Hostname: page-component-586b7cd67f-r5fsc Total loading time: 0 Render date: 2024-11-23T00:01:28.536Z Has data issue: false hasContentIssue false

100 days outcome of severe wasting in hospitalised infants <6 months of age

Published online by Cambridge University Press:  06 August 2021

Jai Prakash Patel
Affiliation:
Department of Pediatrics, University College of Medical Sciences, Associated GTB Hospital, Dilshad Garden, New Delhi110095, India
Rajesh Kumar Meena
Affiliation:
Department of Pediatrics, University College of Medical Sciences, Associated GTB Hospital, Dilshad Garden, New Delhi110095, India
Dheeraj Shah
Affiliation:
Department of Pediatrics, University College of Medical Sciences, Associated GTB Hospital, Dilshad Garden, New Delhi110095, India
Piyush Gupta*
Affiliation:
Department of Pediatrics, University College of Medical Sciences, Associated GTB Hospital, Dilshad Garden, New Delhi110095, India
*
*Corresponding author: Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Objective:

To assess the outcome of severe wasting in infants below 6 months of age.

Design:

A prospective observational study conducted between January 2017 and October 2018.

Setting:

A medical college-affiliated hospital in Eastern Delhi, catering mainly to the urban poor population.

Participants:

All children with severe wasting (weight-for-length Z-score (WLZ) < −3 sd) between 1 and 6 months of age, requiring hospitalisation.

Results:

Out of fifty children enrolled, during hospitalisation, forty-two (84 %) recovered (WLZ > −3 sd) and discharged; the median (interquartile range (IQR)) duration of stay was 9·5 (6·5, 13·0) d. After 100 d of enrolment, sustained cure (WLZ > −2 SD) could be achieved in only fifteen (30 %) infants, while another fourteen (28 %) recovered from severe wasting, but remained in moderately wasted state (WLZ between −2 and −3 sd). Overall, there were three (6 %) deaths (all during first week of hospitalisation); three (6 %) relapses and fifteen (30 %) defaulters (5, 5, 2, 1 and 2 defaulted during hospitalisation at day 15, day 60, day 75 and day 90, respectively).

Conclusions:

The overall recovery rate from severe wasting in infants below 6 months of age was below the acceptable levels. In order to achieve better long-term outcome, community linkage services after discharge from hospital are required for supervised feeding, close monitoring and supportive care.

Type
Research paper
Copyright
© The Author(s), 2021. Published by Cambridge University Press on behalf of The Nutrition Society

According to recent report released by UNICEF, almost half of all deaths in children under 5 years are attributable to poor nutritional status. Malnutrition is not a direct cause of death, but the vicious cycle of infection and undernutrition increases the chances of death from common infections by delaying the recovery and increasing the frequency and severity of infection(1).

India has one of the highest rates of child malnutrition and mortality among children under 5 years of age in the world. Malnutrition is estimated to contribute to almost 68·2 % of the total children under 5 years deaths and 17·3 % of the total disability-adjusted life years in India(2). Anthropometric data from the Comprehensive National Nutrition Survey (CNNS) – 2019 documented suboptimal level of nutrition in 0–5 years age group with one-third (33 per cent) children being underweight (10 % severe), 35 per cent being stunted (13 % severe), 17 per cent being wasted (5 % severe) and with ∼1 % having mid-upper arm circumference (MUAC) < 115 mm (in 6–59 months age group)(3).

Childhood undernutrition is a major global public health problem, and the major focus of research and interventional strategies has been the 6–59 months age group. As breast-feeding is a good nutritional source, it is believed that severe forms of undernutrition are rare in infants under 6 months of age, but rates of exclusive breast-feeding are suboptimal throughout the world(Reference Victora, Bahl and Barros4). Apart from the dietary intake, young infants can have a variety of health problems which can have impact on nutritional status(Reference Goh, How and Ng5). Infants under 6 months of age with severe malnutrition are more vulnerable due to the physiological and immunological immaturity leading to the high morbidity and mortality rates. A meta-analysis comparing the outcome of infants with severe acute malnutrition (SAM) aged under 6 months with that of 6–60 months receiving the same treatment documented that risk of death was significantly higher in <6 months of age group (RR 1·30, 95 % CI (1·09, 1·56); P < 0·01)(Reference Grijalva-Eternod, Kerac and McGrath6). Apart from mortality, long-term effects of early-life severe malnutrition can have significant effects on adult health and wellbeing with a higher likelihood of non-communicable disease-related risks(Reference Ruemmele7Reference Lelijveld, Seal and Wells9).

