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Article

Choosing Anthropometric Indicators to Monitor the Response to Treatment for Severe Acute Malnutrition in Rural Southern Ethiopia—Empirical Evidence

by
Amare Worku Tadesse
1,2,*,
Elazar Tadesse
1,2,
Yemane Berhane
2 and
Eva-Charlotte Ekström
1
1
Department of Women’s and Children’s Health, International Maternal and Child Health Uppsala University, SE-75185 Uppsala, Sweden
2
Addis Continental Institute of Public Health, P.O. Box 26751/1000 Addis Ababa, Ethiopia
*
Author to whom correspondence should be addressed.
Nutrients 2017, 9(12), 1339; https://doi.org/10.3390/nu9121339
Submission received: 13 November 2017 / Revised: 29 November 2017 / Accepted: 2 December 2017 / Published: 8 December 2017

Abstract

:
The World Health Organization (WHO) recommends the assessment of nutritional recovery using the same anthropometric indicator that was used to diagnose severe acute malnutrition (SAM) in children. However, related empirical evidence from low-income countries is lacking. Non-oedematous children (n = 661) aged 6–59 months admitted to a community-based outpatient therapeutic program for SAM in rural southern Ethiopia were studied. The response to treatment in children admitted to the program based on the mid-upper arm circumference (MUAC) measurement was defined by calculating the gains in average MUAC and weight during the first four weeks of treatment. The children showed significant anthropometric changes only when assessed with the same anthropometric indicator used to define SAM at admission. Children with the lowest MUAC at admission showed a significant gain in MUAC but not weight, and children with the lowest weight-for-height/length (WHZ) showed a significant gain in weight but not MUAC. The response to treatment was largest for children with the lowest anthropometric status at admission in either measurement. MUAC and weight gain are two independent anthropometric measures that can be used to monitor sufficient recovery in children treated for SAM. This study provides empirical evidence from a low-income country to support the recent World Health Organization recommendation.

1. Introduction

Severe acute malnutrition (SAM) is estimated to cause 540,000 child deaths every year [1]. Since being introduced in 2007, the community management of SAM (CMAM) is the recommended treatment guideline, which combines an outpatient therapeutic program (OTP) with ready-to-use therapeutic foods (RUTF) for uncomplicated cases, and inpatient treatment for complicated cases [2,3]. The introduction of the OTP has improved the coverage, access, and cost-effectiveness of SAM management [3,4,5].
The current guidelines recommend the use of values of mid-upper arm circumference (MUAC) lower than 115 mm or of weight-for-height/length (WHZ) below the −3 Z score of the WHO standard [2,3,6] as two independent anthropometric criteria for identifying children with SAM for treatment [7]. Although both indicators are commonly used in nutritional rehabilitative programs, WHZ and MUAC were shown to identify different sets of children as having SAM [2,8,9,10]. Such discrepancy was also shown to vary in different settings [7,8] and according to the age and sex of the children identified as having SAM [10]. Although both indicators measure the nutritional status [6,11], uncertainty exists about the appropriate indicator to use for monitoring the response to treatment, recovery, and discharge from programs providing care for SAM.
When the admission was based on WHZ, the indicators to define recovery from SAM used to be based on WHZ [12]. For programs using MUAC as the admission criteria, the WHZ-based discharge criteria were not applicable as some children might have already fulfilled the WHZ discharge criteria at the time of admission into the program [2,13]. To avoid this problem and to eliminate the need for height measurement, the discharge criterion was redefined to be based on the percentage weight gain since admission [14]. However, the use of the percent weight gain was problematic because it led the most severely malnourished, and hence lighter, children to require a smaller absolute weight gain to meet the discharge criteria despite the risk of insufficient recovery [15,16,17]. Currently, the WHO guidelines on SAM management recommends that the criteria for discharging children from the treatment should be based on the same indicator that was used to diagnose SAM [7].
The response to treatment of children with SAM admitted to programs on the basis of WHZ is well documented [5,18,19,20,21], and weight gain has been the indicator of choice for monitoring the response to treatment for SAM [2,11]. The application of the standard protocol that uses the same measure for both the admission and discharge criteria aims to enable sufficient nutritional rehabilitation and to reduce mortality in children with SAM. The follow-up of severely malnourished children on the basis of MUAC alone was used in some settings [16,17], and this strategy is now included in the WHO updated recommendations [7]. However, there is limited evidence that the mid-upper arm circumference is an indicator of the progress in recovery during nutritional rehabilitation.
A good monitoring indicator needs to be responsive to the changes in the nutritional status and should predict a negative or positive outcome. The decision to use either the weight gain or the MUAC change as an indicator for monitoring the response to treatment in programs providing care for SAM needs to be based on understanding the relationship between these indicators to ensure that sufficient nutritional rehabilitation is achieved during the treatment of SAM children in the OTP. It is also imperative to generate empirical evidence in support of the current treatment guidelines [7]. Thus, we analyzed the average MUAC and weight gains of SAM children admitted to the OTP after 4 weeks of rehabilitation.

