Skip to main content
Cureus logoLink to Cureus
. 2024 Feb 1;16(2):e53432. doi: 10.7759/cureus.53432

A Retrospective Study on the Outcome of Coronavirus Disease 2019 (COVID-19) Patients Admitted to a District General Hospital and Predictors of High Mortality

Zahid Khan 1,2,3,4,, Gideon Mlawa 5, Saiful Islam 6, Suhier Elshowaya 5, Mohammad Saleem 7
Editors: Alexander Muacevic, John R Adler
PMCID: PMC10908435  PMID: 38435221

Abstract

Background: The clinical features and severity of coronavirus disease 2019 (COVID-19) vary between patients and countries. Patients with certain conditions are predisposed to poor outcomes compared with those without medical conditions, such as diabetes, dementia, and hypertension (HTN).

Methods: The aim of this retrospective study was to assess factors associated with higher mortality in patients with COVID-19 infections and to identify the reason for hospital admission in these patients. The study was performed on patients admitted between 1 and 31 March 2020. Data collection was done retrospectively from electronic medical records.

Results: There were 269 patient admissions during this period, of which 147 were included in this audit. The mean age of COVID-19-positive patients was 62.8 years and 65.9 years for COVID-19-negative patients during this period. Forty-seven patients requiring hospital admission were COVID-19 positive and 93 were COVID-19 negative. There were no COVID-19 swabs in the seven patients included in the audit. Approximately 50% of the COVID-19-positive patients presented with fever and shortness of breath (sob), followed by dyspnea and cough (seven patients). The most common comorbidity was HTN, followed by type 2 diabetes mellitus (T2DM) and ischemic heart disease (IHD). The survival rate was 72.3% in COVID-19-positive patients and 80% in COVID-19-negative patients. The average length of stay was 14.4 days for COVID-19-positive survivors compared to 7.8 days for COVID-19-negative survivors. Most patients who tested positive for COVID-19 infection received oseltamivir vaccination and antibiotics. The presence of HTN, diabetes mellitus (DM), age, and organ failure was associated with a high mortality risk.

Conclusion: Our study supports the findings of previous studies that diabetes, HTN, coronary artery disease, old age, and organ failure were associated with high mortality in patients admitted to hospitals with COVID-19 infections.

Keywords: risk factors for covid-19, covid-19 mortality predictors, risk of covid-19 mortality, coronavirus disease 2019 (covid-19), covid-19 outbreak

Introduction

The coronavirus disease 2019 (COVID-19) pandemic that started in China and spread rapidly worldwide continues to cause occasional outbreaks in various parts of the world. The manifestation can vary from minor asymptomatic illness to fulminant systemic inflammatory syndrome unleashed by a cytokine storm [1]. There is some variation in the data for COVID-19 morbidity and mortality across various regions due to underreporting in some regions because of poor health infrastructure [1,2]. The World Health Organization (WHO) reported a significant difference in the outcomes of patients with COVID-19, and the case fatality rate was far higher in certain parts of the world compared to others. The fatality rate reported in South Europe and the United States is significantly higher compared to China and North Europe [2]. Similarly, the case fatality rate in Italy was far higher than in China and was linked to male sex, older age, and comorbidities [2]. Other studies have highlighted similar findings and have attributed advanced age, male sex, and comorbidities such as diabetes mellitus (DM), obesity, hypertension (HTN), renal disease, coronary artery disease (CAD), and malignancy to poor outcomes in patients with COVID-19 infections [3-8]. The spectrum of presentation can vary from asymptomatic infection to lower respiratory tract infective symptoms, such as cough, shortness of breath (sob), fever, sore throat, anosmia, and acute respiratory distress syndrome in severe cases [9].