A study published in 2011 analysed the Demographic and Health Survey (DHS) datasets of twenty-one countries and estimated that globally ∼8·5 million infants under 6 months of age had wasting and among these ∼3·8 million had severe wasting(Reference Kerac, Blencowe and Grijalva-Eternod10). Subsequently, analysis of National Family Health Survey-3 (NFHS-3) data from India showed that 31 % of infants less than 6 months of age had wasting, while 13 % had severe wasting(Reference Patwari, Kumar and Beard11). A recent analysis based on NFHS-4 documented a variable prevalence of severe wasting across different Indian states, ranging from 3·5 % to 21 % (median 14·8 %) among infants less than 6 months of age(Reference Choudhary, Srivastava and Chowdhury12). As this translates into a huge number of infants aged under 6 months having severe wasting and a higher risk of mortality as compared to older children, this age group needs to be prioritised for research and targeted interventions. Limited data, mainly from African settings, are available regarding the course and outcome of severe wasting in children aged less than 6 months. Most such information is from retrospective studies describing the immediate outcome of hospitalised children(Reference Desta13Reference Dhanalakshmi and Devi15). Follow-up studies after discharge are available mainly for older children(Reference Dhanalakshmi and Devi15,Reference Bhatnagar, Kumar and Dua16) . We conducted this study to assess the course and outcome of severe wasting during a period of 3 months following discharge and to evaluate the risk factors for unsatisfactory outcome in children below 6 months of age.

Methods

This was a prospective observational hospital-based study conducted between January 2017 and October 2018 on inpatients at a hospital attached to a medical college and catering mainly to the urban low-income population of the Eastern part of Delhi and adjoining state of Uttar Pradesh. The study was approved by the Institutional Ethics Committee. Informed consent was obtained from parents or caregivers of all the participants.

All consecutive children with severe wasting between 1 and 6 months of age, presenting to outpatient department or paediatric casualty and requiring hospitalisation, were enrolled. Severe wasting was defined as weight-for-length Z-score (WLZ) less than −3 of the median reference WHO standard(17). Infants having any structural abnormalities such as cleft lip, cleft palate or any other major malformations, those with features suggestive of inborn error of metabolism such as seizures, recurrent vomiting, prolonged jaundice, those with the presence of chronic systemic illness (congenital heart disease, chronic renal disease, neurological conditions, chronic liver disease, primary or secondary immunodeficiency, and congenital hypothyroidism) or those born to a HIV-positive mother were excluded.

At the time of enrolment, a baseline assessment of all children was done and findings were recorded in a pre-designed case record form. Detailed clinical history, including dietary, immunisation and socio-economic history, was elicited from the parents/guardian, and demographic details including residential address, occupation, educational qualification and family income were recorded. Modified Kuppuswamy Scale 2017 update was used for the classification of socio-economic status. In this scale, a composite score is calculated based on the education and occupation of the head of the family along with total monthly income of the family, and socio-economic status of urban and peri-urban population is classified into upper, upper middle, lower middle, upper lower and lower(Reference Singh, Sharma and Nagesh18).

Baseline anthropometry (weight, length and head circumference) and detailed clinical examination for ruling out other causes of malnutrition were performed, and findings were recorded in a pre-designed case record form. Anthropometric measurements were taken using standard techniques(Reference Gupta and Gupta19,20) . Z-scores were calculated using age and sex appropriate WHO standards using the WHO Anthro software (21). Relevant investigations including blood sugar, electrolytes, Hb, cultures and X-rays were conducted at admission according to the clinical diagnosis. All enrolled children were managed according to the facility-based guidelines for the management of children with SAM prescribed by the National Rural Health Mission, Ministry of Health and Family Welfare (India) 2013(22). These infants received the similar general medical care as older children with SAM, including thermoregulation, maintaining normoglycemia, correction of dehydration and dyselectrolytemia, treatment and prevention of micronutrient deficiencies, antibiotics for presumed sepsis, and appropriate treatment of other medical complications. Initial feeding approach consisted of establishing or re-establishing effective exclusive breast-feeding by mother or caregiver. Support was given to re-lactate in the form of supplement suckling approach, wherever needed. In case of no prospect or failure of above approach, feeding with F-75 was started.

