Abstract
Purpose
To characterize the clinical features and outcome of patients treated at a specialized hospital for coronavirus disease 2019 (COVID-19).
Methods
We retrospectively reviewed the symptoms on admission, treatment, and outcome of a total of 300 patients with mild (peripheral oxygen saturation (SpO2) ≥ 96%), moderate I (93% < SpO2 < 96%), moderate II (SpO2 ≤ 93%) and severe (requiring admission to the ICU or mechanical ventilation) COVID-19.
Results
Median age was 53 (interquartile range [IQR] 33–72) years and 57% was male. The number of patients with mild, moderate I, II and severe condition was 85, 138, 61 and 16, respectively. Common presenting symptoms were cough (n = 71), loss of taste (42), loss of smell (39), fever ≥ 37.5 °C (36). Dyspnea was observed only 21 cases; 57 reported no symptoms on admission. Favipiravir, ciclesonide, dexamethasone, and heparin were administered in 106, 168, 65, and 38 patients, respectively, but not remdesivir. The median duration of hospitalization was 10 (7–15) days. All patients with mild and moderate I severity were discharged. Among the 77 patients classified as moderate II or severe, 3 were transferred to tertiary hospitals for further treatment on the day of admission. The respiratory condition worsened in 21 patients; 18 required transfer to tertiary hospitals 3 (median) days after admission and 3 died.
Conclusion
Respiratory condition recovered in 92%; whereas it worsened in 7% and the mortality rate was 1%. The ratios of male patients, of patients with diabetes mellitus in those with the decreased respiratory condition, were significantly higher than recovered.
Keywords: COVID-19, Pandemic, Specialized hospital
Coronavirus disease 2019 (COVID-19) is a global pandemic and nearly 73 million cases and 1.5 million deaths have been reported worldwide until November 2020.1 The clinical spectrum of COVID-19 appears to be wide, encompassing asymptomatic infection, mild upper respiratory tract illness, and severe viral pneumonia with respiratory failure and even death [1]. A high proportion of patients (10–32%) requires admission to high dependency or intensive care units [1–3], and the clinical course of those patients, prognostic factors have been repeatedly reported [2, 4, 5]. On the other hand, despite an increasing importance of neighboring hospitals for initial treatment with an outbreak of COVID-19, profiles and clinical course of patients in those hospitals with a wide range of severity are less reported [6, 7]. We aimed to explore the clinical, laboratory characteristics and outcome of patients at the first Japanese hospital designated to treat COVID-19 patients.
Methods
This is a retrospective, observational study at Osaka City Joso Hospital, a public hospital located in the north of Osaka prefecture with a population of 8.8 million. Ours was the first hospital in Japan dedicated to COVID-19 patients when the system was started. It was initially scheduled to admit a maximum of 20 patients, which was expanded to 70 later. After obtaining approval from the institutional ethics committee (No. 2–5, September 28, 2020), all consecutive patients who were admitted to our hospital during the period from March 25 to September 14, phase 2 of COVID-19 pandemic, were included in the study. Written informed consent from each patient was waived by opting out.
Profiles of patients
People with suspected COVID-19 infection underwent reverse transcription-polymerase chain reaction (RT-PCR) test of a nasopharyngeal sample for SARS-CoV-2 at hospitals, clinics and drive-through testing stations. Information of all infected patients is collected at the Osaka Prefectural Follow-up Center via the local public health centers in each city, and triage doctors order them to stay home, in the hotels, to be admitted to hospitals providing regular medical care or tertiary hospitals, according to the severity classification made by the Ministry of Health, Labour and Welfare,2 where mild, peripheral oxygen saturation (SpO2) ≥ 96%, with no respiratory symptoms or coughing only, no shortness of breath; moderate I (patient does not suffer respiratory failure), 93% < SpO2 < 96%, with shortness of breath and pneumonia findings; moderate II (patient suffers respiratory failure), SpO2 ≤ 93% and oxygen administration is required; severe, requiring admission to the ICU or mechanical ventilation. Our hospital, as one of the neighboring hospitals, mainly received patients with COVID-19 of mild, moderate I or II severity, and those with severe COVID-19 requiring no life-prolonging treatment.
