Clinical characteristics of coronavirus disease 2019 patients with diarrhea in Daegu.

BACKGROUND/AIMS: Coronavirus disease 2019 (COVID-19) can reportedly cause gastrointestinal symptoms. Therefore, we investigated the clinical characteristics of COVID-19 patients with diarrhea.
METHODS: We included 118 COVID-19 patients admitted to a single hospital from February 20 to March 31, 2020. Medical records with clinical characteristics, laboratory data, treatment course, and clinical outcomes were compared based on the presence or absence of diarrhea. Prognostic factors for disease severity and mortality in COVID-19 were also assessed.
RESULTS: Among patients, 54 (45.8%) had diarrhea, whereas seven (5.9%) had only diarrhea. The median age of patients with diarrhea was 59 years (44 to 64), and 22 (40.7%) were male. Systemic steroid use, intensive care unit admission, septic shock, and acute respiratory distress syndrome were less frequent in the diarrhea group than in the non-diarrhea group. No significant differences were observed in total hospital stay and mortality between groups. On multivariate analysis, age (odds ratio [OR], 1.06; 95% confidence interval [CI], 1.01 to 1.12; p = 0.044), diabetes (OR, 3.00; 95% CI, 1.25 to 20.47; p = 0.042), and dyspnea (OR, 41.19; 95% CI, 6.60 to 823.16; p < 0.001) were independent risk factors for septic shock. On Cox regression analysis, diabetes (hazard ratio [HR], 4.82; 95% CI, 0.89 to 26.03; p = 0.043) and chronic obstructive pulmonary disease (HR, 16.58; 95% CI, 3.10 to 88.70; p = 0.044) were risk factors for mortality.
CONCLUSION: Diarrhea was present in 45.8% of patients and was a common symptom of COVID-19. Although patients with diarrhea showed less severe clinical features, diarrhea was not associated with disease severity or mortality.

INTRODUCTION

The coronavirus disease 2019 (COVID-19) outbreak initially occurred in Wuhan, Hubei province of China [1]. After the first outbreak, Daegu, the third largest city in South Korea, became the second outbreak hotspot in the world on February 20, 2020. Since then, COVID-19 has been declared a pandemic, thereby becoming a threat to global health and worsening socio-economic conditions [2-4].

COVID-19 is caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) [5]. This virus can cause serious respiratory disease, and its diagnosis and treatment have been mainly focused on respiratory symptoms such as fever, chills, cough, and sputum production. However, a recent Chinese multicenter study reported that the prevalence of extrapulmonary symptoms such as gastrointestinal symptoms was not insignificant [6], and some other studies have reported the prevalence of gastrointestinal symptoms to be approximately 50% in COVID-19 patients [6,7]. The gastrointestinal symptoms associated with COVID-19 are diarrhea, anorexia, nausea, and vomiting. Among these, diarrhea is one of the most frequently reported symptoms [6]. Since the presence or absence of nausea or discomfort might be subjective, diarrhea would be a more reliable symptom for assessment. Therefore, we investigated the prevalence, baseline clinical characteristics, therapy, and clinical outcomes, including mortality, of COVID-19 patients in Daegu who were classified according to the presence or absence of diarrhea. Additionally, we evaluated the prognostic factors and whether diarrhea could be a predictor of severe disease or mortality for COVID-19.

METHODS

Patients

From February 20 to March 31, 2020, 118 confirmed COVID-19 patients (> 19 years) were hospitalized at our institution. All patients underwent chest radiography and laboratory tests, including complete blood cell count, liver, and kidney function tests, with careful patient interviews on the day of admission. The medical records, which included data on age, sex, body mass index, epidemiological history such as comorbidities, clinical characteristics such as diarrhea and respiratory symptoms on admission, laboratory parameters, treatment course, and clinical outcomes such as mortality were retrospectively reviewed. Clinical outcomes were followed up until April 15, 2020. This study was approved by the Institutional Review Board of Yeungnam University Medical Center, and the requirement of written informed consent by the patients was waived owing to the retrospective nature of the study (IRB No: 2020-04-030).

Definitions

In accordance with the World Health Organization (WHO) interim guidelines, real-time polymerase chain reaction (PCR) from nasopharyngeal and/or oropharyngeal swabs was used to confirm COVID-19 cases. Sputum and/or endobronchial aspirate were obtained from patients with severe respiratory disease. Duration from symptom onset to admission was defined as the interval between the potential earliest date of symptom (fever, chill, cough, sputum production, diarrhea, myalgia, and headache) and the date of hospital admission at our institution. After the COVID-19 outbreak in Daegu, even asymptomatic COVID-19 patients were tested early for COVID-19 using real-time PCR. Therefore, we considered the duration from symptom onset to admission instead of the duration from symptom onset to test day for COVID-19 in this study.

