Volume 24, Number 2—February 2018
Research
Development of a Pediatric Ebola Predictive Score, Sierra Leone1
Table 1
Characteristic |
All children,
no. (%) or median (IQR) |
EVD negative | EVD positive | p value |
|||
---|---|---|---|---|---|---|---|
No./no. available or median (IQR) |
% (95% CI) |
No./no. available or median (IQR) |
% (95% CI) |
||||
Total† |
1,006 (100) |
697 |
69 |
309 |
31 |
– |
|
Sex | |||||||
F | 512 (51) | 348/697 | 50 (46–54) | 164/309 | 47 (41–53) | 0.357 | |
M |
494 (49) |
349/697 |
50 (46-54) |
145/309 |
53 (47–59) |
0.380 |
|
Median age, y (IQR) | 4 (1.3–8) | 3 (1–7) | – | 6 (3–10) | – | <0.001 | |
Age 0–2 y | 392 (39) | 336/697 | 48 (44–52) | 56/309 | 18 (14–23) | <0.001 | |
Positive contact, n = 754‡ |
275 (36) |
108/541 |
20 (17–24) |
167/213 |
78 (72–84) |
<0.001 |
|
Days from symptoms to EHU admission, n = 772 | 2 (1–4) | 2 (1–3) | – | 3 (2–4) | – | 0.001 | |
Admitted with caregiver, n = 822 |
822 (82) |
516/621 |
83 (80–86) |
127/201 |
63 (56–70) |
<0.001 |
|
Signs/symptoms§ | |||||||
Fever, n = 787 | 740 (94) | 528/566 | 93 (91–95) | 212/221 | 96 (92–98) | 0.160 | |
Fatigue/weakness, n = 587 | 568 (97) | 393/407 | 97 (94–98) | 175/180 | 97 (94–99) | 0.676 | |
Vomiting/nausea, n = 777 | 472 (61) | 345/556 | 62 (58–66) | 127/221 | 57 (51–64) | 0.238 | |
Diarrhea, n = 763 | 351 (46) | 252/548 | 46 (42–50) | 99/215 | 46 (39–53) | 0.988 | |
Conjunctivitis, n = 669 | 152 (23) | 73/463 | 16 (13–19) | 79/206 | 38 (32–45) | <0.001 | |
Anorexia, n = 779 | 621 (80) | 452/560 | 81 (77–84) | 169/219 | 77 (71–83) | 0.269 | |
Abdominal pain, n = 594 | 269 (45) | 155/392 | 40 (35–45) | 114/202 | 56 (49–63) | <0.001 | |
Muscle pain, n = 577 | 212 (21) | 127/377 | 34 (29–39) | 85/200 | 43 (36–50) | 0.037 | |
Joint pain, n = 569 | 192 (34) | 102/368 | 28 (23–33) | 90/201 | 45 (38–52) | <0.001 | |
Headache, n = 598 | 370 (62) | 256/397 | 65 (60–69) | 114/201 | 57 (50–64) | 0.065 | |
Difficulty breathing, n = 738 | 199 (27) | 169/533 | 32 (28–36) | 30/205 | 15 (10–20) | <0.001 | |
Difficulty swallowing, n = 687 | 177 (26) | 130/481 | 27 (23–31) | 47/206 | 23 (17–29) | 0.247 | |
Rash, n = 728 | 98 (13) | 88/522 | 17 (14–20) | 10/206 | 5 (2–9) | <0.001 | |
Cough, n = 587 | 70 (12) | 57/407 | 14 (11–18) | 13/180 | 7 (4–12) | 0.019 | |
Hiccups, n = 723 | 62 (9) | 52/519 | 10 (8–13) | 10/204 | 5 (2–9) | 0.027 | |
Unexplained bleeding, n = 726 |
22 (3) |
19/518 |
4 (2–6) |
3/208 |
1 (0–4) |
0.114 |
|
Treatment¶ | |||||||
Antimicrobial drug, n = 657 | 556 (85) | 407/494 | 82 (79–86) | 149/163 | 91 (86–95) | 0.006 | |
Antimalarial drug, n = 657 | 567 (86) | 416/494 | 84 (81–87) | 151/163 | 93 (87–96) | 0.007 | |
IV treatment |
115 (11) |
101/697 |
14 (12–17) |
14/309 |
5 (2–7) |
<0.001 |
|
Malaria RDT+, n = 74 | 33 (45) | 31/57 | 54 (41–68) | 2/17 | 12 (15–36) | 0.002 | |
Median days of EHU stay# | 2 (1–3) | 2 (1–2) | – | 2 (1–3) | – | <0.001 |
*n values and denominators indicate no. children with recorded data available for variable (i.e., for binary variables children with neither “yes” nor “no” populated in their source notes were not included in the denominator, and for the median days symptoms to EHU admission variable those without date of start of symptoms were not included). EHU, Ebola holding unit; EVD, Ebola virus disease; RDT, rapid diagnostic test.
†z-test of proportions, comparing whether the proportion of children with the variable was the same for EVD-negative and EVD-positive children (apart from numerical variables, for which a Wilcoxon rank-sum test was performed to test the hypothesis that the distribution of the variable was the same for EVD-negative and EVD-positive children).
‡Total no. children admitted to holding units with test results available.
§Recorded on presentation at EHU.
¶At EHU.
#Time from EHU admission until death, discharge, or transfer.
1Preliminary results from this study were presented at the 26th European Congress of Clinical Microbiology and Infectious Diseases, Amsterdam, Netherlands, April 9–12, 2016; and the 34th Annual Meeting of the European Society for Pediatric Infectious Diseases, Brighton, UK, May 10–14, 2016.
2These authors contributed equally to this article.