Literature DB >> 33883900

Predictors of Length of Hospital Stay, Mortality, and Outcomes Among Hospitalised COVID-19 Patients in Saudi Arabia: A Cross-Sectional Study.

Hassan Alwafi1, Abdallah Y Naser2, Sultan Qanash3,4, Ahmad S Brinji5, Maher A Ghazawi5, Basil Alotaibi6, Ahmad Alghamdi7, Aisha Alrhmani7, Reham Fatehaldin7, Ali Alelyani7, Abdulrhman Basfar7, Abdulaziz AlBarakati7, Ghaidaa F Alsharif7, Elaf F Obaid7, Mohammed Shabrawishi7,8.   

Abstract

BACKGROUND: COVID-19 pandemic is a major strain on health and economic systems, with rapidly increasing demand for in patients' facilities. Disease diagnosis and estimating patients at higher risk is important for the optimal management during the pandemic. This study aimed to identify the predictors of mortality and length of hospital stay in COVID-19 patients.
METHODS: A retrospective cross-sectional study was conducted between March 2020 and August 2020 at Al-Noor Specialist Hospital in Mecca, Saudi Arabia. All patients who were admitted and had a confirmed COVID-19 diagnosis by a real-time polymerase chain reaction (PCR) were included in the study. Descriptive statistics were used to describe patients' demographic characteristics, laboratory findings, and clinical outcomes. Multiple logistic/linear regression analysis was used to identify predictors of death and length of stay at the hospital.
RESULTS: A total of 706 patients were hospitalised for COVID-19. The mean age was 48.0 years (SD: 15.6 years). More than half of the patients (68.5%; n= 292) were males. The median duration of stay at the hospital was 6.0 days (IQR: 300-10:00). The prevalence rate of venous thromboembolism (VTE) among the patients was 3.0% (n= 21). In the multivariate logistic regression analysis, age (AOR: 1.05; 1.02-1.09), patients with end-stage renal disease (AOR: 6.44; 2.20-18.87), low Oxygen saturation SPO2 (AOR: 9.92; 4.19-23.50), D.dimer >0.5 (AOR: 13.31; 5.45-32.49), ESR>10 mm/h (AOR: 4.08; 1.72-9.68), Ferritin>400mcg/L (AOR: 18.55; 6.89-49.96), and Procalcitonin>0.5ug/L (AOR: 8.23; 1.81- 37.40) were associated with a higher risk of death among patients with COVID-19. Patients with VTE (AOR: 12.86; 3.07- 53.92) were at higher risk of death due to COVID-19.
CONCLUSION: Hospitalised COVID-19 patients have multiple negative consequences in terms of their laboratory findings, signs and symptoms. Age and end-stage renal diseases have a significant impact on the mortality rate and the length of hospital stay among COVID-19 patients.
© 2021 Alwafi et al.

Entities:  

Keywords:  COVID-19; ICU; Saudi Arabia; hospitalisation; length of stay; survival

Year:  2021        PMID: 33883900      PMCID: PMC8055273          DOI: 10.2147/JMDH.S304788

Source DB:  PubMed          Journal:  J Multidiscip Healthc        ISSN: 1178-2390


Introduction

The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), which was discovered in China in 2019, is an ongoing pandemic.1 In March 2021, it was reported that there are more than 117 million confirmed cases in the world, and the total number of deaths in the world is around 2,600,000 in 220 countries, with a mortality rate of around 2%.2 In Saudi Arabia, there were around 380,000 confirmed infected cases by January 2021, and a mortality rate of around 1.7%.3 Patients with COVID-19 usually complain of fever, cough, fatigue, anorexia, myalgia, and diarrhoea,4 but in severe illness, usually dyspnoea is the most common symptom often accompanied by hypoxemia.4 Mortality rates depend on patients who have severe respiratory failure related to interstitial pneumonia and acute respiratory distress syndrome,5 but higher mortality is found in association with older age, male sex, pre-existing cardiovascular diseases, uncontrolled diabetes, hypertension, asthma, chronic lung disease, and d-dimer greater than 1 μg/mL at admission.6 Length of hospital stay due to the COVID-19 depends on patients’ clinical situation, however, it also depends on local guidelines in the institution or local health authority and the capacity of hospitals.7,8 COVID-19 pandemic is a major strain on health and economic systems, and the demand for inpatients’ facilities is increasing with the increase in the number of infected cases.9 Predicting factors associated with the need for hospitalisation and length of stay can be important to help in aid prioritizing patients, decision-making and contingency planning.10 This study aimed to identify the predictors of mortality and length hospital of stay in COVID-19 patients.

Methods

Study Design and Participants

A retrospective cross-sectional study was conducted at Al-Noor Specialist Hospital in Mecca, Saudi Arabia. Al-Noor Specialist Hospital is a tertiary hospital in Mecca, Saudi Arabia, and it is part of the Ministry of Health. The description of the study settings and the hospital has been described previously.11 All patients had a confirmed COVID-19 diagnosis by a real-time polymerase chain reaction (PCR). The PCR samples were obtained through a nasopharyngeal swap. All patients were admitted between March 15, 2020, and June 15, 2020 and they were followed up for a time to assess the clinical outcome; and the final date of follow-up was August 15, 2020. Data collection were between March 2020, and August 2020. All patients who were admitted and had a confirmed diagnosis of COVID-19 during the study period were included in the study.

Data Collection and Study Variables

Data were collected from patients’ files and electronic records using a unique medical record number (MRN) for each patient. All data were collected, reviewed and checked by a medical team, including medical residents and a consultant pulmonologist. Data included the patient’s demographics, clinical symptoms, comorbidity, and laboratory findings. Data were collected at the time of admission to the hospital. Patients were classified according to their severity based on the following category: mild, moderate, severe and, critically severe disease. The definition of these categories has been described previously.11

Outcomes

The primary outcome was predictors of patients’ admission to an intensive care unit. Secondary outcomes were to identify predictors of length of hospital stay and mortality.

