was "not political" or intimidated by "the
parade of doctors and the stench of specimens." In
response to the patient's request, the psychiatrist met
with Mr. C. frequently throughout his prolonged hospitalization
to facilitate his profound grief response and to
help explain the bewildering array of tests and procedures.
Mr. C. met "the approaching shadow" without
the panic and awesome loneliness he had feared.
Discussion
On the basis of a retrospective review of the charts of
52 hospitalized patients, mood disturbance and cognitive
dysfunction were found to be a pervasive clinical feature
of AIDS. Although neuropsychiatric symptoms could be
identified in every record, they were rarely diagnosed or
treated. Only one patient received a psychiatric discharge
diagnosis, and psychiatric consultation was requested for
fewer than one in five patients. Thus, AIDS patients are
at high risk for psychological problems, but these problems
tend to be underdiagnosed and undertreated. Five factors may help explain these observed tendencies: sample bias, rater bias, preoccupation with severe
medical complications, failure to appreciate the high incidence of OMS in AIDS patients and the benefits of palliative treatment, and avoidance of emotional issues in homosexual, "contagious," and fatally-ill patients. 

1. Sample bias. The population was mainly composed
of white middle-class homosexuals in their 30s.
Only one patient (1.9 percent) was a heterosexual intravenous
drug abuser,

Psychiatric complications may be more readily recognized
in drug abusers or indigent patients either because
their problems are more pronounced or because health
personnel are less inclined to overidentify with patients
who are more obviously different in their sociocultural
background and lifestyle.


2. Rater bias. Because the assessments were made on
the basis of face validity, the psychological orientation of
the raters may have prejudiced the findings, increased the
significance of references to neuropsychiatric problems,
and underestimated implicit therapeutic interventions.
3. Severe medical complications. By design, this review
included only those subjects requiring hospitalization.
All the patients were critically ill; at least 19 (36.5
percent) died during the 2-year study period. The need
for intensive medical care may have diverted attention
from neuropsychiatric problems that neither the staff nor
the patients considered life-threatening. Possibly more
attention would have been given to psychological issues
if acute medical problems were not an overwhelming
preoccupation.
4. Unrecognized organic mental syndrome (OMS).
Twenty-one patients (40.4 percent) met DSM III criteria
for an OMS; confusion, disorientation, loss of memory,
and other organic signs were described in 13 additional
patients (25 percent). The high incidence of cognitive
dysfunction in these patients is consistent with recent
studies that have described the frequent neurological
complications of AIDS (25,26), yet only those patients
seen in psychiatric consultation were explicitly given an
OMS diagnosis. More importantly, according to the
medical records, palliative treatment for dementia or
delirium was given to only those patients whose OMS
was identified.
The general failure to diagnose and treat OMS in
hospitalized medical patients has been documented
(28-31). The cases of Mr. A. and Mr. B. illustrate that
the staff may not realize that mild cognitive impairment
is a factor contributing to noncompliance, depression,
and altered behavior.
5. Avoidance of emotional issues. Although the subtle
attitude of caretakers cannot be adequately substantiated
by a chart review, the relatively low incidence of
recorded psychopathological reactions raises the possibility
that staff members consciously or unconsciously
avoided emotional issues with these patients. The rate of
requests for psychiatric consultation was one-third the
usual rate for ward medical services that have an active
consultation-liaison program. Furthermore, no consultation
was requested by the staff to help patients cope with
March-April 1984, Vol. 99, No. 2 203
the psychological stresses of the illness; the requests
were for management problems, for diagnostic assessment,
or at the patient's request.
There are a few explanations for this lapse in psychiatric
consultation. Staff members may have believed psychiatric
intervention would be futile for patients who
were critically ill, or they may have wished to remain
detached from the difficult emotional issues in dying
patients. These general tendencies have been described
with other kinds of patients (32-34), but may be compounded
with AIDS patients by fears of contagion (35),
homophobia (36), or, as illustrated by the case of Mr. B.,
the staff's own hopelessness in treating a large series of
enigmatic terminally ill patients. Additionally, patients
themselves may have wished to minimize their neuropsychological
problems or may have chosen to discuss
these problems with their own friends and counselors
because they considered the medical staff to be unsympathetic,
or at least unfamiliar, with homosexual issues.
Recommendations for Psychiatric Intervention
Based on the results of this study at the New York
Hospital, we recommend the following measures to deal
with the neuropsychiatric complications of AIDS during
medical hospitalization:
1. Document mental status. The high incidence of
OMS recently associated with this population (25,26)
provides a compelling argument for routine monitoring
of the mental status of every AIDS patient. The Mini-
Mental State examination (37,38) may help detect the
mild OMS that frequently occurs early in the course of
the disease. Disorders of mood, thinking, or behavior
should not presumptively be viewed as psychogenic until
a systematic mental status examination has ruled out
possible cognitive (organic) determinants. Depression,
lethargy, impulsivity, explosive episodes, and noncompliance
may be secondary to the nervous system
dysfunctions associated with subacute encephalitis, lymphomas
of the central nervous system, vascular complications,
and other neurological and systemic problems.
If the diagnosis of an OMS is recognized and
recorded, the staff will be alerted to provide specific
palliative treatment, including neuroleptics; correction of
misinterpretations; and simplified instructions and explanations
(39-41).
2. Identify and treat avoidance of psychological issues.
The limited requests for psychiatric consultation
and the paucity of recorded information regarding psychological
aspects suggest that the staff may be inclined
to avoid emotional issues with these AIDS patients,
thereby enhancing their sense of being different. Staff
education can be helpful in (a) explaining what is known
about the transmission of the disease, thus reducing unreasonable
precautions and fears of contagion (35); (b)
providing information about homosexual behavior to correct
distortions and decrease homophobia; and (c) indicating
(as with Mr. C.) that the psychiatric reactions of
patients hospitalized with AIDS are not dissimilar to
reactions of other kinds of patients who have a lifethreatening
illness (fears of pain, abandonment, debility,
dependency, and separation). These familiar reactions
can potentially respond to the same psychotherapeutic
and psychopharmacological interventions proven to be
effective for other medically ill patients.
3. Arrange for aftercare. Hospitalization provides an
opportunity to marshal family, peer, legal, and social
support. Psychological problems may surface or at least
become more apparent after the acute medical crises
pass. In communities where AIDS is most prevalent,
homosexual organizations provide support groups,
trained counselors, supervised social activities, homemakers,
and a buddy system to accompany AIDS victims
to outpatient appointments.
Conclusion
Neuropsychiatric complications, especially cognitive
dysfunction and mood impairment, were pervasive
clinical features in AIDS patients hospitalized during
acute illness, but those complications were seldom explicitly
diagnosed or treated. The results of any retrospective
chart review must be interpreted cautiously, but
there is a strong suggestion that a thorough mental status
examination will detect neuropsychiatric complications
in an overwhelming majority of hospitalized AIDS patients.
When these complications are detected and diagnosed
and when the sources of distress are appreciated,
effective supportive and palliative interventions can be
prescribed.


Our findings are a preliminary step in alerting clinicians
to the neuropsychiatric problems of AIDS patients.
To document the prevalence and severity of these problems
more systematically, we are conducting a controlled
prospective study of newly diagnosed AIDS patients.