Determinants of linear growth faltering among children with moderate-to-severe diarrhea in the Global Enteric Multicenter Study

被引:27
作者
Brander, Rebecca L. [1 ]
Pavlinac, Patricia B. [2 ]
Walson, Judd L. [3 ]
John-Stewart, Grace C. [4 ]
Weaver, Marcia R. [5 ]
Faruque, Abu S. G. [6 ]
Zaidi, Anita K. M. [7 ,8 ]
Sur, Dipika [9 ,10 ]
Sow, Samba O. [11 ]
Hossain, M. Jahangir [12 ]
Alonso, Pedro L. [13 ,14 ]
Breiman, Robert F. [15 ,16 ]
Nasrin, Dilruba [17 ]
Nataro, James P. [18 ,19 ]
Levine, Myron M. [20 ]
Kotloff, Karen L. [21 ]
机构
[1] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
[2] Univ Washington, Dept Global Hlth, Seattle, WA 98195 USA
[3] Univ Washington, Dept Epidemiol Global Hlth Pediat Med Childhood A, Seattle, WA 98195 USA
[4] Univ Washington, Dept Epidemiol, Global Hlth, Pediat Med, Seattle, WA 98195 USA
[5] Univ Washington, Hlth Metr Sci, Dept Global Hlth, Hlth Serv, Seattle, WA 98195 USA
[6] Int Ctr Diarrhoeal Dis Res, Dhaka, Bangladesh
[7] Aga Khan Univ, Dept Pediat & Child Hlth, Karachi, Pakistan
[8] Bill & Melinda Gates Fdn, Enter & Diarrheal Dis Program, Seattle, WA USA
[9] Natl Inst Cholera & Enter Dis, Kolkata, India
[10] Translat Hlth Sci & Technol Inst, Faridabad, India
[11] Ctr Dev Vaccines, Bamako, Mali
[12] Gambia London Sch Hyg & Trop Med, Med Res Council Unit, Banjul, Gambia
[13] Ctr Invest Saude Manh, Maputo, Mozambique
[14] WHO, Global Malaria Programme, Geneva, Switzerland
[15] US Ctr Dis Control & Prevent, Kenya Off, Global Dis Detect Div, Nairobi, Kenya
[16] Emory Univ, Global Hlth Inst, Atlanta, GA 30322 USA
[17] Univ Maryland, Sch Med, Dept Med, Ctr Vaccine Dev, Baltimore, MD 21201 USA
[18] Univ Maryland, Sch Med, Dept Med, Ctr Vaccine Dev,Dept Pediat, Baltimore, MD 21201 USA
[19] Univ Virginia, Sch Med, Dept Pediat, Charlottesville, VA 22908 USA
[20] Univ Maryland, Sch Med, Dept Pediat, Dept Pediat & Med,Ctr Vaccine Dev & Global Hlth, Baltimore, MD 21201 USA
[21] Univ Maryland, Sch Med, Dept Pediat & Med, Ctr Vaccine Dev & Global Hlth, Baltimore, MD USA
关键词
Diarrheal diseases; Malnutrition; Stunting; Growth retardation; Nutritional deterioration; Diarrhea sequelae; Clinical prediction; CATCH-UP GROWTH; DEVELOPING-COUNTRIES; YOUNG-CHILDREN; LOW-INCOME; WEIGHT; UNDERNUTRITION; INFANTS; DISEASE; LENGTH; GEMS;
D O I
10.1186/s12916-019-1441-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Moderate-to-severe diarrhea (MSD) in the first 2 years of life can impair linear growth. We sought to determine risk factors for linear growth faltering and to build a clinical prediction tool to identify children most likely to experience growth faltering following an episode of MSD. Methods: Using data from the Global Enteric Multicenter Study of children 0-23 months old presenting with MSD in Africa and Asia, we performed log-binomial regression to determine clinical and sociodemographic factors associated with severe linear growth faltering (loss of >= 0.5 length-for-age z-score [LAZ]). Linear regression was used to estimate associations with Delta LAZ. A clinical prediction tool was developed using backward elimination of potential variables, and Akaike Information Criterion to select the best fit model. Results: Of the 5902 included children, mean age was 10 months and 43.2% were female. Over the 50-90-day follow-up period, 24.2% of children had severe linear growth faltering and the mean Delta LAZ over follow-up was - 0.17 (standard deviation [SD] 0.54). After adjustment for age, baseline LAZ, and site, several factors were associated with decline in LAZ: young age, acute malnutrition, hospitalization at presentation, non-dysenteric diarrhea, unimproved sanitation, lower wealth, fever, co-morbidity, or an IMCI danger sign. Compared to children 12-23 months old, those 0-6 months were more likely to experience severe linear growth faltering (adjusted prevalence ratio [aPR] 1.97 [95% CI 1.70, 2.28]), as were children 6-12 months of age (aPR 1.72 [95% CI 1.51, 1.95]). A prediction model that included age, wasting, stunting, presentation with fever, and presentation with an IMCI danger sign had an area under the ROC (AUC) of 0.67 (95% CI 0.64, 0.69). Risk scores ranged from 0 to 37, and a cut-off of 21 maximized sensitivity (60.7%) and specificity (63.5%). Conclusion: Younger age, acute malnutrition, MSD severity, and sociodemographic factors were associated with short-term linear growth deterioration following MSD. Data routinely obtained at MSD may be useful to predict children at risk for growth deterioration who would benefit from interventions.
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