Ethical Approval and Consent-to-Participate

The study protocol and study methodology were approved by the Ministry of Health’s Institutional Review Board (IRB), as well as the hospital (No H-02-K-076-0920-386). Patients informed consent were obtained and patients were informed that their clinical data would be used for clinical or research purposes, while keeping all their personal information confidential. The ethical principles of the Declaration of Helsinki were adhered to during collection, handling, and storage of data, and all care was taken to protect patient confidentiality.

Statistical Analysis

Descriptive statistics were used to describe patients’ demographics, laboratory findings, and clinical outcomes. Independent sample t-test was used to compare the mean value for continuous variables. A Chi-squared test/Fisher test was used to compare proportions for categorical variables. Multiple logistic/linear regression analysis was used to identify predictors of death and length of stay at the hospital, and a confidence interval of 95% (p < 0.05) was applied to represent the statistical significance of the results. All statistical analyses were conducted using SPSS (Statistical Package for the Social Sciences) version 25.0 software (SPSS Inc.).

Results

Patients’ Clinical Characteristics

Table 1 below shows the characteristics of COVID-19 patients at presentation to the hospital. A total of 706 patients were hospitalised for COVID-19. The mean age was 48.0 years (SD: 15.6 years). More than half of the patients (68.5%; n= 292) were males. The majority of them were having mild to moderate cases. Twenty-five patients (3.5%) reported working in the healthcare sector. More than half of them (61.9%; n= 435) were non-Saudi. Around 17.4% (n= 122) reported a history of smoking. The most common comorbidities were diabetes mellitus (DM) (36.0%, n= 254), hypertension (30.2%, n= 213), and coronary heart diseases (10.9%; n= 77). Around 9.8% of the patients (n= 69) reported a recent travel history. Regarding the severity of the patients’ case, 33.7% were mild, 30.3% were moderate, and 24.2% were severe, and 11.8% were critical and required intensive care unit (ICU) care. Regarding patients’ vital signs upon arrival to hospital, 47.3% (n= 334) had fever (body temperature > 38 °C), 9.5% (n= 67) had respiratory rate (RR) more than 30, 22.1% (n= 156) had SPO2 < 93, and 4.2% (n= 30) had heart rate (HR) > 125.
Table 1

Patients Demographic Characteristics at Presentation

DemographicsAll Patients (n=706)Mild Cases (n= 238)Moderate Cases (n= 214)Severe Cases (n= 171)Critical Cases (n= 83)P-value
Age (years; mean (SD))48.0 years (15.6)41.4 years (14.1)48.4 years (14.3)51.5 years (16.0)58.4 years (14.5)0.001**
Gender (Total n= 426, Mild n= 168, Moderate n= 154, Severe n= 58, Critical n= 46)
 Male No. (%)292 (68.5)116 (69.0)96 (62.3)49 (84.5)31 (67.4)0.022*
Healthcare worker (Total n= 705, Mild n= 238, Moderate n= 214, Severe n= 170, Critical n= 83)
 Yes No. (%)25 (3.5)11 (4.6)6 (2.8)6 (3.5)2 (2.4)0.691
Nationality No. (%)
 Non-Saudi435 (61.6)160 (67.2)135 (63.1)90 (52.6)50 (60.2)0.026*
Smoking history (Total n= 698, Mild n= 234, Moderate n= 212, Severe n= 169, Critical n= 83)
 Yes No. (%)122 (17.3)46 (19.7)31 (14.6)36 (21.3)9 (10.8)0.102
Body mass index (BMI)
 BMI >30 kg/m288 (15.8)18 (11.1)27 (16.7)30 (18.9)13 (17.8)0.250
Comorbidities No. (%)
 Diabetes mellitus254 (36.0)55 (23.1)72 (33.6)73 (42.7)54 (65.1)0.000***
 Hypertension213 (30.2)38 (16.0)68 (31.8)62 (36.3)45 (54.2)0.000***
 Coronary artery disease77 (10.9)4 (1.7)19 (8.9)35 (20.5)19 (22.9)0.000***
 End-Stage Renal Disease64 (9.1)8 (3.4)20 (9.4)13 (7.6)23 (27.7)0.000***
 Asthma28 (4.0)11 (4.6)7 (3.3)8 (4.7)2 (2.4)0.730
 Congestive heart failure27 (3.8)1 (0.4)5 (2.3)13 (7.6)8 (9.6)0.000***
 Cerebrovascular accident17 (2.4)1 (0.4)07 (4.1)9 (10.8)0.000***
 Chronic obstructive pulmonary disease14 (2.0)2 (0.8)4 (1.9)5 (2.9)3 (3.6)0.320
 Chronic liver disease4 (0.6)01 (0.5)1 (0.6)2 (2.4)0.095
 Cancer3 (0.4)01 (0.5)02 (2.4)0.024*
Tracing history No. (%)
 Recent travel history (Total n= 704, Mild n= 238, Moderate n= 212, Severe n= 171, Critical n= 83) (Yes) No. (%)69 (9.8)30 (12.6)32 (15.1)6 (3.5)1 (1.2)0.000***
 Contact with traveller (Total n= 706, Mild n= 238, Moderate n= 214, Severe n= 171, Critical n= 83) (Yes) No. (%)84 (11.9)38 (16.0)39 (18.2)5 (2.9)2 (2.4)0.000***
 Contact with COVID-19 patient (Total n= 706, Mild n= 238, Moderate n= 214, Severe n= 171, Critical n= 83) (Yes) No. (%)324 (45.9)127 (53.4)101 (47.2)65 (38.0)31 (37.3)0.007**
Vital signs upon arrival to hospital No. (%)
 Fever (≥ 38°C) (Yes) No. (%)334 (47.3)71 (29.8)84 (39.3)127 (74.3)52 (62.7)0.000***
 Respiratory rate > 30 (Yes) No. (%)67 (9.5)1 (0.4)1 (0.5)38 (22.2)27 (32.5)0.000***
 SPO2<93 (Yes) No. (%)156 (22.1)6 (2.5)6 (2.8)97 (56.7)47 (56.6)0.000***
 Heart rate>125 (Yes) No. (%)30 (4.2)04 (1.9)8 (4.7)18 (21.7)0.000***
Outcome No. (%) (n= 680)
 Deceased54 (7.6)001 (0.6)53 (71.6)0.000***
 Not recovered3 (0.4)0003 (4.1)0.000***
 Recovered623 (91.6)235 (100)214 (100)156 (99.4)18 (24.3)0.000***
Respiratory diseases
 Venous thromboembolism21 (3.0)03 (1.4)4 (2.3)14 (16.9)0.000***
 Pneumonia (radiologically)450 (63.6)0215 (99.5)155 (90.6)80 (96.4)0.000***

Notes: *p < 0.05; **p < 0.01; ***p < 0.001.

