Table 3.
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.