Skip to main content
Health Science Reports logoLink to Health Science Reports
. 2023 Jun 14;6(6):e1329. doi: 10.1002/hsr2.1329

Predictors of hospital length of stay and mortality among COVID‐19 inpatients during 2020–2021 in Hormozgan Province of Iran: A retrospective cohort study

Zahra Mastaneh 1, Ali Mouseli 2, Shokrollah Mohseni 2, Sara Dadipoor 2,
PMCID: PMC10265171  PMID: 37324249

Abstract

Background and Aims

About one‐fifth of patients with COVID‐19 need to be hospitalized. Predicting factors affecting the hospital length of stay (LOS) can be effective in prioritizing patients, planning for services, and preventing the increase in LOS and death of patients. The present study aimed to identify the factors that predict LOS and mortality in COVID‐19 patients in a retrospective cohort study.

Methods

A total of 27,859 patients were admitted to 22 hospitals from February 20, 2020 to June 21, 2021. The data collected from 12,454 patients were screened according to the inclusion and exclusion criteria. The data were captured from the MCMC (Medical Care Monitoring Center) database. The study tracked patients until their hospital discharge or death. Hospital LOS and mortality were assessed as the study outcomes.

Results

As the results revealed, 50.8% of patients were male and 49.2% were female. The mean hospital LOS of the discharged patients was 4.94. Yet, 9.1% of the patients (n = 1133) died. Among the predictors of mortality and long hospital LOS were the age above 60, admission to the ICU, coughs, respiratory distress, intubation, oxygen level less than 93%, cigarette and drug abuse, and a history of chronic diseases. Masculinity, gastrointestinal symptoms, and cancer were the effective variables in mortality, and positive CT was a factor significantly affecting the hospital LOS.

Conclusion

Paying special attention to high‐risk patients and modifiable risk factors such as heart disease, liver disease, and other chronic diseases can diminish the complications and mortality rate of COVID‐19. Providing training, especially for those who care for patients experiencing respiratory distress such as nurses and operating room personnel can improve the qualifications and skills of medical staff. Also, ensuring the availability of sufficient supply of medical equipment is strongly recommended.

Keywords: COVID‐19, Iran, length of stay, mortality rate, predictors, SARS‐CoV‐2


Abbreviations

COVID‐19

Coronavirus disease 2019

LOS

hospital length of stay

1. INTRODUCTION

In December 2019, a new kind of respiratory distress disorder emerged in Wuhan, China, which the World Health Organization (WHO) designated COVID‐19 on January 11, 2020. 1 It has been one of the greatest challenges of the world in the past century. COVID‐19 has had the greatest global uncertainty index in recent years. 2 Statistical evidence confirms that COVID‐19 has been the most serious pandemic since the emergence of Spanish flu in 1918, when between 40 and 50 million people died worldwide. 3 From the time the disease was proclaimed to be a global threat by WHO, to date (February 13, 2023) more than 755,703,002 people have been infected in the world and more than 6,836,825 people have died. In Iran at the time of the study, 7,224,701 were infected with COVID‐19 among whom 141,165 died. 4

Patients with COVID‐19 infection frequently report fever, coughing, fatigue, anorexia, myalgia, and diarrhea; however, in severe cases, dyspnea is typically the most prominent symptom, frequently accompanied by hypoxemia. 5 Patients with severe respiratory failure brought on by interstitial pneumonia and acute respiratory distress syndrome have a higher fatality rate. 6 Furthermore, older age, male gender, pre‐existing cardiovascular conditions, asthma, hypertension, uncontrolled diabetes, chronic lung disease, and a d‐dimer larger than 1 g/mL at admission were all linked to a higher mortality rate. 7

In a meta‐analysis study, patients with a history of chronic diseases, smoking, being female, and aging had increased mortality rates. The most likely independent predictor of mortality among hospitalized patients was acute respiratory distress syndrome. 8

There was no consistent cutoff point for prolonged LOS. However, it was described as the total number of bed days a patient spent in the hospital when their stay lasted longer than anticipated for a particular procedure. 9 The COVID‐19 hospital LOS is dependent on the clinical condition of the patients, but it is also influenced by guidelines within the institution or local healthcare authority, as well as the capacity of hospitals. 5

The collected data showed that 5%–20% of COVID‐19‐infected patients need to be hospitalized and of these patients, 14%–20% require admission to the intensive care unit (ICU). 10 According to a study, the health system, which only has 3.2 hospital beds for every 1000 people, reached the breaking point due to the rapid rise in COVID‐19 infection cases and the associated requirement for hospitalization. 11 Hospital LOS is a crucial predictor for healthcare planning. According to reports, shorter hospital stays are linked to lower mortality rates, fewer nosocomial infections, lower patient financial burden, and higher hospital bed turnover rates. 9 , 12

Predicting LOS‐related factors and mortality rate in COVID‐19 patients can help better prioritize patients, make emergent decisions, provide healthcare services, and seek useful and necessary solutions to reduce mortality and hospital LOS. Although the predictors of mortality and hospital LOS have been previously reported in studies, 1 , 13 , 14 according to the epidemiological characteristics of patients and the specific socioeconomic features of each region, it is necessary to examine the correlates of hospital LOS and mortality in each region separately. It was recommended in an investigation that these factors be repeated in several studies to ensure comprehensive literature coverage. 15 Therefore, the present study was conducted to identify the predictors of mortality and hospital LOS in COVID‐19‐infected patients in Hormozgan Province in the south of Iran.

