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Published in final edited form as: N Engl J Med. 2024 Jul 18;391(3):285–287. doi: 10.1056/NEJMc2313183

Sudan Virus Disease among Health Care Workers, Uganda, 2022

Abdullah Wailagala 1, Paul W Blair 2, Kenneth Kobba 3, Kayiira Mubaraka 4, Hellen Aanyu-Tumukahebwa 5, Daniel Kiiza 6, Musoke T Sekikongo 7, John D Klena 8, Peter Waitt 9, Rony R Bahatungire 10, Henry S Kyobe 11, Diana Atwine 12, Alex Adaku 13, Bodo Bongomin 14, Bruce Kirenga 15, Amy Boore 16, Danielle V Clark 17, David Kaggwa 18, Melissa Gregory 19, Wilberforce Kabweru 20, Willy Kayondo 21, Stacy K Mbabazi 22, Hannah Kibuuka 23, Ivan Kimuli 24, Sophie Mulei 25, Michael Mutegeki 26, Batibwe Emmanuel 27, Henry Mwebesa 28, Prossy Naluyima 29, Stephen Okello 30, Alex Tumusiime 31, Joel Montgomery 32, Vamsi Vasireddy 33, Charles Olaro 34, Misaki Wayengera 35, Mohammed Lamorde 36
PMCID: PMC11997613  NIHMSID: NIHMS2063280  PMID: 39018540

To the Editor:

Infections among health care workers represented a high proportion of cases during the first weeks of the 2022 Ebola outbreak in Uganda.1 This Ebola outbreak, which was caused by Sudan virus, resulted in 19 infections in health care workers among 142 confirmed cases.1 Not only are health care workers vulnerable to infection, but cases that occur early after detection of an Ebola outbreak carry an increased risk of death2 as health systems scramble to set up well-functioning Ebola treatment units. Ethical priority for immediate and quality care of infected health care workers is buttressed by the need to minimize fear, burnout, and strikes among these workers, since such complications could ultimately lead to deaths among patients with or without Ebola disease.3

On September 20, 2022, Uganda declared an Ebola outbreak due to Sudan virus in the Mubende district. We report on seven health care workers who contracted Sudan virus disease, most likely through two nosocomial transmission events that occurred before the identification of the outbreak. On September 15, 2022, an exposure event occurred during an emergency exploratory laparotomy that was performed in a patient who was thought to have a perforated bowel (Figs. S1 through S3 in the Supplementary Appendix, available with the full text of this letter at NEJM.org). Unfortunately, this patient died during the procedure and is considered to have had a probable case of Sudan virus disease. The patient was found to be a member of the same household as the patient with the first confirmed case of Sudan virus disease in this outbreak. All five of the providers in the operating room were infected (Patients A1 through A5 in Table 1) and were subsequently admitted to the Fort Portal Regional Referral Hospital (FPRRH) Isolation Unit in western Uganda.

Table 1.

Epidemiologic and Clinical Characteristics of the Patients.*

Patient No. Age in Yr (Sex) Suspected Exposure Incubation Period Initial Symptoms Diagnostic Plasma Ct Clinical Laboratory Abnormalities during Hospitalization Ultrasound Abnormalities Complications Outcome
Peak Creatinine Peak Proteinuria Peak Liver AST/ALT Platelet-Count Nadir
days mg/dl U/liter ×10−3/μl
A1 37 (M) Exploratory laparotomy 2 Myalgias, arthralgias, and subjective fever 22.6 NA NA NA NA NA Respiratory failure Death
A2 27 (M) Exploratory laparotomy 3 Malaise and subjective fever 29.1 1.2 Severe 528/175 84.3 Discrete and thick B lines with irregular pleural lines, small pericardial effusion Low oxygen saturation leading to provision of supplemental oxygen Discharge
A3 58 (F) Exploratory laparotomy 3 Generalized weakness, back pain, and arthralgias 22.9 10.4 Severe >2000/461 148.4 Discrete B lines, hyperdynamic LV function, >50% IVC collapsibility Respiratory failure, renal failure, liver failure, encephalopathy Death
A4 39 (M) Exploratory laparotomy 2 Back pain and progressive generalized weakness 28.1 1.0 Trace 97/65 183.5 Small subpleural consolidation Low oxygen saturation leading to provision of supplemental oxygen Discharge
A5 39 (M) Exploratory laparotomy 3 Loose stools, subjective fevers, and diaphoresis 21.5 15.3 Moderate 227/53 139.9 Discrete B lines Renal failure Discharge
B1 25 (M) Care of child with probable SVD 2 Mild headache, generalized weakness, and subjective fever 38.1 0.8 NA 41/49 293.8 Discrete B lines with one area with an irregular pleural line None Discharge
C1 34 (M) Care of Patient B1 4–7 Mild headache and generalized weakness 23.0 0.8 Trace 759/375 72.3 Discrete B lines with one area with an irregular pleural line None Discharge
*

The seven health care workers included two medical students, two assistant surgeons, two house officers, and an anesthetist. ALT denotes alanine aminotransferase, AST aspartate aminotransferase, Ct cycle threshold, IVC inferior vena cava, LV left ventricular, NA not available, and SVD Sudan virus disease.