Several studies have investigated mortality predictors in patients with COVID-19 pneumonia and identified age, sex, cardiovascular and metabolic abnormalities, and C-reactive protein (CRP) as significant prognostic factors [10-12]. Genetic factors may play a role in the progression of acute respiratory distress syndrome severity in patients with COVID-19, whereas the opposite effects were found with blood group types. Blood group type A has been associated with a higher risk of disease severity or progression, while blood group O was found to exhibit protective effects [10,13]. After the initial decline in the number of cases, there was an increase in the number of patients requiring hospital and intensive care admission in parts of the European Union and European Economic Area (EU/EEA) countries, attributed to the Delta variant (B.1.617.2) and the Omicron variant (B.1.1.529) and inadequate vaccination in some of these countries [14]. The mortality rate of the severe form of infection varies among studies, and the rate is higher in patients admitted to intensive care units (ICU), with rates ranging from 8.1% to 30% for hospitalized patients in medical wards and 16% to 78% for patients admitted to ICU [9].

Several biomarkers, such as high neutrophil-to-lymphocyte ratio, high creatinine, lactate dehydrogenase (LDH), direct bilirubin, alanine aminotransferase (ALT), D-dimer, CRP, serum ferritin, interleukin-6 (IL-6), and procalcitonin (PCT), were associated with a higher mortality risk in patients with COVID-19 [1]. Most patients had mild infections without requiring hospitalization; however, 5-10% of patients developed pneumonia after a week of infection requiring hospitalization. Only a small number of patients develop further complications requiring intensive care support, with a mortality rate of approximately 1.4%. The risk of severe adverse outcomes was associated with an increasing number of comorbidities and patients aged ≥60 years, and underlying comorbidities such as cardiovascular disease, DM, chronic respiratory disease, malignancy, immunodeficiency, obesity, and male sex were associated with a higher mortality risk [15]. This study aimed to identify factors, including comorbidities and features of COVID-19 infection, associated with high mortality in patients with suspected COVID-19. The data is presented in tabular and graphical forms, and comparisons are made with other national and international studies.

Materials and methods

Methodology

This was a retrospective audit of patients presenting to Queen's Hospital, Barking, Havering and Redbridge University Hospitals NHS Trust, in Romford with suspected COVID-19 requiring admission. The audit was approved by the Audit and Research Department of Queen's Hospital, Barking, Havering and Redbridge University Hospitals NHS Trust (approval number: 074-21), and access was granted to patients' medical and electronic records. Patient confidentiality was maintained during this process, the collected data was saved on hospital local computer drivers, and access was granted to all the researchers involved in the data collection

Aims and objectives

The primary aim of this audit was to determine associated symptoms, reasons for admission, factors associated with a higher chance of hospital admission, and predictors of poor outcomes. We aimed to assess factors associated with poor outcomes in patients admitted with COVID-19 and to compare our findings with published national and international data. The audit was approved by the local audit and research departments. We collected data for patients admitted to the hospital between 1 and 31 March 2020 and presented local findings, and data collection was performed by three participants. The final data were reviewed by two reviewers for any discrepancies, and data were excluded or included after discussion between the two independent reviewers based on the inclusion and exclusion criteria.

Inclusion and exclusion criteria

The inclusion criteria were patients aged >18 years, suspected to have COVID-19 based clinically and confirmed biochemically or radiologically, and requiring hospital admission. The exclusion criteria were patients aged <18 years, those admitted for surgical reasons, and those who were not suspected to have COVID-19. Patients with missing data were excluded from this study, and tremendous efforts were made to retrieve data for all patients; however, patients with missing data despite our maximum efforts were excluded from the study to minimize the risk of selection bias. This was unanimously agreed upon by all researchers involved in the study.

Data collection and analysis

Data were collected from the patients who met the inclusion and exclusion criteria. The collected data included patient demographics, presenting problems, and medical histories. Patient records were retrieved from patients' medical notes, and biochemical and radiological test results were retrieved from the electronic data system. We collected data on patient demographics, length of stay, blood cultures, flu swabs, administration of antibiotics or antiviral therapy, COVID-19 swabs, mortality data, past medical history, and factors associated with high mortality risk. A significant number of patients had missing data and were excluded from the audit, resulting in a lower number of patients included in the study. We reviewed these patients' records at least three times including paper records and electronic records to look for the missing data before excluding these patients and to minimize the risk of bias. A few patients did not undergo COVID-19 tests on the electronic system and were excluded from the final analysis. Microsoft Excel and the Statistical Package for the Social Sciences (SPSS) Statistics were used for data analysis. We analyzed variables associated with poor prognosis and prolonged hospital stay. Data was collected about patient demographics, comorbidities, and treatment received during hospital stay, and we performed the chi-squared test and Kaplan-Meier curve to measure survival analysis in patients with suspected COVID-19 admitted to hospital. We divided patients into COVID-19-positive and COVID-19-negative groups to compare the outcome and management of patients during admission and to measure survival analysis for both groups. 