Outcomes were assessed as immediate outcome, that is, at discharge from hospital and overall outcome after 3 months of discharge (approximately 100 d from admission). Infants were discharged if all clinical conditions or medical complications, including oedema, were resolved; the infant had good appetite and was clinically well and alert; and weight gain on either exclusive breast-feeding or replacement feeding was satisfactory, that is, more than 5 g/kg/d for three successive days. Children received any pending immunisation and treatment of any comorbidity before discharge.

At discharge, mothers were counselled for dietary rehabilitation and childcare and advised to maintain a regular fortnightly follow-up with the hospital for 3 months. They were provided with the telephone numbers of the investigators and were told to contact them for any problem at any time during the follow-up. Clinical course and anthropometry were recoded every fortnightly following discharge for 3 months. Overall outcome after the completion of 3-month follow-up was categorised as recovered, cured, relapsed, lost to follow-up or died. Recovery was considered when an infant gained WLZ > −3 SD (recovered from severe wasting), cure was considered when WLZ > −2 SD (recovery from wasting) and this gain in weight for length was sustained over the follow-up period. Any infant who had achieved WLZ > −3 Z-score on treatment but again falls below it anytime during the follow-up was considered as relapse(17).

Statistical analysis

Data were analysed using IBM SPSS Statistics version 25.0. For analysis of risk factors of unsatisfactory outcome, enrolled infants were divided into two groups: favourable outcome group (recovered or cured) and unsatisfactory outcome group (those who died/left against medical advice/lost to follow-up/relapse). Chi-square or Fisher’s exact test, Cochran–Mante–Haenszel statistics and multivariable logistic regression were applied for calculating P-value, OR (95 % CI) and adjusted OR (95 % CI), respectively. Multivariable logistic regression was performed for the risk factors with P > 0·3 on univariate analysis.

Results

During the study period, sixty-four infants below 6 months of age with severe wasting were hospitalised, of which fifty were enrolled, and fourteen were excluded (six congenital heart disease, five suspected metabolic disorders and three congenital anomalies) (Fig. 1).

Fig. 1 Flow of participants in the study

The median (interquartile range (IQR)) age of enrolled infants was 108 (70, 148) d. These included twenty-nine (58 %) boys and twenty-one (42 %) girls. Only half of them had institutional delivery. Birth details were available for only twenty-three participants (median birth weight (IQR) 2500 (2250, 2900) g); 43 % of these were born as low birth weight. None of the enrolled infants had early initiation of breast-feeding. All of them were receiving replacement milk. Only eleven (22 %) were completely immunised for age. Diarrhoea was the presenting complaint in thirty-three (66 %) infants followed by fever, vomiting, cough, fast breathing, and decreased oral acceptance in 29, 28, 23,15 and 9 infants, respectively. None had edematous malnutrition, pallor was present in thirty-four (68 %) children and twenty-three (46 %) had dehydration (sixteen severe dehydration). Table 1 presents the socio-demographic profile of enrolled infants. Almost three-fourth of cases were from urban areas, two-third cases were from lower socio-economic strata (42 % fathers were illiterate or studied up to primary only and 50 % doing a desk job with an average earning < Rs. 6213 in three-fourth cases). More than 50 % mothers (n 28) were either illiterate or studied up to primary school only. Majority (∼80 %) of the families had a pucca (bricked or cemented) house with attached toilet and two-thirds were using municipal water supply.

Table 1 Socio-demographic profile of enrolled infants (n 50)

LAZ, length-for-age Z-score.

In the short-term, forty-two (84 %) infants were discharged, five (10 %) left against medical advice and three (6 %) died (Table 2). All deaths occurred within 1 week of hospitalisation, and the cause of death included – sepsis with acute gastroenteritis in two infants and meningitis in one infant. For those who were discharged (n 42), the median (IQR) duration of stay was 9·5 (6·5, 13·0) d. Overall, at the end of 3-month follow-up, twenty-nine (58 %) infants recovered, fifteen (30 %) cured, fifteen (30 %) left treatment in between/lost to follow-up, three (6 %) died and three (6 %) relapsed (Table 2).