Treatment
Blood test, chest X-ray, and if required, CT scan were performed on admission. Symptoms and complaints on admission were recorded by the attending nurses. Supplemental oxygen was administered in order to maintain SpO2 ≥ 93%. Patients received medications for COVID-19 pneumonia according to the methods suggested by the Ministry of Health, Labour and Welfare (see Footnote 2). Oral favipiravir, an RNA polymerase inhibitor, and inhalational ciclesonide, corticosteroid for bronchial asthma, were administered in the form of a clinical trial after obtaining approval from the ethics committee of our institute (No. 1–10 and 1–11, respectively, March 30, 2020) as well as from each patient, based on the decision by the individual physicians. Intravenous dexamethasone 6.6 mg/day was administered for 10 days in case SpO2 decreased below 93% with inhalational oxygen. Subcutaneous heparin 10,000 units/day was added to dexamethasone in patients with abnormal increase of plasma fibrinogen. Remdesivir was not used because its use has been limited to those with severe cases requiring the introduction of extracorporeal membrane oxygenation or mechanical ventilation. In case a decrease of SpO2 below 93% with inhalational oxygen at 5 L/min lasted for > 12 h, patients were transferred to tertiary hospitals for intensive care unless they required no life-prolonging treatment. Discharge criteria were (1) 10 days after the date of onset and 72 h after the resolution of symptoms, or (2) 24 h after the resolution of symptoms if the patient has tested negative for the PCR test twice with at least 24 h between tests (see Footnote 2). The last follow-up date was October 2020, when all the subjects were discharged or died.
Data collection and statistical analysis
We collected data from the electronic medical records (MegaOak, NEC Corporation, Tokyo). Information of past histories was obtained from the patients, their families, and previous institutes where they stayed. We did not calculate the Sequential Organ Failure Assessment Score or APACHE II score because consciousness disturbance or hypotension was observed in no patients on admission, and arterial blood gas was not measured in most of them. No statistical sample size calculation was performed a priori owing to the nature of the study. We defined recovery as an improvement of the grade of severity from moderate I or II on admission to mild. Patients’ condition was also construed as being recovered if they satisfy the aforementioned criteria for discharge. We defined worsening as SpO2 decreasing to < 93% with inhalational oxygen at 5 L/min for > 12 h.
Statistical analyses were performed by SigmaPlot 12 (Systat Software Inc., San Jose, California, USA). Continuous variables are presented as median (range), if not specified. Categorical variables are presented as frequency (percentage). Categorical data of the severity and outcome among the three age groups were analyzed by chi-square test or Fisher’s exact test. For univariate comparisons between patients with recovered and worsened respiratory condition Mann–Whitney’s U-test was used. Duration of hospitalization among the three age groups was analyzed by Kruskal–Wallis test, followed by Dunn’s multiple comparisons. P < 0.05 was regarded as statistically significant.
Results
Profiles
A total of 300 patients, including one who was readmitted and calculated as two individuals, were included (median age, 53 years [interquartile range {IQR}, 33–72; range 15–100 years]; 57% male). The median time from illness onset to admission was 7 (IQR, 4–9; range, 1–44) days, including a young female in whom results of the retest for SARS-CoV-2 RNA was positive and was admitted to our hospital 44 days after initial onset. Among the 300 patients, 223 (74%) including 10 pregnant women were classified as mild or moderate I severity (n = 85 and 138, respectively) requiring no supplemental oxygen, and the remaining 77 patients were accompanied with moderate II or severe respiratory condition (n = 61 and 16, respectively, Table 1). Of the 16 patients with a severe condition on admission, 13 (81%) were transferred from tertiary hospitals, of whom 10 patients had undergone mechanical ventilation under tracheal intubation in those hospitals. They were still requiring supplemental oxygen ≥ 5 L/min for maintaining SpO2 ≥ 93% after extubation.
Table 1.