Results

Among 269 patients, only 153 were included in the study. The mean age of the COVID-19 and non-COVID-19 patients was 62.8 years and 65.9 years respectively. Male and female patients accounted for 47% and 53%, respectively, in the COVID-19 group, whereas male and female patients accounted for 51.6% and 48.4%, respectively, in the non-COVID-19 group. In terms of demographic distribution, the majority of the patients were white (57.4%), followed by Asians (19.1%) and Afro-Caribbean (10.6%), respectively, as shown in Table 1. There were no COVID-19 swabs for the seven patients included in the audit, but they were suspected to have COVID-19 based on clinical and radiological findings.

Table 1. Demographic distribution .

COVID-19: coronavirus disease 2019

    COVID-19 Non-COVID-19
Age (years) Mean 62.8 65.9
  Median 65 69
Gender Male 22 (46.8%) 48 (51.6%)
  Female 25 (53.2%) 45 (48.4%)
Ethnicity  White 27 (57.4%) 64 (68.8%)
  Asian  9 (19.1%) 10 (10.8%)
  Afro-Caribbean 5 (10.6%) 8 (8.6%)
  Others 6 (12.8%) 11 (11.8%)

Most patients (n=28) presented with sob and fever, sob and cough (nine patients), and fever and body aches (eight patients). Only two patients experienced other symptoms, such as sore throat, chest tightness, rigors, and joint aches, as shown in Figure 1. Based on the comorbidities of patients admitted to the hospital during this time, HTN and DM were the major long-term illnesses, followed by chronic kidney disease. Most patients (n=24) had HTN, 17 had type 2 diabetes mellitus (T2DM), and nine had chronic kidney disease. Other comorbidities included asthma, ischemic heart disease (IHD), and chronic obstructive pulmonary disease (COPD), and six patients were affected by these comorbidities (Figure 2).

Figure 1. Clinical features of COVID-19 patients.

Figure 1

COVID-19: coronavirus disease 2019

Figure 2. Comorbidities in COVID-19 group .

Figure 2

COVID-19: coronavirus disease 2019; COPD: chronic obstructive pulmonary disease

Based on the survival analysis, more non-COVID-19 patients survived during hospital admission than did COVID-19 patients. Approximately 73% of the patients survived in the COVID-19 group compared to 81% in the non-COVID-19 group (Figure 3). Patients who were COVID-19 positive had longer hospital stays than those who were negative for the disease. The average length of stay was 14.4 days for COVID-19-positive survivors compared to 7.8 days for COVID-19-negative survivors (Figure 4). Based on the treatment received, approximately 62% of the COVID-19-positive patients received oseltamivir, whereas only one-third of this group (34.4%) received antibiotics during admission (Figure 5).

Figure 3. Percentage of survival.

Figure 3

Figure 4. Length of stay in days for suspected COVID-19 patients .

Figure 4

The x-axis shows patient status and the y-axis shows the length of patient stay in days.

COVID-19: coronavirus disease 2019

Figure 5. Percentage of patients who either received or did not receive antibiotics and antiviral therapy.

Figure 5

This could be because COVID-19 is considered primarily a viral illness, and antibiotics were not prescribed during the initial outbreak. On the other hand, over 90% of the patients in the non-COVID-19 group received both oseltamivir and antibiotics which could be because these patients were considered to have influenza and possible chest infections. Most patients (81.8%) admitted to the hospital had nasopharyngeal swabs sent for COVID-19 polymerase chain reaction (PCR), whereas 49% of patients had blood cultures and 32% of patients had flu swabs taken (Figure 6). Furthermore, 35.5% and 18.3% of the patients in both groups had atypical pneumonia screening and sputum cultures, respectively (Figure 6).

Figure 6. Sepsis workup in suspected COVID-19 patients.

