Mohiuddin Chowdhury ATM, Kamal A, Abbas MKU, Karim MR, Ali MA, Talukder S, Hamidullah Mehedi HM, Hassan H, Shahin AH, Li Y, He S. Role of H2 receptor blocker famotidine over the clinical recovery of COVID-19 patients: A randomized controlled trial. World J Clin Cases 2022; 10(23): 8170-8185 [PMID: 36159508 DOI: 10.12998/wjcc.v10.i23.8170]
Corresponding Author of This Article
Shui-Xiang He, PhD, Professor, Department of Gastroenterology, The First Affiliated Hospital of Xi'an Jiaotong University, Yanta Road, Xi'an 710061, Shaanxi Province, China. dyyyjxk@mail.xjtu.edu.cn
Research Domain of This Article
Infectious Diseases
Article-Type of This Article
Clinical Trials Study
Open-Access Policy of This Article
This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
Table 2 Subgroup analysis according to sex and duration
Variables
Duration
Male (%)
Female (%)
Group A, ICU stay
< 10 d (71)
51 (65.3)
n = 78
20 (76.9)
n = 26
11-20 d (30)
24 (30.76)
6 (23.1)
21-30 d (3)
3 (3.8)
0 (0)
≥ 31 d (0)
0 (0)
0 (0)
Group B, ICU stay
≤ 10 d (68)
55 (69.6)
n = 79
13 (52)
n = 25
11-20 d (25)
16 (20.2)
9 (36)
21-30 d (9)
8 (10.1)
1 (4)
≥ 31 d (2)
0 (0)
2 (8)
Group A (n = 101), duration of total hospital stays
≤ 10 d (51)
37 (47.4)
n = 78
14 (53.8)
n = 26
11-20 d (43)
33 (42.3)
10 (38.5)
21-30 d (10)
8 (10.3)
2 (7.7)
≥ 31 d (0)
0 (0)
0 (0)
Group B (n = 104), duration of total hospital stays
≤ 10 d (40)
31 (39.2)
n = 79
9 (36)
n = 25
11-20 d (49)
40 (50.6)
9 (36)
21-30 d (13)
8 (10.1)
5 (20)
≥ 31 d (2)
0 (0)
2 (8)
Group A (n = 78), time to clinical improvement
≤ 10 d (50)
31 (55.4)
n = 56
19 (86.3)
n = 22
11-20 d (24)
21 (37.5)
3 (13.6)
21-30 d (4)
4 (7.1)
0 (0)
Group B (n = 73), time to clinical improvement
≤ 10 d (21)
20 (32.7)
n = 61
1 (8.3)
n = 12
11-20 d (41)
34 (55.7)
7 (58.3)
21-30 d (11)
7 (11.4)
4 (33.3)
Group A (n = 78), recovered cases, duration of ICU stay
≤ 10 d (49)
33 (59)
n = 56
16
n = 22
11-20 d (27)
21 (37.5)
6
21-30 d (2)
2 (3.5)
0
≥ 31 d (0)
0 (0)
0
Group B (n = 73), recovered cases, duration of ICU stay
≤ 10 d (41)
37 (60)
n = 61
4 (33.3)
n = 12
11-20 d (24)
16 (17)
8 (66.6)
21-30 d (8)
8 (13)
0 (0)
≥ 31 d (0)
0 (0)
0 (0)
Group A (n = 26), expired cases; Time to clinical failure/death
≤ 10 d (1)
1 (4.5)
n = 22
0 (0)
n = 4
11-20 d (22)
18 (82)
4 (100)
21-30 d (3)
3 (13.5)
0 (0)
Group B (n = 31), expired cases, time to clinical failure/death
≤ 10 d (27)
18 (100)
n = 18
9 (70)
n = 13
11-20 d (1)
0 (0)
1 (7.5)
21-30 d (1)
0 (0)
1 (7.5)
