Table 1.
HD | EBOV_S | P value | |
---|---|---|---|
No. of participants | 39 | 35 | N/A |
Median age (years) | 25 [21–36] | 30 [25–36] | 0.2 |
Sex (male) | 31 (80%) | 19 (54%) | 0.03 |
Median time from ETC discharge to inclusion (months) | N/A | 23 [19–25] | N/A |
EBOV RT-PCRa | N/A | Negative (100%) | |
Clinical eventsb | |||
All symptoms | N/A | 23 (66%) | N/A |
Joint pain | N/A | 13 (37%) | N/A |
Fatigue | N/A | 12 (34%) | N/A |
Ocular disorders | N/A | 6 (17%) | N/A |
Headache | N/A | 6 (17%) | N/A |
Muscle pain | N/A | 5 (14.3%) | N/A |
Fever | N/A | 4 (11.4%) | N/A |
Abdominal pain | N/A | 2 (5.7%) | N/A |
Anorexia | N/A | 1 (2.8%) | N/A |
The differences between healthy donors (HDs) and survivors (EBOV_S) were evaluated in nonparametric Mann–Whitney U tests or χ2 test. Median values ± IQR are shown. Source data are provided as a Source Data file.
aBlood samples were taken from patients enrolled in the Postebogui cohort. Before PBMC and serum freezing, EBOV RT-PCR was performed on each sample to exclude the presence of EBOV in the blood.
bSymptoms and findings on physical examination for the EBOV_S on inclusion in the Postebogui cohort.