Abbreviations: COVID-19, coronavirus disease-2019; SD, standard deviation; No, number (frequency).

Patients Demographic Characteristics at Presentation Notes: *p < 0.05; **p < 0.01; ***p < 0.001. Abbreviations: COVID-19, coronavirus disease-2019; SD, standard deviation; No, number (frequency). Fever was the most common symptom at presentation (72.4%, n= 511), followed by cough (63.0%, n= 445), and shortness of breath (56.4%, n= 398) (Table 2). Fever, cough, shortness of breath, nausea/vomiting, headache, loss of taste and smell, sputum were more common across severe and critical cases compared to others.
Table 2

Patient Signs and Symptoms Stratified by Severity

VariableAll Patients (n=706)Mild Cases (n= 238)Moderate Cases (n= 214)Severe Cases (n= 171)Critical Cases (n= 83)P-value
Fever511 (72.4)143 (60.1)152 (71.0)150 (87.7)66 (79.5)0.000***
Cough445 (63.0)140 (58.8)128 (59.8)117 (68.4)60 (72.3)0.047*
Shortness of breath398 (56.4)90 (37.8)97 (45.3)143 (83.6)68 (81.9)0.000***
Fatigue176 (25.0)52 (21.8)43 (20.1)61 (35.9)20 (24.1)0.002**
Nausea/vomiting118 (16.7)38 (16.0)23 (10.7)43 (25.1)14 (16.9)0.003**
Sore throat115 (16.3)54 (22.7)29 (13.6)25 (14.6)7 (8.5)0.006**
Myalgia108 (15.3)31 (13.0)24 (11.3)42 (24.6)11 (13.3)0.002**
Headache102 (14.4)31 (13.0)28 (13.1)31 (18.1)12 (14.5)0.460
Loss of taste98 (13.9)30 (12.6)21 (9.8)21 (12.3)26 (31.3)0.000***
Loss of smell90 (12.7)28 (11.8)19 (8.9)18 (10.5)25 (30.1)0.000***
Diarrhea52 (7.4)19 (8.0)13 (6.1)15 (8.8)5 (6.0)0.705
Sputum35 (5.0)10 (4.2)8 (3.7)11 (6.4)6 (7.2)0.447
Runny nose25 (3.5)16 (6.7)5 (2.3)2 (1.2)2 (2.4)0.012*
Haemoptysis2 (0.3)001 (0.6)1 (1.2)0.228

Notes: *p<0.05; **p<0.01; ***p<0.000.

Patient Signs and Symptoms Stratified by Severity Notes: *p<0.05; **p<0.01; ***p<0.000.

Laboratory Findings

Around 16.5% (n= 116) of the patients had white blood cell (WBC)> 10,000, 13.9% (n= 98) had WBC< 4000, and 21.0% (n= 148) of them had lymphocyte count <1500. About 12.6% (89) had platelet count < 150 and 29.9% (n= 210) had D.dimer >0.5. The proportion of patients who had WBC >10,000, lymphocyte count <1500, platelet count < 150, and D.dimer >0.5 increase as the severity of the disease increase in a statistically significant pattern (p<0.001). The mean Neutrophil-lymphocyte ratio (NLR) value was 9.9 (SD:33.5). The most common blood groups of COVID-19 patients were A+, O+, and B+ accounting for 35.7%, 28.6%, and 20.5% respectively (Table 3).
Table 3

Laboratory Findings of the Study Participants Stratified by Severity

VariableAll Patients (n=706)Mild Cases (n= 238)Moderate Cases (n= 214)Severe Cases (n= 171)Critical Cases (n= 83)P-value
Complete Blood Count
WBC >10,000 (Total n= 701, Mild n= 234, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)116 (16.5)17 (7.3)22 (10.3)32 (18.7)45 (54.9)0.000***
WBC <4000 (Total n= 705, Mild n= 238, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)98 (13.9)34 (14.3)34 (15.9)21 (12.3)9 (11.0)0.638
Lymphocyte count <1500 (Total n= 704, Mild n= 237, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)148 (21.0)25 (10.5)40 (18.7)43 (25.1)40 (48.8)0.000***
NLR (Mean (SD))9.9 (33.5)1.17 (2.33)1.23 (2.28)9.2 (66.9)12.8 (18.8)0.000***
Platelet < 150 (Total n= 704, Mild n= 238, Moderate n= 214, Severe n= 170, Critical n= 82) (Yes) No. (%)89 (12.6)21 (8.8)23 (10.7)22 (12.9)23 (28.0)0.000***
D.dimer >0.5 (Total n= 703, Mild n= 236, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)210 (29.9)27 (11.4)35 (16.4)91 (53.2)57 (69.5)0.000***
Blood Groups (Total n= 322, Mild n= 82, Moderate n= 86, Severe n= 114, Critical n= 40) (Yes) No. (%)
A+115 (35.7)34 (41.5)21 (24.4)44 (38.6)16 (40.0)0.000***
A-2 (0.6)002 (1.8)0
AB+22 (6.8)5 (6.1)5 (5.8)9 (7.9)3 (7.5)
AB-1 (0.3)1 (1.2)000
B+66 (20.5)16 (19.5)24 (27.9)20 (17.5)6 (15.0)
B-3 (0.9)1 (1.2)2 (2.3)00
O+92 (28.6)19 (23.2)27 (31.4)32 (28.1)14 (35.0)
O–21 (6.5)6 (7.3)7 (8.1)7 (6.1)1 (2.5)
Inflammatory measures
ESR>10 mm/h (Total n= 704, Mild n= 238, Moderate n= 214, Severe n= 170, Critical n= 82) (Yes) No. (%)366 (52.0)67 (28.2)99 (46.3)139 (81.8)61 (74.4)0.000***
CRP>0.3 mg/dl (Total n= 704, Mild n= 238, Moderate n= 213, Severe n= 171, Critical n= 82) (Yes) No. (%)340 (48.3)65 (27.3)97 (45.6)132 (77.2)46 (56.1)0.000***
Ferritin>400mcg/L (Total n= 705, Mild n= 238, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)204 (28.9)40 (16.8)43 (20.1)76 (44.4)45 (54.9)0.000***
Procalcitonin>0.5ug/L (Total n= 705, Mild n= 237, Moderate n= 216, Severe n= 170, Critical n= 82) (Yes) No. (%)13 (1.8)1 (0.4)6 (2.8)2 (1.2)4 (4.9)0.041*
Liver Function Tests (Total n= 705, Mild n= 238, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)
AST>40251 (35.6)58 (24.4)61 (28.5)81 (47.4)51 (62.2)0.000***
ALT>40237 (33.6)55 (23.1)56 (26.2)81 (47.4)45 (54.9)0.000***
LDH>230 U/L (Total n= 704, Mild n= 238, Moderate n= 213, Severe n= 171, Critical n= 82) (Yes) No. (%)282 (40.1)51 (21.4)62 (29.1)108 (63.2)61 (74.4)0.000***
Bilirubin>18.7 umol/L44 (6.2)6 (2.5)9 (4.2)11 (6.4)18 (22.0)0.000***
Renal function tests (Total n= 705, Mild n= 238, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)
Creatinine>115umol/L121 (17.2)13 (5.5)28 (13.1)34 (19.9)46 (56.1)0.000***
Urea>6.04 mmol/L (Total n= 704, Mild n= 237, Moderate n= 214, Severe n= 171, Critical n= 82) (Yes) No. (%)171 (24.3)19 (8.0)46 (21.5)57 (33.3)49 (59.8)0.000***