> 31 d (2)
0 (0)
2 (15)
Group A (survived patients) (n = 78), time to symptomatic recovery
< 10 d (21)
20 (32.8)
n = 61
1 (8.3)
n = 12
11-20 d (41)
34 (55.7)
7 (58.3)
21-30 d (11)
7 (11.5)
4 (33.3)
> 31 d (0)
0 (0)
0 (0)
Group B (survived patients) (n = 73), time to symptomatic recovery
< 10 d (3)
3 (3.91)
n = 61
0 (0)
n = 12
11-20 d (45)
41 (67.2)
4 (33.3)
21-30 d (19)
12 (19.7)
7 (58.3)
>31 d (6)
5 (8.1)
1 (8.3)
Group A (n = 78) time to negative PCR recovery
11-20 d (41)
n = 56
n = 22
21-30 d (32)
31-40 d (5)
Group B (survived patients) (n = 73), time to negative PCR recovery
11-20 d (26)
n = 61
n = 12
21-30 d (35)
31-40 d (12)
Group A (n = 78), CT chest involvement on admission
< 20%
26 (46.4)
n = 56
15 (68.2)
n = 22
21%-40%
16 (28.6)
5 (22.7)
41%-60%
11 (19.6)
2 (9.0)
> 61%
3 (5.3)
0 (0)
Group B (n = 73), CT chest involvement on admission
< 20
26 (42.6)
n = 61
3 (25)
n = 12
21-40
22 (36)
7 (58.3)
41-60
13 (21.3)
1 (8.3)
> 61
0 (0)
1 (8.3)
Group A (n = 78), CT chest involvement during discharge
< 20
47 (83.9)
n = 56
16 (72.7)
n = 22
21-40
9 (16)
6 (12.2)
Group B (n = 73), CT chest involvement during discharge
< 20
47 (77)
n = 61
8 (36.4)
n = 12
21-40
14 (23)
4 (33.3)
Group A (n = 78), chest CT improvement
< 20
44 (74.6)
n = 56
19 (86.6)
n = 22
21-40
5 (8.5)
3 (13.6)
41-60
7 (11.9)
0 (0)
Group B (n = 73), CT improvement
< 20
54 (88.5)
n = 61
10 (83.3)
n = 12
21-40
4 (6.6)
1 (8.3)
41-60
3 (4.9)
1 (8.3)
Table 3 Analysis of the total duration of hospitalization and intensive care unit stay against the age group
Variables
Age group (yr)
Group A (famotidine)
Group B (control)
1-10 d
11-20 d
21-30 d
> 31 d
1-10 d
11-20 d
21-30 d
> 31 d
Duration of hospital stay, group A (n = 104), group B (n = 104)
11-20
1
1
0
0
4
0
0
0
21-30
1
1
0
0
8
8
0
0
31-40
4
5
0
0
12
8
0
0
41-50
7
8
1
0
4
8
4
0
51-60
18
11
5
0
0
17
5
2
61-70
11
10
4
0
12
4
4
0
71-80
6
6
0
0
0
4
0
0
> 81
3
1
0
0
4
0
0
0
Total (%)
51 (49)
43 (41.5)
10 (9.5)
0 (0)
40 (38.5)
49 (47.1)
13 (12.5)
2 (1.9)
Duration of ICU stay, group A (n = 104), group B (n = 104)
11-20
2
0
0
0
4
0
0
0
21-30
2
0
0
0
12
4
0
0
31-40
6
3
0
0
20
0
0
0
41-50
8
8
0
0
12
0
4
0
51-60
23
10
1
0
8
13
1
2
61-70
17
6
2
0
12
4
4
0
71-80
9
3
0
0
0
4
0
0
> 81
4
0
0
0
4
0
0
0
Total (%)
71 (68)
30 (29)
3 (3)
0 (0)
68 (65.4)
25 (24)
9 (8.6)
2 (1.9)
Table 4 Subgroup analysis of the study group patients depending on age group
Age group (yr)
Total study population (%)
Over all (%)
Recovered patients (%)
Death cases (%)