Figure 6

COVID-19: coronavirus disease 2019

All patients admitted to the hospital during this period had an escalation plan in place. This was probably due to the fact that clinicians wanted to identify patients with poor prognoses and patients at risk of deterioration to make escalation plans in advance. We were not able to identify from the documentation discussions with families and how many of these patients' families were consulted about escalation plans. Figure 7 shows the treatment escalation plan for patients admitted to the hospital during this period. Numerous predictors of survival to hospital discharge have been identified. Chronic diseases play an important role in mortality and extended hospital stays. T2DM was the most common condition among COVID-19-positive patients, followed by HTN, acute kidney injury (AKI), elevated inflammatory marker levels, age, and organ failure. Patients with COVID-19 infection features in both lungs have poor outcomes (unilateral vs. bilateral, hazard ratio (HR) 8.32 (1.11-62.3), p=0.039) (Table 2). We performed the chi-squared test to check the association between various variables such as HTN, diabetes, acute kidney injury, accommodation, organ failure, inflammatory markers, and unilateral or bilateral COVID-19 features and outcomes.

Table 2. Predictors of the survival to hospital discharge in COVID-19.

The chi-squared test was performed for these variables.

COVID-19: coronavirus disease 2019; OR: odds ratio; CI: confidence interval; ACEi: angiotensin-converting enzyme inhibitor; ARB: angiotensin II receptor blocker; AKI: acute kidney injury; CRP: C-reactive protein

Characteristics Characteristics outcome OR (99% CI) P-value
Age (years) >70 years 10.53 (1.017-1.091) P=0.003
Accommodation House/flat  1 (1.53-127) P=0.019
Nursing/residential home 13.9
Hypertension Absent   1 (1.27-10.6) P=0.016
Present 3.67
Diabetes mellitus Absent   1 (1.04-7.58) P=0.042
Present 2.81
ACEi/ARB Not taking   1   (1.07-7.93) P=0.037
Taking 2.91
Location of COVID-19 Unilateral   1 (1.32-81.3) P=0.031
Bilateral 10
Leukocyte count Raised 12.5 (1.017-1.245) P=0.022
AKI Absent   1 (1.67-13.9) P=0.004
Present 4.82
CRP >100 1.008 (1.004-1.012) P=0.0002
D-dimer Elevated 1.416 (0.338-5.935) P=0.634
Any organ failure Single   1 (1.44-20.3) P=0.012
Multiple 5.42

Figure 7. Treatment escalation plan for patients with suspected COVID-19 infection.

Figure 7

Level 1 care patients require acute medical ward care with input from critical care due to the risk of deterioration.

Level 2 care patients require more regular monitoring including single-organ support.

Level 3 care patients require respiratory and two or more organ support.

COVID-19: coronavirus disease 2019

Patients from nursing and residential homes had poorer outcomes than those from homes or flat homes. The HR for nursing home vs. house/flat was 9.68 (3.03-30.9), p=0.0001 (Figure 8). This is most likely because patients from nursing homes have more comorbidities and poorer reserves compared to patients living in their own homes. Additionally, patients living independently at home are likely to be more active than nursing home residents. Similarly, patients with AKI and COVID-19 had poorer outcomes and longer hospital stays than patients positive for COVID-19 but without AKI (Figure 9). Renal impairment was associated with poor outcomes in our study group, and similar findings have been reported in other national and international studies. Patients with COVID-19 infiltrates in both lungs on CT imaging had poor outcomes or higher HRs than patients with unilateral COVID-19 lung features (Figure 10). The overall survival of patients with COVID-19 is presented in the Kaplan-Meier curves (Figures 8-10).

Figure 8. Kaplan-Meier curve showing overall survival in patients living in nursing homes/residential homes vs. house/flat.

Figure 8

Figure 9. Kaplan-Meier curve showing overall survival in patients with AKI vs. without AKI.

Figure 9

AKI: acute kidney injury

Figure 10. Kaplan-Meier curve showing overall survival in patients with unilateral COVID-19 vs. bilateral COVID-19.

