Malnutrition
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P18 - Can Constraints Observed in the Case-Management of Severely Malnourished Children be addressed through the IMCI Program?

G Tom Heikens, theikens@knmg.nl, Emma Kinderziekenhuis. AMC. University of Amsterdam, the Netherlands (formerly Tropical Metabolism Research Unit, Kingston Jamaica) WN Schofield, Dept. Public Health & Community Medicine, Westmead Hospital, Westmead NSW 2146, Australia. BJ Brabin, Emma Kinderziekenhuis, AMC, University of Amsterdam, the Netherlands and Liverpool School of Tropical Medicine, Liverpool, UK

Severe malnutrition, can successfully be reversed by case-management based on knowledge of the pathophysiology and effective use of different tiers of the health system. Despite this, case-fatality often remains unnecessarily high. The Kingston Project (KP: 1983-91) showed that short- and long-term (1 and 36 m) rehabilitation of severely malnourished children can be successful.1 Survival occurred in >95%. After initial resuscitation and recovery in hospital (18 days), these children were successfully rehabilitated in the community. An additional admission period of 22 d resulted not only in a full correction of wasting but also showed significant advantages in weight and length at discharge (p <0.05 to <0.001). Irrespective of their initial treatment regime (short or long-term), mortality was <4%, and the attained anthropometric indices were not different from peers in the community. These results are compared to data from 34 available studies (1950-2000) and an additional dozen recent experiences in African District Health Systems (1990-2000). The presented analysis suggests that reasons for failure of such case-management are:

a limited knowledge of the pathophysiology resulting in inadequate therapies,
b poor anticipation on the child’s compromised condition,
c inability to distinguish and monitor stages in clinical recovery,
d lack of nutritional knowledge resulting in inappropriate dietary therapies.

Even after intensive exposure to adequate educational material, faulty practices may not be the main obstacle to lowering case-fatality. District health systems failing to achieve acceptable results can have a weak institutional knowledge and offer poor continuum of care. WHOs programme for the Integrated Management of Childhood Illnesses (IMCI) contains the elements to reverse these. Adequate in-service training with continuous supervision and motivation of local staff should improve the continuum of care and hence reduce case-fatality rates to figures as low as 5% as seen with the case management used in the Kingston Project.

1 Heikens GT, Schofield WN, Dawson S & Waterlow JC. Long-stay versus short-stay hospital treatment of children suffering from severe protein-energy malnutrition. Eur J Clin Nutr1994; 48: 873-882.

P19 - Integrated Management of Childhood Illnesses : Lessons Learned from the Egyptian Experience

Said Madkour. Director General of Childhood Diseases Programme, IMCI National Coordinator, Ministry Of Health and Population, Egypt

Egypt is not an exception of the developing countries, where the toll of childhood morbidity and mortality is high. During the past 15 years, the country managed to control under-5 years mortality through implementing vertical programmes. Those programmes have resulted in appreciable reduction of mortality and morbidity, however, the initial net decrease reached a plateau phase. A further gain in reducing these indicators would need a new strategy. In 1997, the Ministry of Health & Population has adopted the "Integrated Management of Childhood Illnesses" (IMCI) strategy developed by WHO and UNICEF. Following the decision to implement IMCI under the umbrella of PHC sector, preparatory steps were undertaken, primarily in the three IMCI components. These are improving providers’ skills, improving the health system and improving family and community practices. Much effort was devoted to case management materials and preparing the heath facilities for implementing the IMCI strategy. At the same time, efforts were directed towards introducing IMCI approach in medical curricula. The experience, so far, entails a number of challenges. Some of those challenges are the initiation of health sector reforms, reaching a consensus on case management materials, interactions between academic community and service responsible, drug policy, working with communities, capacity building at central and district levels, documenting the experience … etc. The paper will present the pertinent aspects of the experience, evidence that IMCI works, and lessons learned.

