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
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
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