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. 2019 Nov 26;9(11):e030793. doi: 10.1136/bmjopen-2019-030793

Table 3.

Summary of articles with models predicting mortality in adult severe malaria

N Study Year Period of participant recruitment Country Type of study Sample size Statistics used Name of model Method internal of validation Age profiles Sex
profiles
Outcome predicted Variables used Diagnostic properties External validation Use in clinical settings
Mortality
1 Wilairatana and Looareesuwan41 1995 July 1991 to
May 1993
Thailand Cohort 72 Validation of APACHE II model (Original APACHE II score use clinical judgement and physiological relationships to assign weightings) APACHE II score58 ROC analysis Mean age: 29.9 Females—33.3% Mortality in adult patients with cerebral falciparum malaria MAP, temperature, heart rate, respiratory rate, arterial pH, PaO2, haematocrit, WBC count, creatinine, sodium, potassium and Glasgow coma score Predicted mortality with 95.8% accuracy None NE
2 Dondorp et al17 2004 NC Vietnam Cohort 268 Logistic regression None Hosmer-Lemeshow goodness-of-fit test 15–79 years Females—19% Mortality in adults with severe falciparum malaria Plasma lactate, plasma strong anion gap and plasma creatinine AUROC: 0.81 None NE
3 Mishra et al24 2007 NC India Cohort 212 Linear regression MSA (malaria score for adults) Not done NC NC Mortality in adults with severe malaria severe anaemia, acute renal failure, respiratory distress, cerebral malaria Sensitivity: 89.9%, specificity: 70.6%, positive predictive value: 94.1% with cut-off of 5/10 Yes43 NE
MPS (malaria prediction score) Not done NC NC Mortality in severe malaria Age, serum creatinine level, haemoglobin level, cerebral malaria, presence of a pregnancy, use of a ventilator NE Yes43 NE
4 Hanson et al18 2010 June 2003 to May 2005 Bangladesh, India, Indonesia and Myanmar Retrospective analysis of a randomised control trial 789 Logistic regression CAM (coma acidosis malaria) score Hosmer-Lemeshow goodness-of-fit NC NC Mortality in adults with severe malaria Coma and acidosis (base deficit AUROC: 0.81 (95% CI 0.77 to 0.84) Yes59 NE
5 Mohapatra and Das26 2009 January 200 to December 2004 India Cohort study 2089 Logistic regression MSS (Malaria severity score) Hosmer-Lemeshow goodness-of-fit (internal validation by splitting data—2089 vs 509) 18–71 years Female—34.6% Mortality in adult patients with severe falciparum malaria Neurological, renal, haematological, hepatic, respiratory, cardiovascular, and metabolic organ systems AUROC: 0.9 None NE
6 Newton et al29 2013 1986–2002 Thailand Retrospective analysis 988 Logistic regression MPI (malaria prognostic index) ROC curve analysis and internal validation by data splitting 15–74 years Females—43% Mortality in adult severe falciparum malaria Glasgow coma scale, parasitaemia, plasma lactate, serum bilirubin, pigmented parasites and treatment with ACT AUROC: 0.97 None NE
7 Mohapatra et al25 2014 NC India Cohort 112 NC GCBRS (GCS, creatinine, respiratory rate, bilirubin and systolic BP) score NC Mean: 35.8±15.1 years Females—16.1 Mortality in severe falciparum malaria Cerebral malaria, renal failure, respiratory distress, jaundice and shock Sensitivity: 85.3%. Specificity: 95.6% None NE
8 Hanson et al19 2014 1996–2013 Bangladesh, India, Indonesia, Vietnam and Myanmar Randomised control trials and cohort studies 1801 Logistic regression None Hosmer-Lemeshow goodness-of-fit 21–45 Females—24.4 48 hours survival and survival to discharge in patients with severe malaria Shock, oligo-anuria, dysglycaemia, respiratory rate, Glasgow Coma Score and absence of fever PPV for 48 hour-survival: 99.4% (95% CI 97.8 to 99.9). PPV for survival to discharge: 96.9% (95% CI 94.3 to 98.5) None NE

ACT, artemisinin combined therapy;AUROC, area under the receiver operating curve; NC, not clear; NE, no evidence; PPV, positive predictive value; WBC, white blood cells.