P20 - Characteristics of Adopted Young Children in Urban Slums of Bangladesh

1N.R. Sarkar. 2A. S. G. Faruque. 1Helen Keller International, Dhaka, Bangladesh, 2Clinical Sciences Division, International Center for Diarrhoeal Disease Research, Dhaka, Bangladesh

We studied health and nutritional status, feeding practices, and the reasons behind adoption of infants, in urban slums of Dhaka, the capital city of Bangladesh. Foster mothers of 46 young children (0 to 24 months old) were interviewed. Of these children (n=40, without pedal oedema), 93 % were underweight, 62% had wasting, and 70% were stunted while 13% had marasmic-kwashiorkor. Ninety-percent children were fed animal and/or formula milk and 7% received gruel with milk in their first month of life. The practice of giving gruel with milk increased with advancing age. These children often suffered from diarrhoea, cough and/or fever, skin diseases, oral thrush etc. Fifty four percent of these mothers had no biological relationship with the adopted child and 76% of them owned no child. Aunt adopted 35% of these children, and rests were by grand mother. Sixty five percent of them lost their own mother, of them 83% died during their complicated delivery while 11% mother died due to diseases of diverse cause. Thirty three percent of adopted children had own mother still alive, however, 73% of the children were given to others to be adopted because of mothers’ poverty. Maternal death, childlessness of mother, and poverty were important factors for adoption.

P21 - Identification of Key Components for the Establishment of Successful Breastfeeding in the Primary Health Care System

Abu Yusuf Choudhury, Joyeeta Saha Piwoo, et at, PIACT Bangladesh.

Studies conducted in several areas of Bangladesh have identified serious problems in practices of infant feeding. Mothers discard colostrum, delay in initiation of breastmilk and give newborns pre-lacteal feeds like honey, sugar water, cow's milk or artificial milk or even water. Exclusive breastfeeding for the first 5-6 months is practised by about 4 percent mothers. A study was conducted to identify the factors associated with colostrum feeding; pre-lacteal feeds; and failure to exclusive breastfeed for the first 5 months of life in Bangladesh. The study was carried out among a total of 582 children, of which 126 were exclusively breastfed and 456 were partially breastfed. Logistic regression analysis yielded certain factors causing mothers to exclusively breastfeed the child for 4 months or more. The analysis showed that a mother was more likely to exclusively breastfeed her child a) if she had more than 2 children; b) if she belonged to lower economic class; c) if she believed that a child should be exclusively breastfed for 5 months or more; and d) mothers who had sufficient breastmilk. It was also found that if the newborns were not separated from the mothers they were more likely to be exclusively breastfed. The logistic regression analysis also yielded some factors causing mothers to feed colostrum. Such factors were education of husband, exposure to health workers during pregnancy and types of persons attending the delivery. Feeding pre-lacteal foods was found to be almost universal. It was recommended that the primary health care programs should address the following issues: irrespective of sex of children, they should be exclusively breastfed for 5 months; the concept of exclusive breastfeeding should be promoted at the community level with special attention to the better off families, newborns should be kept in touch of mothers immediately after birth; and health workers should advocate for colostrum feeding during pregnancy of mothers.

P22 - From General to Baby friendly Hospital: what gain? (Experience of an industrial hospital in India)

Radhanath Satpathy. Head of the Department of Pediatrics, Ispat General Hospital, Rourkela, Orissa , India

Ispat General Hospital in Orissa State of India with 750 beds includes 70 beds for children. In an average 3300 deliveries take place and 4000 children are hospitalised in a year. Since inception (1960) bottle-feeding was in practice till 1990. From 1990 onwards active counselling, education of healthcare staff, seminars in the social circle, celebration of World Breastfeeding Week, review of the hospital policies and practices, developing a written breastfeeding policy and administrative communications continued. The hospital was assessed in 1995 and was declared by the National Task Force as a Baby- friendly Hospital. Since breastfeeding is of immense benefit to infants, it was decided to study of the benefits of this achievement to the hospital and community. Method: Hospital admissions, sickness and deaths of infants before and after the achievement were studied in retrospect. Mothers immunising their children were asked about the feeding practices with reference to exclusive breast-feeding. Doctors, nurses and paramedical staffs of the hospital were exposed to knowledge, attitude and practice (KAP) study on infant feeding. Results were analysed. Result: The exclusive breastfeeding incidence has improved fro 45% to 82%. There has been reduction in childhood hospitalisation. The hospital based infant (IMR) rate has been reduced. Morbidity changes showed a shift from common infectious diseases. KAP study showed improved attitude of the health-care personnel. From among the doctors and nurses more advocates of breastfeeding were identified. Conclusion: Baby friendly hospital initiative has been able to inculcate hospital as well as community benefits.