2. METHODOLOGY

2.1. Study setting and design

The present retrospective study was conducted between February 20, 2020 and June 21, 2021 among patients in Hormozgan Province in the south of Iran. The patients were definitely diagnosed with COVID‐19 according to the “Diagnosis and Treatment Scheme for Novel Coronavirus Pneumonia (Trial), 6th Edition” adopted by the People's Republic of China's National Health Commission on February 19, 2021. 16

Hormozgan Province lies between the coordinates of 2524′ to 2857′N latitude and 5341′ to 5915′E longitude. With an area of about 68,000 square kilometers (about the size of Georgia), Hormozgan is the eighth largest province in Iran.

2.2. Research population and eligibility criteria

The research population consisted of all COVID‐19‐infected inpatients (with confirmed test results) who were either discharged from hospital (actually survived) or deceased. These patients were sampled from 22 active hospitals throughout the province that admitted COVID‐19 patients. Patients diagnosed with confirmed COVID‐19, discharged patients, and the deceased were included in this study. The exclusion criteria were incomplete information and outpatients.

2.3. Research variables

2.3.1. Dependent variables

Within‐hospital mortality and hospital length of stay (LOS)

LOS: This variable was measured as the average length of hospitalization. Patients who remained in the hospital longer than the median length of stay were categorized as “long‐term LOS” and those who remained below the median LOS were referred to as “short‐term LOS.”

2.3.2. Independent variables

The demographic variables included: age, gender, ward, history of cigarette, or drug abuse

Clinical symptoms: fever, coughs, sore muscles, respiratory distress, headache or dizziness, sore throat, respiratory distress, gastrointestinal symptoms (vomiting, diarrhea, anorexia, abdominal pain, nausea), sore muscles, coughs, fever, CT result, PO2 level, intubation

History: diabetes, heart disease, hypertension, renal disease, asthma or chronic pulmonary disease, chronic liver disease, chronic neurological disorder, cancer

2.3.3. Sample size estimation and sampling procedure

The required data were collected from patients' information recorded in the MCMC (Medical Care Monitoring Center) database. This national system covers the information of all patients admitted to the country's hospitals by province, city, and hospital name. This study was conducted on 12,454 patients who were admitted to 22 hospitals in Hormozgan Province from February 20, 2020 to June 21, 2021 with a definitive diagnosis of COVID‐19.

2.3.4. Data collection instrument, process, and management

The data were obtained from the electronic health records of the patients using a distinct medical record number (MRN) for each patient. A medical team, including medical residents and a consultant pulmonologist, evaluated and double‐checked all the data.

In the MCMC system of Hormozgan Province from February 20, 2020 to the June 21, 2021, a total number of 28,759 people were diagnosed with the acute respiratory syndrome, out of which 15,405 were excluded for certain reasons. For instance, 10,761 patients tested negative for COVID‐19, 4045 received outpatient care, and 599 had missing data. Finally, the data from 12,454 patients who tested positive for COVID‐19 and had complete information about all the variables were included in the final analysis (Figure 1).

Figure 1.

Figure 1

Sampling procedure.

2.3.5. Outcomes

The expected outcome was identifying the predictors of hospital LOS and mortality.

2.4. Statistical analysis

The data recorded in MCMC system were punched into SPSS16. Descriptive statistics, including frequency, percentage, mean with SD, and median with interquartile range (IQR) were used to describe the participants. Chi‐square assumption was tested before the statistical analysis. For each predictor variable, bivariate binary logistic regressions were fitted. The variables with p values less than 0.25 were candidate for multivariable logistic regression models to test their effects after adjusting for the potential confounders. In the multivariable logistic regressions, predictor variables were provided using adjusted odds ratios (AORs) at 95% confidence intervals (CIs). Finally, the statistical significance was substantiated at a p value lower than 0.05.

2.5. Ethical statement

The ethics board at Hormozgan University of Medical Sciences approved this study (Ref. no. IR.HUMS.REC.1399.036). Informed consent was obtained from patients and they were assured that their personal information would be kept confidential and used for research purposes. The ethical principles of the Declaration of Helsinki were followed during the collection, handling, and storage of data, and all care was taken to protect patient confidentiality.

3. RESULTS

3.1. Sociodemographic features

The data from 12,454 patients were analyzed. In all, 50.8% of these patients (n = 6321) were male and 49.2% of patients (n = 6133) were female. The mean and SD of age were 50.25 ± 17.20 years for men and 50.97 ± 16.46 years for women. Out of the 12,454 patients, 1133 (9.1%) died. Of the deceased, 676 (59.7%) were male and 457 (40.3%) were female. Of the deaths, 737 (65.05%) occurred in patients aged 60 years or older. The details of participants' features and the clinical symptoms were compared between two groups of “survived” and “deceased” as indicated in Table 1.

Table 1.

Research participants’ sociodemographic features (N = 12,454).

