Child Wasting Risk Effects
Risk Overview
Child wasting, defined as low weight for heigh/length, is a measure of acute malnutrition that is associated with increased mortality and susceptibility to infectious disease. More information can be found in the wasting risk exposure model document.
GBD Modeling Strategy
The GBD 2019 risk effects of child wasting are informed by [Olofin-et-al-2013], which evauated the relative risk of cause-specific mortality rate (CSMR) by child wasting categories [GBD-2019-Risk-Factors-Appendix-Child-Wasting-Risk-Effects]. Notably, given that \(CSMR = EMR * prevalence\), the relative risks may be attributable to increased disease incidence (increases prevalence), duration (increases prevalence), or severity (increases excess mortality rate (EMR)), or some comination of these factors. The 2019 GBD applies the child wasting risk effects equally to both morbidity and mortality estimates (YLDs and YLLs).
Note
The acute malnutrition simulation uses GBD 2020 relative risks for child wasting. The data source for these potentially updated relative risks needs to be investigated.
Vivarium Modeling Strategy
Note
This section will describe the Vivarium modeling strategy for risk effects. For a description of Vivarium modeling strategy for risk exposure, see the wasting risk exposure model document.
For the acute malnutrition simulation, we will make different assumptions about how to apply the child wasting risk effects for diarrheal diseases than for measles and lower respiratory infections due to the inclusion of diarrheal diseases in the “vicious cycle”/positive feedback model with child wasting, which required this change to solve for the steady state model (discussed here).
Diarrheal diseases (to be used when the risk effect of diarrheal diseases on wasting is included in model)
For the acute malnutrition simulation, the relative risks for wasting on diarrheal diseases should be applied to the diarrheal diseases excess mortality rate and not the diarrheal diseases incidence rate in the following manner:
Where, for wasting state \(X\) in wasting states cat1, cat2, cat3, and cat4:
Note
Parameters \(p_{D1}, p_{D2}, p_{D3}, p_{D4}\) are defined on the diarrheal diseases risk effects document
The GBD 2020 wasting relative risks should be used in tandem with the GBD 2020 wasting risk exposure
NOTE: we use a custom PAF calculation rather than the GBD PAF that uses the wasting risk exposure distribution specific to those infected with diarrheal diseases to avoid bias in our application of the PAF to the population at-risk for diarrheal diseases mortality
Validation and Verification Criteria
Verification and validation criteria from the diarrheal diseases cause model should remain true.
Verification and validation criteria from the dynamic child wasting exposure model should remain true.
Todo
List additional V&V criteria
Assumptions and Limitations
Todo
List assumptions and limitations
Lower respiratory infections and measles (and diarrheal diseases when risk effect of diarrheal diseases on wasting is not included in the model)
For the acute malnutrition simulation, the relative risks for wasting on lower respiratory infections and measles should be applied to the diarrheal diseases excess mortality rate and not the diarrheal diseases incidence rate in the following manner:
Note
The GBD 2020 wasting relative risks should be used in tandem with the GBD 2020 wasting risk exposure
Validation and Verification Criteria
Verification and validation criteria from the LRI and measles cause model documents should remain true.
Verification and validation criteria from the dynamic child wasting exposure model should remain true.
Todo
List additional V&V criteria
Assumptions and Limitations
Todo
List assumptions and limitations
References
Pages 157-161 in Supplementary appendix 1 to the GBD 2019 Risk Factors Capstone:
(GBD 2019 Risk Factors Capstone) GBD 2019 Risk Factor Collaborators. Global burden of 87 risk factors in 204 countries and territories, 1990–2019: a systematic analysis for the Global Burden of Disease Study 2019. Lancet 2020; 396: 1223-1249. DOI: https://doi.org/10.1016/S0140-6736(20)30752-2
Olofin I, McDonald CM, Ezzati M, et al. Associations of Suboptimal Growth with All‐Cause and Cause‐ Specific Mortality in Children under Five Years: A Pooled Analysis of Ten Prospective Studies. PLOS ONE 2013; 8: e64636