Clinical Trials Study
Copyright ©The Author(s) 2022.
World J Clin Cases. Aug 16, 2022; 10(23): 8170-8185
Published online Aug 16, 2022. doi: 10.12998/wjcc.v10.i23.8170
Table 1 Patient demographics, characteristics, and treatment outcomes among the study groups
Variables
Group A (famotidine)
Group B (control)
t-test (95%CI)
Patient demographics and characteristics during hospitalizationSexn = 104, male: 78, female: 26n = 104, male: 77, female: 27
Age (yr)57.06 ± 14.97 (23-83)57.24 ± 13.87 (18-85)P = 0.92
Body weight (Kg) 65.9 ± 9.0 (55-93) 66.5 ± 7.7 (53-90)P = 0.61
BMI24.3 ± 5.8 (19.7-35.4)22.7 ± 5.0 (20.4-34.5)P = 0.58
Comorbidity61 (58.7%)46 (44.2%)
Oxygen saturation (%)85.23 ± 6.961; 73-9887.77 ± 8.971; 34-99P = 0.0243a
PaO2 (mm of Hg)47.9 ± 6.8; 27-8552.0 ± 9.8; 28-84P = 0.005b
P:F ratio (on admission)62.9 ± 28.1; 38-21071.3 ± 35.8; 23-192P = 0.015a
Oxygen requirement 19.44 ± 16.56; 4-60 L/min18.38 ± 10.51; 2-40 L/minP = 0.643
CT chest (%)39.87 ± 14.3; 15-7027.08 ± 16.7; 15-65P ≤ 0.0001d
Respiratory rate 29.07 ± 10; 12-55/min30.37 ± 6.865; 18-45/minP = 0.299
Temperature 100.7 ± 1.865; 98-104 °F101.4 ± 1.453; 98-104 °FP = 0.398
Serum creatinine (mg/dL)1.2 ± 0.61; 0.5-3.31.26 ± 0.62; 0.6-3.5P = 0.24
Serum Bilirubin (mg/dL)1.62 ± 1.0; 0.2-5.01.59 ± 1.1; 0.4-5.8P = 0.80
Platelet count (103/mL)206.3 ± 995.2; 85000-400000221 ± 82.6; 78000-395000P = 0.24
MAP (in mm of Hg) 87.0 ± 12.27; 54-11687.2 ± 11.5; 54-116P = 0.91
GCS score12.1 ± 1.7; 7-1512.6 ± 1.9; 7-15P = 0.06
NEWS-2 score (on admission)8.3 ± 1.8; 3-128.7 ± 2.0; 5-13P = 0.11
SOFA day-1 score6 ± 1.68; 3-115.3 ± 1.44; 3-9P = 0.004b
Characteristics of study group patients during discharge (recovered cases)NEWS-2 score (on discharge; Recovered cases)0.89 ± 0.8; 0-21.2 ± 0.8; 0-2P = 0.0221a
Oxygen saturation (%) (on discharge; Recovered cases)95.9 ± 2.07; 90-10096.3 ± 1.5; 93-99P = 0.080
Oxygen requirement (on discharge; Recovered cases)1.36 ± 2.2; 0-10 L/min1.5 ± 2.4; 0-12 L/minP = 0.279
CT chest (%) (on discharge; Recovered cases)18.0 ± 7.5; 5-3513.86 ± 9.9; 0-35P = 0.004b
Respiratory rate (on discharge; recovered cases)19.4 ± 4.7; 12-34/min19.1 ± 2.2; 15-26/minP = 0.638
Temperature (on discharge; Recovered cases)99.9 ± 1.6; 98-104 °F100.3 ± 1.7; 97.5-103.6 °FP = 0.252
Treatment outcomes among the study groupsRecoveredn = 78 (75%), male: 58 (74.4%), female 20 (25.6%)n = 73 (70%), male: 59 (81%), female: 14 (19%)
Deadn = 26 (25%), male: 20 (76.9%), female: 6 (23.1%)n = 31 (30%), male: 18 (58.1%), female: 13 (41.9%)
Time to clinical improvement9.53 ± 5.0; 3-27 d14.21 ± 5.6; 6-28 dP ≤ 0.0001d
CT difference (%) (on admission and before discharge)21.7 ± 9.5; 8-4013.2 ± 8.9; 0%-40%P ≤ 0.0001d
Time to symptomatic recovery17.9 ± 5.4; 8-37 d19.3 ± 6.3; 10-35 dP = 0.14
duration of ICU stay9.28 ± 4.96; 1-27 d10.23 ± 7.13; 2-42 dP = 0.26
Total duration of hospitalization11.73 ± 6.0; 1-30 d14.13 ± 7.6; 3-42 dP = 0.013a
Duration of hospitalization (recovered patients)13.04 ± 5.5; 4-30 d16.31 ± 6.1; 7-30 dP = 0.0009c
Duration of ICU stay (recovered patients)9.7 ± 4.6; 1-26 d10.6 ± 6.3; 2-26 dP = 0.33
Time to clinical failure/death6.9 ± 6.1; 1-27 d10.4 ± 12.2; 3-42 dP = 0.1986
Time to viral clearance (negative PCR)20.7 ± 5.9; 13-39 d23.8 ± 6.4; 13-42 dP = 0.002b
Table 2 Subgroup analysis according to sex and duration
Variables
Duration
Male (%)
Female (%)
Group A, ICU stay< 10 d (71)51 (65.3)n = 7820 (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 = 7913 (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 = 7814 (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 = 799 (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 = 5619 (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 = 611 (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 = 5616n = 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 = 614 (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 = 220 (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 = 189 (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 = 611 (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 = 610 (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 recovery11-20 d (41)n = 56n = 22
