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BMJ No 7111 Volume 315

Papers - Abstracts Saturday 27 September 1997


Mortality associated with HIV-1 infection over five years in a rural Ugandan population: cohort study
Epidemiology and clinical management of meningococcal disease in west Gloucestershire: retrospective, population based study
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 years
Effects on birth weight and perinatal mortality of maternal dietary supplements in rural Gambia: 5 year randomised controlled trial

Mortality associated with HIV-1 infection over five years in a rural Ugandan population: cohort study

Andrew J Nunn, Daan W Mulder, Anatoli Kamali, Anthony Ruberantwari, Jane-Frances Kengeya-Kayondo, Jimmy Whitworth

Abstract

Objective: To assess the impact of HIV-1 infection on mortality over five years in a rural Ugandan population.

Design: Longitudinal cohort study followed up annually by a house to house census and medical survey.

Setting: Rural population in south west Uganda.

Subjects: About 10,000 people from 15 villages who were enrolled in 1989-90 or later.

Main outcome measures: Number of deaths from all causes, death rates, mortality fraction attributable to HIV-1 infection.

Results: Of 9,777 people resident in the study area in 1989-90, 8833 (90%) had an unambiguous result on testing for HIV-1 antibody; throughout the period of follow up adult seroprevalence was about 8%. During 35,083 person years of follow up, 459 deaths occurred, 273 in seronegative subjects and 186 in seropositive subjects, corresponding to standardised death rates of 8.1 and 129.3 per 1,000 person years. Standardised death rates for adults were 10.4 (95% confidence interval 9.0 to 11.8) and 114.0 (93.2 to 134.8) per 1,000 person years respectively. The mortality fraction attributable to HIV-1 infection was 41% for adults and was in excess of 70% for men aged 25-44 and women aged 20-44 years. Median survival from time of enrolment was less than three years in subjects aged 55 years or more who were infected with HIV-1. Life expectancy from birth in the total population resident at any time was estimated to be 42.5 years (41.4 years in men; 43.5 years in women), which compares with 58.3 years (56.5 years in men; 60.5 years in women) in people known to be seronegative.
Conclusions: These data confirm that in a rural African population HIV-1 infection is associated with high death rates and a substantial reduction in life expectancy.

Medical Research Programme on AIDS in Uganda,
Uganda Virus Research Institute,
Entebbe
Andrew J Nunn, senior statistician
Anatoli Kamali, epidemiologist
Anthony Ruberantwari, statistician
Jane-Frances Kengeya-Kayondo, epidemiologist
Jimmy Whitworth, head of MRC AIDS programme in Uganda

Institute of Social Medicine,
Academic Medical Centre,
University of Amsterdam,
1105 AZ Amsterdam,
Netherlands
Daan W Mulder, former head of MRC AIDS programme in Uganda

Correspondence to: Mr A J Nunn

MRC HIV Clinical Trials Centre,
University College London Medical School,
London WC1E 6AU
ajn@mrc.ucl.ac.uk

Full text on BioMedNet

Epidemiology and clinical management of meningococcal disease in west Gloucestershire: retrospective, population based study

Philip AL Wylie, David Stevens, William Drake III, James Stuart, Keith Cartwright

See Editorial by Cartwright, p 757

Abstract

Objective: To study changes in the epidemiology and management of meningococcal disease in one health district during a period of high local incidence of disease.

Design: Prospective case ascertainment and data collection over 14 years, with retrospective analysis of cases.

Setting: West Gloucestershire (population 320,000).

Subjects: Residents developing meningococcal disease between 1 January 1982 and 31 December 1995.

Results: 252 cases of invasive meningococcal disease were identified, of which 102 (40%) were officially notified and 191 (76%) were confirmed by culture from a deep site. The observed disease incidence of 5.6/100,000/year was about 2.7 times the national incidence (as measured by either statutory notifications or reference laboratory reports). The period 1983-90 was characterised by a prolonged localised outbreak due to serogroup B serotype 15 sulphonamide resistant (B15R) strains. General practitioners gave benzylpenicillin before hospital admission to 18% of patients who presented with meningococcal disease in the first half of the study period and to 40% who presented in the second half. The overall case fatality rate was 6.7% (17/252). Four deaths were directly or indirectly related to lumbar puncture. Of 120 patients whose lumbar puncture yielded meningococci, nine (8%) showed no abnormality on initial examination.
Conclusions: Neither laboratory records nor formal notifications alone can give an accurate estimate of the incidence of meningococcal disease. Because of the dangers of lumbar puncture, the frequency of misleading negative initial findings, and the advent of new diagnostic techniques, the need for samples of cerebrospinal fluid should be critically questioned in each case of suspected meningococcal disease.

Paediatric Department,
Gloucestershire Royal Hospital,
Gloucester GL1 3NN
Philip AL Wylie, senior registrar
William Drake III, senior registrar
David Stevens, consultant paediatrician

Public Health Laboratory,
Gloucestershire Royal Hospital
James Stuart, regional epidemiologist
Keith Cartwright, consultant microbiologist

Correspondence to: Dr Cartwright

kcartwright@phls.co.uk

Full text on BioMedNet

Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 years

B Modell, M Petrou, M Layton, L Varnavides, C Slater, R H T Ward, C Rodeck, K Nicolaides, S Gibbons, A Fitches, J Old

Abstract

Objectives: To audit services for prenatal diagnosis for haemoglobin disorders in the United Kingdom.