2. Methods

2.1. Study Design and Setting

This cohort study was part of a larger study (COMSAM) which aimed at evaluating the effectiveness of a community-based management of a severe acute malnutrition program in four adjacent districts in southern Ethiopia. The details of the study were described previously [15,22], but a brief description is provided here. In Ethiopia, the OTP has been scaled up and integrated into the existing public health system, including health posts (the lowest tier in the Ethiopian health system hierarchy). As part of CMAM, the children in the study area are screened for signs of malnutrition by community health workers. The OTP offers services to severely malnourished children aged 6–59 months. According to the Ethiopian national SAM management protocol [23], the children are admitted to the programme when their MUAC is lower than 11 cm or nutritional oedema is present. After admission, the children receive RUTF based on their weight on a weekly basis and additional supportive therapies based on their needs [23]. The study area is known for its recurrent nutritional emergencies and chronic food insecurity [24]. As a result, severe acute malnutrition in children is highly prevalent in the districts, and child mortality is also reported to be one of the highest in this part of the country [25].

2.2. Participants and Data Collection

The children admitted to the OTP in health posts of the study districts were identified using the health post registry. The research team collected independent anthropometric measurements, including mid-upper arm circumference, weight, height, and presence of bilateral oedema within one week of admission and 4 weeks after admission. Follow-up measurements were taken at the children’s homes. The mid-upper arm circumference of children aged 6 to 59 months was measured. Oedema on the feet was checked in children by pressing the foot. Other household, caregiver, and child information was also collected through household interviews conducted during these home visits [15,22].
In this paper, we used a subset of children admitted to the OTP during a 6 months period, from July to December 2011 (n = 1048), who had complete information on anthropometry at admission. Children with oedema at admission or follow-up were excluded from the analyses, as the changes in the anthropometric measurements could be obscure because of the fluid retained in the body [13]. Further, only children whose anthropometric measurements were taken at the 4th week of follow-up (n = 661) were included in the analysis for the assessment of the response to treatment at the 4th week of follow-up (Figure 1).

2.3. Measures

2.3.1. Anthropometry

The weight of each child was measured to the nearest 0.1 kg using the UNICEF electronic scale. Their MUAC was taken using the WHO-recommended MUAC tape and procedure, and their length and height were measured to the nearest 0.1 cm using the UNICEF recommended model of the wooden board, as per the WHO protocol [26,27]. Nutritional indices of malnutrition were calculated using the WHO Anthro (Version 3.2.2, WHO, Geneva, Switzerland) to produce the Z-scores for weight and length and height data, using the 2006 WHO Growth Standards [28]. To set categories based on the nutritional status at admission and distinguish between the gains in MUAC or weight that occurred during the process of normal growth and response to treatment, MUAC measurements and WHZ-scores were categorized into three groups, i.e, MUAC < 110 mm, 110–114 mm, and ≥115 mm; and WHZ < −3, −3 ≤ WHZ < −2 and WHZ ≥ −2, respectively.

2.3.2. Outcome

The response to treatment was defined by two anthropometric indicators: the average MUAC gain per day and the average weight gain per day. The average MUAC gain, expressed as mm/day, was calculated by taking the difference in the MUAC measurements between the admission and the 2nd visit conducted after 4 weeks of follow-up in the programme and dividing this value by the total number of days between each measurement. The average weight gain, expressed as g/kg/day, was calculated by dividing the rate of weight gain between the admission and the 4th week of follow-up by the child’s average weight, in line with the recommendations [27].

2.3.3. Sociodemographic Characteristics

Data on housing quality, caregiver characteristics such as occupation, education, and age (years), child age, child sex, and child length and height were collected. The housing quality was used as a proxy indicator of the household’s overall material resources. This measure was based on the type of material used in the construction of the house, the sources of drinking water, and the latrine facilities. Each characteristic was coded from 1 to 3, where a value of “1” referred to the lowest housing quality and a value of “3” to the highest. The household variables were summed up to create a housing quality score ranging from 3 to 9, which was further divided into tertiles to define the lowest, middle, and highest housing quality level.

2.4. Statistical Analysis

Descriptive statistics, including proportions and 95% confidence intervals, were computed to describe age and sex distributions according to the children’s nutritional status at admission and the change in anthropometric indicators. The ages of the children were dichotomized to correspond to categories usually used in field nutrition programs: young (age < 24 months) and older children (age ≥ 24 months). We created continuous variables to define the response to treatment by using average MUAC and average weight gain values, as described above. We used the general linear model (GLM) to estimate the gain in anthropometric indicators (as continuous outcome variables) according to MUAC and WHZ at admission.
Based on the UNICEF conceptual model of child growth and development [29] as well as on previous research on the determinants of treatment outcome for the OTP [30,31,32], certain child, caregiver, and household characteristics that can influence child growth and nutrition were selected as potential confounders. Three statistical models were then created: the first unadjusted, the second adjusted for child age, sex, and length and height, and the third adjusted for housing quality, caregiver characteristics (occupation, age in years, education), and duration of the follow-up until the 2nd visit, in addition to the child characteristics. The regression diagnostic procedure and visual impressions of the standard errors of the regression coefficients in the multivariable model showed no evidence of multicollinearity (variance inflation factor < 1 and tolerance > 0.9). The data were analysed using SPSS 20 (International Business Machines Corporation, New York, NY, USA) statistical software package for Windows.

2.5. Ethics

Ethical approval was received from the institutional ethical review board of the Addis Continental Institute of Public Health (ACIPH), Ethiopia, and the regional ethical review board in Uppsala, Sweden. Permission to conduct the study was obtained from regional and district health offices. The Declaration of Helsinki was followed when conducting the study. A verbal informed consent was obtained from the caregiver of the child prior to conducting the interviews.