Severity on admission, duration of hospitalization, and outcome of the three age groups
| Age | Severity on admission | Duration of hospitalization (days) | Outcome | |||||||
|---|---|---|---|---|---|---|---|---|---|---|
| Mild | M I | M II | Severe | Total (%) | Improve | Unchange | Worsen | Died | ||
| [Mild + M I] | [M II + severe] | [worsen + died] | ||||||||
| < 40 | 52 | 36 | 6 | 1 | 95 (32%) | 9 ([7–12], 1–39) | 93 | 1 | 1 | 0 |
| [88] | [7] | [1] | ||||||||
| 40–69 | 19 | 60 | 31 | 7 | 117 (39%) | 10 ([7–18], 1–52) | 103 | 1 | 13 | 0 |
| [79] | [38]** | [13] | ||||||||
| ≤ 70 | 14 | 42 | 24 | 8 | 88 (29%) | 14 ([9–22], 1–85)‡ | 80 | 1 | 4 | 3 |
| [56] | [32]** | [7]¶ | ||||||||
| Total | 85 | 138 | 61 | 16 | 300 | 10 ([7–15], 1–85) | 276 | 3 | 18 | 3 |
| [223] | [77] | |||||||||
The number of patients is expressed as the absolute value (percentage), [sum of the two severity groups] or [sum of the worsen and died]. The duration of hospitalization is expressed as median days ([25–75% interquartile range], range)
MI moderate I, M II moderate II
**P < 0.001 compared with the ratio of patients to the total number in the age group < 40 years
‡P < 0.001 compared with the duration of hospitalization of patients < 40 years and 40–69 years
¶P = 0.03 compared with the ratio of patients in the age group < 40 years
The ratio of patients classified as moderate II or severe condition to the total number of patients between 40 and 69 years (38/117) and ≥ 70 years (32/88) was significantly higher than those < 40 years (7/95) (P < 0.001 for both, Table 1). Patients had been staying in their homes (206 [69%]), hospitals (62 [21%]), hotels (16 [5%]) or care homes (16 [5%]) before admission to our hospital. A cluster of COVID-19 cases occurred in hospitals and care homes, from where 31 patients were transferred to our hospital. Among the 62 patients who had been staying in other hospitals, 34 were transferred for treatment of COVID-19 based on the positive results of RT-PCR; the remaining 28 were for follow-up treatment of COVID-19 after recovering from severe stage in the tertiary hospitals in Osaka.
Symptoms and laboratory data
Common presenting symptoms on admission were cough, loss of taste, loss of smell, fever ≥ 37.5 °C, and general fatigue. Only 21 (7%), much fewer than 77 cases with moderate II or severe condition, complained of dyspnea (Table 2). Notably, 57 (19%) cases reported no symptoms on admission. The most common comorbidities were hypertension, followed by diabetes mellitus, cerebral vascular disease and dementia. Chest XP demonstrated abnormal shadows indicative of pneumonia in 186 (62%) patients. Ground-glass opacity and consolidation typical for COVID-19 pneumonia were detected in 177 (83%) of a total of 214 patients underwent chest CT scan. More than 50% of the patients presented with abnormally increased levels of C-reactive protein (CRP), ferritin, and fibrinogen within 4 h after admission (Table 3). Lymphocytopenia (< 1.1 × 109/L) was detected in 44%.
Table 2.
Symptoms on admission and comorbidities
| Symptoms | |
| Cough | 71 (24) |
| Loss of taste | 42 (14) |
| Loss of smell | 39 (13) |
| Fever ≥ 37.5 °C | 36 (12) |
| General fatigue | 36 (12) |
| Dyspnea | 21 (7) |
| Comorbidities | |
| Hypertension | 68 (23) |
| Diabetes mellitus | 60 (20) |
| Cerebral vascular disease without dementia | 13 (4) |
| Dementia | 12 (4) |
| Psychiatric disease | 9 (3) |
| Chronic obstructive lung disease | 8 (3) |
| Ischemic heart disease | 7 (2) |
| Chronic heart failure | 7 (2) |
| Obstructive sleep apnea | 6 (2) |
Data are expressed as the number of patients (percentage)
Table 3.