Notes: *p < 0.05; ***p < 0.001. Reference values; WBC: 4000–1000; lymphocyte: 1500–4000; NLR: 0.78–3.53; platelet: 150–400; D.dimer: 0–0.55; ESR: 0–10; CRP: 0–0.3; ferritin: 10–291; procalcitonin: 0–0.5; AST: 10–34; ALT: 46–120; LDH: 80–230; bilirubin: 0–18.7; creatinine: 44–90; urea: 3.2–8.2.

Abbreviations: AST, aspartate transaminase; ALT, alanine transaminase; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; NLR, neutrophil-lymphocyte ratio; LDH, lactate dehydrogenase; WBC, white blood cell.

Laboratory Findings of the Study Participants Stratified by Severity Notes: *p < 0.05; ***p < 0.001. Reference values; WBC: 4000–1000; lymphocyte: 1500–4000; NLR: 0.78–3.53; platelet: 150–400; D.dimer: 0–0.55; ESR: 0–10; CRP: 0–0.3; ferritin: 10–291; procalcitonin: 0–0.5; AST: 10–34; ALT: 46–120; LDH: 80–230; bilirubin: 0–18.7; creatinine: 44–90; urea: 3.2–8.2. Abbreviations: AST, aspartate transaminase; ALT, alanine transaminase; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; NLR, neutrophil-lymphocyte ratio; LDH, lactate dehydrogenase; WBC, white blood cell. Regarding patients’ inflammatory measures, around half of the patients had erythrocyte sedimentation rate (ESR)>10 mm/h and C-reactive protein (CRP)>0.3 mg/dl. One-third of the patients had Ferritin>400mcg/L, and 1.8% of them had Procalcitonin>0.5ug/L. Concerning patients’ liver function tests, around one-third of the patients had AST>40 and ALT>40. Additionally, 40.1% of them had lactate dehydrogenase (LDH)>230 U/L, and 6.2% had Bilirubin>18.7 umol/L. Regarding patients’ kidney function tests, 17.2% of them had Creatinine>115 umol/L, and 24.3% had Urea>6.04 mmol/L (Table 3).

Factors Associated with Death

The median duration of stay at the hospital was 6.0 days (IQR: 300– 10:00). The duration of stay in the hospital ranged from one day to 55 days. The prevalence rate of venous thromboembolism (VTE) among the patients was 3.0% (n= 21). More than half of the patients (63.6%; n= 450) pneumonia radiologically. At the end of the follow-up period, a total of 623 patients (91.6%) recovered. Three patients (0.4%) did not recover at the end of the follow-up, and 7.6% of the patients (n= 54) deceased while the remaining either transferred to other facility or still in the hospital, at last, follow up. The severity of the cases affected the recovery rate and mortality rate in a statistically significant way (p>0.001) (Table 1). In the multivariate logistic regression analysis, the following risk factors were associated with a higher risk of death among patients with COVID-19. Age (AOR: 1.05; 1.02–1.09), high respiratory rate (RR) (AOR: 153.90; 9.80–2416.60), low Oxygen saturation SPO2 (AOR: 9.92; 4.19–23.50), D.dimer >0.5 (AOR: 13.31; 5.45–32.49), ESR>10 mm/h (AOR: 4.08; 1.72–9.68), Ferritin>400mcg/L (AOR: 18.55; 6.89–49.96), and Procalcitonin>0.5ug/L (AOR: 8.23; 1.81–37.40). Patients with VTE (AOR: 12.86; 3.07–53.92) were at higher risk of death due to COVID-19. End-stage renal diseases were identified to increase the risk of COVID-19. For further details, please refer to Table 4.
Table 4