21-30 d (32)
31-40 d (5)
Group B (survived patients) (n = 73), time to negative PCR recovery11-20 d (26)n = 61n = 12
21-30 d (35)
31-40 d (12)
Group A (n = 78), CT chest involvement on admission< 20%26 (46.4)n = 5615 (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< 2026 (42.6)n = 613 (25)n = 12
21-4022 (36)7 (58.3)
41-6013 (21.3)1 (8.3)
> 610 (0)1 (8.3)
Group A (n = 78), CT chest involvement during discharge< 2047 (83.9)n = 5616 (72.7)n = 22
21-409 (16)6 (12.2)
Group B (n = 73), CT chest involvement during discharge< 2047 (77)n = 618 (36.4)n = 12
21-4014 (23)4 (33.3)
Group A (n = 78), chest CT improvement< 2044 (74.6)n = 5619 (86.6)n = 22
21-405 (8.5)3 (13.6)
41-607 (11.9)0 (0)
Group B (n = 73), CT improvement< 2054 (88.5)n = 6110 (83.3)n = 12
21-404 (6.6)1 (8.3)
41-603 (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 11004000
21-30 11008800
31-40 450012800
41-50 78104840
51-60 18115001752
61-70 11104012440
71-80 66000400
> 81 31004000
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 20004000
21-30 200012400
31-40 630020000
41-50 880012040
51-60 23101081312
61-70 1762012440
71-80 93000400
> 81 40004000
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
11-202 (1)2 (2)0 (0)2 (2.5)0 (0)0 (0)0 (0)
21-306 (2.9)2 (2)4 (4)2 (2.5)0 (0)0 (0)4 (13)
31-4025 (12)9 (8.5)16 (16)8 (10)16 (22)1 (4)0 (0)
41-5036 (17.3)16 (15)20 (19)9 (11.5)8 (11)7 (27)12 (39)
51-6050 (24)34 (33)16 (15)24 (31)16 (22)10 (38)0 (0)
61-7049 (23.6)25 (24)24 (23)19 (24.5)20 (27)6 (23)4 (13)
71-8032 (15.4)12 (11.5)20 (19)10 (13)9 (12)2 (8)11 (35)
> 818 (3.8)4 (4)4 (4)4 (5)4 (6)0 (0)0 (0)
Total20810410478732631
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 0200200000
21-30 0110200000
31-40 34108880016
41-50 4500908008
51-60 1383024484016
61-70 51310190164020
71-80 54101014409
> 811210404004
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 2000200000
21-30 1100200000
31-40 620081240016
41-50 5400980008
51-60 20400241204016
61-70 81100198120020
71-80 63101014409
> 81 1210404004
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 0000000000
21-30 0000040004
31-40 0100100000
41-50 070071200012
51-60 18101000000
61-70 0420601124
71-80 020021100011
> 81 0000000000
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 2000200000
21-30 1100200000
31-40 620083103016
41-50 5310923308
51-60 1761024790016
61-7010810196113020
71-80 54101026109
> 81 4000412104
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 0200200000
21-30 0020200000
31-40 07108097016
41-50 0711904408
51-60 01211124085316
61-70 06121190411520
71-80 04511001449
> 81 0301400404
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 0200200000
21-30 0200200000
31-40 260082131016
41-50 4410906208
51-60 111210241113116
61-70 71110190118120
71-80 37001003249
> 81 1300401304
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)022 (21.1) 8 (44.4)6 (42.8)7 (87.5)1 (50)
IHD, 11 (5.5)8 (7.9)3 (25)04 (33.3)1 (33.3)3 (2.8)1 (10)2 (14.2)00
Diabetes mellitus, 28 (14)15 (14.5)6 (50)1 (11.1)8 (66.6)013 (12.5)5 (27.8)1 (7.1)6 (75)1 (50)
COPD5 (4.8)1 (8.3)1 (11.1)3 (25)04 (3.9)3 (30)1 (7.1)00
BPH9 (8.9)5 (41.6)02 (16.6)2 (66.6)3 (2.8)1 (10)02 (25)0
Rheumatoid arthritis4 (3.8)4 (33.3)0002 (1.9)1 (10)1 (7.1)00
Osteoarthritis5 (4.8)1 (8.3)3 (33.3)01 (33.3)1 (0.9)01 (7.1)00
Hypothyroid3 (2.9)2 (16.6)1 (11.1)001 (0.9)01 (7.1)00
Ischemic stroke2 (1.9)1 (8.3)1 (11.1)001 (0.9)01 (7.1)00
Heart failure2 (1.9)1 (8.3)01 (8.3)02 (1.9)0020
Chronic kidney disease1 (1)0001 (33.3)1 (0.9)01 (7.1)00
Bronchial asthma1 (1)1 (8.3)0002 (1.9)002 (25)0
IBD1 (1)0001 (33.3)0 (0)0000
IBS000001 (0.9)01 (7.1)00
Hepatitis B1 (1)01 (8.3)001 (0.9)01 (7.1)00
Migraine1 (1)1 (8.3)0003 (2.8)01 (7.1)2 (25)0
Carcinoma (early)1 (1)1 (8.3)00000000