P23 - Dietary Management of Protein Energy Malnutrition

M. El- Mougi. K Rashid, I Hegazi, A Hendawi. Alazhar Faculty of Medicine, Cairo, Egypt

The present study intended to evaluate the effectiveness of a dietary algorithm in hospital management of protein energy malnutrition (PEM) Study patients (n=45) had mean age 8.9±1.8 months, weight for length < 75% of median reference, oedema (in only 13 cases). All except 9 had haemoglobin < 10 g/ dL , associated pneumonia was present in 9 cases. Patients were submitted to clinical examination, anthropometric measurements and routine laboratory tests. Associated pneumonia or diarrhoea were treated according to standard guidelines. Diet started immediately after admission or after rehydration (4-6 hr). All patients were given diet I (yoghurt 100 mL, sucrose 5g, palm oil 2g) by nasogastric tube. Failure cases as expressed by development of diarrhoea with weight loss at any time or no weight gain within 7 days, were shifted to diet II (skimmed milk powder 6g, rice powder 6g, sucrose 6g, water to make 100 mL) and if failed patient was shifted to diet III (cooked chicken meat 6g, rice powder 1.5g, palm oil 2g, glucose 1.5g , water to make 100 mL ). The amount supplied was 150 mL /kg divided into 8-12 feeds daily. Vitamins and minerals were supplied in double the daily requirements. Results revealed that 38 (84.4 %) responded to diet I, 4 ( 8.9 %) to diet II and 1 (2.2% ) to diet III . Two patient died from septicaemia while on diet I. Patients who did not respond to diet I were younger and more severely malnourished. On follow-up after two months (n=31), satisfactory weight gain was observed in 20 cases (64.5%), the remaining 11 cases (35.5%) had nearly stationary weight with recurrent diarrhoeal episodes. It is concluded that this dietary algorithm is suitable to treat severe forms of PEM and even diet I can be prepared at home for ambulatory patients. However, intensive nutrition education and follow-up is required to prevent recurrence.

P24 - Study of Malnutrition and Food Insecurity among Urban Adolescent Girls in North and South-west of Iran

Egtesadi S, Zargari F, Hoseinalizadeh L, Ansari N, Berenji S,Faqhi S,Amani R, Dastgiri S. Tabriz University of Medical Sciences, School of Public Health & Nutrition, Department of Biochemistry and Clinical Nutrition, Tabriz Iran.

To study the prevalence of malnutrition and food insecurity in adolescent girls in Iran, a cross-sectional study was conducted on 2000 adolescent high school female students aged 11-18 years old in north and south-west of Iran using stratified sampling through Socioeconomic Questionnaires, Nutrition history, Food frequency list , 24-hour recall, two days food record and measurement of growth parameters. Data were computerised and analysed using Foxpro, N3 and SPSS. The results are as follows: 49%, 13.5%, 52%, 100%, 84%, 78%, 57%, 61%, 80%, 99.5%, 98%, 97%, 91%, 17.5% and 87% of girls had low intakes of energy, protein, Vitamin A, Vitamin D, Vitamin B2, Vitamin B1, Niacin, Vitamin B6, Vitamin B12, Folate, Calcium, Phosphorous, Zinc, Iron and Iodine, respectively. Prevalences of wasting, stunting and obesity were 13%, 10.5% and 9.5% respectively. 25% of subjects did not consume breakfast. The results indicate that the major nutritional problem of adolescent subjects in this study was low energy intake underlaid by food inequity, which leads to low growth rate and deficient nutrient intake.