Characteristics Level Discharged (survived the disease) Deceased Total
f. % f. %
Age groups ≥60 3217 28.42 737 65.05 3954
20–59 7938 70.12 393 34.69 8331
0–19 166 1.47 3 0.26 169
Gender Male 5645 49.86 676 59.66 6321
Female 5676 50.14 457 40.34 6133
Ward ICU 276 2.44 852 75.20 1128
Ordinary or isolated 11,045 97.56 281 24.80 11,326
Fever Yes 4579 40.45 445 39.28 5024
No 6742 59.55 688 60.72 7430
Coughs Yes 6299 55.64 564 49.78 6863
No 5022 44.36 569 50.22 5591
Sore muscles Yes 4796 42.36 344 30.36 5140
No 6525 57.64 789 69.64 7314
Respiratory distress Yes 4408 38.94 763 67.34 5171
No 6913 61.06 370 32.66 7283
Gastrointestinal symptoms Yes 2923 25.82 233 20.56 3156
No 8398 74.18 900 79.44 9298
Headache/dizziness Yes 2100 18.55 145 12.80 2245
No 9221 81.45 988 87.20 10,209
Sore throat Yes 585 5.17 63 5.56 648
No 10,736 94.83 1070 94.44 11,806
Intubated Yes 231 2.04 681 60.11 912
No 11,090 97.96 452 39.89 11,542
PO2 <93 2124 18.76 769 67.87 2893
>93 9197 81.24 364 32.13 9561
CT Positive 11,073 97.81 1117 98.59 12,190
Negative 248 2.19 16 1.41 264
Cigarette or drug abuse Yes 215 1.90 56 4.94 271
No 11,106 98.10 1077 95.06 12,183
Cancer Yes 94 0.83 31 2.74 125
No 11,227 99.17 1102 97.26 12,329
Chronic liver disease Yes 26 0.23 7 0.62 33
No 11295 99.77 1126 99.38 12,421
Diabetes Yes 1715 15.15 362 31.95 2077
No 9606 84.85 771 68.05 10,377
Cardiac disease Yes 1042 9.20 324 28.60 1366
No 10,279 90.80 809 71.40 11,088
Renal disease Yes 169 1.49 88 7.77 257
No 11,152 98.51 1045 92.23 12,197
Asthma/chronic pulmonary disease Yes 356 3.14 70 6.18 426
No 10,965 96.86 1063 93.82 12,028
Chronic neurological disease Yes 88 0.78 17 1.50 105
No 11,233 99.22 1116 98.50 12,349
Hypertension Yes 2033 17.96 467 41.22 2500
No 9288 82.04 666 58.78 9954

3.2. Predictors of mortality

In the multivariate regression analysis, the adjusted odds ratio of mortality for those at or above 60 compared to those in the 0–19 age group was OR = 10.02 (CI 95%: 1.61, 62.47). For patients admitted to the ICU in comparison to those admitted to the ordinary or isolated ward, the odds ratio was OR = 47.47 (CI 95%: 37.54, 60.03). The same value for intubated patients was OR = 31.73 (CI 95%: 24.03, 41. 89). For individuals with PO2 less than 93, the odds ratio was OR = 3.29 (CI 95%: 2. 63, 4.12). The other mortality predictors are listed in Table 2.

Table 2.

Predictors of patient mortality (N = 12,454).

Covariates Level Univariate Multivariate
OR 95% CI for OR p Value OR 95% CI for OR p Value
Lower Upper Lower Upper
Age groups ≥60 12.68 4.04 39.82 <0.001 10.02 1.61 62.47 0.014
20–59 2.74 0.87 8.62 0.085 3.75 0.60 23.28 0.157
0–19 Reference Reference
Gender Male 1.49 1.31 1.68 <0.001 1.58 1.26 1.99 <0.001
Female Reference Reference
Ward ICU 121.34 101.34 145.28 <0.001 47.47 37.54 60.03 <0.001
Ordinary or isolated Reference Reference
Fever Yes 0.95 0.84 1.08 0.444
No Reference Reference
Coughs Yes 0.79 0.70 0.89 <0.001 1.05 0.84 1.31 0.677
No
Sore muscles Yes 0.59 0.52 0.68 <0.001 0.85 0.67 1.09 0.199
No Reference Reference
Respiratory distress Yes 3.23 2.84 3.68 <0.001 1.87 1.50 2.37 <0.001
No Reference Reference
Gastrointestinal disorder Yes 0.74 0.64 0.86 <0.001 0.75 0.57 0.98 0.036
No Reference Reference
Headache/dizziness Yes 0.644 0.54 0.77 <0.001 0.82 0.58 1.14 0.241
No Reference Reference
Sore throat Yes 1.081 0.83 1.41 0.570
No Reference Reference
Intubated Yes 72.33 60.63 86.28 <0.001 31.73 24.03 41.89 <0.001
No Reference Reference
PO2 <93 9.15 8.00 10.45 <0.001 3.29 2.63 4.12 <0.001
>93 Reference Reference
CT Positive 1.56 0.94 2.60 0.085 1.19 0.53 2.68 0.673
Negative Reference Reference
Cigarette or drug abuse Yes 2.67 1.99 3.63 <0.001 2.31 1.37 3.89 0.002
No Reference Reference
Cancer Yes 3.36 2.23 5.07 <0.001 2.69 1.27 5.70 0.010
No Reference Reference
Chronic liver disease Yes 2.70 1.17 6.24 0.020 1.04 0.14 7.66 0.969
No Reference Reference
Diabetes Yes 2.63 2.30 3.01 <0.001 1.37 1.05 1.78 0.020
No Reference Reference
Cardiac disease Yes 3.95 3.42 4.56 <0.001 2.53 1.93 3.32 <0.001
No Reference Reference
Renal disease Yes 5.56 4.26 7.24 <0.001 3.08 1.83 5.18 <0.001
No Reference Reference
Asthma/chronic pulmonary disease Yes 2.03 1.56 2.64 <0.001 1.93 1.18 3.15 0.008
No Reference Reference
Chronic neurological disease Yes 1.94 1.15 3.28 0.013 1.02 0.35 2.95 0.978
No Reference Reference
Hypertension Yes 3.20 2.82 3.64 <0.001 1.55 1.20 2.00 0.001
No Reference Reference

Overall, the mean and SD of hospital LOS was 4.94 ± 3.72 with a median of 4 days. In the “survived” group, the mean and SD of hospital LOS was 3.86 ± 5.03. In women, the mean and SD of LOS was 4.85 ± 3.57 with a median of 4 days.

