BACKGROUND: Identifying severe, life-threatening falciparum malaria in African children allows for the prompt institution of appropriate management. In the past 2 decades, hyperlactatemia and acidosis have been identified as being associated with mortality in patients with severe malaria, but measurement of blood lactate concentration and base excess is expensive and technically demanding. In this large, prospective study, we examined the prognostic value of acidosis and hyperlactatemia and compared these markers to clinically assessed variables. METHODS: We examined several clinical and laboratory measurements as prognostic markers of mortality in 14,605 parasitemic children admitted to 3 hospitals in Africa. Whole-blood lactate concentration and acid/base status were used to identify subjects who had hyperlactatemia and acidosis. RESULTS: Using cut-points established by sensitivity and specificity curves, the sensitivities and positive predictive values for both lactate concentration and base excess were low, the specificities were moderate, and the negative predictive values were high (>97%). No reliable clinical surrogates for hyperlactatemia or acidosis were identified. Addition of lactate concentration and base excess to predictive models with previously identified clinical features (Blantyre Coma Score, deep breathing, prostration, and weight-for-age Z score) and 1 laboratory measure (blood glucose level) did not appreciably improve models to predict mortality. CONCLUSIONS: Measurements of lactate concentration and acid/base balance are expensive to perform, and performance of the latter can be problematic. Severe falciparum malaria may be readily recognized in children at admission to hospitals in sub-Saharan Africa with use of simple, inexpensive means and does not require knowledge of lactate concentration and base excess.
BACKGROUND: Identifying severe, life-threatening falciparum malaria in African children allows for the prompt institution of appropriate management. In the past 2 decades, hyperlactatemia and acidosis have been identified as being associated with mortality in patients with severe malaria, but measurement of blood lactate concentration and base excess is expensive and technically demanding. In this large, prospective study, we examined the prognostic value of acidosis and hyperlactatemia and compared these markers to clinically assessed variables. METHODS: We examined several clinical and laboratory measurements as prognostic markers of mortality in 14,605 parasitemic children admitted to 3 hospitals in Africa. Whole-blood lactate concentration and acid/base status were used to identify subjects who had hyperlactatemia and acidosis. RESULTS: Using cut-points established by sensitivity and specificity curves, the sensitivities and positive predictive values for both lactate concentration and base excess were low, the specificities were moderate, and the negative predictive values were high (>97%). No reliable clinical surrogates for hyperlactatemia or acidosis were identified. Addition of lactate concentration and base excess to predictive models with previously identified clinical features (Blantyre Coma Score, deep breathing, prostration, and weight-for-age Z score) and 1 laboratory measure (blood glucose level) did not appreciably improve models to predict mortality. CONCLUSIONS: Measurements of lactate concentration and acid/base balance are expensive to perform, and performance of the latter can be problematic. Severe falciparum malaria may be readily recognized in children at admission to hospitals in sub-Saharan Africa with use of simple, inexpensive means and does not require knowledge of lactate concentration and base excess.
Authors: D Waller; S Krishna; J Crawley; K Miller; F Nosten; D Chapman; F O ter Kuile; C Craddock; C Berry; P A Holloway Journal: Clin Infect Dis Date: 1995-09 Impact factor: 9.079
Authors: Michael Hawkes; Robert Opika Opoka; Sophie Namasopo; Christopher Miller; Andrea L Conroy; Lena Serghides; Hani Kim; Nisha Thampi; W Conrad Liles; Chandy C John; Kevin C Kain Journal: Med Hypotheses Date: 2011-07-13 Impact factor: 1.538
Authors: Andrea L Conroy; Simon J Glover; Michael Hawkes; Laura K Erdman; Karl B Seydel; Terrie E Taylor; Malcolm E Molyneux; Kevin C Kain Journal: Crit Care Med Date: 2012-03 Impact factor: 7.598
Authors: Mayfong Mayxay; Ann M Taylor; Maniphone Khanthavong; Siamphay Keola; Tiengkham Pongvongsa; Samlane Phompida; Rattanaxay Phetsouvanh; Nicholas J White; Paul N Newton Journal: Trop Med Int Health Date: 2007-03 Impact factor: 2.622
Authors: Peter Gottfried Kremsner; Clarissa Valim; Michel A Missinou; Christopher Olola; Sanjeev Krishna; Saadou Issifou; Maryvonne Kombila; Lloyd Bwanaisa; Sadik Mithwani; Charles R Newton; Tsiri Agbenyega; Margaret Pinder; Kalifa Bojang; David Wypij; Terrie Taylor Journal: J Infect Dis Date: 2009-01-01 Impact factor: 5.226
Authors: Michael Hawkes; Andrea L Conroy; Robert O Opoka; Sophie Namasopo; W Conrad Liles; Chandy C John; Kevin C Kain Journal: Am J Trop Med Hyg Date: 2014-03-03 Impact factor: 2.345
Authors: Abdullah Al-Taiar; Shabbar Jaffar; Ali Assabri; Molham Al-Habori; Ahmed Azazy; Nagiba Al-Mahdi; Khaled Ameen; Brian M Greenwood; Christopher J M Whitty Journal: BMJ Date: 2006-10-21