3. Results

Figure 1 illustrates the complete participant flow from admission to 4 weeks of therapy in the OTP. Of 1659 children admitted to the OTP, 179 were excluded because ineligible and 355 because their nutritional status was not assessed within seven days of admission. After assessing the nutritional status of 1125 children, 77 children with missing key information at admission and 215 children with oedema were excluded from the analysis in this study. Of 833 children who were followed for 4 weeks, 77 exited from the OTP before the 4th week follow-up assessment by the study team. Of the 756 eligible children for this study, 661 children with a complete follow-up at 4 weeks were included in the analysis. We compared the excluded group of children with that of children included in this study and found no significant differences in their ages or sex (for those with available information) or in the caregivers’ and household characteristics of the children. The background household, caregiver, and child characteristics of those who participated in the OTP are shown in Table 1. Nearly three out of four households had a house with a thatched roof with wood and mud/grass walls, open-pit latrine, and access to a protected source of drinking water. A majority of the mothers were married, aged between 20 and 39 years, and had at least some form of primary education. About 60% of the children were females and 70% were under two years of age.
The nutritional status at admission was analysed for 661 children who were admitted to the OTP based on mid-upper arm circumference (MUAC) criteria and who received 4 weeks of therapy. When using the MUAC criteria to define SAM, 75.9% had SAM on admission (57% MUAC < 110 mm and 18.9% MUAC 110–114 mm) and 24% did not have SAM. When using the WHZ criteria to define SAM, 28.1% had SAM and 35.6% did not have SAM. MUAC classified a higher proportion of young children (age < 24 months) compared to the older children (age ≥ 24 months) as severely malnourished. Among the studied children, WHZ classified a higher proportion of boys compared to girls as severely malnourished. Thus, the two indicators classify children in a significantly different way (Table 2).
MUAC and weight increased in all children overtime. However, the average gain for these measures varied between children with different degrees of severity of malnutrition as well as whether the indicator used was based on MUAC or WHZ. The average MUAC and weight gains after 4 weeks of follow-up were 0.17 mm/day (±0.2 SD) and 1.8 g/kg/day (±4.0 SD), respectively (Table 3). When MUAC was used to define SAM at admission, MUAC gain was significantly greater among severely malnourished children (MUAC < 110 mm) compared with children with no SAM (MUAC ≥ 115 mm). Similarly, when WHZ was used to define SAM at admission, weight gain was significantly greater among severely malnourished children (WHZ < −3) compared with children with no SAM (WHZ ≥ −2). The anthropometric changes were marginal for those malnourished children with MUAC 110–114 mm and −3 ≤ WHZ < −2, compared to children with no SAM (MUAC ≥ 115 mm and WHZ ≥ −2). The average gain was two-fold for MUAC (0.20; 95% CI 0.17, 0.23) and three-fold for weight (3.1; 95% CI 2.4, 3.8) (Table 3).
Children with the lowest MUAC (MUAC < 110 mm) showed a significant change on the average MUAC gain after 4 weeks of therapy but no significant difference in weight gain. Children with the lowest WHZ (WHZ < −3) showed a significant change on the average weight gain after 4 weeks of therapy but no significant difference in the average MUAC gain (Table 4). Thus, both MUAC and weight gain detected a good response to treatment in 4 weeks, and the largest response was observed among the severely malnourished children. However, using a measure different from the one used to define SAM at admission did not allow to detect a significant change in the response to treatment.