3.3. Predictors of hospital LOS

In the multivariate regression analysis, the adjusted odds ratio of long‐term LOS for those aged 60 or more compared to the 0–19 age group was OR = 2.29 (CI 95%: 1.55, 3.39). In Mitella patients with asthma or chronic lung disease, the odds ratio was OR = 1.24 (CI 95%: 1.09, 1.49), and in patients with hypertension it was OR = 1.43 (CI 95%: 1.03, 1.98) (Tables 3 and 4).

Table 3.

Research participants' socio‐demographic features (associated with LOS) (N = 11,321).

Characteristics Level Long term stay Short term stay Total
f. % f. %
Age groups ≥60 1545 31.95 1672 25.78 3217
20–59 3237 66.94 4701 72.49 7938
0–19 54 1.12 112 1.73 166
Total 4836 100.00 6485 100.00 11,321
Gender Male 2449 50.64 3196 49.28 5645
Female 2387 49.36 3289 50.72 5676
Total 4836 100.00 6485 100.00 11,321
Ward ICU 166 3.43 110 1.70 276
Ordinary or isolated 4670 96.57 6375 98.30 11,045
Total 4836 100.00 6485 100.00 11,321
Fever Yes 1941 40.14 2638 40.68 4579
No 2895 59.86 3847 59.32 6742
Total 4836 100.00 6485 100.00 11,321
Coughs Yes 2762 57.11 3537 54.54 6299
No 2074 42.89 2948 45.46 5022
Total 4836 100.00 6485 100.00 11,321
Sore muscles Yes 2051 42.41 2745 42.33 4796
No 2785 57.59 3740 57.67 6525
Total 4836 100.00 6485 100.00 11,321
Respiratory distress Yes 2070 42.80 2338 36.05 4408
No 2766 57.20 4147 63.95 6913
Total 4836 100.00 6485 100.00 11,321
Gastrointestinal symptoms Yes 1293 26.74 1630 25.13 2923
No 3543 73.26 4855 74.87 8398
Total 4836 100.00 6485 100.00 11,321
Headache/dizziness Yes 893 18.47 1207 18.61 2100
No 3943 81.53 5278 81.39 9221
Total 4836 100.00 6485 100.00 11,321
Sore throat Yes 286 5.91 299 4.61 585
No 4550 94.09 6186 95.39 10,736
Total 4836 100.00 6485 100.00 11,321
Intubated Yes 130 2.69 101 1.56 231
No 4706 97.31 6384 98.44 11,090
Total 4836 100.00 6485 100.00 11,321
PO2 <93 1261 26.08 863 13.31 2124
>93 3575 73.92 5622 86.69 9197
Total 4836 100.00 6485 100.00 11,321
CT Positive 4758 98.39 6315 97.38 11073
Negative 78 1.61 170 2.62 248
Total 4836 100.00 6485 100.00 11,321
Cigarette or drug abuse Yes 80 1.65 135 2.08 215
No 4756 98.35 6350 97.92 11,106
Total 4836 100.00 6485 100.00 11,321
Cancer Yes 45 0.93 49 0.76 94
No 4791 99.07 6436 99.24 11,227
Total 4836 100.00 6485 100.00 11,321
Chronic liver disease Yes 16 0.33 10 0.15 26
No 4820 99.67 6475 99.85 11,295
Total 4836 100.00 6485 100.00 11,321
Diabetes Yes 811 16.77 904 13.94 1715
No 4025 83.23 5581 86.06 9606
Total 4836 100.00 6485 100.00 11,321
Cardiac disease Yes 542 11.21 500 7.71 1042
No 4294 88.79 5985 92.29 10,279
Total 4836 100.00 6485 100.00 11,321
Renal disease Yes 87 1.80 82 1.26 169
No 4749 98.20 6403 98.74 11,152
Total 4836 100.00 6485 100.00 11,321
Asthma/chronic pulmonary disease Yes 171 3.54 185 2.85 356
No 4665 96.46 6300 97.15 10,965
Total 4836 100.00 6485 100.00 11,321
Chronic neurological disease Yes 41 0.85 47 0.72 88
No 4795 99.15 6438 99.28 11,233
Total 4836 100.00 6485 100.00 11,321
Hypertension Yes 921 19.04 1112 17.15 2033
No 3915 80.96 5373 82.85 9288
Total 4836 100.00 6485 100.00 11,321

Table 4.

Predictors of hospital LOS.