Figure 10

COVID-19: coronavirus disease 2019

Discussion

The COVID-19 pandemic, which started in China and spread rapidly worldwide, has resulted in significant morbidity and mortality. The viral pathogen is highly virulent and can mutate, resulting in outbreaks worldwide. Patient stratification can be useful to identify patients at a higher risk of deterioration, and several studies have been conducted in this regard [1-7]. Several studies have assessed mortality predictors in various countries [16-18]. The main risk factors for mortality in COVID-19 patients reported by various studies include male sex, advanced age, obesity, HTN, coronary artery disease, DM, and malignancy [1,2]. Additionally, certain biochemical and physical signs are also related to higher mortality, including fever, hemoptysis, loss of consciousness, renal impairment, deranged liver function, and elevated levels of inflammatory biomarkers such as CRP, LDH, and procalcitonin. Our study also showed that patients with renal impairment, fever, sob, and raised inflammatory markers had poor outcomes compared to those without these, and similar data was published by the WHO that showed high mortality in Italy compared to China, which was attributed to male gender, advanced age, and comorbidities [2,19]. Similarly, there was a significant difference in mortality among Western countries, and Germany reported a very low fatality rate compared to the United Kingdom, Spain, France, and Italy [2,4]. The high mortality in these studies was attributed to old age, male gender, and comorbidities, and our study showed similar findings.

Bellan et al. reported that mortality was high among older patients, and arterial HTN was the most common comorbidity among these patients [2]. They also noted that coronary artery disease, HTN, malignancy, atrial fibrillation, chronic kidney disease, smoking, COPD, and dementia were associated with poor prognosis [2,3]. This study also reported an association between increased CRP and LDH levels, low platelet and lymphocyte counts, and mortality risk, and our study also showed similar results [2-5]. A previous study reported similar findings, and patients with severe pneumonia, multiorgan dysfunction, interstitial lung disease, heart failure, immunosuppressive conditions, COPD, male sex, malignancy, and sepsis were more likely to have poor outcomes [16].

España et al. performed a retrospective study on COVID-19 patients requiring hospital and ICU admission [18]. The study included patients from nursing homes (3567 patients) and the general population (15,201 patients) [18]. COVID-19 infection requiring hospital admission was associated with an increased mortality risk in both groups. Data from nursing home patients showed that male sex, old age >80 years, COVID-19 infections requiring hospital admission, cardiovascular disease, renal disease, and dementia were associated with increased mortality risk, and our study also showed similar findings. Anticoagulants and lipid-lowering therapy had protective effects in this group of patients in this study although we could not collect data regarding these two variables and were not able to compare this data. On the other hand, for patients in the general population group, predictors of mortality were male gender, age >60 years, cardiovascular disease, dementia, respiratory disease, liver disease, diabetes with end-organ damage, malignancy, COVID-19 infection requiring hospital admission, or hospital admission for any cause within the last month. Our study also showed that diabetes, renal disease, HTN, cardiovascular disease, increased D-dimer levels, being a nursing home resident, and old age were associated with higher mortality risk. Additionally, our study also showed that patients with COVID-19 features in both lungs were associated with a higher mortality risk than single lung features.

Several meta-analyses have previously reported an association between male sex, advanced age, comorbidities, and increased COVID-19 mortality risk; however, a major weakness of these studies is the heterogeneity in the data. Additionally, all of these studies have focused on hospitalized patients using laboratory data that lack uniformity [19-21]. Yang et al. reported a higher rate of hospital and ICU admission and mortality in patients with obesity and COVID-19 infections [21]. Comorbidities such as COPD, diabetes, chronic liver disease, cardiovascular disease, and malignancy were shown to be associated with a higher mortality risk among most patients. From these, diabetes is the most prevalent comorbidity seen among patients with COVID-19 infection, and although the exact etiology is unclear, an exacerbated pro-inflammatory cascade and impaired immune response are believed to be involved in this association [22-24]. Similarly, patients with underlying malignancy and chronic kidney disease are more susceptible to COVID-19, and both are associated with an increased mortality risk [25,26]. These studies also showed that certain medications, such as anticoagulants and statins, have protective roles against COVID-19 infection mortality, which could be due to the anti-inflammatory role of statins as COVID-19 is a pro-inflammatory condition. Anticoagulants are protective due to the prothrombotic nature of COVID-19; however, the use of both these medications is reduced in patients aged >85 years due to functional and cognitive decline [27-30]. We did not collect data regarding the use of anticoagulation and statin use in patients admitted to hospitals with suspected COVID-19 infection.