Laboratory data on admission
| White blood cell count, ×109/L | 5.2 (4.0–7.0) |
| < 3.6* | 45 (15%)* |
| 3.6–8.2 | 218 (73%) |
| > 8.2* | 36 (12%)* |
| Lymphocyte count, × 109/L | 1.2 (0.8–1.6) |
| < 1.1* | 132 (44%)* |
| ≥ 1.1 | 167 (56%) |
| Aspartate aminotransferase, U/L | 27 (20–39) |
| ≤ 38 | 224 (75%) |
| > 38* | 75 (25%)* |
| Alanine aminotransferase, U/L | 24 (14–41) |
| ≤ 43 | 231 (77%) |
| > 43* | 68 (23%)* |
| Lactate dehydrogenase, U/L | 212 (173–272) |
| ≤ 211 | 150 (50%) |
| > 211* | 149 (50%)* |
| Creatinine, mg/dL | 0.76 (0.61–1.0) |
| ≤ 0.80 | 169 (57%) |
| > 0.80* | 130 (43%)* |
| C-reactive protein, mg/L | 1.8 (0.4–4.0) |
| ≤ 0.3 | 69 (23%) |
| > 0.3* | 230 (77%)* |
| Fibrinogen, mg/dL | 420 (327–548) |
| ≤ 400 | 132 (44%) |
| > 400* | 167 (56%)* |
| D-dimer, µg/mL | 0.9 (0.7–1.0) |
| ≤ 1.0 | 181 (61%) |
| > 1.0* | 118 (39%)* |
| Ferritin, ng/mL | |
| Male | 586.5 (354.5–990.3) |
| Female | 184.0 (85.1–363.5) |
| Within normal range | 119 (40%) |
| Out of normal range | 177 (60%)* |
Data are median (interquartile range) or number of patients (% of those with available data)
*Out of normal range
Treatment and outcome
The median duration of hospitalization of all patients was 10 (IQR, 7–15; range, 1–85) days (Table 1). It was significantly longer in patients ≥ 70 years than in those < 40 years and 40–69 years (14 vs. 9 and 14 vs. 10 days, P < 0.001 for both). Favipiravir, ciclesonide, dexamethasone and heparin were administered in 106 (35%), 168 (56%), 65 (22%), and 38 (13%) patients, respectively.
Respiratory condition recovered in 276 (92%) patients including all cases with mild and moderate I severity on admission (n = 223). Of those 276 patients, 229 were discharged home; 33 and 14 were discharged to outside hospitals and nursing facilities, respectively, because of difficulties in daily life after discharge. Most of them stayed in hospitals and nursing homes before transferring to our hospital. In two males initially classified as moderate II and severe, the respiratory condition was poorer than the prehospital information reported by the triage doctor and both of them apparently required tracheal intubation soon after arrival at our hospital. A 30-year-old pregnant woman (36 weeks and 1 day) was transferred from a university hospital. Although the initial classification of severity was moderate II, she developed remarkable tachypnea with SpO2 < 93% with supplemental oxygen 1 h after arrival at our hospital, suggesting that her condition was severe. These three patients were transferred to tertiary hospitals with unchanged conditions on the day of admission to our hospital and were excluded from the outcome evaluation.
Among the 74 patients classified as moderate II and severe COVID-19 (n = 59 and 15, respectively), the respiratory condition worsened in 21 patients (initial classification: mild II, 16 and severe, 5) during hospitalization (Table 1); 18 of them were urgently transferred to tertiary hospitals after staying 3 (1–7) days, and 3 (85, 85 and 77 years, all males) who required no life-prolonging treatment died 14–15 days after transferal from other hospitals or from a care home to our hospital. No patients required emergency tracheal intubation, circulatory support or kidney replacement therapy.
