Saadia Omer1,2,3†
Mehrunnisa Fatima Gondal1
Muhammad Usman4
Muhammad Bilal Sarwar1†
Muhammad Roman1Alam Khan1Nadeem Afzal1Tanveer Ahmed Qaiser5
Muhammad Yasir6Faheem Shahzad1Romeeza Tahir1
Saima Ayub2Javed Akram1Raja Muhammad Faizan7Muhammad Asif Naveed1
Shah Jahan1*- 1Department of Immunology, University of Health Sciences, Lahore, Pakistan
- 2Institute of Public Health, Health Department, Government of Punjab, Lahore, Pakistan
- 3Department of Community Medicine, Fatima Jinnah Medical University, Lahore, Pakistan
- 4Allama Iqbal Medical College, Jinnah Hospital, Lahore, Pakistan
- 5Department of Molecular Biology, Shaheed Zulfiqar Ali Bhutto Medical University, Islamabad, Pakistan
- 6Quadram Institute Bioscience, Norwich Research Park, Norwich, United Kingdom
- 7Department of Medicine, Shifa College of Medicine, Islamabad, Pakistan
SARS-CoV-2 is a causative agent for COVID-19 disease, initially reported from Wuhan, China. The infected patients experienced mild to severe symptoms, resulting in several fatalities due to a weak understanding of its pathogenesis, which is the same even to date. This cross-sectional study has been designed on 452 symptomatic mild-to-moderate and severe/critical patients to understand the epidemiology and clinical characteristics of COVID-19 patients with their comorbidities and response to treatment. The mean age of the studied patients was 58 ± 14.42 years, and the overall male to female ratio was 61.7 to 38.2%, respectively. In total, 27.3% of the patients had a history of exposure, and 11.9% had a travel history, while for 60% of patients, the source of infection was unknown. The most prevalent signs and symptoms in ICU patients were dry cough, myalgia, shortness of breath, gastrointestinal discomfort, and abnormal chest X-ray (p < 0.001), along with a high percentage of hypertension (p = 0.007) and chronic obstructive pulmonary disease (p = 0.029) as leading comorbidities. The complete blood count indicators were significantly disturbed in severe patients, while the coagulation profile and D-dimer values were significantly higher in mild-to-moderate (non-ICU) patients (p < 0.001). The serum creatinine (1.22 μmol L-1; p = 0.016) and lactate dehydrogenase (619 μmol L-1; p < 0.001) indicators were significantly high in non-ICU patients, while raised values of total bilirubin (0.91 μmol L-1; p = 0.054), C-reactive protein (84.68 mg L-1; p = 0.001), and ferritin (996.81 mg L-1; p < 0.001) were found in ICU patients. The drug dexamethasone was the leading prescribed and administrated medicine to COVID-19 patients, followed by remdesivir, meropenem, heparin, and tocilizumab, respectively. A characteristic pattern of ground glass opacities, consolidation, and interlobular septal thickening was prominent in severely infected patients. These findings could be used for future research, control, and prevention of SARS-CoV-2-infected patients.
Introduction
The novel coronavirus (2019-nCoV) was first identified in patients with pneumonia of unknown cause, originating in Wuhan, China, in late December 2019 (Lu et al., 2020; Zhou et al., 2020). The virus that caused this infection belongs to the Conronaviridae family (Lvov and Alkhovsky, 2020), which was later named “severe acute respiratory syndrome coronavirus 2” (SARS-CoV-2) by the World Health Organization (WHO) and caused coronavirus disease 2019 (COVID-19) (WHO, 2020). In January 2020, WHO declared the COVID-19 outbreak, a public health emergency of international concern, and a pandemic in March 2020 (Sun et al., 2020a). There have been around half a billion confirmed cases, with approximately 5 million deaths attributed to the ongoing COVID-19 pandemic, while the confirmed cases in Southeast Asia are in the range of 50 million (WHO, 2021; WHO, 2022).