A study based on data from COVIDENCE UK, a prospective population-based UK study of acute respiratory infections (ARIs) in adults, demonstrated that both COVID-19 and non-COVID-19 infections related to severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2 infection) were associated with increased symptoms and decreased health-related quality of life (HRQoL) [31]. Patients with COVID-19 infection-related ARIs were more likely to have problems with taste/smell, lightheadedness, or dizziness than those with non-COVID-19 ARIs [31]. Similarly, patients with COVID-19 were more likely to experience hair loss, unusual sweating, unexpected palpitations, and memory problems than non-COVID-19 ARI. Another study showed that patients with prolonged COVID-19 were more likely to have anterior pituitary deficiencies [32]. The prevalence of symptoms in patients with a long COVID-19 infection has been reported to range from low to 93% in this study [32]. The presence of endocrine abnormalities in acute COVID-19 infections has been reported previously; however, few studies have reported long-term endocrine problems in patients with long-term COVID-19 infections [32-34]. 

Limitations

There are several limitations to our study, including its retrospective nature, small sample size, and missing data for a significant number of patients, resulting in the exclusion of these patients from the study. We however made maximum efforts to retrieve this missing data before excluding these patients.

Conclusions

COVID-19 is associated with higher mortality and morbidity, and our study showed that certain conditions and variables are associated with a higher mortality risk. Our study showed that male sex was associated with a higher mortality risk and patients with comorbidities were more likely to have a poor prognosis. Patients with diabetes and cardiovascular disease are more likely to have poor outcomes. Nursing or care home residents were at an increased risk of mortality compared to patients from homes and flats. Advanced age was associated with poor outcomes in the study group. These data can be useful for planning future health interventions for cases of disease outbreaks.

Acknowledgments

Zahid Khan and Gideon Mlawa contributed equally to the work and should be considered co-first authors.

The authors have declared that no competing interests exist.

Author Contributions

Concept and design:  Zahid Khan, Gideon Mlawa

Acquisition, analysis, or interpretation of data:  Zahid Khan, Gideon Mlawa, Saiful Islam, Suhier Elshowaya, Mohammad Saleem

Drafting of the manuscript:  Zahid Khan, Gideon Mlawa

Critical review of the manuscript for important intellectual content:  Zahid Khan, Gideon Mlawa, Saiful Islam, Suhier Elshowaya, Mohammad Saleem

Supervision:  Zahid Khan, Gideon Mlawa

Human Ethics

Consent was obtained or waived by all participants in this study. Audit and Research Department, Queen's Hospital, Barking, Havering and Redbridge University Hospitals NHS Trust issued approval 074-21

Animal Ethics

Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.