Compared with patients who recovered, those with the decreased respiratory condition were significantly older, predominantly male sex, with larger body mass index, and had a higher proportion with diabetes mellitus (Table 4). Compared with patients with recovered respiratory condition, for patients with decreased respiratory condition, aspartate aminotransferase (AST), alanine aminotransferase (ALT), lactate dehydrogenase (LDH), creatinine and inflammation-related indices (CRP, fibrinogen and ferritin), but not D-dimer were significantly elevated, lymphocyte counts were significantly decreased.
Table 4.
Univariate analysis of characteristics, comorbidities, and laboratory data between patients with recovered and worsened respiratory condition
| All (n = 300) | Recovered (n = 276) | Worsened (n = 21) | P value | |
|---|---|---|---|---|
| Age (year) | 53 (33–72) | 52 (32–72) | 63 (48–73) | 0.03 |
| Sex (male) | 171 (57%) | 150 (54%) | 20 (95%) | < 0.001 |
| Body mass index (kg/m2) | 23 (21–26) | 23 (21–26) | 25 (24–26) | 0.04 |
| Comorbidities | ||||
| Hypertension | 68 (23%) | 62 (21%) | 6 (29%) | 0.3 |
| Diabetes mellitus | 60 (20%) | 50 (18%) | 10 (48%) | 0.003 |
| Laboratory data | ||||
| White blood cell count (×109/L) | 5.2 (4.0–7.0) | 5.2 (4.0–6.9) | 5.4 (5.0–6.7) | 0.5 |
| Lymphocyte (× 109/L) | 1.2 (0.9 − 1.6) | 1.2 (0.9 − 1.6) | 1.0 (0.7 − 1.4) | 0.04 |
| Aspartate aminotransferase (U/L) | 27 (20–39) | 27 (20–37) | 36 (31–54) | < 0.001 |
| Alanine aminotransferase (U/L) | 24 (14–41) | 22 (13–40) | 34 (27–57) | 0.003 |
| Lactate dehydrogenase (U/L) | 212 (173–272) | 209 (168–265) | 267 (221–348) | < 0.001 |
| Creatinine (mg/dL) | 0.76 (0.61–1.00) | 0.76 (0.61–0.91) | 0.83 (0.75–0.95) | 0.03 |
| C-reactive protein (mg/dL) | 1.8 (0.4–4.5) | 1.5 (0.3–4.0) | 5.2 (3.5–9.2) | < 0.001 |
| Fibrinogen (mg/dL) | 420 (327–548) | 411 (322–531) | 548 (470–635) | < 0.001 |
| D-dimer (µg/dL) | 0.9 (0.7–1.4) | 0.9 (0.7–1.4) | 1.0 (0.9–1.6) | 0.16 |
| Ferritin (ng/mL) | 397 (189–800) | 362 (166–733) | 1006 (530–1409) | < 0.001 |
Data are expressed as the absolute value (percentage) or median (25–75% interquartile range)
Discussion
Our hospital started receiving patients with COVID-19 on March 25, and was transformed into one specialized for COVID-19 since May 1, 2020 with great efforts of all the medical staff. Similar hospitals are also reported in the US and in Italy [6, 7]. Because the cumulative number of patients of COVID-19 was approximately 9600 until September 14 in the Osaka prefecture,3 we provided medical care for almost 3% of the total number of patients in this area.
The mortality rate was only 1% (3/300), much lower than early reports from China (28%, from December, 2019 to January, 2020) and from the US (21%, from March to April, 2020) [8–10], although the distribution of age, the ratio of male sex and comorbidities were similar to those reports. This might result from the small number of patients with severe respiratory dysfunction admitted to our hospital, as supported by the similarly low mortality rate (1.1%) in non-severe cases in China [5]. The global mortality rate in Japan is approximately 1.5%, still lower than other countries (see Footnote 1). This might result from the reduced susceptibility to COVID-19 due to angiotensin-converting enzyme 2 receptor expression and/or different human leukocyte antigen (HLA) that confers immune resistance to coronavirus specific for Japanese [11], although the precise reason remains unclear.