Logistic Regression to Identify Risk Factors of Death

DemographicsOdds Ratio for Deatha95% CIOdds Ratio for Deathb95% CI
Age1.06(1.04 – 1.08)***1.05(1.02 – 1.09)**
Gender
Female (Reference category)1.001.00
Male0.77(0.39 – 1.54)0.30(0.11 – 0.81)*
Smoking history
No (Reference category)1.001.00
Yes0.36(0.13 – 1.02)0.49(0.13 – 1.91)
BMI
BMI <30 kg/m2 (Reference category)1.001.00
BMI >30 kg/m21.24(0.59 – 2.63)0.25(0.06 – 1.01)
Comorbidities (not having the disease is the reference category)
Diabetes mellitus4.82(2.63 – 8.85)***1.64(0.59 – 4.54)
Hypertension5.91(3.24 – 10.77)***1.63(0.55 – 4.85)
Coronary artery disease3.04(1.54 – 5.99)**1.08(0.28 – 4.17)
End-Stage Renal Disease6.97(3.69 – 13.17)***6.44(2.20 – 18.87)**
Asthma0.42(0.06 – 3.13)0.80(0.07 – 8.82)
Congestive heart failure3.59(1.38 – 9.32)**0.85(0.17 – 4.31)
Cerebrovascular accident10.18(3.63 – 28.54)***2.09(0.37 – 11.92)
Chronic obstructive pulmonary disease0.89(0.11 – 6.90)
Chronic liver disease11.92(1.65 – 86.38)*
Cancer23.96(2.14 – 268.68)*
Vital signs upon arrival to hospital (having the normal range is the reference category)
Fever (≥ 38°C) (Yes)1.28(0.73 – 2.24)1.46(0.68 – 3.13)
Respiratory rate > 30 (Yes)7.09(3.66 – 13.73)***153.90(9.80 – 2416.60)***
SPO2<93 (Yes)2.63(1.46 – 4.73)**9.92(4.19 – 23.50)***
Heart rate>125 (Yes)12.87(5.74 – 28.86)***19.82(5.22 – 75.25)***
Outcome
Venous thromboembolism (Yes)17.54(6.90 – 44.61)***12.86(3.07 – 53.92)***
Pneumonia Radiologically(Yes)2.35(1.19 – 4.61)*1.37(0.95 – 1.98)
Complete Blood Count (having the normal range is the reference category)
WBC >10,000 (Yes)12.36(6.74 – 22.68)***16.47(6.78 – 40.00)***
WBC <4000 (Yes)0.34(0.10 – 1.11)0.31(0.07 – 1.48)
Lymphocyte count <1500 (Yes)5.70(3.19 – 10.17)***10.17(4.29 – 24.14)***
NLR (Mean (SD))1.00(1.00 – 1.01)1.23(1.15 – 1.32)***
Platelet < 150 (Yes)5.73(3.12 – 10.53)***9.92(4.01 – 24.52)***
D.dimer >0.5 (Yes)8.47(4.48 – 16.01)***13.31(5.45 – 32.49)***
Inflammatory measures (having the normal range is the reference category)
ESR>10 mm/h (Yes)2.89(1.54 – 5.42)**4.08(1.72 – 9.68)**
CRP>0.3 mg/dl (Yes)0.90(0.52 – 1.55)0.84(0.39 – 1.80)
Ferritin>400mcg/L (Yes)3.89(2.19 – 6.91)***18.55(6.89 – 49.96)***
Procalcitonin>0.5ug/L (Yes)5.58(1.66 – 18.77)**8.23(1.81 – 37.40)**
Liver Function Tests (having the normal range is the reference category)
AST>40 (Yes)3.71(2.07 – 6.67)***8.85(3.64 – 21.50)***
ALT>40 (Yes)2.41(1.37 – 4.24)**4.78(2.11 – 10.83)***
LDH>230 U/L (Yes)6.09(3.13 – 11.82)***21.26(7.61 – 59.40)***
Bilirubin>18.7 umol/L (Yes)1.51(1.14 – 2.00)**15.06(4.63 – 48.99)***
Renal function tests (having the normal range is the reference category)
Creatinine>115umol/L (Yes)18.00(9.46 – 34.25)***36.33(13.65 – 96.66)***
Urea>6.04 mmol/L (Yes)4.48(2.54 – 7.90)***15.27(6.29 – 37.07)***
Blood Groups (blood group A is the reference category)
B0.35(0.08 – 1.47)0.51(0.11 – 2.36)
AB1.08(0.02 – 54.95)
O1.52(0.77 – 2.99)1.50(0.57 – 3.96)

Notes: *p < 0.05; **p < 0.01; ***p < 0.001. aBinary logistic regression. bMultiple logistic regression adjusted for the following variables (age, gender, and comorbidities). Reference values; WBC: 4000–1000; lymphocyte: 1500–4000; NLR: 0.78–3.53; platelet: 150–400; D.dimer: 0–0.55; ESR: 0–10; CRP: 0–0.3; ferritin: 10–291; procalcitonin: 0–0.5; AST: 10–34; ALT: 46–120; LDH: 80–230; bilirubin: 0–18.7; creatinine: 44–90; urea: 3.2–8.2.

Abbreviations: AST, aspartate transaminase; ALT, alanine transaminase; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; NLR, neutrophil-lymphocyte ratio; LDH, lactate dehydrogenase; WBC, white blood cell.

Logistic Regression to Identify Risk Factors of Death Notes: *p < 0.05; **p < 0.01; ***p < 0.001. aBinary logistic regression. bMultiple logistic regression adjusted for the following variables (age, gender, and comorbidities). Reference values; WBC: 4000–1000; lymphocyte: 1500–4000; NLR: 0.78–3.53; platelet: 150–400; D.dimer: 0–0.55; ESR: 0–10; CRP: 0–0.3; ferritin: 10–291; procalcitonin: 0–0.5; AST: 10–34; ALT: 46–120; LDH: 80–230; bilirubin: 0–18.7; creatinine: 44–90; urea: 3.2–8.2. Abbreviations: AST, aspartate transaminase; ALT, alanine transaminase; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; NLR, neutrophil-lymphocyte ratio; LDH, lactate dehydrogenase; WBC, white blood cell.