Diarrhea was defined as the presence of any of the following criteria: (1) change in bowel habit to loose stools with frequency of diarrhea > 3 times/day and (2) diosmectite use for symptom control. Duration of diarrhea was defined as the interval from the potential earliest date of diarrhea or diosmectite use for symptom relief to the recorded date of no diarrhea in medical charts. After admission, we included the patients’ diosmectite use in their medical records.

Fever was defined as a tympanic temperature of 37.5°C or higher. Systemic inflammatory response syndrome (SIRS) on admission was defined as the presence of at least two symptoms: (1) body temperature < 36°C or > 38°C, (2) heart rate > 90 beats/min, (3) tachypnea > 20 breaths/min, and (4) white blood cell count < 4,000 or > 12,000 cells/mm3 [8]. Shock and acute respiratory distress syndrome (ARDS) was defined in accordance with the WHO interim guidelines [9]. Acute kidney injury was defined as an increase in the serum creatinine level of > 0.3 mg/dL within 48 hours or 1.5 times the baseline level within 7 days; and decreased urine output of < 0.6 mL/kg/hr for 6 hours [10]. Patients who needed high oxygen including the necessity of mechanical ventilation and high-flow oxygen therapy were admitted to the intensive care unit (ICU). Abnormal parenchymal finding was defined as a ground glass appearance with hazy opacity and consolidation; this was detected using chest radiography and analyzed by an experienced chest radiologist.

Statistical analysis

All continuous variables were expressed as a mean with standard deviation (mean ± SD) or median with range. The clinical characteristics and outcomes were compared using Student’s t test or Mann-Whitney U test for continuous variables. The categorical values were compared using chi-square test or Fischer’s exact test. Factors related to septic shock were identified with univariate and multivariate logistic regression analysis. Cox proportional hazard regression analysis was used to assess prognostic factors for mortality. p values < 0.05 were considered statistically significant. All statistical analyses were performed using SPSS version 23.0 (IBM Co., Armonk, NY, USA).

RESULTS

Baseline and clinical characteristics of patients

Among the 118 COVID-19 patients, diarrhea accompanied other symptoms in 54 patients (45.8%), whereas diarrhea was the only symptom in seven patients (5.9% of all the COVID-19 patients and 13.0% of COVID-19 patients with diarrhea) (Fig. 1). The baseline characteristics of the patients are shown in Table 1. The median age was 61.0 years (range, 50.0 to 70.0), and 52 subjects (44.1%) were male. Among COVID-19 patients, 84 (71.2%) had at least one comorbidity, such as hypertension (34.7%) and diabetes mellitus (DM) (16.1%). On admission, there were 77 (65.3%) patients with fever or chills, 84 (71.2%) with cough or sputum production, 49 (41.5%) with dyspnea, 47 (39.8%) with myalgia, 43 (36.4%) with headache, and seven (5.9%) with only diarrhea. The mean duration from symptom onset to admission was 5.4 ± 8.2 days.

Figure 1.

Flow chart of coronavirus disease 2019 (COVID-19) patients according to the presence of diarrhea.

Table 1.

Baseline characteristics of the patients according to presence or absence of diarrhea