4. Discussion

In this cohort study, we found that SAM children showed changes in both MUAC and weight measurements following treatment. For the MUAC-based definition of SAM at admission, the gain in MUAC was the indicator of choice to monitor the treatment response in children treated for SAM. Likewise, when WHZ was used to define SAM at admission, weight gain was the indicator used to monitor the response to treatment.
An average MUAC gain of 0.17 mm/day and weight gain of 1.8 g/kg/day for the children in our cohort compared unfavorably to those reported by other community-based nutritional programs, where the average MUAC and weight gains for children recovering from acute malnutrition varied between 0.2 to 0.52 mm/day [17,33] and 3 to 6.8 g/kg/day [33,34], respectively. The lower MUAC and weight gain compared to the recommended standards and other studies [17,35] may possibly be explained by differences in the adherence to optimal management of children with SAM under the OTP. Low frequency of feeding per day and sharing of the RUTF with other members of the household are likely to cause poor recovery of the children treated at home [22,34,36]. Results from our previous study area also indicated that the sharing of RUTF with other family members, mostly children, was justified by social norms favouring food sharing, shortage of food in the household, the good taste of RUTF, and its high-energy properties [22,36]. The lower MUAC and weight gains may also be due to the providers’ nonadherence to the guidelines on SAM management where the follow-up of the children being managed at the OTP was inadequate in relation to the monitoring of the children’s response to treatment and the provision of the recommended amount of RUTF [7,22,36].
In our study, the rate of MUAC gain was the largest in children with the smallest MUAC at admission. This gain could reveal, besides the normal physiologic growth, changes in the lean tissue during recovery [37,38]. Thus, children with low MUAC had a larger gain in MUAC, suggesting that they experienced rapid catch-up growth in response to a therapeutic diet [16,17]. Our results also show that children with the lowest WHZ at admission had higher proportional weight gain than the children with a higher WHZ at admission. A rapid weight gain happens during recovery for children with a deficit in WHZ [39], whereas the rates of weight gain fall substantially when children approach a normal WHZ [39]. However, our findings on the gains in MUAC and weight differed according to the indicator that was used to define SAM at admission. These gains are likely to reflect normal growth during rehabilitation to achieve sufficient recovery from SAM [13]. Thus, it is worth noting the importance of using the same indicator to monitor the response to treatment as the one used on admission for diagnosing SAM. Moreover, our analysis showed no effect of child age, sex, and length and height on the rate of weight or MUAC gain (Table A1), which may support a reasonable argument that MUAC and weight may be used independently to monitor the response to treatment.
In children being treated for SAM in OTPs, the gains in MUAC and weight were shown to be closely correlated and follow a similar recovery trajectory [40]. As weight loss or the failure to gain weight in children may suggest that follow-up in the community or referral to hospital are necessary [7,40], the failure to gain MUAC in children may similarly be indicative of the need for such a procedure. Our findings are also in line with the results of the above studies. Furthermore, using the same measurement tool for admission, treatment monitoring, follow-up, and discharge could make programs more coherent and understandable to caregivers [17].
Decreasing the growth velocity measures based on weight and MUAC were shown to be useful in identifying children at high risk of dying [41,42,43,44,45]. The application of these measures in the field by minimally trained community health workers is a challenge, as calculating the growth velocity requires mathematical skills similar to those used for completing growth charts [13]. Decreased gains in weight and MUAC could reflect a recent drop in the growth curve and could possibly identify children at an increased risk of death [44]. However, it may be possible to develop simpler monitoring tools and protocols for the appropriate management of SAM based on changes in MUAC and weight with field testing and refinement [41], as the children’s nutritional status is typically monitored for progress at the OTP [13,17].
In anthropometric assessment, the reliability of the measurements is an important requirement as it directly influences the admission and discharge criteria for children in nutrition interventions [46]. The reliability reflects the repeatability of the results when several measurements are performed by the same (intraobserver) or different (interobserver) observers under the same conditions [47]. Previous studies of reliability were conducted within a carefully controlled hospital or research environment and reported high reliability scores for absolute measures of weight, length and height, and MUAC [48,49]. As variations in the reliability of the measurements could influence the interpretation of the children’s responses to the treatment of SAM, all enumerators went through training to ensure the standardization of the measurements, and used the WHO-recommended MUAC tapes and the UNICEF-recommended weight and height boards. A rigorous measurement technique is a means to minimize random errors in anthropometric measurements and the regression to the mean and thus to reduce the risk of insufficient reliability as an explanation to our findings.
A potential limitation of this study was that the analysis was based on data collected from children admitted to the OTP by MUAC criteria. However, because there was no significant difference in terms of their background characteristics in the proportion of children with low WHZ between the population [10] and the study sample, our estimation of the gains in anthropometric measures is likely to reflect a valid estimate of the response in the children treated for SAM.

5. Conclusions

The gains in MUAC and weight are two independent anthropometric measures that can be used to monitor the response to treatment for severe acute malnutrition and ensure sufficient recovery. This study provides empirical evidence that supports the recent recommendation to use the same anthropometric indicator to identify children for the treatment of SAM and to monitor their response to nutritional rehabilitation programs.

Acknowledgments

We would like to express our gratitude to the study participants and the district health offices that participated in the study. We are also grateful to the Swedish International Development Cooperation (SIDA) Department for Research for funding the project (SWE-2010-179). The Department of Women’s and Children’s Health, Uppsala University, also contributed funds to the project and covered the publication costs. UNICEF Addis Ababa provided weighing scales and height boards.

Author Contributions

E.E. and Y.B. conceived and designed the study. E.T. and A.W. performed the field work. A.W. analysed data. A.W. wrote the paper in close collaboration with Y.B. and E.E. All authors revised and approved the final version of the paper.

Conflicts of Interest

All authors declare no conflict of interest.

Appendix A

Table A1. GLM results for the estimated effect of child, caregiver, and household characteristics on average MUAC and weight gain after 4 weeks of follow-up.
Table A1. GLM results for the estimated effect of child, caregiver, and household characteristics on average MUAC and weight gain after 4 weeks of follow-up.
Average MUAC Gain (mm/day)Average Weight Gain (g/kg/day)
Variablesβ95% CIβ95% CI
Housing quality
  Lowest0.13−0.11, 0.380.87−2.80, 4.54
  Middle0.14−0.11, 0.390.89−2.84, 4.62
  HighestRef Ref
Caregivers’ education
  Never attended school−0.07−0.20, 0.06−1.40−3.35, 0.55
  In but did not complete primary school−0.01−0.06, 0.04−0.01−0.76, 0.74
  Completed primary school or aboveRef Ref
Caregivers’ occupation
  Non-salaried0.08−0.02, 0.15−0.01−1.03, 0.99
  Farmer0.03−0.14, 0.810.27−0.45, 0.99
  Petty trade & wage workRef Ref
Caregivers’ age (years)0.001−0.01, 0.01−0.04−0.09, 0.01
Duration of follow up−0.005−0.01, 0.01−0.06−0.15, 0.03
Child age
  <24 months−0.03−0.09, 0.03−0.12−1.12, 0.88
  ≥24 monthsRef Ref
Child sex
  Boys−0.002−0.05, 0.04−0.14−0.80, 0.53
  GirlsRef Ref
Child length/height0.003−0.01, 0.01−0.02−0.07, 0.03
β, Coefficients for variables in final model (GLM).