Factors Associated with Increased Length of Stay

Several factors were associated with increased risk of the length of stay, including comorbidities such as congestive heart failure, cerebrovascular accident, and COPD, fever, D.dimer value of more than >0.5, WBC>10,000, ESR>10 mm/h, CRP>0.3 mg/dl, ferritin > 400 mcg/L, procalcitonin >0.5 ug/L, LDH>230 U/L, creatinine >115 umol/L, and blood group O (p<0.05), for further details, please refer to Table 5.
Table 5

Linear Regression to Identify Predictors of Length of Stay

DemographicsModel aModel b
BSEßBSEß
Age0.070.020.145***−0.0130.02−0.03
Gender
Female0.930.68−0.07−1.210.66−0.09
Smoking history
Yes3.040.71−0.16***−1.751.03−0.11
BMI
BMI >30 kg/m20.120.770.014.276.700.04
Comorbidities (not having the disease is the reference category)
Diabetes mellitus2.460.560.17***0.730.760.05
Hypertension3.070.580.20***0.550.820.04
Coronary artery disease3.060.860.13***−1.001.21−0.04
End-Stage Renal Disease7.680.910.31***−1.042.00−0.03
Asthma1.201.400.03−0.282.16−0.01
Congestive heart faliure3.771.400.10**−1.042.00−0.03
Cerebrovascular accident5.311.740.12**7.822.180.17***
Chronic obstructive pulmonary disease3.931.920.08*3.633.960.05
Chronic liver disease3.083.590.032.764.830.03
Cancer−0.604.14−0.01−4.883.98−0.06
Vital signs upon arrival to hospital
Fever (≥ 38°C) (Yes)2.190.540.15***1.830.640.13**
Respiratory rate > 30 (Yes)5.150.900.21***0.832.380.02
SPO2<93 (Yes)1.900.480.15***0.210.970.01
Heart rate>125 (Yes)4.951.320.14***0.541.820.01
Outcome
Venous thromboembolism (Yes)5.041.620.12**2.192.060.05
Pneumonia (Yes)2.790.420.24***1.190.440.13**
Complete Blood Count
WBC >10,000 (Yes)4.020.720.21***2.370.870.13**
WBC <4000 (Yes)−0.380.79−0.021.690.930.09
Lymphocyte count <1500 (Yes)1.020.670.061.130.890.06
NLR (Mean (SD))0.000.010.020.070.060.06
Platelet < 150 (Yes)0.240.810.010.451.070.02
D.dimer >0.5 (Yes)3.570.580.23***2.570.870.15**
Inflammatory measures
ESR>10 mm/h (Yes)2.090.540.15***1.640.640.12*
CRP>0.3 mg/dl (Yes)2.100.540.15***2.740.640.20***
Ferritin>400mcg/L (Yes)4.590.570.29***3.700.720.24***
Procalcitonin>0.5ug/L (Yes)4.462.000.08*4.941.780.13**
Liver Function Tests
AST>40−0.270.57−0.02−0.810.69−0.06
ALT>40−0.120.57−0.01−0.820.71−0.06
LDH>230 U/L (Yes)2.090.550.14***2.320.700.16**
Bilirubin>18.7 umol/L0.610.430.051.031.480.04
Renal function tests
Creatinine>115umol/L4.900.690.26***2.441.090.13*
Urea>6.04 mmol/L (Yes)2.890.540.20***1.690.910.10
Blood Groups
B−1.380.92−0.06−1.031.12−0.04
AB−3.583.22−0.042.704.830.03
O0.520.740.033.430.950.17***

Notes: *p < 0.05; **p < 0.01; ***p < 0.001. Model a: Univariate linear regression. Model b: Multiple linear regression adjusted for the following variables (age, gender and comorbidities).

Abbreviations: AST, aspartate transaminase; ALT, alanine transaminase; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; NLR, neutrophil-lymphocyte ratio; LDH, lactate dehydrogenase; WBC, white blood cell; B, the average change in the dependent variable associated with a 1 unit change in the independent variable, statistically controlling for the other independent variables; SE, it is the standard deviation of its sampling distribution or an estimate of that standard deviation; ß, a statistical measure that compares the strength of the effect of each individual independent variable to the dependent variable.

Linear Regression to Identify Predictors of Length of Stay Notes: *p < 0.05; **p < 0.01; ***p < 0.001. Model a: Univariate linear regression. Model b: Multiple linear regression adjusted for the following variables (age, gender and comorbidities). Abbreviations: AST, aspartate transaminase; ALT, alanine transaminase; CRP, C-reactive protein; ESR, erythrocyte sedimentation rate; NLR, neutrophil-lymphocyte ratio; LDH, lactate dehydrogenase; WBC, white blood cell; B, the average change in the dependent variable associated with a 1 unit change in the independent variable, statistically controlling for the other independent variables; SE, it is the standard deviation of its sampling distribution or an estimate of that standard deviation; ß, a statistical measure that compares the strength of the effect of each individual independent variable to the dependent variable.