Table 2 Outcomes of children under 6 months of age with severe wasting (n 50)

WLZ, weight-for-length Z-score.

* Includes the cured cases.

The anthropometric parameters at baseline, at discharge and during 3-month follow-up are shown in Table 3. Out of forty-two infants discharged, ten were lost to follow-up over 90 d. Of 32 remaining infants, 3, 9 and 15 achieved cure (WLZ > −2 SD) at the end of 1 month-, 2 month- and 3-month follow-up, respectively. Three infants relapsed and had to be re-hospitalised. In univariate analysis, none of the risk factors evaluated had a significant association with favourable or unsatisfactory outcome. On multivariable logistic regression, the adjusted OR for adverse outcomes was higher (>1) for higher birth order, low education status of the parents, absence of in-house toilet and father’s occupation, but these were not statistically significant (Table 4).

Table 3 Anthropometric parameters of infants less than 6 months with severe wasting from enrolment to 3 months after discharge

* All values are represented as median (interquartile range (IQR)).

Table 4 Association of risk factors and unsatisfactory outcome

Figure 2 depicts the trends for weight-for-age Z-score, length-for-age Z-score and WLZ for thirty-two infants in whom complete 100 d of outcome (including hospital stay) was available (Online Fig. 3). And it depicts the pattern of (a) weight-for-age Z-score, (b) WLZ and (c) length-for-age Z-score of the individual children over the study period)

Fig. 2 Trends in (a) weight for age Z-score; (b) length-for-age Z-score and (c) weight-for-length Z-score during 3 months of follow-up (n 32)

Fig. 3 Pattern of (a) weight-for-age Z-score; (b) weight-for-length Z-score and (c) length-for-age Z-score of the individual children over the study period

Discussion

In the present study that enrolled fifty infants with severe wasting under 6 months of age, the discharge rate from the hospital was 84 %, but cure could be achieved in only 30 % infants after 100 d of enrolment. Another 28 % recovered from severe wasting but remained in moderately wasted state. Overall mortality was 6 % and all deaths occurred in the first week. Overall relapse and default rates were 6 % and 30 %, respectively.

In a secondary analysis of data of 24 045 children (0–60 months) with SAM from 10 countries, 2939 (12 %) were aged below 6 months, and the outcomes in this age group at discharge were: 76 % recovered, 6 % defaulted and 5 % died(Reference Grijalva-Eternod, Kerac and McGrath6). A study from Bangladesh evaluating the outcome of SAM in infants enrolled at 4–8 weeks of age documented an overall recovery rate of 66 %, death rate of 4 % and default rate of 7 %, at the age of 6 months. Mother’s low education status and lower monthly family income were the important factors associated with poor outcome in these children(Reference Munirul Islam, Arafat and Connell23). We could not document any risk factor to be significantly associated with unsatisfactory outcome, probably because of inadequate sample size for such comparison.

The recovery rate in our study was lower and the default rate was higher compared to other similar studies(Reference Grijalva-Eternod, Kerac and McGrath6,Reference Dhanalakshmi and Devi15,Reference Vygen, Roberfroid and Captier24) . SPHERE Humanitarian Charter 2018 has suggested that in the management of SAM, the overall deaths should be <10 %, default rate should be < 15 % and recovery rate should be >75 %, where recovery is taken as discharge from the therapeutic care(25). In the present series, only one criteria of the Charter could be fulfilled. Two major reasons for this could be that majority of the parents belonged to the lower social class, working as daily wage earners and majority of the mothers were either illiterate or studied only up to middle school. There was no family or community support to these mothers following discharge, which could to be a major factor for high default and poor recovery.

Regarding the pattern of catch-up growth in our series, infants who completed 3 months of follow-up showed a significant improvement in all anthropometric parameters except in the length-for-age Z-score. This is similar to other studies having reported that during the rehabilitation phase in children with SAM (both in under 6 months and 6–59 months age group), there is minimal or no change in the length for age(Reference Munirul Islam, Arafat and Connell23,Reference Kerac, Bunn and Chagaluka26,Reference Ngari, Iversen and Thitiri27) . Studies from Bangladesh and Kenya had even reported a negative change in the height-for-age Z-score for children with SAM between 1 and 5 years age(Reference Ngari, Iversen and Thitiri27,Reference Khanum, Ashworth and Huttly28) . The postulated reasons for the minimal or no change in the height-for-age Z-score are that the catch-up in the height for age is restricted by the deficit in the weight for height, that is, the linear growth starts after reaching a threshold of for weight-for-age Z-score or WHZ, and persistence of adverse environmental factors like diarrhoea or respiratory illnesses even after recovering from SAM(Reference Ngari, Iversen and Thitiri27,Reference Walker and Golden29Reference Golden34) . In the current study, our patients did not have any episode of diarrhoea or respiratory infection, but there was no increase in the linear growth during the follow-up period, suggesting the formal hypothesis.