The FPRRH Isolation Unit was established in 2017 to support therapeutic trials against filoviruses and continues to be used for clinical research focused on sepsis.4 The symptoms and complications among the health care workers with Sudan virus disease were similar to those described for Ebola virus disease (Table 1 and Figs. S4 and S5). Influenza-like illness was followed by severe diarrheal disease and multiorgan failure among the patients with severe cases. Lung and cardiac ultrasonography informed the choice of fluid resuscitation volumes among the patients with respiratory failure (Fig. S6). Six of the seven infected health care workers received remdesivir on a compassionate-use basis at 5 to 13 days after symptom onset. One of the infected health care workers received a combination of the investigational antibody product MBP1345 with remdesivir at 5 days after symptom onset, had abatement of symptoms and improvement in laboratory measures, and survived. No cases of secondary transmission occurred at the FPRRH Isolation Unit. Five of the seven infected health care workers survived to discharge.

Supplementary Material

Supplemental material

Acknowledgments

In-kind support in the form of clinical and laboratory equipment was provided by the Henry M. Jackson Foundation for the Advancement of Military Medicine.

Footnotes

Disclosure forms provided by the authors are available with the full text of this letter at NEJM.org.

A complete list of authors is available with the full text of this letter at NEJM.org.

The contents of this letter are the sole responsibility of the authors and do not necessarily reflect the views, assertions, opinions, or policies of the Henry M. Jackson Foundation for the Advancement of Military Medicine, the U.S. Department of Defense, the U.S. government, or any other government or agency. Mention of trade names, commercial products, or organizations does not imply endorsement by the U.S. government. The investigators have adhered to the policies for protection of human subjects as prescribed in 45 CFR 46.

Contributor Information

Abdullah Wailagala, Makerere University Infectious Diseases Institute Kampala, Uganda

Paul W. Blair, Vanderbilt University Medical Center Nashville, TN

Kenneth Kobba, Makerere University Infectious Diseases Institute Kampala, Uganda

Kayiira Mubaraka, Makerere University Infectious Diseases Institute Kampala, Uganda

Hellen Aanyu-Tumukahebwa, Mulago National Specialised Hospital Kampala, Uganda

Daniel Kiiza, Makerere University Infectious Diseases Institute Kampala, Uganda

Musoke T. Sekikongo, Mulago National Specialised Hospital Kampala, Uganda

John D. Klena, Centers for Disease Control and Prevention Atlanta, GA

Peter Waitt, Makerere University Infectious Diseases Institute Kampala, Uganda

Rony R. Bahatungire, Uganda Ministry of Health Kampala, Uganda

Henry S. Kyobe, Uganda Ministry of Health Kampala, Uganda

Diana Atwine, Uganda Ministry of Health Kampala, Uganda

Alex Adaku, Fort Portal Regional Referral Hospital Fort Portal, Uganda

Bodo Bongomin, World Health Organization Uganda Kampala, Uganda

Bruce Kirenga, Makerere University Lung Institute Kampala, Uganda

Amy Boore, Centers for Disease Control and Prevention Entebbe, Uganda

Danielle V. Clark, Henry M. Jackson Foundation for the Advancement of Military Medicine Bethesda, MD

David Kaggwa, World Health Organization Uganda Kampala, Uganda

Melissa Gregory, Henry M. Jackson Foundation for the Advancement of Military Medicine Bethesda, MD

Wilberforce Kabweru, Mulago National Specialised Hospital Kampala, Uganda

Willy Kayondo, Makerere University Walter Reed Project Kampala, Uganda

Stacy K. Mbabazi, Makerere University Infectious Diseases Institute Kampala, Uganda

Hannah Kibuuka, Makerere University Walter Reed Project Kampala, Uganda

Ivan Kimuli, Mulago National Specialised Hospital Kampala, Uganda

Sophie Mulei, Uganda Virus Research Institute Entebbe, Uganda

Michael Mutegeki, Uganda Ministry of Health Kampala, Uganda

Batibwe Emmanuel, Mubende Regional Referral Hospital Mubende, Uganda

Henry Mwebesa, Uganda Ministry of Health Kampala, Uganda

Prossy Naluyima, Makerere University Walter Reed Project Kampala, Uganda

Stephen Okello, Makerere University Walter Reed Project Kampala, Uganda

Alex Tumusiime, Uganda Virus Research Institute Entebbe, Uganda

Joel Montgomery, Centers for Disease Control and Prevention Atlanta, GA

Vamsi Vasireddy, Walter Reed Army Institute of Research Bethesda, MD

Charles Olaro, Uganda Ministry of Health Kampala, Uganda

Misaki Wayengera, Uganda Ministry of Health Kampala, Uganda

Mohammed Lamorde, Makerere University Infectious Diseases Institute Kampala, Uganda

References

  • 1.World Health Organization–Uganda, Republic of Uganda Ministry of Health. Ebola virus disease: situation report 93. January 2023. (https://www.afro.who.int/sites/default/files/2023-01/Ug_EVD_SitRep%2393.pdf).
  • 2.Garske T, Cori A, Ariyarajah A, et al. Heterogeneities in the case fatality ratio in the West African Ebola outbreak 2013–2016. Philos Trans R Soc Lond B Biol Sci 2017;372:372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Evans DK, Goldstein M, Popova A. Health-care worker mortality and the legacy of the Ebola epidemic. Lancet Glob Health 2015;3(8):e439–e440. [DOI] [PubMed] [Google Scholar]
  • 4.Martins KA, Ayebare RR, Bhadelia N, et al. Pre-positioned outbreak research: the joint medical emerging diseases intervention clinical capability experience in Uganda. Health Secur 2020;18:114–24. [DOI] [PubMed] [Google Scholar]
  • 5.Wec AZ, Bornholdt ZA, He S, et al. Development of a human antibody cocktail that deploys multiple functions to confer panEbolavirus protection. Cell Host Microbe 2019;25(1):39–48.e5. [DOI] [PMC free article] [PubMed] [Google Scholar]

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