References

  1. Black, R.E.; Victora, C.G.; Walker, S.P.; Bhutta, Z.A.; Christian, P.; de Onis, M.; Ezzati, M.; Grantham-McGregor, S.; Katz, J.; Martorell, R.; et al. Maternal and child undernutrition and overweight in low-income and middle-income countries. Lancet 2013, 382, 427–451. [Google Scholar] [CrossRef]
  2. WHO Child Growth Standards and Identification of Severe Acute Malnutrition in Infants and Children: A Joint Statement by the World Health Organization and the United Nations Children’s Fund. Available online: http://apps.who.int/iris/bitstream/10665/44129/1/9789241598163_eng.pdf (accessed on 17 December 2016).
  3. Community-Based Management of Severe Acute Malnutrition: A Joint Statement by the World Health Organization, the World Food Programme, the United Nations System Standing Committee on Nutrition and the United Nations Children’s Fund. Available online: http://www.who.int/nutrition/topics/Statement_community_based_man_sev_acute_mal_eng.pdf (accessed on 20 September 2016).
  4. Collins, S.; Sadler, K.; Dent, N.; Khara, T.; Guerrero, S.; Myatt, M.; Saboya, M.; Walsh, A. Key issues in the success of community-based management of severe malnutrition. Food Nutr. Bull. 2006, 27, S49–S82. [Google Scholar] [CrossRef] [PubMed]
  5. Manary, M.J.; Ndkeha, M.J.; Ashorn, P.; Maleta, K.; Briend, A. Home based therapy for severe malnutrition with ready-to-use food. Arch. Dis. Child. 2004, 89, 557–561. [Google Scholar] [CrossRef] [PubMed]
  6. WHO Child Growth Standards: Length/Height-for-Age, Weight-for-Age, Weight-for-Length, Weight-for-Height and Body Mass Index-for-Age: Methods and Development. Available online: http://www.who.int/childgrowth/standards/Technical_report.pdf (accessed on 19 September 2016).
  7. Guideline: Updates on the Management of Severe Acute Malnutrition in Infants and Children. Available online: http://apps.who.int/iris/bitstream/10665/95584/1/9789241506328_eng.pdf (accessed on 16 January 2017).
  8. Laillou, A.; Prak, S.; de Groot, R.; Whitney, S.; Conkle, J.; Horton, L.; Un, S.O.; Dijkhuizen, M.A.; Wieringa, F.T. Optimal screening of children with acute malnutrition requires a change in current WHO guidelines as MUAC and WHZ identify different patient groups. PLoS ONE 2014, 9, e101159. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  9. Walters, T.; Sibson, V.; McGrath, M. Mid Upper Arm Circumference and Weight-for-Height Z-Score as Indicators of Severe Acute Malnutrition: A Consultation of Operational Agencies and Academic Specialist to Understand the Evidence, Identify Knowledge Gaps and to Inform Operational Guidance. Available online: http://files.ennonline.net/attachments/1398/muac-wfh-reportweb.pdf (accessed on 23 January 2017).
  10. Tadesse, A.W.; Tadesse, E.; Berhane, Y.; Ekström, E.C. Comparison of mid-upper arm circumference and weight-for-height to diagnose severe acute malnutrition: A study in Southern Ethiopia. Nutrients 2017, 9, 267. [Google Scholar] [CrossRef] [PubMed]
  11. The Harmonised Training Package (HTP): Resource Material for Training on Nutrition in Emergencies, Version 2. Available online: http://www.ennonline.net/ourwork/capacitydevelopment/htpversion2 (accessed on 23 December 2016).
  12. Management of Severe Malnutrition: A Manual for Physicians and Other Senior Health Workers. Available online: http://www.who.int/nutrition/publications/malnutrition/en/index.html (accessed on 23 December 2016).
  13. Myatt, M.; Khara, T.; Collins, S. A review of methods to detect cases of severely malnourished children in the community for their admission into community-based therapeutic care programs. Food Nutr. Bull. 2006, 27, S7–S23. [Google Scholar] [CrossRef] [PubMed]
  14. WHO, UNICEF, and SCN Informal Consultation on Community-Based Management of Severe Malnutrition in Children. Available online: http://www.who.int/nutrition/publications/severemalnutrition/FNB_0379-5721.pdf (accessed on 5 February 2017).
  15. Forsén, E.; Tadesse, E.; Berhane, Y.; Ekström, E.-C. Predicted implications of using percentage weight gain as single discharge criterion in management of acute malnutrition in rural southern Ethiopia. Matern. Child. Nutr. 2013, 11, 962–972. [Google Scholar] [CrossRef] [PubMed]
  16. Dale, N.; Myatt, M.; Prudhon, C.; Briend, A. Using Mid-Upper Arm Circumference to End Treatment of Severe Acute Malnutrition Leads to Higher Weight Gains in the Most Malnourished Children. PLoS ONE 2013, 8, e55404. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  17. Goossens, S.; Bekele, Y.; Yun, O.; Harczi, G.; Ouannes, M.; Shepherd, S. Mid-upper arm circumference based nutrition programming: Evidence for a new approach in regions with high burden of acute malnutrition. PLoS ONE 2012, 7, e49320. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  18. Ciliberto, M.A.; Sandige, H.; Ndekha, M.J.; Ashorn, P.; Briend, A.; Ciliberto, H.M.; Manary, M.J. Comparison of home-based therapy with ready-to-use therapeutic food with standard therapy in the treatment of malnourished Malawian children: A controlled, clinical effectiveness trial. Am. J. Clin. Nutr. 2005, 81, 864–870. [Google Scholar] [PubMed]
  19. Diop, E.H.I.; Dossou, N.I.; Ndour, M.M.; Briend, A.; Wade, S. Comparison of the efficacy of a solid ready-to-use food and a liquid, milk-based diet for the rehabilitation of severely malnourished children: A randomized trial. Am. J. Clin. Nutr. 2003, 78, 302–307. [Google Scholar]
  20. Trehan, I.; Goldbach, H.S.; LaGrone, L.N.; Meuli, G.J.; Wang, R.J.; Maleta, K.M.; Manary, M.J. Antibiotics as part of the management of severe acute malnutrition. Malawi Med. J. 2016, 28, 123–130. [Google Scholar] [CrossRef] [PubMed]
