The effect of HIV and mpox co‐infection on clinical outcomes: Systematic review and meta‐analysis

Author:

Taha Amira Mohamed1,Elrosasy Amr2ORCID,Mahmoud Abdelrahman Mohamed3,Saed Sara Adel Abdelkader45,Moawad Wesam Abd El‐Tawab56,Hamouda Esraa37,Nguyen Dang8,Tran Van Phu9,Pham Hoang Tran10,Sah Sanjit1112,Barboza Joshuan J.13,Sah Ranjit714

Affiliation:

1. Faculty of Medicine Fayoum University Fayoum Egypt

2. Faculty of Medicine Cairo University Cairo Egypt

3. Faculty of Medicine Menoufia University Menoufia Egypt

4. Department of Clinical Pharmacy MOH Cairo Egypt

5. MARS Global London UK

6. Faculty of Pharmacy (Girls) Al‐Azhar University Cairo Egypt

7. Department of Microbiology, Tribhuvan University Teaching Hospital Institute of Medicine Kathmandu Nepal

8. Massachusetts General Hospital, Corrigan Minehan Heart Center Harvard Medical School Boston Massachusetts USA

9. Tra Vinh University Tra Vinh Vietnam

10. Pham Ngoc Thach University of Medicine Ho Chi Minh City Vietnam

11. Research Scientist, Global Consortium for Public Health and Research, Datta Meghe Institute of Higher Education and Research Jawaharlal Nehru Medical College Wardha India

12. SR Sanjeevani Hospital Siraha Nepal

13. Escuela de Medicina Universidad Cesar Vallejo Trujillo Peru

14. Department of Microbiology Dr. D. Y. Patil Medical College, Hospital and Research Centre, Dr. D. Y. Patil Vidyapeeth Pune India

Abstract

AbstractIntroductionCo‐infection with HIV and mpox is a significant issue for public health because of the potential combined impact on clinical outcomes. However, the existing literature lacks a comprehensive synthesis of the available evidence. The purpose of this meta‐analysis is to provide insight into the impact of HIV and mpox co‐infection on clinical outcomes.MethodsWe systematically searched major electronic databases (PubMed, Embase, Cochrane Central, and Web of Science) for pertinent studies published up to June 2023. Included were studies that described the clinical outcomes of people who had both mpox and HIV. We performed the analysis using OpenMeta and STATA 17 software.ResultsWith an overall number of participants of 35 207, 21 studies that met the inclusion criteria were considered. The greatest number of the studies (n = 10) were cohort designs, with three being cross‐sectional and eight being case series studies. The meta‐analysis found that people who had both HIV and mpox had a higher hospitalization rate than those who only had mpox (odds ratio [OR] 1.848; 95% confidence interval [CI] 0.918–3.719, p = 0.085, I2 = 60.19%, p = 0.020). Furthermore, co‐infected patients had higher mortality rates than those who did not have HIV co‐infection (OR 3.887; 95% CI 2.272–6.650, p < 0.001). Meta‐regression analysis showed that CD4 levels can significantly predict the risk of hospitalization (p = 0.016) and death (p = 0.031).DiscussionHIV causes immunosuppression, making it difficult for the body to mount an effective immune response against pathogens such as mpox. Individuals who are co‐infected are at a higher risk of severe disease and death, according to our findings. Although hospitalization rates did not differ significantly between the two groups, it is critical to prioritize interventions and improve management strategies tailored specifically for people living with HIV.ConclusionThis meta‐analysis provides substantial evidence that HIV and mpox co‐infection has a negative impact on clinical outcomes. Co‐infected individuals had higher hospitalization and significantly higher mortality rates. These findings highlight the significance of early diagnosis, prompt treatment initiation, and effective management strategies for people living with HIV and mpox.

Publisher

Wiley

Reference44 articles.

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2. CDC.2022 Mpox Outbreak Global Map.2022https://www.cdc.gov/poxvirus/mpox/response/2022/world-map.html(accessed: September 2023)

3. Clinical features and management of human monkeypox: a retrospective observational study in the UK

4. Human Monkeypox

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