In Pakistan, the first confirmed case of COVID-19 was reported on February 26, 2020, and that spread horrifically in the following months in all parts of the country despite the safety measures adopted (Khalid and Ali, 2020; Mushtaq et al., 2020). Initially, due to the lack of access to essential healthcare services at the Pak-Iran border, the asymptomatic pilgrims returning from Iran to Pakistan introduced the virus in the latter (Javed et al., 2021). Later, over the period, unchecked non-essential international travel to Pakistan has led to its spread in all parts of the country (Nawaz et al., 2020). Considering the severity of the pandemic, the government of Pakistan has established the National Command and Operational Centre (NCOC) to synergize and articulate national efforts against COVID-19 (NCOC, 2021a). The measure taken by NCOC to control the pandemic was quite effective. NCOC adopted the WHO checklist to exercise travel restrictions, placed smart lockdowns, enforced workplace hazard controls, and even implemented facility closures to minimize exposure with the carriers (asymptomatic) as preventive measures (NCOC, 2021b). Pakistan’s overall verified COVID-19 count has reached around one and a half million, with approximately 90% recoveries and 2% fatalities (NCOC 2022). Despite the control measures launched into action, the alarming rise in COVID-19 cases and the increasing fatalities in the region have raised multiple concerns regarding the infrastructure of our healthcare system and the overwhelming burden placed on it. Understanding the relationship between COVID-19 and epidemiological features like clinicopathological characteristics and treatment available for mild-to-moderate and severe patients is essential to suggest preventive measures. The epidemiological features include age, sex, race, and comorbidities, which are the most studied parameters not only in COVID-19 but also in other infectious diseases (Bi et al., 2020; Sun et al., 2020b, Yang et al., 2020).
Practically, most health workers relied upon clinical signs and symptoms, mainly of the respiratory and digestive system, associated fever, fatigue, and lab findings—such as values of IL-6, D-dimer, procalcitonin, complete blood count (CBC), etc.—to assess the disease prognosis (Grant et al., 2020; Lechien et al., 2020; Tian et al., 2020). The SARS-CoV-2-infected patients showed variable symptoms, ranging from mild to severe illness. It primarily affects the pulmonary system, causes symptoms like sore throat, cough, rhinorrhea, nasal congestion, and dyspnea; digestive system-related complaints causing nausea, vomiting, diarrhea, and abdominal pain; and associated systemic symptoms like fever, headache, myalgia, arthralgia, generalized body ache, and fatigue (Mehta et al., 2021). It may affect the nervous system, causing atypical clinical findings such as anosmia, loss of taste, dizziness, and, rarely, seizure (Niazkar et al., 2020; Vohora et al., 2020). The most common symptoms seen were fever, dyspnea, myalgia, etc. One in five patients infected with SARS-CoV-2 did not develop noticeable symptoms, thus acting as a silent carrier (He et al., 2021) and thereby increasing the chances of the further progression of SARS-CoV-2 infection in the community as well as putting at risk old-age patients and those with associated comorbidities like diabetes, hypertension, chronic obstructive pulmonary disease (COPD), acute respiratory distress syndrome (ARDS), ischemic heart disease (IHD), chronic liver disease, chronic kidney disease (He et al., 2020a). The comorbidities and the nature of pathological findings related to organs and tissues are the leading factors that determine the disease severity and outcome (Gu and Korteweg, 2007; Mueller et al., 2020).
The mortality in COVID-19 depends on the virus–host genetic interaction and geographical setting (international and regional spread), as climate differences influence viral transmission via respiratory droplets (Oberemok et al., 2020). Punjab is the largest and most densely populated province of Pakistan and has a population of 110 million, out of which about 64% reside in urban areas (GOP, 2017). It has a high population density of about 536 persons per square kilometer, increasing the susceptibility towards the spread of COVID-19. Out of the total number of confirmed COVID-19 patients, about 37% were located in the province of Punjab (GOP, 2021). Islamabad is the tertiary capital of Pakistan with more than 2 million inhabitants, but due to its limited area, it has the highest average population density of 2,215 persons per square kilometer (GOP, 2017). The city is the gateway to the country for foreign travellers and provides habitation to people from the whole country. Accordingly, the main referral hospital of Islamabad was also selected for this study.