Discussion

In this cross-sectional study, we investigated the predictors of mortality and length of stay in hospital among hospitalised patients with COVID-19. The key findings of this study are that age, patients with chronic comorbidities, patients with VTE and radiological evidence of pneumonia, and higher D-dimer values were important risk factors that were associated with a higher risk of death and increased length of stay in hospital. Our findings revealed the significant impact of age and chronic conditions on the mortality rate and the length of hospital stay. It comes as no surprise that the escalated rate of mortality and prolonged hospital stay was associated with older patients. Thus this study substantiates the previous findings of the literature.12 This may also be due to their weak immune system and some behavioural responses in the measures taken.13,14 Chronic diseases demonstrate a significant influence on the outcomes; diabetes patients were more vulnerable to fatal consequences and longer hospitalisation compared to non-DM patients, which is consistent with results reported from the previous study.15 Hypertensive patients have a propensity to express high mortality rate and stay hospitalised longer. Likewise, pre-existent cardiovascular and cerebrovascular events carry a high risk of death and a longer duration of hospitalisation. The effect of SARS-COV-2 on the vascular endothelium could be explained by the current understanding that angiotensin-converting enzyme 2 (ACE2) cellular receptors as the entry sites of SARS-COV2 as shown in different studies.16,17 There are several explanations for these results, Renin-Angiotensin system (RAAS) and inflammatory cytokines have been mentioned as mediators in severe outcomes among hypertensive patients.18 Furthermore, the frequent utilisation of angiotensin-converting enzyme inhibitors (ACEIs) can lead to a decrease in angiotensin-converting enzyme (ACE) and an increase in the expression of ACE2 in the lungs which eventually facilitates the invasion of Covid-19 virus,19,20 nonetheless this still controversial as illustrated by other studies.21 Further, the severe viral virulence may lead to high oxygen demand, physiological and reflex tachycardia and aggravates the manifestation of coronary artery diseases accompanied by respiratory distress, finally, unfavourable outcomes will present.22 Patients with chronic liver diseases (CLD) were also more susceptible to fatal consequences either death or a longer hospitalisation period. The confirmed laboratory findings emphasise the negative impact of Covid-19 on liver functions. The previous study elucidated the high mortality rate among CLD patient who they are Covid-19 infected.23,24 Our findings also highlighted the high mortality rate and the long period of hospitalisation among cancer patients. The nature of cancer and the antineoplastic agents compromise the immune system. Consequently, it spikes the probability of lethal and severe infection of the Covid-19 virus among these patients. Moreover, the redundant clinical visits for follow up and chemotherapy dose also expose the patients to the infection.25 The hypercoagulability of Covid-19 patients was observed and confirmed by laboratory findings. Venous thrombus embolism was one of the poor outcomes among covid-19 patients with a significant correlation and high odd ratios. The severe infection and long bed-ridden interval in ICU dysregulate the homeostasis of the cascade system by activating the inflammatory cytokines.26 Not withstanding, the pathogeneses of VTE-induced by Covid-19 are complex and multifactorial. Our study provides further evidence of Covid-19 pneumonia as a predictor for the high mortality rate and prolonged hospitalisation. These findings support the aggressive preventive measures that be taken to halt the mortality rate among these patients. In our study, we found no significant difference between blood group type and the risk of death. However, we found a significant difference in the duration of hospital stay for patients with blood group O. Previous reports showed a reduced prevalence of Covid-19 infection in blood group O.27 However, this was later contradicted, as some other published report suggested that there is no link between Covid-19 infection and type of blood group.28,29 Future studies on a larger scale and different populations are needed to investigate this association. In our study and similar to published reports, patients with chronic obstructive pulmonary disease (COPD) were found to be at higher risk for a severe outcome,30 likely due to the fact that these patients usually have reduced lung function along with various comorbidities.31 Interestingly, on the other hand, patients with pre-existent asthma did not have a risk of worse outcome,32 and this could be partly explained by the lower expression of ACE2 in asthmatic bronchial epithelium.33 Obesity is one of the major comorbidities to be considered. Above increasing the risk of different complications such as DM, liver diseases and cardiovascular diseases, we observed obesity also increases the mortality rate and the demand on intensive care facilities among SARS-COV-2 patients, which augments the findings in a previous systematic review.34 Henceforth, obesity is one of the potential predictors for the study outcomes. However, the underlying mechanism behind the bad prognosis of obese patients still unknown. We believe that our results are similar to the literature, it may help in earlier risk stratification, and triage of COVID-19 patients admitted to the hospital and in reducing the overload on emergency departments visits and intensive care units in order to facilitate COVID-19 cases and other emergency care cases. Some factors identified in this study, such as older age and comorbidities, may help policymakers and guidelines in their recommendations about prioritising patients based on their symptoms and may help to improve the patient’s care. Furthermore, the founded risk factors might be helpful in establishing a scoring system that can be applied to predict mortality and appropriate management plan. This study has some limitations. First, the study population only included patients from a single-centre hospital in Saudi Arabia. Second, the cross-sectional study design restricted our ability to identify causality between study variables.

Conclusion

Hospitalised COVID-19 patients have multiple negative consequences in term of their laboratory findings, signs and symptoms. Age and chronic conditions have a significant impact on the mortality rate and the length of hospital stay among COVID-19 patients. Earlier risk stratification of the COVID-19 patients admitted to the hospital is recommended.
  31 in total

Review 1.  Mortality in COPD: Role of comorbidities.

Authors:  D D Sin; N R Anthonisen; J B Soriano; A G Agusti
Journal:  Eur Respir J       Date:  2006-12       Impact factor: 16.671

Review 2.  The use of renin-angiotensin-aldosterone system (RAAS) inhibitors is associated with a lower risk of mortality in hypertensive COVID-19 patients: A systematic review and meta-analysis.

Authors:  Yixuan Wang; Baixin Chen; Yun Li; Lei Zhang; Yuyi Wang; Shuaibing Yang; Xue Xiao; Qingsong Qin
Journal:  J Med Virol       Date:  2020-10-23       Impact factor: 2.327

3.  High mortality rates for SARS-CoV-2 infection in patients with pre-existing chronic liver disease and cirrhosis: Preliminary results from an international registry.

Authors:  Andrew M Moon; Gwilym J Webb; Costica Aloman; Matthew J Armstrong; Tamsin Cargill; Renumathy Dhanasekaran; Joan Genescà; Upkar S Gill; Theodore W James; Patricia D Jones; Aileen Marshall; George Mells; Ponni V Perumalswami; Xiaolong Qi; Feng Su; Nneka N Ufere; Eleanor Barnes; A Sidney Barritt; Thomas Marjot
Journal:  J Hepatol       Date:  2020-05-21       Impact factor: 25.083

4.  Clinical characteristics and manifestations in older patients with COVID-19.

Authors:  Chenchen Wei; Ya Liu; Yapeng Liu; Kai Zhang; Dezhen Su; Ming Zhong; Xiao Meng
Journal:  BMC Geriatr       Date:  2020-10-08       Impact factor: 3.921

5.  Influencing Factors of Understanding COVID-19 Risks and Coping Behaviors among the Elderly Population.

Authors:  Zhonggen Sun; Bingqing Yang; Ruilian Zhang; Xin Cheng
Journal:  Int J Environ Res Public Health       Date:  2020-08-13       Impact factor: 3.390

6.  ABO blood groups and severe outcomes in COVID-19: A meta-analysis.

Authors:  Sukrita Bhattacharjee; Mainak Banerjee; Rimesh Pal
Journal:  Postgrad Med J       Date:  2020-12-24       Impact factor: 2.401

Review 7.  Angiotensin-Converting Enzyme 2: SARS-CoV-2 Receptor and Regulator of the Renin-Angiotensin System: Celebrating the 20th Anniversary of the Discovery of ACE2.