Variable	No diarrhea (n = 64, 54.2%)	Diarrhea (n = 54, 45.8%)	Total (n = 118, 100.0%)	p value
Age, yr	62.5 (50.0–72.0)	59.0 (44.0–64.0)	61.0 (50.0–70.0)	0.079
Male sex	30 (46.9)	22 (40.7)	52 (44.1)	0.629
BMI, kg/m2	24.2 ± 3.3	22.9 ± 3.7	23.6 ± 3.5	0.053
Comorbidities
Diabetes mellitus	9 (14.1)	10 (18.5)	19 (16.1)	0.686
Hypertension	26 (40.6)	15 (27.8)	41 (34.7)	0.205
Coronary artery disease	5 (7.8)	4 (7.4)	9 (7.6)	1.000
COPD	6 (9.4)	2 (3.7)	8 (6.8)	0.393
Chronic liver disease	1 (1.6)	3 (5.6)	4 (3.4)	0.494
Fatty liver	0	2 (3.7)	2 (1.7)	0.403
Chronic hepatitis C	0	1 (1.9)	1 (0.8)	0.932
Malignancy	3 (4.8)	5 (9.3)	8 (6.8)	0.553
Initial symptoms on admission
Fever/chills	39 (60.9)	38 (70.4)	77 (65.3)	0.380
Cough/sputum	44 (68.8)	40 (74.1)	84 (71.2)	0.666
Dyspnea	30 (46.9)	19 (35.2)	49 (41.5)	0.273
Myalgia	24 (37.5)	23 (42.6)	47 (39.8)	0.708
headache	21 (32.8)	22 (40.7)	43 (36.4)	0.484
Only diarrheal symptom	0	7 (13.0)	7 (5.9)	0.010
Duration from symptom onset to admission, day	4.1 ± 6.3	6.8 ± 9.8	5.4 ± 8.2	0.086
Duration of diarrhea on admission, day	0.0 ± 0.0	4.2 ± 3.0		< 0.001
Vital sign on admission
SBP, mmHg	134.0 ± 20.5	125.7 ± 17.8	130.2 ± 19.7	0.023
Heart rate, beats/min	85.1 ± 18.7	83.5 ± 17.7	84.4 ± 18.2	0.65
Body temperature, °C	37.2 ± 0.8	37.4 ± 0.7	37.3 ± 0.7	0.176
RR, breaths/min	21.6 ± 3.3	20.5 ± 1.7	21.1 ± 2.7	0.021
Initial oxygen saturation, %	93.5 ± 7.5	96.6 ± 1.9	94.9 ± 5.9	0.002

Values are presented as median (range), number (%), or mean ± SD.

BMI, body mass index; COPD, chronic obstructive pulmonary disease; SBP, systolic blood pressure; RR, respiratory rate.

Patients were classified based on the presence or absence of diarrhea; there was no significant difference in baseline characteristics between the two groups. In the diarrhea group, the median age was 59.0 years (range, 44.0 to 64.0), and 22 (40.7) were male. The frequency of accompanying symptoms such as fever or chills and cough or sputum production were higher in the diarrhea group, but there were no significant differences (60.9% vs. 70.4% with fever or chills, p = 0.380; 68.8% vs. 74.1% with cough or sputum production). The mean duration from symptom onset to admission was 6.8 ± 9.8 days in patients with diarrhea versus 4.1 ± 6.3 days in those without diarrhea (p = 0.086). The clinical manifestation showed differences in the respiratory rate (21.6 breaths/min in the non-diarrhea group vs. 20.5 breaths/min in the diarrhea group, p = 0.021) and initial oxygen saturation (93.5% in the non-diarrhea group vs. 96.6% in the diarrhea group, p = 0.002) (Table 1).

Laboratory and radiologic results

White blood cell count was lower in the diarrhea group than in the non-diarrhea group (7,124/mm3 vs. 5,843/mm3, p = 0.035). Lymphocyte count was higher in the diarrhea group than in the non-diarrhea group (21.5% vs. 27.0%, p = 0.012). Patients in the diarrhea group had lower levels of blood urea nitrogen (17.3 mg/dL vs. 13.1 mg/dL, p = 0.005) and serum potassium (4.2 mEq/L vs. 4.0 mEq/L, p = 0.033), and a higher estimated glomerular filtration rate (eGFR) (86.7 mL/min/1.73 m2 vs. 102.4 mL/min/1.73 m2, p = 0.004). There were no significant differences in the liver battery tests and C-reactive protein levels between the groups (Table 2).

Table 2.