Only a few studies have been undertaken in Pakistan to determine the epidemiological aspect, clinic pathological characteristics, and comorbidities of COVID-19 patients. A key shortcoming of several COVID-19 studies seems to be the focus on either epidemiological or clinico-pathological factors. This study aims to give insight into the interrelationships between illness and epidemiology, clinicopathological characteristics, co-morbidities, and treatment options for moderately and critically ill patients. The goal of this study is to understand more about the COVID-19 pandemic by evaluating symptomatic hospitalized COVID-19 patients based on their epidemiological, clinical, and laboratory features. This comparative cross-sectional study was conducted in leading hospitals designated for COVID-19 treatments, ie., Mayo Hospital Lahore, Jinnah Hospital Lahore, Sheikh Zaid Hospital Lahore, University of Health Sciences Lahore, Nishtar Hospital Multan, Victoria Hospital Bahawalpur, Pakistan Institute of Medical Sciences Islamabad, and Infectious Treatment Centre Islamabad. The findings of this pioneering study will serve as a foundation for policy development and strategic planning to prevent, diagnose, and cure the COVID-19 pandemic.
Materials and Methods
Sampling Technique
A non-probability convenience sampling technique was used for the selection of the study population. Quantitative real-time polymerase chain reaction (qPCR) confirmed the SARS-CoV-2-infected patients, with age >18 years, who were admitted in the isolation wards of the selected hospitals and selected after taking permission from the respective administration and obtaining their informed consent. None of the patients in this study had previously been vaccinated or had a history of the illness. Furthermore, patients with co-infections were ruled out, with the help of a clinician, using available laboratory tests and other clinical data; however, patients with an asymptomatic illness in the past could not be ruled out entirely. Patients with co-infections of Pseudomonas spp., Klebsiella pneumoniae, Streptococcus pneumoniae, Acinetobacter spp., and Escherichia coli were identified and excluded from this study.
These patients were classified into mild-to-moderate and severe/critical categories using the operational definitions of the “Chinese Clinical Guidance for COVID-19 Pneumonia Diagnosis and Treatment”, published by the Chinese National Health Commission (Gao et al., 2020). The patients in the isolation wards, who meet the case definition for COVID-19 with and without evidence of pneumonia, were categorized in the mild-to-moderate group, whereas the patients in intensive care units who had clinical signs of pneumonia (fever, cough, dyspnea, and tachypnea)—with the following parameters: respiratory rate, >30 breaths min-1; severe respiratory distress; or oxygen saturation (SpO2) <90% on room air—were considered in the severe group. The estimated sample size, using the WHO formula and considering the anticipated population proportion, was ~450 patients (Yang et al., 2020).
Data Collection/Measurements
Before entering the isolation wards, the guidelines and SOPs of each hospital were adopted. A detailed questionnaire was prepared with the assistance of three medical consultants for information collection, which was based on similar studies (Al Mutair et al., 2020; Kirchberger et al., 2021; Yegorov et al., 2021). It included demographic data (age and gender), family type (nuclear and extended), source of infection (travel history and contact with COVID-19 patient), etiology, clinical features (upper and lower respiratory tract and gastro-intestinal tract symptoms), co-morbidities (diabetes mellitus, hypertension, chronic liver disease, chronic obstructive pulmonary disease, ischemic heart disease, cancer, tuberculosis, etc.), laboratory values (complete blood count, biochemical parameters, coagulation profile, inflammatory biomarkers for organ function, and analysis of immunological responses), treatment given (oral/IV antibiotics, antiviral, steroids, I/V fluids, orogastric fluids, antimalarial, and any experimental drug), length of hospitalization, and time taken to get the negative result of qPCR for SARS-CoV-2 (1st qPCR negative report). The digital images of the chest CT scan of COVID-19 patients were also obtained from selected hospitals and shared with experienced radiologists for characteristic disease findings.
Statistical Analysis
The data were entered, cleaned, and analyzed using Statistical Package for Social Sciences, V.23. Quantitative variables like age and laboratory parameters were presented as mean and standard deviation. In contrast, qualitative data like clinical features, comorbidities, and demography were presented in frequency and percentages. The relationship between COVID-19 with clinico-pathological parameters and comorbidities among mild-to-moderate and severe patients was assessed using chi-square test (p ≤ 0.05). The means were compared using Student’s t-test or ANOVA where applicable. Bar and pie diagrams were used to present categorical data where applicable.