P25 – Home management of moderately malnourished children within communities of the Bangladesh Integrated Nutrition Project (BINP)

ASG Faruque, AI Khan, A Malek, K Hahar, MA Wahed, M Khan, GJ Fuchs. ICDDR,B: Centre for Health and Population Research, GPO Box 128, Dhaka 1000, Bangladesh

Objective: To explore effective means to address moderately malnourished children. Methodology: 282 moderately malnourished children aged 6-24 months were assigned to one of three groups 1)intensive nutrition education (INE), 2) INE plus the BINP food supplement (FS), or 3) control. Mothers received intensive nutrition education on food security and a proscriptive diet for their children, disease control, and caring practices and the other intervention group received INE plus a food supplement providing 300 kcal daily x 6 days/wk for a period of 3 months. The control group received only the routine BINP advice on nutrition and health education. The children were observed during the 3 month intervention and for 3 months following the intervention. Focus Group Discussions (FGD) were conducted with the mothers and repeated after the nutrition intervention period. Results: The rate of weight gain (g/kg/d) was greater in both the intervention groups (1.71 in INE and 2.02 in INE plus FS) compared to the control group (1.15), p<0.001 and p<0.0001. A significant change was found in mothers’ behaviour on child feeding frequency (p<0.001), home-based complementary feeding (p<0.001), and the provision of nutrient rich foods for child in both intervention groups. Significant improvements were observed regarding in food taboos on addition of oil to child’s feed, addition of eggs in home made complementary feed, and the frequent feeding of khichuri. Conclusion: These results show that improved nutritional status can be achieved in moderately malnourished children through changes in child feeding behaviour within the context of this study.

P26 - Vitamin A (VA) and Iron Status of Mothers and their Children in Rural Bangladesh.

ASG Faruque, AI Khan, A Malek, K Nahar, MA Wahed, M Khan, GJ Fuchs. ICDDR,B: Centre for Health and Population Research. GPO Box 128, Dhaka 1000, Bangladesh

Objective: Assess the VA and iron status of mothers and children and to examine the relationship among these biochemical indices. Design: A cross-sectional study. Setting: 8 randomly selected sub-districts of rural Bangladesh. Subjects: Mothers (n=1091) aged between 17 and 53 years and children (n=1289) 2-6 years old participated in the study. Results: While anaemia among mothers was common (59%), IDA constituted 23%. Six percent of the mothers had low levels of serum retinol (<0.70 m mol/L) and 7% of mothers had both IDA and low serum retinol. Nearly half of all children were anaemic (Hb <110 mg/dL) and 18% had IDA. Twenty percent of the children had low levels of serum retinol. The proportion of anaemia, iron depletion, and low serum retinol content in women remained same with a progressive increase in age except IDA. Although proportion of low serum retinol and iron depletion remained same, a significant declining trend (p=0.001) in proportion of anaemia, and IDA in children with advancing age was observed. IDA and low serum retinol constituted 13% children. When age, ferritin level, family size, green leafy vegetables consumption, practice of home-gardening, and duration of vitamin A intake were accounted for by multiple regression analysis, a significant relationship of serum retinol content with female child, Hb level, CRP concentration, household expenditure and stunting of children was observed. The study also showed that there is an interaction among serum retinol concentration, BMI, Hb level, CRP concentration, household expenditure, and practice of home-gardening while adjusting for mother’s age, family size, green leafy vegetables consumption, and ferritin concentration. Conclusions: Our observations indicate that the interactions among Hb and vitamin A and other micronutrients need to be more defined. These results may have important implications on the design of effective interventions for mothers and children with concomitant IDA and low serum retinol concentrations.

P27 - Acceptability of Diversified Complementary Foods by Rural Bangladeshi Infants

Professor Mamunar Rashid. Director of the Institute Of Public Health Nutrition, Bangladesh