Laboratory and imaging data of the patients

Variable	No diarrhea (n = 64, 54.2%)	Diarrhea (n = 54, 45.8%)	Total (n = 118, 100.0%)	p value
Laboratory data on admission
White blood count, /mm3	7,124.4 ± 2,883.5	5,843.2 ± 3,648.4	6,538.1 ± 3,304.2	0.035
Lymphocyte, %	21.5 ± 11.5	27.0 ± 11.4	24.0 ± 11.7	0.012
Hemoglobin, g/dL	15.1 ± 17.7	13.1 ± 1.5	14.1 ± 13.1	0.377
Platelet, 103/μL	244.9 ± 107.0	233.4 ± 97.4	239.6 ± 102.4	0.543
C-reactive protein, mg/dL	6.6 ± 9.0	4.2 ± 6.6	5.5 ± 8.1	0.106
Procalcitonin, ng/dL	0.4 ± 1.6	0.1 ± 0.1	0.3 ± 1.2	0.103
AST, IU/L	48.5 ± 55.1	40.2 ± 34.2	44.7 ± 46.8	0.322
ALT, IU/L	35.2 ± 47.2	37.1 ± 43.4	36.1 ± 45.3	0.826
ALP, IU/L	80.7 ± 41.6	79.8 ± 38.5	80.3 ± 40.1	0.904
GGT, IU/L	32.1 ± 35.3	39.2 ± 39.0	35.6 ± 37.1	0.383
LDH, IU/L	667.6 ± 404.9	567.5 ± 187.4	621.7 ± 326.3	0.093
Total bilirubin, mg/dL	0.8 ± 0.5	0.9 ± 0.4	0.8 ± 0.4	0.845
Albumin, g/dL	3.7 ± 0.6	3.8 ± 0.5	3.7 ± 0.5	0.060
PT-INR	1.2 ± 0.1	1.1 ± 0.1	1.1 ± 0.1	0.055
Blood urea nitrogen, mg/dL	17.3 ± 10.1	13.1 ± 5.3	15.4 ± 8.5	0.005
Creatinine, mg/dL	0.9 ± 0.6	0.8 ± 0.2	0.9 ± 0.5	0.062
eGFR, mL/min/1.73 m2	86.7 ± 28.7	102.4 ± 28.6	93.7 ± 29.6	0.004
Sodium, mEq/L	138.7 ± 3.3	138.7 ± 2.8	138.7 ± 3.1	0.741
Potassium, mEq/L	4.2 ± 0.5	4.0 ± 0.5	4.1 ± 0.5	0.033
Abnormal finding on chest radiography	62 (96.9)	52 (96.3)	114 (96.6)	1.000
Ground glass appearance	50 (80.6)	47 (90.4)	91 (85.1)	0.234

Values are presented as mean ± SD or number (%).

AST, aspartate aminotransferase; ALT, alanine aminotransferase; ALP, alkaline phosphatase; GGT, gamma-glutamyl transferase; LDH, lactate dehydrogenase; PT-INR, prothrombin time-international normalized ratio; eGFR, estimated glomerular filtration rate.

Among all patients, 114 (96.6%) had abnormal parenchymal findings, as detected by chest radiography. Interestingly, all patients with only diarrhea also showed abnormal parenchymal findings (data not shown). Similar proportions of abnormal chest radiography findings were noted in both groups (96.9% vs. 96.3%, p = 1.00). Typical ground-glass opacity was the most common finding in 91 (85.1%) patients. A total of 50 (80.6%) and 47 (90.4%) patients in the non-diarrhea and diarrhea groups, respectively, had ground-glass appearance (p = 0.234) (Table 2).

Therapy and clinical outcomes

There were no significant differences in the usage of lopinavir/ritonavir (93.8% vs. 92.6%, p = 1.000) and hydroxychloroquine (89.1% vs. 94.4%, p = 0.475) between the two groups. Systemic steroid (40.6% vs. 20.4%, p = 0.030) and extracorporeal membrane oxygenation (10.9% vs. 0.0%, p = 0.034) were needed more frequently in the non-diarrhea group. More patients in the non-diarrhea group needed ICU care (23.4% vs. 1.9%, p = 0.002). SIRS on admission was noted in 32 (27.1%) patients. SIRS on admission was comparatively lesser in the diarrhea group, but there was no significant difference (34.4% vs. 18.5%, p = 0.085). During hospitalization, septic shock (20.3% vs. 1.9%, p = 0.005) and ARDS (15.6% vs. 0.0%, p = 0.007) developed less in the diarrhea group. However, no significant differences were observed in mortality (7.8% vs. 1.9%, p = 0.295) and length of hospital stay (25.1 days vs. 26.8 days, p = 0.407) between the groups (Table 3).

Table 3.

