Prospective Clinical Surveillance for Severe Acute Respiratory Illness in Kenyan Hospitals during the COVID-19 pandemic

Ruth Khadembu Lucinde, Henry Gathuri, Lynda Isaaka, Morris Ogero, Livingstone Mumelo, Dennis Kimego, George Mbevi, Conrad W Wanyama, Edwin Onyango Otieno, Stella Mwakio, Metrine Saisi, ELizabeth Isinde, Irene Njeri Oginga, Alvin Wachira, Evans Manuthu, Hazel Kariuki, Jared Nyikuli, Cyprian Wekesa, Amos Otedo, Hannah Bosire, Steve Biko Okoth, Winston Ongalo, David Mukabi, Wilber Lusamba, Beatrice Muthui, Isaac Adembesa, Caroline W Mithi, Mohammed Sood, Nadia Aliyan, Bernard Gituma, Matiko Giabe, Charles Omondi,Rashid Aman,Patrick Amoth,Kadondi Kasera,Fred Were, Wangari Nganga,James A Berkley, Benjamin A Tsofa, Joseph Mwangangi, Phillip Bejon, Edwine Barasa,Mike English, J Anthony G Scott, Samuel Akech, E Wangeci Kagucia, Ambrose Agweyu, Anthony O Etyang

medrxiv(2024)

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摘要
There are limited data from sub–Saharan Africa describing the pattern of admissions to public hospitals with severe acute respiratory infections during the COVID–19 pandemic. We conducted a prospective longitudinal hospital-based sentinel surveillance between May 2020 and December 2022 at 16 public hospitals in Kenya. All patients aged above 18 years admitted to adult medical wards in the participating hospitals were included. Demographic and clinical characteristics, COVID–19 infection and vaccination status and outcome data were collected. Of the 52,714 patients included in the study, 18,001 (35%) were admitted with severe acute respiratory illness (SARI). The mean age was 51 years. Patients were equally distributed across sexes. Pneumonia was the most common diagnosis at discharge. Hypertension, HIV and diabetes mellitus were the most common comorbidities. COVID–19 test results were positive in 2,370 (28%) of the 8,517 (47%) patients that underwent testing. Overall inpatient case fatality for SARI was 21% (n=3,828). After adjusting for age, sex and presence of a comorbidity, SARI patients had higher inpatient mortality compared to non-SARI patients regardless of their COVID–19 status (aHR 1.31, 95% CI 1.19 – 1.46). COVID–19 positive SARI patients had a higher inpatient mortality rate compared to their negative counterparts (aHR 1.31, 95% CI 1.12 – 1.54, p value < 0.0001). COVID-19 vaccine effectiveness against mortality due to SARI after adjusting for age, sex and presence of a comorbidity was 34% (95% CI 11% – 51%). We have provided a comprehensive description of the pattern of admissions with respiratory illnesses in Kenyan hospitals during the COVID–19 pandemic period. We have demonstrated the utility of routine surveillance activities within public hospitals in low-income settings which if strengthened can enhance the response to emerging health threats. ### Competing Interest Statement The authors have declared no competing interest. ### Funding Statement This project was funded by the Wellcome Trust (grants 20991/Z/20/Z and 203077/Z/16/Z), a DFID/MRC/NIHR/Wellcome Trust Joint Global Health Trials Award (MR/R006083/1) and The Bill & Melinda Gates Foundation (OPP1131320) ### Author Declarations I confirm all relevant ethical guidelines have been followed, and any necessary IRB and/or ethics committee approvals have been obtained. Yes The details of the IRB/oversight body that provided approval or exemption for the research described are given below: The Scientific and Ethical Review Unit (SERU) of the Kenya Medical Research Institute gave ethical approval for this work (KEMRI/CGMR-C/203/4085) The Oxford Tropical Research Ethics Committee of the University of Oxford gave approval for this work (OxTREC 44-20) The Research Ethics Committee of the London School of Hygiene and Tropical Medicine gave approval for this work (LEO 26950) I confirm that all necessary patient/participant consent has been obtained and the appropriate institutional forms have been archived, and that any patient/participant/sample identifiers included were not known to anyone (e.g., hospital staff, patients or participants themselves) outside the research group so cannot be used to identify individuals. Yes I understand that all clinical trials and any other prospective interventional studies must be registered with an ICMJE-approved registry, such as ClinicalTrials.gov. I confirm that any such study reported in the manuscript has been registered and the trial registration ID is provided (note: if posting a prospective study registered retrospectively, please provide a statement in the trial ID field explaining why the study was not registered in advance). Yes I have followed all appropriate research reporting guidelines, such as any relevant EQUATOR Network research reporting checklist(s) and other pertinent material, if applicable. Yes Data are available upon reasonable request
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