Group A
Group B
Group A
Group B
Group A
Group B
11-20
2 (1)
2 (2)
0 (0)
2 (2.5)
0 (0)
0 (0)
0 (0)
21-30
6 (2.9)
2 (2)
4 (4)
2 (2.5)
0 (0)
0 (0)
4 (13)
31-40
25 (12)
9 (8.5)
16 (16)
8 (10)
16 (22)
1 (4)
0 (0)
41-50
36 (17.3)
16 (15)
20 (19)
9 (11.5)
8 (11)
7 (27)
12 (39)
51-60
50 (24)
34 (33)
16 (15)
24 (31)
16 (22)
10 (38)
0 (0)
61-70
49 (23.6)
25 (24)
24 (23)
19 (24.5)
20 (27)
6 (23)
4 (13)
71-80
32 (15.4)
12 (11.5)
20 (19)
10 (13)
9 (12)
2 (8)
11 (35)
> 81
8 (3.8)
4 (4)
4 (4)
4 (5)
4 (6)
0 (0)
0 (0)
Total
208
104
104
78
73
26
31
Table 5 Analysis of the hospital stay, intensive care unit stay, time to symptomatic recovery, and time to negative polymerase chain reaction among the recovered patients against duration and age
Variables
Age group (yr)
Group A (famotidine)
Group B (control)
1-10 d
11-20 d
21-30 d
> 31 d
Total
1-10 d
11-20 d
21-30 d
> 31 d
Total
Duration of hospital stay (recovered cases), group A (n = 78), group B (n = 73)
11-20
0
2
0
0
2
0
0
0
0
0
21-30
0
1
1
0
2
0
0
0
0
0
31-40
3
4
1
0
8
8
8
0
0
16
41-50
4
5
0
0
9
0
8
0
0
8
51-60
13
8
3
0
24
4
8
4
0
16
61-70
5
13
1
0
19
0
16
4
0
20
71-80
5
4
1
0
10
1
4
4
0
9
> 81
1
2
1
0
4
0
4
0
0
4
Total (%)
31 (40)
39 (50)
8 (10)
0 (0)
78 (100)
13 (18)
48 (66)
12 (16)
0 (0)
73 (100)
Duration of ICU stay (recovered cases), group A (n = 78), group B (n = 73)
11-20
2
0
0
0
2
0
0
0
0
0
21-30
1
1
0
0
2
0
0
0
0
0
31-40
6
2
0
0
8
12
4
0
0
16
41-50
5
4
0
0
9
8
0
0
0
8
51-60
20
4
0
0
24
12
0
4
0
16
61-70
8
11
0
0
19
8
12
0
0
20
71-80
6
3
1
0
10
1
4
4
0
9
> 81
1
2
1
0
4
0
4
0
0
4
Total (%)
49 (63)
27 (34.5)
2 (2.5)
0 (0)
78 (100)
41 (56)
24 (33)
8 (11)
0 (0)
73 (100)
Duration of hospital/ICU stay (death cases), group A (n = 26), group B (n = 32)
11-20
0
0
0
0
0
0
0
0
0
0
21-30
0
0
0
0
0
4
0
0
0
4
31-40
0
1
0
0
1
0
0
0
0
0
41-50
0
7
0
0
7
12
0
0
0
12
51-60
1
8
1
0
10
0
0
0
0
0
61-70
0
4
2
0
6
0
1
1
2
4
71-80
0
2
0
0
2
11
0
0
0
11
> 81
0
0
0
0
0
0
0
0
0
0
Total (%)
1 (4)
22 (84.5)
3 (11.5)
0 (0)
26 (100)
27 (88)
1 (3)
1 (3)
2 (6)
31 (100)
Time to clinical improvement (recovered cases), group A (n = 78), group B (n = 73)
11-20
2
0
0
0
2
0
0
0
0
0
21-30
1
1
0
0
2
0
0
0
0
0
31-40
6
2
0
0
8
3
10
3
0
16
41-50
5
3
1
0
9
2
3
3
0
8
51-60
17
6
1
0
24
7
9
0
0
16
61-70
10
8
1
0
19
6
11
3
0
20
71-80
5
4
1
0
10
2
6
1
0
9
> 81
4
0
0
0
4
1
2
1
0
4
Total (%)
50 (64)
24 (31)
4 (5)
0 (0)
78 (100)
21 (29)
41 (56)
11 (15)
0 (0)
73 (100)
Time to negative PCR (recovered cases), group A (n = 78), group B (n = 73)