Therapy and clinical outcomes of patients on admission

Variable	No diarrhea (n = 64, 54.2%)	Diarrhea (n = 54, 45.8%)	Total (n = 118, 100%)	p value
SIRS on admission	22 (34.4)	10 (18.5)	32 (27.1)	0.085
Therapy
Oxygen therapy	26 (40.6)	14 (25.9)	40 (33.9)	0.137
Lopinavir/ritonavir	60 (93.8)	50 (92.6)	110 (93.2)	1.000
Hydroxychloroquine	57 (89.1)	51 (94.4)	108 (91.5)	0.475
Systemic steroid	26 (40.6)	11 (20.4)	37 (31.4)	0.030
Diosmectite	0	50 (92.6)	50 (42.4)	1.000
CRRT	1 (1.6)	0	1 (0.8)	1.000
ECMO	7 (10.9)	0	7 (5.9)	0.034
Clinical course
ICU care	15 (23.4)	1 (1.9)	16 (13.6)	0.002
Septic shock	13 (20.3)	1 (1.9)	14 (11.9)	0.005
ARDS	10 (15.6)	0	10 (8.5)	0.007
AKI	3 (4.7)	0	3 (2.5)	0.306
Outcomes
Death	5 (7.8)	1 (1.9)	6 (5.1)	0.295
Duration of hospital stay, day	25.1 ± 11.1	26.8 ± 10.6	25.9 ± 10.9	0.407

Values are presented as number (%) or mean ± SD.

SIRS, systemic inflammatory response syndrome; CRRT, continuous renal replacement therapy; ECMO, extracorporeal membrane oxygenation; ICU, intensive care unit; ARDS, acute respiratory distress syndrome; AKI, acute kidney injury.

Prognostic factors for septic shock and mortality in COVID-19 patients

COVID-19 was less severe in patients with diarrhea than in those with non-diarrhea. In multivariate analysis, higher age (odds ratio [OR], 1.06; 95% confidence interval [CI], 1.01 to 1.12; p = 0.044), DM (OR, 3.00; 95% CI, 1.25 to 20.47; p = 0.042), and dyspnea (OR, 41.19; 95% CI, 6.60 to 823.16; p < 0.001) were identified as independent risk factors for septic shock (Table 4). The presence of diarrhea was not a significant prognostic factor (OR, 0.24; 95% CI, 0.05 to 1.03; p = 0.065). In Cox proportional regression analysis, DM (hazard ratio [HR], 4.82; 95% CI, 0.89 to 26.03; p = 0.043) and chronic obstructive pulmonary disease (COPD) (HR, 16.58; 95% CI, 3.10 to 88.70; p = 0.044) were risk factors for mortality (Table 5). The presence of diarrhea was not a prognostic factor for septic shock and mortality in patients with COVID-19.

Table 4.

Independent risk factors for septic shock

Variable	Univariate	Multivariate analysis
	p value[a]	p value[a]	OR (95% CI)
Age, yr	< 0.001	0.044	1.06 (1.01–1.12)
Male sex	0.299
Overweight (BMI ≥ 25 kg/m2)	0.098
Diabetes mellitus	0.002	0.042	3.00 (1.25–20.47)
Hypertension	0.069
Chronic obstructive pulmonary disease	0.034
History of cancer	0.962
Fever/chills	0.60 6
Cough	0.983
Dyspnea	0.002	< 0.001	41.19 (6.60–823.16)
Diarrhea	0.016
Myalgia	0.146
Headache	0.015

OR, odds ratio; CI, confidence interval; BMI, body mass index.

Calculated by logistic regression analysis.

Table 5.

Independent risk factors for death

Variable	Univariate	Multivariate analysis
	p value[a]	p value[a]	OR (95% CI)
Age, yr	0.745
Male sex	0.079
Overweight (BMI ≥ 25 kg/m2)	0.256
Diabetes mellitus	0.031	0.043	4.82 (0.89–26.03)
Hypertension	0.456
Chronic obstructive pulmonary disease	< 0.001	0.010	16.58 (3.10–88.70)
History of cancer	0.215
Fever/chills	0.389
Cough	0.781
Dyspnea	0.084
Diarrhea	0.174
Myalgia	0.794
Headache	0.482

HR, hazard ratio; CI, confidence interval; BMI, body mass index.

Calculated by Cox proportional hazards regression test.

DISCUSSION

To the best of our knowledge, this is the first study in the Korean population that has reported the extrapulmonary manifestations of COVID-19 in patients, after their classification on the basis of the presence or absence of diarrhea. COVID-19, caused by SARS-CoV-2, mainly causes respiratory symptoms including fever, chills, cough, and sputum production [6]. Therefore, patient diagnosis and classification is based on the severity of respiratory symptoms and oxygen demand. However, according to a recent report, it is also possible for COVID-19 to manifest with only gastrointestinal symptoms like other viruses [6].