After the age of 4 months, most nutritionists consider breast milk alone as inadequate to maintain nutritional needs as well as growth of infants. In developing countries, appropriate and sustainable home-based complementary food offers an appropriate strategy to meet this food-gap while breastfeeding is further continued. Any new food to an infant has to undergo the process of acceptability. This intervention study was conducted in a rural setting (in three separate centres) to evaluate the acceptance of different kinds of home based mixed complementary foods. Eight different kinds of recipes were tested among 115 infants, aged 4 to 6 months for a period of 180 days from Oct’ 99 to Mar’ 2000.The infants were purposively selected and divided into cases (n=69) and controls (46). Both the groups were comparable in biological and socio-economic characteristics. Anthropometry was done every month using standard procedures. The infants were grouped into three (around 20-30 in each group), each being placed under the guidance of a community field worker and supervisor. Mothers were brought in the morning, where they took part in the preparation of foods, were made familiar with different kinds of foods for various possible combinations to ensure adequate nutrition for their infants and quantify the amounts of food to be offered at each meal. Acceptance was measured as per mother’s statement by a defined scale used purposively for the study. Basic mix ensured 180 kcal, while multi-mixes provided 270 kcal/100ml. Feeding was given by using spoon and cup. Infants received two varieties of basic mix alternately in all three groups. At conclusion of two weeks, they were introduced to six different recipes of multi mixes, two being given alternatively in each group. The acceptance rate for basic mix ‘a’ was 59.4% whereas for basic mix ‘b’ the rate was more than 80%. For multi mix ‘1a’ and ‘1b’ the acceptance rate was between 61 and 85%, whereas in multi mix ‘2a’ and ‘2b’ the acceptance range was 67-84%. The acceptance range for multi mix recipe ‘3a’ and ‘3b’ was 62-80%. Switching over to multi-mix from basic mix the acceptability was seen to be significantly raised (P<0.003) in analysis of variance. The basic mix showed equal amounts of consumption among the infants in all groups. While comparing the consumption of multi mix recipes between groups it showed significant difference (P<0.006 in group I and II and P<0.002 in group I and III). By conducting both non-parametric tests for acceptance and t-test for consumption of 8 different recipes, 4 recipes were found to be very well accepted by the infants (1 basic mix and 3 multi mix). One striking finding was that after completion of intervention, there was uniform increment in both weight and height. The percent increment for weight was 9.3 (P<0.001) and for height it was 2.1 (P<0.08) in cases compared to that of controls. The study results suggest that home based complementary food has more practical, beneficial as well as sustainable effect on infant’s growth. Careful gradual introduction of diversified basic and multi mixes enhance infant’s acceptance after repeated dietary exposure while breast feeding is also continued.

P28 - Impact of Nutrition Education in Adjunct with Food Supplementation in Rehabilitating Malnourished Children in Urban Slum Community in Dhaka, Bangladesh

A. R. Siddique1, N. R. Sarkar2, K. S. Anwar3, K. B. Biswas2, N. Nahar4. 1EPI Head Quarter, World Health Organization, Dhaka, Bangladesh, 2Helen Keller International, Dhaka, Bangladesh, 3Institute of Public Health, Dhaka, Bangladesh, 4Dhaka Medical College Hospital, Dhaka, Bangladesh

Objectives: Study the impact of nutrition education in adjunct to food supplementation in rehabilitating malnourished children in urban slums of Dhaka, Bangladesh. Methods: Two groups of 68 malnourished children aged 6 to 36 months (having weight for age less than 75% of the median NCHS) were screened out from two distantly located slums in urban Dhaka to enrol for the study. The intervention group received nutrition and health education (for 2 months) in adjunct to food supplementation and the comparison group received only food supplementation. Both groups had received a diet consisting of roasted maize and pulse in powdered eaten when properly cooked which was supposed to allow approx. 200-kcal/day energy for five days a week for a period of 2 consecutive months. Anthropometry was carried out and morbidity profile was recorded on 30th and 60th day of intervention. Results: Significant weight gain was observed on the 30th day of intervention among the children of intervention group (78 g/kg) than their comparison counterparts (52 g/kg), p<0.029. Weight of children from intervention group (50 g/kg) also increased significantly than that of comparison group (36 g/kg) on the 60th day of supplementation, p<0.017. On an average, children from intervention group gained 43 g/kg excess weight, in total, than that of comparison group. Increment of weight for age (W/A) of the median NCHS was also significantly higher among the children in intervention group (4.3) than the comparison one (2.9), p<0.05, after two months of intervention. Mean height increment was found significantly higher at the end of intervention than their baseline height for all the children (1.85 cm, p<0.001) but, however, the height increment didn’t differ between the two groups. Among the study children in both groups, the prevalence of diarrhoea was observed significantly decreased after intervention (25% in baseline to 18% after intervention, p<0.003) and respiratory infection (RI) though decreased but it was not statistically significant (63% at baseline to 41% after intervention). Moreover no significant difference was observed in the prevalence of diarrhoea and RI between the two groups of study children in baseline or after intervention. Conclusion: Health education in conjunction with food supplementation is more effective than only supplementation to improve the nutritional status among the undernourished children. We strongly recommended that further better designed study of this nature is to be carried out to find out the duration and the appropriate food supplementation needed for rehabilitating malnourished children.