  21. Linneman, Z.; Matilsky, D.; Ndekha, M.; Manary, M.J.; Maleta, K.; Manary, M.J. A large-scale operational study of home-based therapy with ready-to-use therapeutic food in childhood malnutrition in Malawi. Matern. Child. Nutr. 2007, 3, 206–215. [Google Scholar] [CrossRef] [PubMed]
  22. Tadesse, E.; Ekström, E.C.; Berhane, Y. Challenges in implementing the Integrated Community-Based Outpatient Therapeutic Program for severely malnourished children in rural Southern Ethiopia. Nutrients 2016, 8, 251. [Google Scholar] [CrossRef] [PubMed]
  23. Protocol for the Management of Severe Acute Malnutrition. Federal Ministry of Health: Addis Ababa, Ethiopia, 2007. Available online: http://files.ennonline.net/attachments/897/ethiopia-sam-guideline-march-2007.pdf (accessed on 20 September 2016).
  24. Ethiopia Southern Nations, Nationalities and Peoples Region (SNNPR) Livelihood Zone Reports: SNNPR Follow-On to Regional Livelihoods Baseline Study. Available online: http://pdf.usaid.gov/pdf_docs/Pnadj866.pdf (accessed on 21 August 2015).
  25. Ethiopia Demographic and Health Survey 2011. Available online: https://www.unicef.org/ethiopia/ET_2011_EDHS.pdf (accessed on 21 August 2015).
  26. Physical Status: The Use and Interpretation of Anthropometry. Available online: http://www.who.int/childgrowth/publications/physical_status/en/ (accessed on 14 November 2015).
  27. Pocket Book of Hospital Care for Children: Guidelines for the Management of Common Childhood Illnesses. Available online: http://apps.who.int/iris/bitstream/10665/81170/1/9789241548373_eng.pdf (accessed on 17 December 2016).
  28. WHO Anthro for Personal Computers, Version 3.2.2. Software for Assessing Growth and Development of the World’s Children. Available online: http://www.who.int/childgrowth/software/en/ (accessed on 20 September 2015).
  29. Engle, P.L.; Menon, P.; Haddad, L. Care and nutrition: Concepts and measurement. World Dev. 1999, 27, 1309–1337. [Google Scholar] [CrossRef]
  30. Kabalo, M.Y.; Seifu, C.N. Treatment outcomes of severe acute malnutrition in children treated within Outpatient Therapeutic Program (OTP) at Wolaita Zone, Southern Ethiopia: Retrospective cross-sectional study. J. Health Popul. Nutr. 2017, 36, 7. [Google Scholar] [CrossRef] [PubMed]
  31. Mengesha, M.M.; Deyessa, N.; Tegegne, B.S.; Dessie, Y. Treatment outcome and factors affecting time to recovery in children with severe acute malnutrition treated at outpatient therapeutic care program. Glob. Health Action 2016, 9, 30704. [Google Scholar] [CrossRef] [PubMed]
  32. Yebyo, H.G.; Kendall, C.; Nigusse, D.; Lemma, W. Outpatient therapeutic feeding program outcomes and determinants in treatment of severe acute malnutrition in Tigray, Northern Ethiopia: A retrospective cohort study. PLoS ONE 2013, 8, e65840. [Google Scholar] [CrossRef] [PubMed]
  33. Maust, A.; Koroma, A.S.; Abla, C.; Molokwu, N.; Ryan, K.N.; Singh, L.; Manary, M.J. Severe and moderate acute malnutrition can be successfully managed with an integrated protocol in Sierra Leone. J. Nutr. 2015, 145, 2604–2609. [Google Scholar] [CrossRef] [PubMed]
  34. Collins, S. Treating severe acute malnutrition seriously. Arch. Dis Child. 2007, 92, 453–461. [Google Scholar] [CrossRef] [PubMed]
  35. Humanitarian Charter and Minimum Standards in Humanitarian Response. Available online: http://www.ifrc.org/PageFiles/95530/The-Sphere-Project-Handbook-20111.pdf (accessed on 4 April 2017).
  36. Tadesse, E.; Berhane, Y.; Hjern, A.; Olsson, P.; Ekstrom, E.C. Perceptions of usage and unintended consequences of provision of ready-to-use therapeutic food for management of severe acute child malnutrition: A qualitative study in Southern Ethiopia. Health Policy Plan. 2015, 30, 1334–1341. [Google Scholar] [CrossRef] [PubMed]
  37. Hop, L.T.; Gross, R.; Sastroamidjojo, S.; Giay, T.; Schultink, W. Mid upper circumeference development and its validity in assessment of undernutrition. Asia Pac. J. Clin. Nutr. 1998, 7, 65–69. [Google Scholar]
  38. Pelletier, D.L. The potentiating effects of malnutrition on child mortality: Epidemiologic evidence and policy implications. Nutr. Rev. 1994, 52, 409–415. [Google Scholar] [CrossRef] [PubMed]
  39. Ashworth, A. Efficacy and effectiveness of community-based treatment of severe malnutrition. Food Nutr. Bull. 2006, 27, S24–S48. [Google Scholar] [CrossRef] [PubMed]
  40. Binns, P.J.; Dale, N.M.; Banda, T.; Banda, C.; Shaba, B.; Myatt, M. Safety and practicability of using mid-upper arm circumference as a discharge criterion in community based management of severe acute malnutrition in children aged 6 to 59 months programmes. Arch. Public Health 2016, 74, 24. [Google Scholar] [CrossRef] [PubMed]
  41. Schwinger, C.; Fadnes, L.T.; van den Broeck, J. Using growth velocity to predict child mortality. Am. J. Clin. Nutr. 2016, 103, 801–807. [Google Scholar] [CrossRef] [PubMed]
  42. O’Neill, S.M.; Fitzgerald, A.; Briend, A.; van den Broeck, J. Child mortality as predicted by nutritional status and recent weight velocity in children under two in rural Africa. J. Nutr. 2012, 142, 520–525. [Google Scholar] [PubMed]
  43. Mwangome, M.K.; Fegan, G.; Fulford, T.; Prentice, A.M.; Berkley, J.A. Mid-upper arm circumference at age of routine infant vaccination to identify infants at elevated risk of death: A retrospective cohort study in the Gambia. Bull. World Health Organ. 2012, 90, 887–894. [Google Scholar] [CrossRef] [PubMed]
  44. Briend, A.; Maire, B.; Fontaine, O.; Garenne, M. Mid-upper arm circumference and weight-for-height to identify high-risk malnourished under-five children. Matern. Child. Nutr. 2012, 8, 130–133. [Google Scholar] [CrossRef] [PubMed]