Several hypotheses have been proposed to understand why COVID-19 causes gastrointestinal symptoms including diarrhea. Molecular studies in the Chinese population have shown that there is an approximately 79% overlap in the sequences of SARS-CoV-2 and SARS-CoV [11,12]. Among these shared sequences, the angiotensin converting enzyme II (ACE2) receptor used for entry by the SARS-CoV was confirmed to be present in SARS-CoV-2 [11,12]. The ACE2 receptor is known to be highly expressed in lung alveolar type 2 cells, cholangiocytes, esophagus epithelial cells, and enterocytes in the ileum [13,14]. Entry of SARS-CoV-2 into the organs of the digestive system might be due to the increased permeability of the enterocytes, subsequently leading to diarrhea. Several studies have revealed that SARS-CoV-2 can be detected in stool samples in approximately 50% of the patients [15-17]. In addition, owing to the systemic immune response to COVID-19, diarrhea may also be caused by the damage to the intestinal mucosa. However, it is difficult to confirm the sequential relationship in this study, and further large-scale studies are promptly needed.

Generally, viral enteritis is accompanied by nausea, vomiting, and anorexia as well as diarrhea; it runs a mild clinical course. In our study, gastrointestinal symptoms other than diarrhea were also noted in hospitalized COVID-19 patients. However, gastrointestinal symptoms other than diarrhea mainly occurred after the administration of drugs such as lopinavir/ritonavir and hydroxychloroquine on admission, and the possibility of side effects due to drugs could not be ruled out.

In our study, there were no significant differences except for those in blood urea nitrogen, eGFR, and serum potassium between the two groups. These laboratory findings are associated with dehydration. Therefore, we could assume that the diarrhea in COVID-19 patients was not severe. Furthermore, steroid use, ICU care, septic shock, and ARDS were also less common in the diarrhea group than in the non-diarrhea group. The overall clinical course of patients in the diarrhea group was likely to be milder than that in the non-diarrhea group, but the mortality was not significantly different between the two groups.

Another study in China showed opposite results for the comparison of clinical courses [6]. We could not explain the exact cause of this discrepancy clearly, but it may be attributable to the severity and duration of diarrhea. All patients with diarrhea showed mild severity and a self-limited course. Alternatively, this could be associated with the limitation of our study design. Since this was a retrospective single center study, there could be several biases. Considering that the average duration from symptom onset to admission was 6.8 days, the patients could not remember their symptoms exactly. In patients who were transferred from other hospitals after their conditions worsened, we could not conclusively determine either the presence of diarrhea at the time of admission, or the treatment course during the stay at secondary-care hospitals.

In this study, old age, DM, and dyspnea were independent risk factors for septic shock in patients with COVID-19. Moreover, DM and COPD were independent risk factors for mortality in COVID-19 patients. However, diarrhea was not associated with disease severity, as indicated by the rates of septic shock and mortality in this study.

This study has several other limitations. First, because it is a retrospective study conducted at a single tertiary-care hospital, it is difficult to generalize our results to the general population. Moreover, there is the possibility of selection bias. Since our hospital is a tertiary university hospital, the COVID-19 patients would present with more severe symptoms than patients at less specialized centers. Since the occurrence of the COVID-19 outbreak on February 18, 2020, the disinfection team of Daegu classified all COVID-19 patients based on severity, and patients with respiratory symptoms and/or those with high oxygen demand were transferred to a tertiary-care hospital preferentially, as per the city’s policy. Second, because both clinicians and patients paid more attention to respiratory symptoms initially, most patients had difficulty in remembering the onset of diarrhea and their accompanying symptoms. This may have introduced recall bias, making it difficult to estimate the amount of stool, the exact duration from the onset of diarrhea to admission, as well as the presence of other gastrointestinal symptoms including nausea and vomiting. Third, because of the very small number of events, it is difficult to ascertain the association of the presence of diarrhea with disease severity and mortality. Despite these limitations, we thought that it could be clinically significant in that, we tried to evaluate the frequency and clinical significance of diarrhea in patients with COVID-19 at early phase of outbreak.

In conclusion, diarrhea could also be one of the main symptoms in COVID-19 patients. Although patients without diarrhea had a more severe clinical course than those with diarrhea, the presence of diarrhea may not be associated with disease severity and mortality. Multicenter studies with large numbers of patients are warranted to elucidate the clinical impact of diarrhea as a prognostic factor for COVID-19 patients.

1. Diarrhea presented along with primary symptoms in approximately 50% of all hospitalized coronavirus disease 2019 (COVID-19) patients.

2. In patients with COVID-19, old age, diabetes mellitus (DM), and dyspnea are independent risk factors for septic shock and DM and chronic obstructive pulmonary disease are independent risk factors for mortality.

3. Presence of diarrhea in COVID-19 patients may not be associated with septic shock and mortality.