P29 - Iron Deficiency Anaemia in Ethnic Minority Children in Birmingham, UK: 15 Years of Research into Prevalence, Consequences and Prevention

R J D Moy. Institute of Child Health, University of Birmingham, UK

Iron deficiency anaemia is the commonest form of malnutrition affecting 43% of the world’s children particularly in Asia and Africa. It is also common among young Asian and Afro-Caribbean children living in Birmingham where local surveys reveal that up to 45% of children have a haemoglobin <110 g/l. Nutritional surveys have indicated that the early introduction of cow’s milk and weaning foods low in iron, feeding behavioural problems, cultural feeding practices and poor access to cheap nutritious food are causal factors. Delayed cognitive development has been identified in anaemic toddlers and a randomised trial of iron therapy versus placebo showed developmental gains in those receiving iron suggesting a causal link between iron deficiency and cognitive deficits independent of environmental and psychosocial confounding. The results of a randomised trial of intensive multimedia nutritional education delivered through home visiting versus routine health education at child health clinics were disappointing and failed to improve the iron content of diets or reduce the prevalence of anaemia. A programme of population screening linked to routine child health surveillance has successfully identified anaemic children but the prevalence remains unchanged over 5 years. A randomised trial of the continued use of cow’s milk from the age of 6 months versus its substitution with an iron-fortified follow-on formula demonstrated how dietary supplementation with iron can eradicate the problem and also confer developmental advantage. Iron deficiency anaemia remains a common child health problem in ethnic minority children in the UK. Whilst dietary supplementation with iron can eliminate the problem, community based solutions to improve dietary intake may ultimately be a more sustainable solution.

P30 - Effect of Iron Supplementation with or without Deworming on the Haemoglobin Level of Ascaris Infested Anaemic Children of a Minority Ethnic Community in a Dhaka Urban Slum, Bangladesh

KS Anwar1, MA Mannan2, MA Karim3, R. Haque4, SK Roy5. 1,3Institute of Public Health (IPH), 2Bangladesh National Nutrition Council (BNNC), 4, 5International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR, B); Mohakhali, Dhaka-1212, Bangladesh.

Objectives: Assess whether iron supplementation increase the haemoglobin (Hb) level among ascaris infested anaemic children belonging to a minority group of Bihari ethnicity (originated from Pakistan) living in Dhaka urban slum, Bangladesh. Subjects and methods: A community based placebo controlled clinical trail was conducted among 2-12 years aged anaemic children (baseline Hb<11g /dL) infested with round worms (Ascaris lumbricoides). One hundred fifty seven children were divided into 2 groups: 79 subjects were dewormed (with pyrantel pamoate at a single dose of 11mg/kg body weight) and the rest 78 were not. Of the 79 dewormed children 39 children were supplemented with iron (receiving an iron syrup at a age-dependent therapeutic dose of 100 to 150 mg ferrous fumerate); and the rest 40 received placebo (receiving a non-iron syrup at similar dose), daily, for 5 consecutive months. Of the 78 non-dewormed children, 37 received iron and the rest 41 did not. Prior to final enrolment, the subjects were screened out for (i) Ascaris lumbricoides infestation (employing a parasitological examination of stool microscopy: FEC method), and, (ii) anaemia (determining haemoglobin level <11mg/dl, estimated employing cyanmethemoglobin method). Results: Statistical analysis revealed significant positive change (p<0.001) in the Hb level among the dewormed children receiving iron supplementation (2.1 g/dL) in comparison to that of receiving placebo (0.4 g/dL). Moreover, dewormed iron supplemented children had better Hb values (p<0.001) than their non-dewormed counterpart receiving placebo (0.3 g/dL); but it did not differ statistically than that of the non-dewormed children receiving iron supplementation (1.9 g/dL). Similarly, post-intervened Hb level of non-dewormed iron-supplemented children increased more in comparison to that of, both, dewormed (p<0.001), and/or, non-dewormed, placebo (p<0.001) groups. Further, in all four groups of children, post-intervened Hb level was increased significantly (p<0.001); but more higher positive changes were revealed among the children of combined iron supplemented group (2.0 g/dL) in comparison to the placebo (0.4 g/dL) ones (p<0.001). However, around 65% iron-supplemented children showed a Hb level of >11g/dl compared to that of 3% in placebo group. Thus the rate of increment of Hb among iron-supplemented children was negatively correlated with that of the baseline data (r= -0.5, p<0.001). Conclusion: Iron supplementation was effective in raising Hb level among these ascaris infested anaemic children, but no significant benefit was observed with anti-helminthic treatment among them.

