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Research Article | Volume 16 Issue 1 (Jan, 2026) | Pages 6 - 9
CLINICO-DEMOGRAPHIC CHARACTERISTICS AND HOSPITAL OUTCOME OF SEVERE COVID-19 PNEUMONIA PATIENTS: A STUDY AT A TERTIARY CARE HOSPITAL
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1
Assistant Professor, Department of Internal Medicine, GMC Srinagar.
2
Senior Resident, Department of Internal Medicine, GMC Srinagar
3
Assistant Professor, Department of Pathology, GMC Srinagar
4
Professor, Department of Internal Medicine, GMC Srinagar
5
Associate Professor, Department of Pathology, GMC Srinagar
Under a Creative Commons license
Open Access
Received
Nov. 12, 2025
Revised
Nov. 28, 2025
Accepted
Dec. 31, 2025
Published
Jan. 3, 2026
Abstract

Background: The clinical profile and outcomes of severe COVID-19 vary across regions and health-care settings. We evaluated the clinico-demographic characteristics and in-hospital outcomes of patients with severe COVID-19 pneumonia admitted to a tertiary hospital in North India. Methods: We performed a prospective observational study of RT-PCR–confirmed COVID-19 patients meeting severity criteria (respiratory rate >24/min, SpO₂ <94% on room air, or organ dysfunction) over seven months. Demographics, symptoms, comorbidities, laboratory tests, and HRCT findings were recorded. Outcomes included in-hospital mortality. Results: Of 179 severe cases, 95 were men (53.1%) and 100 were from rural areas (55.9%). Fever was the most common symptom, followed by cough and breathlessness; universal hypoxaemia was documented on admission. Tachycardia occurred in 89.4%, tachypnoea in 50.3%, bradycardia in 7.3%, and hypotension in 1.7%. Hypertension (48.0%) and diabetes (9.5%) were the leading co-morbidities; one-third had none. Lymphopenia was seen in 19.0% and leukocytosis in 11.2%; HRCT showed a CT severity index >6 in all patients. Overall mortality was 13.4% (24/179) and was higher in males (62.5% of deaths), in those ≥60 years (58.3%), with comorbidities (66.7%), and from rural areas (75%). Conclusion: Severe COVID-19 pneumonia at our centre was characterised by fever with hypoxaemia, frequent hypertension and lymphopenia, and a moderate fatality rate. Male sex, older age, rural residence, co-morbidities, lower SpO₂, and higher CT severity were associated with death, underscoring the need for early risk stratification and intensified management in these subgroups.

Keywords
INTRODUCTION

On December 8, 2019, a case of pneumonia of unknown etiology was detected in Wuhan city, Hubei province, China1. On December 31, China reported a cluster of Pneumonia with unknown etiology to the World Health Organization (WHO), and seven days later, Chinese scientists identified the pathogen as a novel coronavirus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).1 The WHO declared the outbreak a pandemic on 11 March 2020, due to the increasing number of cases outside China2. The pandemic is spreading exponentially, with millions of people across the globe at risk of contracting coronavirus disease 2019 (COVID-19). Coronavirus has caused large respiratory outbreaks previously in the form of severe acute respiratory syndrome (SARS) outbreak in 2003 and Middle East respiratory syndrome (MERS) in 2012 which has caused >10,000 cases globally and mortality around 10 and 37 per cent for SARS and MERS, respectively3,4. In India, the first case of COVID-19 was identified on January 30, 20205 and the number has been increasing steadily due to local transmission and foci of community transmission.

MATERIAL AND METHODS

The study was conducted in a tertiary care hospital of north India to assess the clinico-demographic characteristic and outcome in RTPCR proven cases of severe COVID19 pneumonia. It was a prospective observational study. A focused history including travel and exposure history and comorbidities were recorded. After initial clinical evaluation, patients with dyspnea, respiratory rate (RR) >20/min, or oxygen saturation (SpO2) <94 per cent on room air, clinical diagnosis of pneumonia and those deemed to be at risk for severe disease were subjected to chest radiography. Baseline haemogram, liver and kidney function tests were done for all symptomatic patients. Patients with age >60 years and those with cardiovascular risk factors, immunocompromised state and chronic diseases, were considered at high-risk for progression to severe disease. Severe disease was defined a patient with RR >24/min, SpO2 <94 per cent on room air, confusion, drowsiness, hypotension, sepsis, septic shock or admission to ICU.

RESULTS

Total 179 patients of clinically or radiologically documented severe COVID19 pneumonia were included in study of which 95 were males (53.07%) 84 (46.92%) females 100 (55.86%) patients were from rural area 79 (44.13%) urban area. most common presenting symptom was fever (n=120) followed by cough and breathlessness (n=80) other were myalgia, loose motion, loss of taste and smell the most common sign was hypoxemia (n=179) tachycardia (n=160) tachypnea (n=90) bradycardia (n=13) and hypotension in 3 patients. Most common comorbidity was hypertension 86 (48.04%) followed by diabetes mellitus 17 (9.49%) other were CAD (n=5), COPD (n=3), asthma (n=2), malignancy (n=2), seizure disorder (n=2), active tuberculosis (n=1) and CKD (n=1) whereas 60 (33.51%) were having no underlying comorbidities. Most common CBC abnormality was leukopenia particularly lymphopenia 34 (18.99%) leukocytosis 20 (11.17%) whereas 125 (69.83%) had normal CBC HRTCT revealed CTSI more than 6 in all 179 patients. Out of 179 patients 24 (13.40%) patients expired death were more common in males 15 (62.5%) than females 9 (37.5) elderly 14 (58.33%) were more than 60 years and patients with underlying comorbidities 16 (66.66%) rural 18 (75%) than urban.

