Introduction Hematocrit, an essential indicator of blood health, is significantly affected in patients co-infected with HIV and malaria. This review delves into how co-infection impacts hematocrit levels, complicating disease progression and clinical outcomes in endemic regions.
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In HIV patients, hematocrit fluctuations are common due to anemia induced by immune dysregulation and opportunistic infections. Antiretroviral therapy (ART) improves hematocrit levels by suppressing viral load and reducing inflammation; however, certain ART drugs may negatively affect bone marrow function.
Malaria infection leads to a drop in hematocrit due to red blood cell destruction by Plasmodium parasites. Severe malaria cases show marked decreases in hematocrit, indicative of anemia. Hematocrit recovery post-treatment reflects effective parasite clearance and red blood cell restoration.
The combined effects of HIV and malaria further reduce hematocrit, intensifying anemia in co-infected individuals. Immune modulation, including increased cytokine release, exacerbates red blood cell destruction. Monitoring hematocrit levels in co-infected patients provides insights into disease severity and guides treatment.
Regular hematocrit monitoring is crucial for managing anemia in HIV-malaria co-infection. Addressing hematocrit fluctuations through targeted therapies, including ART and antimalarial drugs, can help mitigate complications and improve outcomes. Preventative measures, such as malaria prophylaxis, are essential for at-risk populations.
Hematocrit levels serve as a vital indicator in co-infected patients, where fluctuations reflect the impact of both infections. A multidisciplinary approach integrating ART, antimalarial therapies, and hematocrit monitoring is recommended to manage the complex dynamics of HIV-malaria co-infection.
Journal article: Obeagu EI, Okwuanaso CB, Edoho SH, Obeagu GU. Under-nutrition among HIV-exposed Uninfected Children: A Review of African Perspective. Madonna University Journal of Medicine and Health Sciences. 2022; 2(3):120-127.
Summary by Faith Oluwamakinde