Authors:  Mahmoud Gheblawi; Kaiming Wang; Anissa Viveiros; Quynh Nguyen; Jiu-Chang Zhong; Anthony J Turner; Mohan K Raizada; Maria B Grant; Gavin Y Oudit
Journal:  Circ Res       Date:  2020-04-08       Impact factor: 17.367

8.  Association of respiratory allergy, asthma, and expression of the SARS-CoV-2 receptor ACE2.

Authors:  Daniel J Jackson; William W Busse; Leonard B Bacharier; Meyer Kattan; George T O'Connor; Robert A Wood; Cynthia M Visness; Stephen R Durham; David Larson; Stephane Esnault; Carole Ober; Peter J Gergen; Patrice Becker; Alkis Togias; James E Gern; Mathew C Altman
Journal:  J Allergy Clin Immunol       Date:  2020-04-22       Impact factor: 10.793

9.  Clinical characteristics of chronic liver disease with coronavirus disease 2019 (COVID-19): a cohort study in Wuhan, China.

Authors:  Chaowei Li; Qingshi Chen; Jianwen Wang; Huasong Lin; Yalan Lin; Jinhuang Lin; Fangzhan Peng; Jiangmu Chen; Zhirong Yang
Journal:  Aging (Albany NY)       Date:  2020-08-28       Impact factor: 5.682

10.  Characteristics of and Important Lessons From the Coronavirus Disease 2019 (COVID-19) Outbreak in China: Summary of a Report of 72 314 Cases From the Chinese Center for Disease Control and Prevention.

Authors:  Zunyou Wu; Jennifer M McGoogan
Journal:  JAMA       Date:  2020-04-07       Impact factor: 56.272

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  23 in total

1.  Assessment of caregiver willingness to vaccinate their children against COVID-19 in Saudi Arabia: a cross-sectional study.

Authors:  Mohammed Samannodi; Hassan Alwafi; Abdallah Y Naser; Renan Alabbasi; Nouf Alsahaf; Rawan Alosaimy; Faisal Minshawi; Mohammad Almatrafi; Rami Khalifa; Rakan Ekram; Emad Salawati
Journal:  Hum Vaccin Immunother       Date:  2021-12-02       Impact factor: 3.452

2.  Coronavirus disease 2019 in Saudi Arabia: A nationwide real-world characterization study.

Authors:  Khalidah A Alenzi; Wafi F Albalawi; Tahani S Alanazi; Najah S Alanazi; Deemah S Alsuhaibani; Nouf Almuwallad; Thamir M Alshammari
Journal:  Saudi Pharm J       Date:  2022-02-25       Impact factor: 4.562

3.  The Impact of Vaccination Against SARS-CoV-2 Virus on the Outcome of COVID-19 Disease.

Authors:  Dania M AlKhafaji; Reem J Al Argan; Salma AlBahrani; Abrar J Alwaheed; Safi G Alqatari; Abdulmohsen H Al Elq; Waleed Albaker; Marwan Alwazzeh; Amal S AlSulaiman; Reem S AlSulaiman; Hussain M Almadan; Ali A Alhammad; Ali N Almajid; Fatimah H Hakami; Wafa K Alanazi
Journal:  Infect Drug Resist       Date:  2022-07-02       Impact factor: 4.177

4.  Factors associated with prolonged length of hospital stay among COVID-19 cases admitted to the largest treatment center in Eastern Ethiopia.

Authors:  Abdi Birhanu; Bedasa Taye Merga; Galana Mamo Ayana; Addisu Alemu; Belay Negash; Yadeta Dessie
Journal:  SAGE Open Med       Date:  2022-01-19

5.  Community Knowledge of and Attitudes towards COVID-19 Prevention Techniques in Saudi Arabia: A Cross-Sectional Study.

Authors:  Amal Khalil AbuAlhommos; Fatimah Essa Alhadab; May Mohammed Almajhad; Rahmah Almutawaa; Sara Taleb Alabdulkareem
Journal:  Int J Environ Res Public Health       Date:  2021-12-03       Impact factor: 3.390

6.  COVID-19 Vaccine Acceptability Among Women Who are Pregnant or Planning for Pregnancy in Saudi Arabia: A Cross-Sectional Study.

Authors:  Mohammed Samannodi
Journal:  Patient Prefer Adherence       Date:  2021-11-23       Impact factor: 2.711

7.  The incubation period of COVID-19: a global meta-analysis of 53 studies and a Chinese observation study of 11 545 patients.

Authors:  Cheng Cheng; DongDong Zhang; Dejian Dang; Juan Geng; Peiyu Zhu; Mingzhu Yuan; Ruonan Liang; Haiyan Yang; Yuefei Jin; Jing Xie; Shuaiyin Chen; Guangcai Duan
Journal:  Infect Dis Poverty       Date:  2021-09-17       Impact factor: 4.520

8.  Negative Nasopharyngeal SARS-CoV-2 PCR Conversion in Response to Different Therapeutic Interventions.

Authors:  Hassan Alwafi; Mohammed H Shabrawishi; Abdallah Y Naser; Ahmad M Aldobyany; Sultan A Qanash; Abdelfattah A Touman
Journal:  Cureus       Date:  2022-01-20

9.  Cumulative Evidence for the Association of Thrombosis and the Prognosis of COVID-19: Systematic Review and Meta-Analysis.

Authors:  Dongqiong Xiao; Fajuan Tang; Lin Chen; Hu Gao; Xihong Li
Journal:  Front Cardiovasc Med       Date:  2022-01-25

10.  Clinical characteristics and treatment outcomes of severe (ICU) COVID-19 patients in Saudi Arabia: A single centre study.

Authors:  Saleh Alghamdi
Journal:  Saudi Pharm J       Date:  2021-08-04       Impact factor: 4.330

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