  45. Lapidus, N.; Minetti, A.; Djibo, A.; Guerin, P.J.; Hustache, S.; Gaboulaud, V.; Grais, R.F. Mortality risk among children admitted in a large-scale nutritional program in Niger, 2006. PLoS ONE 2009, 4, e4313. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Mwangome, M.K.; Berkley, J.A. The reliability of weight-for-length/height Z scores in children. Matern. Child. Nutr. 2014, 10, 474–480. [Google Scholar] [CrossRef] [PubMed]
  47. Hennekens, C.H.; Buring, J.E. Epidemiology in Medicine; Lippincott Williams and Wilkins: Boston, MA, USA, 1987. [Google Scholar]
  48. Johnson, W.; Cameron, N.; Dickson, P.; Emsley, S.; Raynor, P.; Seymour, C.; Wright, J. The reliability of routine anthropometric data collected by health workers: A cross-sectional study. Int. J. Nurs. Stud. 2009, 46, 310–316. [Google Scholar] [CrossRef] [PubMed]
  49. World Health Organization. Reliability of anthropometric measurements in the WHO Multicentre Growth Reference Study. Acta Paediatr. 2006, 95, 38–46. [Google Scholar]
Figure 1. Flowchart of children admitted to the outpatient therapeutic program (OTP).
Figure 1. Flowchart of children admitted to the outpatient therapeutic program (OTP).
Nutrients 09 01339 g001
Table 1. Household, caregiver, and child characteristics of children admitted to the OTP.
Table 1. Household, caregiver, and child characteristics of children admitted to the OTP.
Household Characteristicsn (%)
Sanitation (n = 660)
   Pit latrine with slab17 (2.6)
   Open pit510 (77.2)
   Open space (Bush/farm land, other)123 (20.2)
Source of drinking water (n = 659)
   Protected source ( public tap, protected well/spring)501 (76.0)
   Unprotected source (spring, well, other)158 (24.0)
House construction (n = 660)
   Corrugated iron roof with wood and mud wall168 (25.5)
   Thatched roof with wood and mud/grass wall492 (74.6)
Number of children under five in the household (n = 661)
   One396 (59.9)
   More than one265 (40.1)
Caregiver Characterstics
Relationship to child (n = 660)
   Biological mother586 (88.8)
Marital status (n = 638)
   Married575 (90.1)
Age (in years) (n = 653)
   15–199 (1.4)
   20–29268 (41.0)
   30–39314 (48.1)
   ≥4062 (9.5)
Current occupation (n = 661)
   Nonsalaried job96 (14.5)
   Farmer349 (52.8)
   Petty trade & wage work216 (32.7)
Educational status (n = 661)
   Never attended school20 (3.0)
   In but did not complete primary school355 (69.4)
   Completed primary and above182 (27.6)
Child Characteristics
Sex (n = 661)
   Female389 (58.9)
Age (in Months) (n = 661)
   6–11 months289 (43.7)
   12–23 months207 (31.3)
   24–35 months66 (10.0)
   36–47 months63 (9.5)
   48–59 months36 (5.4)
Table 2. MUAC and WHZ of children categorized by sex and age at admission to the outpatient therapeutic program.
Table 2. MUAC and WHZ of children categorized by sex and age at admission to the outpatient therapeutic program.
MUAC at AdmissionWHZ at Admission
MUAC < 110 mmMUAC 110–114 mmMUAC ≥ 115 mmWHZ < −3−3 ≤ WHZ < −2WHZ ≥ −2
Nn%95% CIn%95% CIn%95% CIn%95% CIn%95% CIn%95% CI
Sex
 Girls38922858.653.5, 63.57118.314.6, 22.59023.119.1, 27.78822.618.6, 27.214838.133.2, 43.115339.334.5, 44.4
 Boys27214954.848.7, 60.85419.915.4, 25.26925.320.4, 31.19836.130.4, 42.19233.828.3, 39.88230.124.8, 36.0
Age
 <24 months49631062.558.1, 66.88617.314.2, 21.010020.216.8, 24.014629.425.5, 33.718637.533.3, 41.916433.129.0, 37.4
 ≥24 months1656740.633.1, 48.53923.617.5, 31.05935.828.6, 43.64024.218.1, 31.65432.725.8, 40.57143.135.4, 51.0
Table 3. Average MUAC gain and weight gain of children categorized by their anthropometric status at admission to the outpatient therapeutic program after 4 weeks of therapy.
Table 3. Average MUAC gain and weight gain of children categorized by their anthropometric status at admission to the outpatient therapeutic program after 4 weeks of therapy.
Average MUAC Gain, mm/day Average Weight Gain, g/kg/day
Mean95% CIMean95% CI
All children0.170.15, 0.191.81.5, 2.2
  MUAC at admission
  MUAC < 110 mm0.200.17, 0.232.01.5, 2.4
  MUAC 110–114 mm0.170.13, 0.211.91.4, 2.4
  MUAC ≥ 115 mm0.100.04, 0.131.50.8, 2.1
  WHZ at admission
  WHZ < −30.170.12, 0.223.12.4, 3.8
  −3 ≤ WHZ < −20.170.13, 0.201.71.3, 2.2
  WHZ ≥ −20.170.14, 0.200.90.5, 1.4
Table 4. GLM results for the estimated effect of the anthropometric status at admission on average MUAC and weight gains after 4 weeks of follow-up.
Table 4. GLM results for the estimated effect of the anthropometric status at admission on average MUAC and weight gains after 4 weeks of follow-up.
Average MUAC Gain (mm/day)
Anthropometric Status at AdmissionUnadjustedModel I Model II
β95% CIR2β95% CIR2β95% CIR2
MUAC < 110 mm0.12 **0.07, 0.170.0310.14 **0.09, 0.200.0460.14 **0.09, 0.200.063
MUAC 110–114 mm 0.09 **0.02, 0.15 0.09 **0.03, 0.16 0.10 **0.04, 0.17
MUAC ≥ 115 mmRefRefRef
Average Weight Gain (g/kg/day)
Anthropometric Status at AdmissionUnadjustedModel I Model II
β95% CIR2β95% CIR2β95% CIR2
WHZ < −32.16 **1.37, 2.950.0422.16 **1.34, 2.960.0432.17 **1.34, 3.000.054
−3 ≤ WHZ < −20.81 *0.07, 1.55 0.79 *0.05, 1.54 0.81 *0.05, 1.57
WHZ ≥ −2 Ref Ref Ref
The regression coefficients (β) represent the mean increase in the dependent variables (average MUAC and weight gain) between the categories of the independent variables. MUAC, mid upper circumference; WHZ, weight-for-height Z-score; Ref, reference category; * p < 0.05, ** p < 0.01; Adjusted for child sex, age (months), and length and height; Adjusted for housing quality, caregiver characteristics (occupation, education, and age in years), duration of follow-up, child sex, child age (months) and child length and height using the general linear model (GLM).