Covariates Level Univariate Multivariate
OR 95% CI for OR p Value OR 95% CI for OR p Value
Lower Upper Lower Upper
Age group ≥60 1.92 1.37 2.67 <0.001 2.29 1.55 3.39 <0.001
20–59 1.43 1.03 1.98 0.033 1.45 0.98 2.13 0.062
0–19 Reference Reference
Gender Male 1.06 0.98 1.14 0.153 1.05 0.97 1.14 0.185
Female Reference Reference
Ward ICU 2.06 1.61 2.63 <0.001 1.81 1.41 2.32 <0.001
Ordinary or isolated Reference Reference
Fever Yes 0.98 0.91 1.06 0.561 Not included in the multivariate analysis
No Reference
Coughs Yes 1.11 1.03 1.19 0.006 1.15 1.06 1.24 0.000
No Reference Reference
Sore muscles Yes 1.00 0.93 1.08 0.930 Not included in the multivariate analysis
No Reference
Respiratory distress Yes 1.33 1.23 1.43 <0.001 1.19 1.10 1.29 <0.001
No Reference Reference
Gastrointestinal symptoms Yes 1.09 0.99 1.18 0.054 1.06 0.97 1.16 0.219
No Reference Reference
Headache/dizziness Yes 0.99 0.90 1.09 0.843 Not included in the multivariate analysis
No Reference
Sore throat Yes 1.30 1.10 1.54 0.001 1.30 0.97 1.72 0.076
No Reference Reference
Intubated Yes 1.75 1.33 2.29 <0.001 1.74 1.35 2.25 <0.001
No Reference Reference
PO2 <93 2.30 2.09 2.53 <0.001 1.94 1.74 2.16 <0.001
>93 Reference Reference
CT Positive 1.64 1.25 2.15 <0.001 1.45 1.10 1.90 0.008
Negative Reference Reference
Cigarette or drug abuse Yes 1.50 1.13 1.98 <0.001 1.58 1.38 2.29 0.003
No Reference Reference
Cancer Yes 1.23 0.82 1.85 0.311 Not included in the multivariate analysis
No Reference
Chronic liver disease yes 2.15 0.97 4.74 0.058 1.13 0.97 1.27 0.088
No Reference Reference
Diabetes Yes 1.24 1.12 1.38 <0.001 1.16 1.04 1.30 0.007
No Reference Reference
Cardiac disease Yes 1.51 1.33 1.72 <0.001 1.27 1.11 1.46 0.000
No Reference Reference
Renal disease Yes 1.43 1.06 1.94 0.021 1.47 1.08 2.02 0.016
No Reference Reference
Asthma/chronic pulmonary Yes 1.32 1.07 1.64 0.008 1.24 1.09 1.49 0.010
No Reference Reference
Chronic neurological Yes 1.17 0.77 1.78 0.461 Not included in the multivariate analysis
No Reference
Hypertension Yes 1.14 1.03 1.25 0.009 1.43 1.03 1.98 0.034
No Reference Reference

4. DISCUSSION

The present study aimed to identify the predictors of mortality and hospital LOS in COVID‐19‐infected patients. The factors that independently affected mortality and hospital LOS were age over 60, admission to ICU, coughs, respiratory distress, intubation, oxygen level below 93%, cigarette or drug abuse, diabetes, cardiovascular disease, renal disease, asthma or chronic pulmonary disease and hypertension. Masculinity, gastrointestinal symptoms and cancer specifically affected mortality, and positive CT specifically affected the LOS.

In Hormozgan Province, there were 215,847 infected cases up to May 8, 2022 of whom 2614 died. In the present study, the within‐hospital mortality rate was 9,097. A study reported that the increasing incidence and mortality of COVID‐19 worldwide is a significant issue. 17 Sadeghifar et al. 13 reported a mortality rate of 3.9% among COVID‐19 patients in Ilam. Shahriarirad et al. carried out a retrospective multicenter study to assess the clinical characteristics of COVID‐19 patients in Fars Province. The findings revealed that individuals with COVID‐19 had an overall mortality rate of 8%, 18 which was lower than the mortality rate of the present study. In addition, a meta‐analysis of mortality in COVID‐19 patients was reported to be 15%. 8 These divergent findings can be explained by different demographic features of patients, different geographies, time and setting of research and the severity of disease.

As the present findings showed, the mean days of hospital stay for survivors were 4.72 ± 3.72 with a median of 4 days and a range of 1–68 days. For the deceased patients, the mean duration was 8.342 ± 9.56 with a median of 7 days and a range of 1–64. In a number of studies, the mean days of hospital stay were 12 and 13 days. 19 , 20 However, in Saudi Arabia, the mean duration was 6 days, 5 while patients not admitted to the ICU in the United States had a mean duration of 6 days. 21 In France, Peru, the Mediterranean, London, and Tehran, the mean hospital LOS was respectively 9, 22 7, 22 8.5, 23 6, 24 and 7.5 days 25 These variations in hospital stay could be attributed to differences in countries, geographical regions, health facilities, and the severity of patients' conditions. 26 Other demographic factors, such as age, may also contribute to these differences.

According to the present findings, old age was associated with higher mortality rates and longer hospital stays. This is consistent with other studies that have identified age as a significant predictor of both mortality and hospital length of stay. 7 , 19 , 25 In a retrospective, multicenter cohort study conducted in China, patients who died from COVID‐19 had a mean age of approximately 69 years, which was significantly higher than those who survived. 7 It appears that as age increases, the probability of death induced by COVID‐19 and the LOS increases too. This could be attributed to weakened immune systems in older patients, as well as various behavioral reactions to treatments. 27

In the present study, admission to the ICU was identified as a predictor of both mortality and longer hospital stay. A meta‐analysis found a high mortality rate among ICU patients. 8 , 28 In another study, ICU patients had a high probability of mortality. 21 This result was quite expected since patients with acute medical conditions often require critical care. Therefore, they have a higher risk of mortality compared to those in regular hospital wards.

Respiratory distress and intubation were the other predictors of increased mortality and longer hospital LOS. Patients who experience respiratory problems face a higher risk of complications that can lead to death or prolonged hospitalization. This study supports previous findings that respiratory distress was a significant factor in COVID‐19 patients' mortality. 19 Additionally, Zhang et al. 29 reported a 100% increase in mortality rates for patients with damaged lungs. 29 A study in Iran found that patients with shortness of breath, sore throat, and abnormal chest radiographic test results were at greater risk of dying compared to other patients. 13 In another study, patients with respiratory distress had an eight times higher mortality rate than those without respiratory issues. 8 Moreover, studies on patients with respiratory problems consistently showed longer hospital stays. 21 , 30

Low oxygen levels (below 93%) have been identified as a predictor of mortality and length of hospital stay in COVID‐19 patients. Several studies have found that lower O2 levels are linked to an increased risk of death. 30 , 31 , 32 , 33 , 34 This may be due to alveolar damage, which can interfere with the exchange of oxygen and carbon dioxide, ultimately leading to early mortality in COVID‐19 patients. 35

The current study found that patients with comorbidities had higher rates of mortality and longer hospital stays. These findings are supported by other research studies. 20 , 36 , 37 In contrast, Yuriy Pya 31 reported no association between comorbidities and mortality in their study. However, they suggested that this may have been due to certain comorbidities going undiagnosed or incomplete data, indicating a need for further research in this area.