P31 - Growth Evaluation and Occurrence of Malnutrition in Children Aged 0-59 Months in Cameroon.

Cécile Omoloko1 and Michel Tenukue2 1 Department of internal medicine, Faculty of medicine and biomedical sciences, University of Yaounde I. Email: omoloko@cm.refer.org 2 Department of statistics and national account, Ministry of economy and finances.

In 1996 a household survey was carried out in Cameroon during which anthropometric measures were performed on 1078 children aged 0-59 months. Weight for age (W/A), weight for height (W/H) and height for age (H/A) indices were expressed as Z-score with cutoff < -2 STD using NCHS reference median. 19% of children were underweight, 8.1% were wasted and 30% were stunted. W/A and H/A showed a significant sex group difference. The proportions of underweight and stunted individuals were statistically higher among boys than among girls, 22.2% vs 16.6% and 33.1% vs 26.8% respectively. The protein-energy malnutrition was statistically higher in rural area than in urban area regarding the three indices: 25.4% vs 14.7% for W/A; 10.0% vs 6.4% for W/H and 40.8% vs 24.9% for H/A. Boys showed higher prevalence in stunting and wasting in rural area than in urban area and than girls as well. The prevalence of underweight was statistically higher among children from poor standard of living (PSL, 25.6%) followed by children from intermediate standard living (ISL, 17.4%), then children from high standard of living (HSL, 11.3%). The same trends prevailed in wasting and stunting (p=0.000). The distribution of the three indices showed a significant sex group difference among the three standards of living in children. The proportions were higher among boys than among girls. The findings seemed to indicate that there was a high prevalence of protein-energy malnutrition among children aged 0-59 months which might have been caused by the long lasting economic crisis. (Funded by the European Union and the World Bank)

P32 - Sepsis and Growth in Severely Malnourished Children

Doherty C.P, Crofton P.M, Sarkar M.A.K, Shakur M.S, Wade J.C, Stephen R, Kelnar C.J.H, Cutting W.A. University of Glasgow, Glasgow, Scotland, UK

The growth, collagen turnover, insulin like growth factor/binding protein levels and inflammatory status of 104 severely malnourished children aged 6 to 36 months old were assessed on days 1, 15 and 30 of nutritional rehabilitation. Children were divided into 3 groups depending on their inflammatory status: 1) well i.e. normal plasma C reactive protein (CRP) levels throughout (n=54), 2) recovering i.e. abnormal initial CRP only (n=25) and 3) unwell i.e. septic throughout or developed new infections (n=25). There were significant differences in weight gain (p=0.03) and lower leg length growth (p=0.02) at day 15 but not 30 between groups. Type 1 bone predominate collagen synthesis (measured as plasma procollagen type 1 C terminal propeptide level) and type 3 soft tissue predominate collagen synthesis (measured as plasma procollagen type 3 N terminal propeptide level) were significantly different between groups at day 15 (p=0.04, p=0.04) but not 30. There were no differences in collagen degradation (measured as plasma cross-linked telopeptide of type I collagen and urinary pyridinoline and deoxypyridinoline crosslinks) or bone alkaline phosphatase levels. Insulin like growth factor binding protein 2 but not insulin like growth factor 1 or binding protein 3 was significantly different between groups at day 15 (p=0.02) but not 30. In conclusion, sepsis affected weight gain and lower leg growth only transiently in these children. Collagen synthesis but not degradation or bone osteoblastic activity was affected possibly through the mediation of the growth hormone/insulin like growth factor axis.