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MDPI and ACS Style

Tadesse, A.W.; Tadesse, E.; Berhane, Y.; Ekström, E.-C. Choosing Anthropometric Indicators to Monitor the Response to Treatment for Severe Acute Malnutrition in Rural Southern Ethiopia—Empirical Evidence. Nutrients 2017, 9, 1339. https://doi.org/10.3390/nu9121339

AMA Style

Tadesse AW, Tadesse E, Berhane Y, Ekström E-C. Choosing Anthropometric Indicators to Monitor the Response to Treatment for Severe Acute Malnutrition in Rural Southern Ethiopia—Empirical Evidence. Nutrients. 2017; 9(12):1339. https://doi.org/10.3390/nu9121339

Chicago/Turabian Style

Tadesse, Amare Worku, Elazar Tadesse, Yemane Berhane, and Eva-Charlotte Ekström. 2017. "Choosing Anthropometric Indicators to Monitor the Response to Treatment for Severe Acute Malnutrition in Rural Southern Ethiopia—Empirical Evidence" Nutrients 9, no. 12: 1339. https://doi.org/10.3390/nu9121339

APA Style

Tadesse, A. W., Tadesse, E., Berhane, Y., & Ekström, E. -C. (2017). Choosing Anthropometric Indicators to Monitor the Response to Treatment for Severe Acute Malnutrition in Rural Southern Ethiopia—Empirical Evidence. Nutrients, 9(12), 1339. https://doi.org/10.3390/nu9121339

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