The correlation found between comorbidities and mortality rate in the present study could be due to the fact that the coexistence of COVID‐19 infection with other diseases could have an immunosuppressive effect and poor treatment response, which might adversely affect the treatment outcome of the infected patients. 38 Additionally, comorbidities can contribute to the development of an acute hyperinflammatory response known as a cytokine storm, which can further increase the risk of mortality in COVID‐19 patients. 32

In the present study, it was found that men had a higher mortality rate than women. This is consistent with the findings of a systematic review, which indicated that masculinity was one of the predictors of patient death. 39 One possible explanation for this disparity is the higher prevalence of COVID‐19 among men as compared to women. The incidence of COVID‐19 was higher in men than in women, as evidenced by the Sadeghifar et al. 13 It is thought that the natural immunity of women, which is bolstered by chromosome X protection and sex hormones, makes them less susceptible to viral infections. 40

In the present study, the odds of mortality were higher in patients with cancer. Similar studies revealed that patients with cancer are at greater risk of mortality compared to the general population. 37 , 38 , 39 Williams et al. 41 reported that the mortality rate increased for at least 2.5‐fold in patients with hematologic malignancy. 41 This increased risk is likely due to both the nature of cancer and the effects of antineoplastic medications, which compromise the immune system. As a result, these patients are more vulnerable to severe and potentially fatal COVID‐19 infections. In addition, frequent clinical visits for follow‐up and chemotherapy treatment may expose cancer patients to infection. 42

According to Li et al., 19 coughing and sputum production are common symptoms among patients with severe or acute COVID‐19, and were found to be significant predictors of mortality in the present study. While coughing is a symptom often associated with pulmonary conditions such as asthma and lung cancer, it was also found to be prevalent in COVID‐19 patients. In fact, a previous study showed that coughing was the most commonly reported symptom among patients with chronic pulmonary disease and lung cancer. 43

According to the results of this study, cigarette and drug abuse were identified as significant predictors of mortality and longer hospital stay. Similarly, another study found that smoking was a major predictor of mortality among COVID‐19 patients. 32 , 43 This may be due to the fact that smoking and drug abuse can lead to compromised lung function, which could exacerbate COVID‐19 infections and ultimately lead to fatalities. 7

4.1. Conclusion

The present study confirmed the impact of effective demographic variables such as age, gender, cigarette smoking, and drug abuse along with clinical symptoms such as coughs, respiratory distress, intubation, oxygen level less than 93, and chronic comorbidities on mortality and hospital LOS. To reduce complications and mortality rates associated with COVID‐19, it is essential to focus on high‐risk patients and address modifiable risk factors, such as heart disease, liver disease, and other chronic illnesses. The medical team, notably nurses and operating room staff should receive proper training to improve their readiness and skills in dealing with patients experiencing respiratory distress, given the high hospitalization rate for these individuals.

To accelerate diagnosis and treatment processes, medical facilities must ensure an adequate supply of medical equipment like oxygen generators, ECMO devices, and portable digital imaging machines for respiratory ICU. Early classification of COVID‐19 patients' risk factors upon admission can also facilitate more effective care delivery.

4.2. Strengths and limitations

Retrospective studies have certain limitations including incorrect classification, low coding accuracy, and missing data. Additionally, lack of access to laboratory findings can be a challenge in such studies. The retrospective nature of the data necessitates careful interpretation of the current findings. Furthermore, the cross‐sectional design of the study prevents the researcher from inferring causal relationships between the independent and dependent variables. However, using a secondary data set in the analyses can lead to a larger sample size, increasing the statistical power and external validity of the study.

4.3. Implications

We believe that our results are somehow in line with the findings of similar studies, which can help to better classify the risk factors. By identifying high‐risk patients more accurately, these findings have the potential to prevent healthcare facilities from becoming overcrowded and limit treatment to specialized centers where severe illness is more likely to occur. Additionally, healthcare professionals can utilize our findings to predict mortality rates associated with specific risk factors, enabling them to make informed decisions and provide better care for infected individuals. However, further large‐scale research is needed to validate our findings.

AUTHOR CONTRIBUTIONS

Zahra Mastaneh: Conceptualization; data curation; investigation; methodology; writing—original draft. Ali Mouseli: Conceptualization; investigation; methodology; writing—original draft. Shokrollah Mohseni: Data curation; formal analysis; methodology. Sara Dadipoor: Conceptualization; investigation; methodology; supervision; writing—original draft.

CONFLICT OF INTEREST STATEMENT

The authors declare no conflict of interest.

ETHICS STATEMENT

All methods adhere to the Helsinki Declaration. The Hormozgan University of Medical Sciences ethics committee approved the study (ethical code ref. no. IR.HUMS.REC.1399.036). To participate in this study, all individuals completed an online consent form.

TRANSPARENCY STATEMENT

The lead author Sara Dadipoor affirms that this manuscript is an honest, accurate, and transparent account of the study being reported; that no important aspects of the study have been omitted; and that any discrepancies from the study as planned (and, if relevant, registered) have been explained.