References

  • 1.Predictors of mortality among hospitalized COVID-19 patients and risk score formulation for prioritizing tertiary care-an experience from South India. Gopalan N, Senthil S, Prabakar NL, et al. PLoS One. 2022;17:0. doi: 10.1371/journal.pone.0263471. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Fatality rate and predictors of mortality in an Italian cohort of hospitalized COVID-19 patients. Bellan M, Patti G, Hayden E, et al. Sci Rep. 2020;10:20731. doi: 10.1038/s41598-020-77698-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.A clinical risk score to identify patients with COVID-19 at high risk of critical care admission or death: an observational cohort study. Galloway JB, Norton S, Barker RD, et al. J Infect. 2020;81:282–288. doi: 10.1016/j.jinf.2020.05.064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Clinical course and risk factors for mortality of adult inpatients with COVID-19 in Wuhan, China: a retrospective cohort study. Zhou F, Yu T, Du R, et al. Lancet. 2020;395:1054–1062. doi: 10.1016/S0140-6736(20)30566-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Risk factors for severity and mortality in adult COVID-19 inpatients in Wuhan. Li X, Xu S, Yu M, et al. J Allergy Clin Immunol. 2020;146:110–118. doi: 10.1016/j.jaci.2020.04.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.Risk stratification of patients admitted to hospital with COVID-19 using the ISARIC WHO Clinical Characterisation Protocol: development and validation of the 4C Mortality Score. Knight SR, Ho A, Pius R, et al. BMJ. 2020;370:0. doi: 10.1136/bmj.m3339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Epidemiological, clinical, and laboratory predictors of in-hospital mortality among COVID-19 patients admitted in a tertiary COVID dedicated hospital, Northern India: a retrospective observational study. Ahmad S, Kumar P, Shekhar S, Saha R, Ranjan A, Pandey S. J Prim Care Community Health. 2021;12:21501327211041486. doi: 10.1177/21501327211041486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Clinical and laboratory predictors of mortality in COVID-19 infection: a retrospective observational study in a tertiary care hospital of Eastern India. Rai D, Ranjan A, H A, Pandey S. Cureus. 2021;13:0. doi: 10.7759/cureus.17660. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.Predictors for adult COVID-19 hospitalized inpatient mortality rate in North West Ethiopia. Kebede F, Kebede T, Gizaw T. SAGE Open Med. 2022;10:20503121221081756. doi: 10.1177/20503121221081756. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Mortality predictors in severe COVID-19 patients from an East European tertiary center: a never-ending challenge for a no happy ending pandemic. Timpau AS, Miftode RS, Petris AO, et al. J Clin Med. 2021;11 doi: 10.3390/jcm11010058. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Risk factors of critical & mortal COVID-19 cases: a systematic literature review and meta-analysis. Zheng Z, Peng F, Xu B, et al. J Infect. 2020;81:0–25. doi: 10.1016/j.jinf.2020.04.021. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Factors associated with disease severity and mortality among patients with COVID-19: a systematic review and meta-analysis. Chidambaram V, Tun NL, Haque WZ, et al. PLoS One. 2020;15:0. doi: 10.1371/journal.pone.0241541. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Association between HLA gene polymorphisms and mortality of COVID-19: an in silico analysis. Tomita Y, Ikeda T, Sato R, Sakagami T. Immun Inflamm Dis. 2020;8:684–694. doi: 10.1002/iid3.358. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Prognostic factors for mortality, intensive care unit and hospital admission due to SARS-CoV-2: a systematic review and meta-analysis of cohort studies in Europe. Vardavas CI, Mathioudakis AG, Nikitara K, et al. Eur Respir Rev. 2022;31:220098. doi: 10.1183/16000617.0098-2022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Predictors of in-hospital mortality in Covid-19: a study across two peripheral district general hospitals in UK. Samanta NK, Bandyopadhyay SK, Herman D, et al. https://www.bjmp.org/content/predictors-hospital-mortality-covid-19-study-across-two-peripheral-district-general-hospitals-uk Br J Medical Pract. 2021;14:0. [Google Scholar]