11-20
0
2
0
0
2
0
0
0
0
0
21-30
0
0
2
0
2
0
0
0
0
0
31-40
0
7
1
0
8
0
9
7
0
16
41-50
0
7
1
1
9
0
4
4
0
8
51-60
0
12
11
1
24
0
8
5
3
16
61-70
0
6
12
1
19
0
4
11
5
20
71-80
0
4
5
1
10
0
1
4
4
9
> 81
0
3
0
1
4
0
0
4
0
4
Total (%)
0 (0)
41 (53)
32 (41)
5 (6)
78 (100)
0 (0)
26 (36)
35 (48)
12 (16)
73 (100)
Time to symptomatic improvement (recovered cases), group A (n = 78), group B (n = 73)
11-20
0
2
0
0
2
0
0
0
0
0
21-30
0
2
0
0
2
0
0
0
0
0
31-40
2
6
0
0
8
2
13
1
0
16
41-50
4
4
1
0
9
0
6
2
0
8
51-60
11
12
1
0
24
1
11
3
1
16
61-70
7
11
1
0
19
0
11
8
1
20
71-80
3
7
0
0
10
0
3
2
4
9
> 81
1
3
0
0
4
0
1
3
0
4
Total (%)
28 (36)
47 (60)
3 (4)
0 (0)
78 (100)
3 (4)
45 (62)
19 (26)
6 (82)
73 (100)
Table 6 Distribution of comorbidity among the study groups
Comorbidity, n (%)
Group A, n (%): Male 46 (75.4), female 15 (24.59)
Group B n (%): Male 33 (71.7), female 13 (28.3)
Total 61 (58.7)
Recovered cases 21 (34.42)
Death cases 15 (24.59)
Total 46 (44.2)
Recovered cases 24 (52.1)
Death cases 10 (21.7)
≥ 2 (12)
< 2 (9)
≥ 2 (12)
< 2 (3)
≥ 2 (10)
< 2 (14)
≥ 2 (8)
< 2 (2)
HTN, 22 (19)
16 (15.8)
6 (50)
5 (55.5)
5 (50)
0
22 (21.1)
8 (44.4)
6 (42.8)
7 (87.5)
1 (50)
IHD, 11 (5.5)
8 (7.9)
3 (25)
0
4 (33.3)
1 (33.3)
3 (2.8)
1 (10)
2 (14.2)
0
0
Diabetes mellitus, 28 (14)
15 (14.5)
6 (50)
1 (11.1)
8 (66.6)
0
13 (12.5)
5 (27.8)
1 (7.1)
6 (75)
1 (50)
COPD
5 (4.8)
1 (8.3)
1 (11.1)
3 (25)
0
4 (3.9)
3 (30)
1 (7.1)
0
0
BPH
9 (8.9)
5 (41.6)
0
2 (16.6)
2 (66.6)
3 (2.8)
1 (10)
0
2 (25)
0
Rheumatoid arthritis
4 (3.8)
4 (33.3)
0
0
0
2 (1.9)
1 (10)
1 (7.1)
0
0
Osteoarthritis
5 (4.8)
1 (8.3)
3 (33.3)
0
1 (33.3)
1 (0.9)
0
1 (7.1)
0
0
Hypothyroid
3 (2.9)
2 (16.6)
1 (11.1)
0
0
1 (0.9)
0
1 (7.1)
0
0
Ischemic stroke
2 (1.9)
1 (8.3)
1 (11.1)
0
0
1 (0.9)
0
1 (7.1)
0
0
Heart failure
2 (1.9)
1 (8.3)
0
1 (8.3)
0
2 (1.9)
0
0
2
0
Chronic kidney disease
1 (1)
0
0
0
1 (33.3)
1 (0.9)
0
1 (7.1)
0
0
Bronchial asthma
1 (1)
1 (8.3)
0
0
0
2 (1.9)
0
0
2 (25)
0
IBD
1 (1)
0
0
0
1 (33.3)
0 (0)
0
0
0
0
IBS
0
0
0
0
0
1 (0.9)
0
1 (7.1)
0
0
Hepatitis B
1 (1)
0
1 (8.3)
0
0
1 (0.9)
0
1 (7.1)
0
0
Migraine
1 (1)
1 (8.3)
0
0
0
3 (2.8)
0
1 (7.1)
2 (25)
0
Carcinoma (early)
1 (1)
1 (8.3)
0
0
0
0
0
0
0
0
Citation: Mohiuddin Chowdhury ATM, Kamal A, Abbas MKU, Karim MR, Ali MA, Talukder S, Hamidullah Mehedi HM, Hassan H, Shahin AH, Li Y, He S. Role of H2 receptor blocker famotidine over the clinical recovery of COVID-19 patients: A randomized controlled trial. World J Clin Cases 2022; 10(23): 8170-8185