ACKNOWLEDGMENTS

This work was supported by a grant from the Hormozgan University of Medical Sciences. The authors sincerely thank all the participants for their sincere cooperation in this study.

Mastaneh Z, Mouseli A, Mohseni S, Dadipoor S. Predictors of hospital length of stay and mortality among COVID‐19 inpatients during 2020–2021 in Hormozgan Province of Iran: a retrospective cohort study. Health Sci Rep. 2023;6:e1329. 10.1002/hsr2.1329

DATA AVAILABILITY STATEMENT

The corresponding author will provide the data supporting the study's finding on reasonable request. Sara Dadipoor had full access to all of the data in this study and took complete responsibility for the integrity of the data and the accuracy of the data analysis.

REFERENCES

  • 1. Guo A, Lu J, Tan H, et al. Risk factors on admission associated with hospital length of stay in patients with COVID‐19: a retrospective cohort study. Sci Rep. 2021;11(1):7310. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2. Baker SR, Bloom N, Davis SJ, Terry SJ. Covid‐Induced Economic Uncertainty. National Bureau of Economic Research; 2020. [Google Scholar]
  • 3. Ferguson NM, Laydon D, Nedjati‐Gilani G, et al. Impact of nonpharmaceutical interventions (NPIs) to reduce COVID‐19 mortality and healthcare demand. Imperial College COVID‐19 Response Team. 2020;20(10.25561):77482. [Google Scholar]
  • 4. World Health Organization . Coronavirus Disease (COVID‐19). Accessed February 13, 2023.  https://www.who.int/emergencies/diseases/novel-coronavirus-2019
  • 5. Alwafi H, Naser AY, Qanash S, et al. Predictors of length of hospital stay, mortality, and outcomes among hospitalised COVID‐19 patients in Saudi Arabia: a cross‐sectional study. J Multidiscip Healthc. 2021;14:839‐852. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6. Force ADT, Ranieri V, Rubenfeld G, et al. Acute respiratory distress syndrome. JAMA. 2012;307(23):2526‐2533. [DOI] [PubMed] [Google Scholar]
  • 7. Zhou F, Yu T, Du R, et al. Clinical course and risk factors for mortality of adult inpatients with COVID‐19 in Wuhan, China: a retrospective cohort study. Lancet. 2020;395(10229):1054‐1062. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Abate SM, Checkol YA, Mantefardo B. Global prevalence and determinants of mortality among patients with COVID‐19: a systematic review and meta‐analysis. Ann Med Surg. 2021;64:102204. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. Tefera GM, Feyisa BB, Umeta GT, Kebede TM. Predictors of prolonged length of hospital stay and in‐hospital mortality among adult patients admitted at the surgical ward of Jimma University medical center, Ethiopia: prospective observational study. J Pharmaceut Policy Pract. 2020;13(1):1‐11. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. Miethke‐Morais A, Cassenote A, Piva H, et al. COVID‐19‐related hospital cost‐outcome analysis: the impact of clinical and demographic factors. Braz J Infect Dis. 2021;25:101609. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11. Rees EM, Nightingale ES, Jafari Y, et al. COVID‐19 length of hospital stay: a systematic review and data synthesis. BMC Med. 2020;18(1):1‐22. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Agarwal N, Biswas B, Singh C, et al. Early determinants of length of hospital stay: a case control survival analysis among COVID‐19 patients admitted in a tertiary healthcare facility of east India. J Prim Care Community Health. 2021;12:21501327211054281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Sadeghifar J, Jalilian H, Momeni K, et al. Outcome evaluation of COVID‐19 infected patients by disease symptoms: a cross‐sectional study in Ilam Province, Iran. BMC Infect Dis. 2021;21(1):903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Vekaria B, Overton C, Wiśniowski A, et al. Hospital length of stay for COVID‐19 patients: data‐driven methods for forward planning. BMC Infect Dis. 2021;21(1):700. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15. Crankson S, Pokhrel S, Anokye NK. Determinants of COVID‐19‐related length of hospital stays and long COVID in Ghana: a cross‐sectional analysis. Int J Environ Res Public Health. 2022;19(1):527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16. National Health Commission & State Administration of Traditional Chinese Medicine . The Diagnosis and Treatment Protocol for Novel Coronavirus Pneumonia (Trial Version Seven). March 3, 2020.  https://www.chinadaily.com.cn/pdf/2020/1.Clinical.Protocols.for.the.Diagnosis.and.Treatment.of.COVID-19.V7.pdf
  • 17. Bazrafshan M‐R, Eidi A, Keshtkaran Z, Shokrpour N, Zand P, Delam H. Epidemiological and clinical aspects of the coronavirus disease 2019 (COVID‐19) outbreak based on global data: a review article. J Health Sci Surv Syst 2020;8(3):100‐104. [Google Scholar]
  • 18. Shahriarirad R, Khodamoradi Z, Erfani A, et al. Epidemiological and clinical features of 2019 novel coronavirus diseases (COVID‐19) in the South of Iran. BMC Infect Dis. 2020;20:427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Li K, Zhang C, Qin L, et al. A nomogram prediction of length of hospital stay in patients with COVID‐19 pneumonia: a retrospective cohort study. Dis Mark. 2021;2021:1‐9. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Birhanu A, Merga BT, Ayana GM, Alemu A, Negash B, Dessie Y. Factors associated with prolonged length of hospital stay among COVID‐19 cases admitted to the largest treatment center in Eastern Ethiopia. SAGE Open Med. 2022;10:205031212110703. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Nguyen NT, Chinn J, Nahmias J, Yuen S, Kirby K, Hohmann S. Outcomes and mortality among adults hospitalized with COVID‐19 at US medical centers. JAMA Network Open. 2021;4(3):e210417. