Abstract

Co-infection with falciparum malaria and leptospirosis is uncommon. The aim of this study is to report a case of severe sepsis secondary to dual infection with falciparum malaria and leptospirosis. The literature is also reviewed on the clinical course of such co-infections, and the possible mechanisms and treatment of patients with life-threatening malaria and leptospirosis with activated protein C. The patient was a 25-year old male admitted in the Respiratory Intensive Care Unit (RICU) with fever, haemolysis, acute renal failure, hepatitis, acute lung injury (ALI) and altered sensorium. A syndromic evaluation was done and investigations revealed falciparum parasitaemia. He was treated with parenteral artesunate, ceftriaxone and doxycycline, and adjunctive therapies as for severe sepsis. Infusion of activated protein C was started 20 hours after onset of organ dysfunction, and intensive haemodialysis was instituted. Over the next four days the patient became afebrile with progressive resolution of ALI, renal failure and hepatitis. His Leptospira serology (requested as part of the evaluation) was reported positive on day 5. Dual infections are common and under-recognized in the tropics. Failure to treat potential co-infections may lead to poor outcomes. Acute lung injury in falciparum malaria has high mortality rates and therapy as for severe sepsis may improve survival. Adjunctive therapies, including activated protein C, cannot replace source eradication.

Highlights

  • The world-wide distribution of malaria [1] overlaps with that of other infectious diseases, including leptospirosis

  • Clinical features are unreliable to separate single from dual infections because of the markedly similar clinical syndrome

  • Patients with dual infections have a severe clinical presentation and their clinical course may be worsened by lack of appropriate therapy for both [2,3]

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Summary

Introduction

The world-wide distribution of malaria [1] overlaps with that of other infectious diseases, including leptospirosis. Co-infection of malaria with a wide variety of infectious diseases has been reported. Patients with dual infections have a severe clinical presentation and their clinical course may be worsened by lack of appropriate therapy for both [2,3]. Patients with severe falciparum malaria, especially those with acute lung injury, have a high mortality rate. Falciparum malaria is due to sequestration of parasites in visceral capillaries with endothelial dysfunction and leptospirosis is an infectious vasculitis; as a result, therapies which improve endothelial function might positively impact the clinical outcomes of both diseases. Newer adjuncts are needed because of the present high mortality rates and the limited benefit conferred by current ancillary therapies. Activated protein C (aPC) has anti-thrombotic, pro-fibrinolytic and anti-inflammatory properties and confers a relative mortality reduction of 22% in patients with severe sepsis and (page number not for citation purposes)

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