The strength of our study is that it is a prospective study focusing on the long-term outcome of children with severe wasting under 6 months of age. The present study was limited by the short duration of follow-up and high loss to follow-up. As we have considered lost to follow-up as an unsatisfactory outcome, we might have underestimated the actual recovery rate. Request for early discharge and high attrition is a reality in urban low-income settings where families have no social support to compensate for the wage losses. Other limitations were lack of exact birth details in all infants, absence of the community linkage for home-based care of the discharged infants and small sample size. Also, our results may be applicable only to infants who have been identified to be undernourished based on the criteria of weight-for-length below −3 sd (severe wasting). Traditionally, children with severe wasting are classified as having SAM, but there is currently a move away from this terminology towards the use of ‘wasting’ or only ‘malnutrition’ due to high rates of co-existence of low length for age (stunting) in children identified as having SAM, and lack of clear differentiation between acute and chronic forms of malnutrition(35,Reference Kerac, McGrath and Connell36) . The validity of our results for less severe form of wasting (weight-for-length below −2 sd) and other forms of undernutrition identified on the basis of low weight-for-age or length-for-age needs to be documented in future studies.

We conclude that facility-based initial management, home-based rehabilitation and follow-up on outpatient basis does not appear to be an appropriate strategy for managing severely malnourished children below 6 months of age. These children may need longer hospitalisation with closer observation, supervised feeding and supportive care. A community linkage service is probably the most vital missing string, and further studies should evaluate the outcome of young infants with malnutrition throughout the continuum of care. Young children with wasting seem to need much more than facility-based initial care to improve compliance, food security and environment. Management of At-risk Mothers and Infants under 6 months of age (MAMI) Care Pathway approach can help the peripheral health workers to screen, assess and manage nutritionally at-risk infants under 6 months of age and their mothers and, thus, can help in achieving the better outcome in this age group(37).

Acknowledgements

Acknowledgements: Not applicable. Financial support: This research received no specific grant from any funding agency in the public, commercial or not-for-profit sectors. Conflict of interest: There are no conflicts of interest. Authorship: D.S. and P.G. conceptualised the project, developed the protocol, supervised the enrolment and outcome assessment, and helped in writing the manuscript; J.P. had primary responsibility of patient screening, enrolment and data collection; R.K.M. performed the data analysis and writing the manuscript. All authors approved manuscript submitted. Ethics of human subject participation: This study was conducted according to the guidelines laid down in the Declaration of Helsinki, and all procedures involving research study participants were approved by the Institutional Ethics Committee-Human Research (IEC-HR) of University College of Medical Sciences, Delhi. Written informed consent was obtained from all guardians/caregivers of all the participants.

Supplementary material

For supplementary material accompanying this paper visit https://doi.org/10.1017/S1368980021003268