  • 16.The predictors of COVID-19 mortality in a nationwide cohort of Turkish patients. Kokturk N, Babayigit C, Kul S, et al. Respir Med. 2021;183:106433. doi: 10.1016/j.rmed.2021.106433. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 17.Risk factors of fatal outcome in hospitalized subjects with coronavirus disease 2019 from a nationwide analysis in China. Chen R, Liang W, Jiang M, et al. Chest. 2020;158:97–105. doi: 10.1016/j.chest.2020.04.010. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Predictors of mortality of COVID-19 in the general population and nursing homes. España PP, Bilbao A, García-Gutiérrez S, et al. Intern Emerg Med. 2021;16:1487–1496. doi: 10.1007/s11739-020-02594-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Coronavirus Disease (COVID-19): Situation report - 119. [ Dec; 2023 ]. 2020. http://www.who.int/docs/default-source/coronaviruse/situation-reports/20200518-covid-19-sitrep-119.pdf?sfvrsn=4bd9de25_4 http://www.who.int/docs/default-source/coronaviruse/situation-reports/20200518-covid-19-sitrep-119.pdf?sfvrsn=4bd9de25_4
  • 20.Risk factors for mortality in patients with coronavirus disease 2019 (COVID-19) infection: a systematic review and meta-analysis of observational studies. Parohan M, Yaghoubi S, Seraji A, Javanbakht MH, Sarraf P, Djalali M. Aging Male. 2020;23:1416–1424. doi: 10.1080/13685538.2020.1774748. [DOI] [PubMed] [Google Scholar]
  • 21.Obesity aggravates COVID-19: an updated systematic review and meta-analysis. Yang J, Tian C, Chen Y, Zhu C, Chi H, Li J. J Med Virol. 2021;93:2662–2674. doi: 10.1002/jmv.26677. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 22.COVID-19: is there a link between the course of infection and pharmacological agents in diabetes? Filardi T, Morano S. J Endocrinol Invest. 2020;43:1053–1060. doi: 10.1007/s40618-020-01318-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Clinical characteristics and risk factors for mortality of COVID-19 patients with diabetes in Wuhan, China: a two-center, retrospective study. Shi Q, Zhang X, Jiang F, et al. Diabetes Care. 2020;43:1382–1391. doi: 10.2337/dc20-0598. [DOI] [PubMed] [Google Scholar]
  • 24.Prognostic factors in patients with diabetes hospitalized for COVID-19: findings from the CORONADO study and other recent reports. Scheen AJ, Marre M, Thivolet C. Diabetes Metab. 2020;46:265–271. doi: 10.1016/j.diabet.2020.05.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25.Management recommendations for patients with chronic kidney disease during the novel coronavirus disease 2019 (COVID-19) epidemic. Li J, Li SX, Zhao LF, Kong DL, Guo ZY. Chronic Dis Transl Med. 2020;6:119–123. doi: 10.1016/j.cdtm.2020.05.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Kidney disease is associated with in-hospital death of patients with COVID-19. Cheng Y, Luo R, Wang K, et al. Kidney Int. 2020;97:829–838. doi: 10.1016/j.kint.2020.03.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Statins and the COVID-19 main protease: in silico evidence on direct interaction. Reiner Ž, Hatamipour M, Banach M, et al. Arch Med Sci. 2020;16:490–496. doi: 10.5114/aoms.2020.94655. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 28.Statins: could an old friend help in the fight against COVID-19? Rodrigues-Diez RR, Tejera-Muñoz A, Marquez-Exposito L, et al. Br J Pharmacol. 2020;177:4873–4886. doi: 10.1111/bph.15166. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 29.COVID-19 mortality in patients on anticoagulants and antiplatelet agents. Sivaloganathan H, Ladikou EE, Chevassut T. Br J Haematol. 2020;190:0–5. doi: 10.1111/bjh.16968. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.COVID-19 and the liver. Jothimani D, Venugopal R, Abedin MF, Kaliamoorthy I, Rela M. J Hepatol. 2020;73:1231–1240. doi: 10.1016/j.jhep.2020.06.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31.Long-term symptom profiles after COVID-19 vs other acute respiratory infections: an analysis of data from the COVIDENCE UK study. Vivaldi G, Pfeffer PE, Talaei M, Basera TJ, Shaheen SO, Martineau AR. EClinicalMedicine. 2023;65:102251. doi: 10.1016/j.eclinm.2023.102251. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Explaining long COVID: a pioneer cross-sectional study supporting the endocrine hypothesis. Ach T, Ben Haj Slama N, Gorchane A, et al. J Endocr Soc. 2024;8:0. doi: 10.1210/jendso/bvae003. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Prevalence and outcomes of hyponatremia among COVID-19 patients: a systematic review and meta-analysis. Khidir RJ, Ibrahim BA, Adam MH, Hassan RM, Fedail AS, Abdulhamid RO, Mohamed SO. https://pubmed.ncbi.nlm.nih.gov/36101848/ Int J Health Sci (Qassim) 2022;16:69–84. [PMC free article] [PubMed] [Google Scholar]
  • 34.Central diabetes insipidus secondary to COVID-19 infection: a case report. Yavari A, Sharifan Z, Larijani B, Mosadegh Khah A. BMC Endocr Disord. 2022;22:134. doi: 10.1186/s12902-022-01048-w. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Cureus are provided here courtesy of Cureus Inc.

RESOURCES