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Volume 30, Number 4—April 2024
CME ACTIVITY - Research

Deaths Associated with Pediatric Hepatitis of Unknown Etiology, United States, October 2021–June 2023

Olivia Almendares1Comments to Author , Julia M. Baker1, David E. Sugerman, Umesh D. Parashar, Sarah Reagan-Steiner, Hannah L. Kirking, Paul A. Gastañaduy, Jacqueline E. Tate, and Hepatitis of Unknown Etiology Group2
Author affiliation: Centers for Disease Control and Prevention, Atlanta, Georgia, USA

Main Article

Table 3

Clinical and demographic characteristics of 8 children with hepatitis of unknown etiology, United States, October 1, 2021–June 6, 2023 *

Characteristic Value
Demographic characteristics
Age
Median age (range) 2.4 (0.2–6.3)
0–11 mo 2 (25.0)
1–2 y 4 (50.0)
3–9 y 2 (25.0)
Sex
F 3 (37.5)
M 5 (62.5)
Race/ethnicity
Hispanic or Latino 5 (62.5)
Black, non-Hispanic 2 (25.0)
White, non-Hispanic
1 (12.5)
Clinical characteristics
Underlying conditions at initial visit
Immunocompromised† 2 (25.0)
Comorbidities that may have increased risk for hepatitis‡ 2 (25.0)
No underlying conditions 4 (50.0)
Reported signs and symptoms§
Respiratory 6/8 (75.0)
Gastrointestinal 7/8 (87.5)
Hepatic 8/8 (100.0)
Systemic 7/8 (87.5)
Laboratory findings
Highest alanine transaminase, median (range), U/L 4,852 (219–5,648)
Highest aspartate aminotransferase, median (range), U/L 7,500 (786–10,000)
Highest total bilirubin, median (range), mg/dL 13.7 (1.3–19.4)
Highest international normalized ratio, median (range) 8.0 (1.4–13.0)
Highest ammonia, median (range), µmol/L
126.0 (60.3–801.0)
Duration of symptoms before admission, d
Median (range) 7 (1–36)
0–7 5 (62.5)
8–14 1 (12.5)
>15 2 (25.0)
Duration of hospital stay, d
Median (range) 14.5 (<1– 18)
0–2 2 (25.0)
3–14 2 (25.0)
>15 4 (50.0)
Physical findings
Hepatomegaly 5/8 (62.5)
Hepatic encephalopathy 4/8 (50.0)
Splenomegaly 2/7 (28.6)
Ascites 3/7 (42.9)
Outcomes¶
Acute liver failure 7 (87.5)
Liver transplant 2 (25.0)

*Values are no. (%) except as indicated. †Immunocompromised at the time of initial presentation. One child immunosuppressed due to ongoing cancer treatment. One child immunocompromised due to a liver transplant. ‡One child was small for gestational age and 1 child had a history of poor weight gain and possible gastrointestinal disorder. §Symptoms are not mutually exclusive; all children reported multiple symptoms. Respiratory signs/symptoms include cough, congestion, runny nose, shortness of breath, conjunctivitis, sore throat, or wheezing. Gastrointestinal signs/symptoms include diarrhea, nausea, vomiting, or abdominal pain. Hepatitis signs/symptoms include dark colored urine, pale stool, jaundice, or scleral icterus. Systemic signs/symptoms include fatigue, decreased appetite, or fever. See Appendix Table 2 for data by patient. ¶Not mutually exclusive. Acute liver failure was defined based on documentation written in the medical chart or medical chart abstraction indicating acute liver failure occurred.

Main Article

1These authors contributed equally to this article.

2Members of the group are listed at the end of this article.

Page created: March 12, 2024
Page updated: March 19, 2024
Page reviewed: March 19, 2024
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
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