References

UNICEF Data (2020) Malnutrition in Children. https://data.unicef.org/topic/nutrition/malnutrition (accessed December 2020).Google Scholar
India State-Level Disease Burden Initiative Malnutrition Collaborators (2019) The burden of child and maternal malnutrition and trends in its indicators in the states of India: the Global Burden of Disease Study 1990–2017. Lancet Child Adolesc Health 3, 855870.CrossRefGoogle Scholar
Nutritionindia.info (2019) Comprehensive National Nutrition Survey 2016 Bihar Fact Sheet. https://www.nutritionindia.info/portal/portal/wp-content/uploads/2019/10/CNNS-v6-factsheet-Bihar.pdf (accessed December 2020).Google Scholar
Victora, CG, Bahl, R, Barros, AJ et al. (2016) Breastfeeding in the 21st century: epidemiology, mechanisms, and lifelong effect. Lancet 387, 475490.CrossRefGoogle ScholarPubMed
Goh, LH, How, CH & Ng, KH (2016) Failure to thrive in babies and toddlers. Singapore Med J 57, 287291.CrossRefGoogle ScholarPubMed
Grijalva-Eternod, CS, Kerac, M, McGrath, M et al. (2017) Admission profile and discharge outcomes for infants aged less than 6 months admitted to inpatient therapeutic care in 10 countries. A secondary data analysis. Matern Child Nutr 13, e12345.CrossRefGoogle ScholarPubMed
Ruemmele, FM (2011) Early programming effects of nutrition: life-long consequences? Ann Nutr Metab 58, Suppl. 2, S5S6.CrossRefGoogle ScholarPubMed
Tarry-Adkins, JL & Ozanne, SE (2011) Mechanisms of early life programming: current knowledge and future directions. Am J Clin Nutr 94, S1765S1771.CrossRefGoogle ScholarPubMed
Lelijveld, N, Seal, A, Wells, JC et al. (2016) Chronic disease outcomes after severe acute malnutrition in Malawian children (ChroSAM): a cohort study. Lancet Glob Health 4, e654e662.CrossRefGoogle ScholarPubMed
Kerac, M, Blencowe, H, Grijalva-Eternod, C et al. (2011) Prevalence of wasting among under 6-month-old infants in developing countries and implications of new case definitions using WHO growth standards: a secondary data analysis. Arch Dis Child 96, 10081013.CrossRefGoogle ScholarPubMed
Patwari, AK, Kumar, S & Beard, J (2015) Undernutrition among infants less than 6 months of age: an underestimated public health problem in India. Matern Child Nutr 11, 119126.CrossRefGoogle ScholarPubMed
Choudhary, TS, Srivastava, A, Chowdhury, R et al. (2019) Severe wasting among Indian infants < 6 months: findings from the National Family Health Survey 4. Matern Child Nutr 15, e12866.CrossRefGoogle ScholarPubMed
Desta, KS (2015) A survival status and predictors of mortality among children aged 0–59 months with severe acute malnutrition admitted to stabilization center at Sekota Hospital Waghemra Zone. J Nutr Disorders Ther 5, 160.Google Scholar
Oumer, A, Mesfin, F & Demena, M (2016) Survival status and predictors of mortality among children aged 0–59 months admitted with severe acute malnutrition in Dilchora Referral Hospital, Eastern Ethiopia. East Afr J Health Biomed Sci 1, 1322.Google Scholar
Dhanalakshmi, K & Devi, CG (2017) The outcome of severe acute malnutrition children admitted to nutrition rehabilitation centre of a tertiary level care hospital. Int J Contemp Pediatr 4, 801803.Google Scholar
Bhatnagar, S, Kumar, R, Dua, R et al. (2019) Outcome of children with severe acute malnutrition and diarrhea: a cohort study. Pediatr Gastroenterol Hepatol Nutr 22, 242248.CrossRefGoogle ScholarPubMed
Ministry of Health Family Welfare. Govt of India (2011) Operational Guidelines on Facility Based Management of Children with Severe Acute Malnutrition. http://rajswasthya.nic.in/MTC%20Guideline-%20MOHFW.pdf (accessed August 2020).Google Scholar
Singh, T, Sharma, S & Nagesh, S (2017) Socio-economic status scales updated for 2017. Int J Res Med Sci 5, 32643267.CrossRefGoogle Scholar
Gupta, P (2017) Anthropometry: assessment of growth. In Clinical Methods in Pediatrics, pp. 58110 [Gupta, P, editor]. New Delhi: CBS Publishers.Google Scholar
World Health Organization (2006) The WHO Child Growth Standards. http//www.who.int/tools/child-growth-standards (accessed August 2020).Google Scholar