Design: Comparison of the annual number of cases recorded in a United Kingdom register of prenatal diagnoses for haemoglobin disorders, with the annual number of pregnancies at risk of these disorders, by ethnic group and regional health authority. The number of pregnancies at risk was estimated using data on ethnic group from the 1991 census and data from the United Kingdom thalassaemia register, which records the number of babies born with thalassaemia.

Setting: The three national prenatal diagnosis centres for haemoglobin disorders.

Subjects: 2,068 cases of prenatal diagnosis for haemoglobin disorders in the United Kingdom from 1974 to 1994.

Main outcome measures: Utilisation of prenatal diagnosis by risk, ethnic group, and regional health authority. Proportion of referrals in the first trimester and before the birth of any affected child.

Results: National utilisation of prenatal diagnosis for haemoglobin disorders was around 20%. During the past 10 years it has remained steady at about 50% for thalassaemias and risen from 7% to 13% for sickle cell disorders. Utilisation for sickle cell disorders varies regionally from 2% to 20%. Utilisation for thalassaemias varies by ethnic group. It is almost 90% for Cypriots and ranges regionally for British Pakistanis from 0% to over 60%. About 60% of first prenatal diagnoses are done for couples without an affected child. Less than 50% of first referrals are in the first trimester.
Conclusions: National utilisation of prenatal diagnosis for haemoglobin disorders is far lower than expected, and there are wide regional variations. A high proportion of referrals are still in the second trimester and after the birth of an affected child. The findings point to serious shortcomings in present antenatal screening practice and in local screening policies and to inadequate counselling resources, especially for British Pakistanis.

Department of Obstetrics and Gynaecology,
University College London Medical School,
London WC1E 6HX
B Modell, professor of community genetics
M Petrou, clinical molecular geneticist
C Slater, research assistant
R H T Ward, senior lecturer
C Rodeck, head

Department of Haematological Medicine,
King's College Hospital,
London SE5 9RS
M Layton, senior lecturer
Lysandros Varnavides, clinical molecular geneticist

Department of Obstetrics and Gynaecology,
King's College School of Medicine and Dentistry,
London SE5 8RX
K Nicolaides, head

Department of Primary Care and Population Sciences,
University College London Medical School,
Whittington Hospital,
Archway Site,
London N19 5HT
S Gibbons, consultant in computing

Institute of Molecular Medicine,
Oxford OX3 9DU
Alison Fitches, clinical scientist
John Old, clinical molecular geneticist

Correspondence to: Professor B Modell

Department of Primary Care and Population Sciences,
University College London and the Royal Free School of Medicine,
Archway Resource Centre,
Archway Site,
Whittington Hospital,
London N19 5HT

b.modell@ucl.ac.uk

Full text on BioMedNet

Effects on birth weight and perinatal mortality of maternal dietary supplements in rural Gambia: 5 year randomised controlled trial

Sana M Ceesay, Andrew M Prentice, Timothy J Cole, Frances Foord, Lawrence T Weaver, Elizabeth M E Poskitt, Roger G Whitehead

Abstract

Objective: To test the efficacy in terms of birth weight and infant survival of a diet supplement programme in pregnant African women through a primary healthcare system.

Design: 5 year controlled trial of all pregnant women in 28 villages randomised to daily supplementation with high energy groundnut biscuits (4.3MJ/day) for about 20 weeks before delivery (intervention) or after delivery (control).

Setting: Rural Gambia.

Subjects: Chronically undernourished women (twin bearers excluded), yielding 2,047 singleton live births and 35 stillbirths.

Main outcome measures: Birth weight; prevalence of low birth weight (<2500 g); head circumference; birth length; gestational age; prevalence of stillbirths; neonatal and postneonatal mortality.

Results: Supplementation increased weight gain in pregnancy and significantly increased birth weight, particularly during the nutritionally debilitating hungry season (June to October). Weight gain increased by 201 g (P<0.001) in the hungry season, by 94 g (P<0.01) in the harvest season (November to May), and by 136 g (P<0.001) over the whole year. The odds ratio for low birthweight babies in supplemented women was 0.61 (95% confidence interval 0.47 to 0.79, P<0.001). Head circumference was significantly increased (P<0.01), but by only 3.1 mm. Birth length and duration of gestation were not affected. Supplementation significantly reduced perinatal mortality: the odds ratio was 0.47 (0.23 to 0.99, P<0.05) for stillbirths and 0.54 (0.35 to 0.85, P<0.01) for all deaths in first week of life. Mortality after 7 days was unaffected.
Conclusion: Prenatal dietary supplementation reduced retardation in intrauterine growth when effectively targeted at genuinely at-risk mothers. This was associated with a substantial reduction in the prevalence of stillbirths and in early neonatal mortality. The intervention can be successfully delivered through a primary healthcare system.

MRC Dunn Nutrition Unit,
Keneba,
Gambia,
West Africa
Sana M Ceesay, senior scientist
Frances Foord, research midwife
Elizabeth M E Poskitt, consultant paediatrician

MRC Dunn Clinical Nutrition Centre,
Cambridge CB2 2DH
Andrew M Prentice, senior scientist
Timothy J Cole, senior scientist
Lawrence T Weaver, consultant paediatrician
Roger G Whitehead, director

Correspondence to: Dr Prentice
andrew.prentice@MRC-Dunn.cam.ac.uk

Full text on BioMedNet


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