 

 

 

DISCUSSION

In this prospective study we aimed to assess the clinical characteristics demographic and outcome in severe covid19 pneumonia patients admitted in tertiary care hospital in north India. Majority of admitted patients to our hospital were men (53.07%), this agrees with emerging studies showing that men with COVID-19 are at higher risk for developing severe outcomes including death than women6,7 rural population had severe disease than urban this difference could be attributed to living habit, poor cough etiquette, overcrowding and delayed presentation to hospital. The most common presenting symptom was fever followed by cough and breathlessness, Fever a respiratory manifestation, is the most commonly reported symptom in patients infected with SARSCoV-2. Accordingly, fever may be a clinical sign of poor prognosis in patients and response to the release of inflammatory mediators such as cytokines and chemokine8,9, The most common co‑morbidity reported was hypertension in 48.04% and diabetes in 9.49% and others had COPD, CKD, CAD Malignancy, tuberculosis seizure disorder and asthma which were in par with other studies.8,10,11. We observed a hospital case fatality rate of 13.40%, which seemed to be lower than those reported by other studies12. However, this is unlikely to reflect the true fatality rate of the disease, as out-patients and those with missing data were excluded. Independent risk factors associated with in-hospital death in this study included older age, males, rural population lower SpO2, lymphopenia and higher CTSI. Association of age and death12 as well as lower SpO2 and death was also reported in China13. Oxygen saturation has appeared to be a reliable surrogate marker of COVID-19 illness severity and death.

CONCLUSION

In this prospective cohort of 179 patients with severe COVID-19 pneumonia from a North Indian tertiary centre, fever with hypoxaemia was the dominant presentation and hypertension was the commonest co-morbidity. Overall in-hospital mortality was 13.4% and was significantly concentrated among men, older adults (≥60 years), patients from rural areas, and those with underlying co-morbidities. Lymphopenia and high HRCT severity (CTSI >6 in all) were frequent among severe cases. Early recognition of hypoxaemia, aggressive monitoring of high-risk groups, and timely referral of rural patients may reduce adverse outcomes.

REFERENCES

1.       Wu Z, McGoogan JM. Characteristics of and important lessons from the coronavirus disease 2019 (COVID-19) outbreak in China: summary of a report of 72314 cases from the Chinese Center for Disease Control and Prevention. JAMA. 2020;323.

2.       WHO Director-General’s opening remarks at the media briefing on COVID-19: 11 March 2020; Published March 11, 2020. Accessed March 30 2020. https://www. who.int/ dg/speeches/detail/who-director-general-s-openingremarks-at-the-media-briefing-on-covid-19—11-march-2020. No title.

3.       World Health Organization. Middle East respiratory syndrome coronavirus (MERSCoV)Availablefrom:https://www.who.int/newsroom/factsheets/detail/middleeast-respiratorysyndrome-coronavirus-(mers-cov), assessed on June 1, 2020.

4.       World Health Organization. Summary of probable SARS cases with onset of illness from 1 November 2002 to July 2003. Available from: https://www.who.int/csr/sars/country/ table2004_04_21/en/ accessed on assessed on June 1, 2020.

5.       Andrews M A, Areekal B, Rajesh K R, Krishnan J, Suryakala R, Krishnan B, et al. First confirmed case of COVID-19 infection in India: A case report. Indian J Med Res 2020; 151: 490-2.

6.       Jin JM, Bai P, He W, Wu F, Liu XF, Han DM et al. Gender Differences in Patients With COVID-19: Focus on Severity and Mortality. Front Public Health. 2020 Apr 29;8:152. doi: 10.3389/fpubh.2020.00152. 

7.       Chen N, Zhou M, Dong X, Qu J, Gong F, Han Y et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study. Lancet. 2020 Feb 15;395(10223):507-513. 

8.       Gupta N, Agrawal S, Ish P, Mishra S, Gaind R, Usha G, et al. Clinical and epidemiologic profile of the initial COVID‑19 patients at a tertiary care centre in India. Monaldi Arch Chest Dis 2020; 90:1294‑6.

9.       Dosi R, Jain G, Mehta A. Clinical characteristics, comorbidities, and outcome among 365 patients of Coronavirus disease 2019 at a Tertiary care centre in Central India. J Assoc Physicians India 2020; 68:20‑3.

10.    Mohan A, Tiwari P, Bhatnagar S, Patel A, Maurya A, Dar L, et al. Clinico‑demographic profile and hospital outcomes of COVID‑19 patients admitted at a Tertiary care centre in North India. Indian J Med Res 2020; 152:61‑9.

11.    Sanyaolu A, Okorie C, Marinkovic A, Patidar R, Younis K, Desai P, et al. Comorbidity and its impact on patients with COVID‑19. SN Compr Clin Med 2020; 25:1‑8

12.    Zhou F, Yu T, Du R, Fan G, Liu Y, Liu Z 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: 1054–62. 

13.    Xie J, Covassin N, Fan Z, Singh P, Gao W, Li G et al. Association Between Hypoxemia and Mortality in Patients With COVID-19. Mayo Clin Proc 2020, 95: 1138–47.

 

Conflict of interest: none

Acknowledgement: none.

Funding: none.

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