All the patients initially classified as mild or moderate I severity (n = 223) were discharged without requiring invasive respiratory treatment. On the other hand, respiratory condition further deteriorated in 21 out of 74 patients (28%) with moderate II or severe respiratory conditions on admission, most of whom required transferal to tertiary hospitals for intensive therapy. This is comparable with the proportion of patients requiring invasive care units among those with a severe condition in the US [2] and in China [5] (17% for both), suggesting that the low mortality rate in Japan would result from the decreased proportion of patients with the severe respiratory condition compared with other countries. Although the severity classification defined by the Ministry of Health, Labour and Welfare, Japan (see Footnote 2) is different from those used in other studies [12], it would be practical and useful for prompt evaluation and prediction of the prognosis based on this study.
A rapid transferal system to tertiary hospitals would be an urgent issue because most of the surrounding hospitals, including ours, do not have enough capacity including equipment or medical staffs for managing severe cases requiring tracheal intubation, mechanical ventilation, and extracorporeal membrane oxygenation. There were 28 patients who were transferred from the tertiary hospitals after recovery from the severe state. Besides receiving patients with new-onset of COVID-19, it is also an important role of our hospital to receive these patients to facilitate the transferal of severe patients to tertiary hospitals because of the full capacity of the ICU.
Regarding laboratory data, abnormalities in CRP, LDH, fibrinogen and ferritin were consistent with previous studies [9, 13]. D-dimer exceeded the normal range (1.0 µg/dL) in 39% cases in our study, similar to the value reported previously [8]; however, it was not higher in patients whose respiratory condition worsened compared with those recovered in the present study. Possible reasons for this would be that the number of elderly patients ≥ 70 years was small (29%) and the outcome was generally favorable. Although few reports evaluate CRP and refer to it in patients with poor prognosis [13, 14], it is regulated by inflammatory cytokines such as interleukin-1 and 6, and systemic inflammation would significantly contribute to the outcome. Longer elapsed time from the onset of COVID-19 to admission (median, 7 days) compared with other reports [2] may be one of the reasons for remarkably elevated CRP.
There are several limitations in this study. This is a retrospective data collection from a small number of patients in a single institute. Most of the patients were classified as mild or moderate severity, and the number of patients with the deteriorated condition or died was too small to elucidate more factors for worsening of the respiratory condition, according to a previous study for statistical analysis [15]. Moreover, the outcome of patients with severe conditions is not known because they were transferred to tertiary care hospitals. The admission policy of patients with COVID-19 to our hospital has changed after the completion of this study, to admit patients with moderate severity or those aged ≥ 65 years on a priority basis because of an increase of affected patients. Patients’ profiles and outcomes in our institute remarkably changed after 2020 October.
In conclusion, we received 300 COVID-19 patients with predominantly mild and moderate severity as a specialized hospital. Respiratory conditions worsened in 7% and in-hospital mortality rate was as low as 1%, probably because of relatively young age. The ratios of male patients, of patients with diabetes mellitus in those with decreased respiratory condition were significantly higher than recovered.
Author contributions
YO conceptualized the study. YO, SS, and MS collected data. YO drafted the manuscript and OK provided critical comments.
Data availability
The datasets used and/o analyzed during the current study are available from the corresponding author on reasonable request.
Declarations
Conflict of interests
The authors declare that they have no conflict of interests.
Footnotes
https://coronavirus.jhu.edu/map.html, accessed Dec. 16, 2020.
https://www.mhlw.go.jp/content/000646531.pdf, accessed Dec. 23, 2020.
This study was carried out at the Department of Anesthesiology, Respiratory Medicine, Gastroenterology and Hepatology, Osaka City Juso Hospital
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Contributor Information
Yutaka Oda, Email: yutakaodayutaka@gmail.com.
Satoshi Shiraishi, Email: s-shiraishi@med.osakacity-hp.or.jp.
Motoko Shimada, Email: m0m017@hotmail.com.
Osamu Kurai, Email: kuraion2@gmail.com.
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Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Data Availability Statement
The datasets used and/o analyzed during the current study are available from the corresponding author on reasonable request.