P33 - A Study of the Impact of Zinc Supplementation in Malnourished Bangladeshi Children

Abu Yusuf Choudhury and S.K. Roy. International Centre for Diarrhoeal Disease Research, Bangladesh (ICDDR, B); Mohakhali, Dhaka-1212, Bangladesh

A study was conducted in 1998 in a rural area of Bangladesh to see the impact of Zinc and Vitamin A supplementation on improvement of growth of children 6-36 months and reduction of severity of diarrhoea and ARI. It was also planned to see the comparative and additive effect of Vitamin A on growth and morbidity of children. The study was conducted on the children who were moderately malnourished and aged between 6 and 36 months. After recruitment and selection, the subjects were randomly allocated to either Zinc, Vitamin A, or both in multivitamin syrup in a double blind randomised control trial. The treatment groups received 40 mg Zinc, Vitamin A 200,000 IU above one year, 100000 IU Vitamin A to below 1 year and both Zinc and vitamin A in a similar MV masked syrup per day in two divided doses for seven days, and repeated at 6 months intervals and followed up for 1 year. Patients were followed up at 15 days interval for anthropometry and weekly for morbidity record. The study showed mixed results of Zinc supplementation in young infants. After the first dose there was significant difference in weight gain after 3 months of Zinc supplementation compared to Vitamin A. Children receiving Vitamin A always showed less growth than children receiving Zinc. After the second dose, children in Zinc group showed increased weight gain than those in Vitamin A. Children above 2 years in combined Zinc & Vitamin-A group increased in length during 1 year of follow-up significantly more than those in Vitamin-A alone. Similarly children above 18 months increased in weight in Zinc supplemented group compared to those with Vitamin A after 3 months of the first dose supplements. Likewise, more increase in length was seen in these groups after 1 year of follow-up with 2 week doses of Zinc supplementation compared to Vitamin A supplementation. In our study we observed that Zinc supplementation reduced diarrhoea and respiratory infection in malnourished children. The mean number of days with blood dysentery was significantly less in children with Zinc + Vitamin A compared to those with Zinc supplementation alone and dysentery was significantly low in combined group compared to Vitamin A. The mean number of attacks was less in Zinc + Vitamin A supplemented group compared to Zinc or Vitamin A alone. Children with Zinc supplementation had significantly low duration of diarrhoea per attack compared to combined group and also had less duration than Vitamin A, but not significantly. There was a significantly shorter period of illness in children with Zinc supplementation alone compared to the combined group. Mean duration (in days) of ARI per attack in Zinc and Vitamin A supplementation group was less than the Vitamin A group.

P34 - Determinants of Severe Stunting in Children in Rural Bangladesh: Maternal Short Stature and Environment.

S. M. Akramuzzaman, T. Ahmed, G. J. Fuchs. ICDDR, B, Bangladesh

Objective: To evaluate the association of maternal short stature and severe stunting in under-five children in a rural area of Bangladesh. Design: A Nutritional survey during November and December 1999. Setting: Chilmari, a rural area of Northern Bangladesh. Subjects: Eight hundred and forty-two children between 6 and 59 months of age from 744 households were randomly selected for the survey. Main outcome measure: Severe stunting. Results: The prevalence of short stature (height < 145 cm) among mothers was 14%, the prevalence of stunting (Height-for-age Z--score (HAZ): less than –2 SD of NCHS reference) among children was 51%, and prevalence of severe stunting (HAZ < -3 SD) was 20%. In the crude analysis, mothers with short stature were more likely to have severely stunted children (Odds ratio (OR) = 2.5; 95% confidence interval (CI) = 1.5 to 4.0; P-value <0.001). In a multiple regression model, the odds ratio for severe child stunting was reduced, but remained significant with OR = 2.0; 95% CI = 1.2 to 3.5; P-value = 0.01 after adjustment of child age, birth order, illness, mother’s age at birth, mother’s body mass index (BMI), mother’s education, possession of cultivable lands, source of rice for consumption, total expenditure for food, education of the household head, crowding, and vulnerability to crisis. However, there was no significant association between short maternal stature and moderate child stunting (HAZ –2 to –3) (OR = 1.1; 95% CI = 0.7 to 1.9; P = 0.574). Conclusion: Maternal stature, reflecting her potential height and early environment, appeared to be an independent risk factor for severe child stunting in rural Bangladesh. However, a part of the association between short maternal stature and severe stunting could be explained by the environmental factors.

 

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