WHO (2010) Anthro for Personal Computers, Version 3.2.2, 2016: Software for Assessing Growth and Development of the World’s Children. Geneva: WHO. http://www.who.int/childgrowth/software/en/ (accessed August 2020).Google Scholar
Ministry of Health Family Welfare. Govt of India (2013) Participant Manual for Facility-Based Care of Severe Acute Malnutrition. New Delhi: Ministry of Health and Family Welfare, Government of India.Google Scholar
Munirul Islam, M, Arafat, Y, Connell, N et al. (2019) Severe malnutrition in infants aged <6 months – outcomes and risk factors in Bangladesh: a prospective cohort study. Matern Child Nutr 15, e12642.CrossRefGoogle ScholarPubMed
Vygen, SB, Roberfroid, D, Captier, V et al. (2013) Treatment of severe acute malnutrition in infants aged <6 months in Niger. J Pediatr 162, 515521.CrossRefGoogle ScholarPubMed
Spherestandards.org (2018) Humanitarian Charter and Minimum Standards in Humanitarian Response. https://spherestandards.org/wp-content/uploads/Sphere-Handbook-2018-EN.pdf (accessed August 2020).Google Scholar
Kerac, M, Bunn, J, Chagaluka, G et al. (2014) Follow-up of post-discharge growth and mortality after treatment for severe acute malnutrition (FuSAM study): a prospective cohort study. PLoS One 9, e96030.Google ScholarPubMed
Ngari, MM, Iversen, PO, Thitiri, J et al. (2019) Linear growth following complicated severe malnutrition: 1-year follow-up cohort of Kenyan children. Arch Dis Child 104, 229235.CrossRefGoogle ScholarPubMed
Khanum, S, Ashworth, A & Huttly, SRA (1998) Growth, morbidity, and mortality of children in Dhaka after treatment for severe malnutrition: a prospective study. Am J Clin Nutr 67, 940945.CrossRefGoogle ScholarPubMed
Walker, SP & Golden, MHN (1988) Growth in length of children recovering from severe malnutrition. Eur J Clin Nutr 42, 395404.Google ScholarPubMed
Waterlow, JC (1994) Relationship of gain in height to gain in weight. Eur J Clin Nutr 48, Suppl. 1, S72S74.Google Scholar
Ashworth, A (1975) Regulation of weight and height during recovery from severe malnutrition. In Proceedings of the 9th International Congress of Nutrition, Mexico, pp. 280285 [Chavez, A, Bourges, H and Basta, S, editors]. Basel, Switzerland: Karger.Google Scholar
Bredow, MT & Jackson, AA (1994) Community based, effective, low cost approach to the treatment of severe malnutrition in rural Jamaica. Arch Dis Child 71, 297303.CrossRefGoogle ScholarPubMed
Martorell, R, Khan, LK & Schroeder, DG (1994) Reversibility of stunting: epidemiological findings in children from developing countries. Eur J Clin Nutr 48, Suppl. 1, S45S57.Google ScholarPubMed
Golden, MHN (1994) Is complete catch-up possible for stunted malnourished children? Eur J Clin Nutr 48, Suppl. 1, S58S71.Google ScholarPubMed
WHO International (2020) Global Action Plan on Child Wasting: A Framework for Action to Accelerate Progress in Preventing and Managing Child Wasting and the achievement of the Sustainable Development Goals. https://www.who.int/publications/m/item/global-action-plan-on-child-wasting-a-framework-for-action (accessed July 2021).Google Scholar
Kerac, M, McGrath, M, Connell, N et al. (2020) ‘Severe malnutrition’: thinking deeply, communicating simply. BMJ Glob Health 5, e003023.CrossRefGoogle Scholar
ENN, LSHTM & Collaborators (2021) MAMI Care Pathway Package, Version 3. https://www.ennonline.net/mamicarepathway (accessed July 2021).Google Scholar
Figure 0

Fig. 1 Flow of participants in the study

Figure 1

Table 1 Socio-demographic profile of enrolled infants (n 50)

Figure 2

Table 2 Outcomes of children under 6 months of age with severe wasting (n 50)

Figure 3

Table 3 Anthropometric parameters of infants less than 6 months with severe wasting from enrolment to 3 months after discharge

Figure 4

Table 4 Association of risk factors and unsatisfactory outcome

Figure 5

Fig. 2 Trends in (a) weight for age Z-score; (b) length-for-age Z-score and (c) weight-for-length Z-score during 3 months of follow-up (n 32)

Figure 6

Fig. 3 Pattern of (a) weight-for-age Z-score; (b) weight-for-length Z-score and (c) length-for-age Z-score of the individual children over the study period

Supplementary material: PDF

Patel et al. supplementary material

Figure 3

Download Patel et al. supplementary material(PDF)
PDF 805.7 KB