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22. Wargny M, Potier L, Gourdy P, et al. Predictors of hospital discharge and mortality in patients with diabetes and COVID‐19: updated results from the nationwide CORONADO study. Diabetologia. 2021;64(4):778‐794. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Moreno‐Pérez O, Merino E, Leon‐Ramirez J‐M, et al. Post‐acute COVID‐19 syndrome. Incidence and risk factors: a Mediterranean cohort study. J Infect. 2021;82(3):378‐383. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24. Fraser S, Baranowski R, Patrini D, et al. Maintaining safe lung cancer surgery during the COVID‐19 pandemic in a global city. EClinicalMedicine. 2021;39:101085. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Jalilvand H, Abdi M, Hejazi Zadeh N, et al. Factors affecting hospitalization and length of hospitalization of the patients with Covid‐19. Depiction Health. 2021;12(4):320‐332. [Google Scholar]
  • 26. Huang C, Soleimani J, Herasevich S, et al. Clinical characteristics, treatment, and outcomes of critically ill patients with COVID‐19: a scoping review. Mayo Clin Proc. 2021;96:183‐202. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27. Bartleson JM, Radenkovic D, Covarrubias AJ, Furman D, Winer DA, Verdin E. SARS‐CoV‐2, COVID‐19 and the aging immune system. Nat Aging. 2021;1(9):769‐782. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28. Yang J, Zheng Y, Gou X, et al. Prevalence of comorbidities in the novel Wuhan coronavirus (COVID‐19) infection: a systematic review and meta‐analysis. Int J Infect Dis. 2020;94:91‐95. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29. Zhang B, Zhou X, Qiu Y, et al. Clinical characteristics of 82 cases of death from COVID‐19. PLoS One. 2020;15(7):e0235458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30. Mejía F, Medina C, Cornejo E, et al. Oxygen saturation as a predictor of mortality in hospitalized adult patients with COVID‐19 in a public hospital in Lima, Peru. PLoS One. 2020;15(12):e0244171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Pya Y, Bekbossynova M, Gaipov A, et al. Mortality predictors of hospitalized patients with COVID‐19: retrospective cohort study from Nur‐Sultan, Kazakhstan. PLoS One. 2021;16(12):e0261272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Ayana GM, Merga BT, Birhanu A, Alemu A, Negash B, Dessie Y. Predictors of mortality among hospitalized COVID‐19 patients at a tertiary care hospital in Ethiopia. Infect Drug Resist. 2021;14:5363‐5373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33. Díaz‐Vélez C, Urrunaga‐Pastor D, Romero‐Cerdán A, et al. Risk factors for mortality in hospitalized patients with COVID‐19 from three hospitals in Peru: a retrospective cohort study. F1000Research. 2021;10:224. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Friedman J, Calderón‐Villarreal A, Bojorquez I, Vera Hernández C, Schriger DL, Tovar Hirashima E. Excess out‐of‐hospital mortality and declining oxygen saturation: the sentinel role of emergency medical services data in the COVID‐19 crisis in Tijuana, Mexico. Ann Emerg Med. 2020;76(4):413‐426. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35. Yuan S, Jiang S‐C, Zhang Z‐W, Fu Y‐F, Hu J, Li Z‐L. The role of alveolar edema in COVID‐19. Cells. 2021;10(8):1897. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 36. Fiorentino G, Coppola A, Izzo R, et al. Effects of adding L‐arginine orally to standard therapy in patients with COVID‐19: a randomized, double‐blind, placebo‐controlled, parallel‐group trial. Results of the first interim analysis. EClinicalMedicine. 2021;40:101125. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37. Choi YJ, Park J‐Y, Lee HS, et al. Variable effects of underlying diseases on the prognosis of patients with COVID‐19. PLoS One. 2021;16(7):e0254258. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Bigdelou B, Sepand MR, Najafikhoshnoo S, et al. COVID‐19 and preexisting comorbidities: risks, synergies, and clinical outcomes. Front Immunol. 2022;13:2077. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Sepandi M, Taghdir M, Alimohamadi Y, Afrashteh S, Hosamirudsari H. Factors associated with mortality in COVID‐19 patients: a systematic review and meta‐analysis. Iran J Publ Health. 2020;49(7):1211. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40. Jaillon S, Berthenet K, Garlanda C. Sexual dimorphism in innate immunity. Clin Rev Allergy Immunol. 2019;56(3):308‐321. [DOI] [PubMed] [Google Scholar]
  • 41. Williamson EJ, Walker AJ, Bhaskaran K, et al. Factors associated with COVID‐19‐related death using OpenSAFELY. Nature. 2020;584(7821):430‐436. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42. Corso CR, Mulinari Turin de Oliveira N, Maria‐Ferreira D. Susceptibility to SARS‐CoV‐2 infection in patients undergoing chemotherapy and radiation therapy. J Infect Public Health. 2021;14(6):766‐771. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 43. Ayhan M, Odabas H, Turan N, et al. Factors affecting the mortality rate of patients with cancer hospitalized with COVID‐19: a single center's experience. J Chemother. 2021;33(7):499‐508. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The corresponding author will provide the data supporting the study's finding on reasonable request. Sara Dadipoor had full access to all of the data in this study and took complete responsibility for the integrity of the data and the accuracy of the data analysis.


Articles from Health Science Reports are provided here courtesy of Wiley

RESOURCES