Results
Demography
Four hundred fifty-two (452) patients confirmed to have COVID-19 diseases and admitted to five leading hospitals in different cities of the country were included in this study. Among these, 279 (61.7%) patients were male, and 173 (38.2%) were female (Figure 1). The mean age of the studied patients was 58 ± 14.42 years old. The overall patients’ age of <50 years was less in number (126, 27.88%; with a mean age of 40 ± 7.83 years) compared with patients aged ≥50 years (326, 72.12%; with a mean age of 65 ± 9.13 years). The mild-to-moderate (non-ICU) cases were higher with patients aged <50 years (83, 34.73%), whereas only 43 (20.19%) were severe (ICU) cases in this age group. In a group with patients >50 years old, more severe cases were seen, i.e., 170 (79.81%) compared with the 156 moderate cases (65.27%). Most of the patients belonged to the extended family type (294, 65%) compared with those who came from a nuclear family (158, 35%). However, the severity of the disease was insignificant between the extended and the nuclear family types (p = 0.429). Overall, 127 (27.3%) patients had a known history of exposure to the infected environment; 54 (11.9%) patients were with a travel history, while for 274 (60.6%) patients the cause of acquiring the infection was unknown. The severity of the disease was insignificant between the sources of COVID-19 infection (p = 0.496). The detailed demographic information is summarized in Table 1.
Figure 1 Gender-wise distribution of the SARS-CoV-2-infected patients in the different age groups studied in this study.
Table 1 Epidemiological data of 452 symptomatic COVID-19 patients.
Clinical Features of SARS-CoV-2-Infected Patients
The most common symptom of illness in the COVID-19 patients was fever (n = 364, 80%), followed by dyspnea at rest (n = 343, 75%) and cough (n = 261, 57%). In a small percentage of COVID-19 patients, fatigue (n = 138, 30%), pneumonia (n = 89, 19%), myalgia and generalized body aches (n = 75, 16%), vomiting (n = 61, 13%), headache (n = 36, 7.9%), sore throat (n = 33, 7.3%), diarrhea (n = 33, 7.3%), sputum production (n = 19, 4.2%), nausea (n = 13, 2.9%), loss of taste (n = 12, 2.7%), rhinorrhea (n = 12, 2.7%), anosmia (n = 7, 1.5%), nasal congestion (n = 5, 1.1%), and abnormal chest X-ray (n = 36, 7.9%) were also observed. Some clinical manifestations differed significantly between mild-to-moderate and severe patients. The symptoms of dyspnea, pneumonia, and respiratory distress and abnormal chest X-ray findings were more pronounced in severe patients compared with the mild-to-moderate cases (p < 0.001). On the contrary, symptoms of fatigue (p < 0.001) and loss of taste (p = 0.04) were seen in the mild-to-moderate cases. A tabulated summary of the clinical features of SARS-CoV-2-infected patients is shown in Table 2.
Table 2 Clinical features of 452 symptomatic COVID-19 patients.
COVID-19 Patients With Comorbidities
Compared with the mild-to-moderate patients, the severe patients had underlying co-morbidities, such as hypertension (n = 104, 48.8%), type 2 diabetes (n = 82, 38.5%), and ischemic heart disease (n = 36, 16.9%). Other diseases included chronic kidney disease (n = 10, 4.7%), asthma (n = 6, 2.8%), immunocompromised state (n = 6, 2.8%), COPD (n = 7, 3%), liver disease (n = 2, 0.9%), and history of smoking (n = 3, 1.4%). The severe patients included a significantly high percentage of hypertension (p = 0.007) and COPD (p = 0.029) cases. These co-morbidities impact the outcome of disease severity and COVID-19 mortality. A comprehensive comparison is shown in Table 3.
Table 3 Comorbidities of 452 symptomatic COVID-19 patients.
Laboratory Parameters
The mean values of CBC were significantly high in severe patients, compared with mild-to-moderate cases, in terms of WBC (14,864.70 ± 5,821.73 vs. 11,055.94 ± 4,344.7, p < 0.001), platelets (249,672 ± 104,826.59 vs. 246,447.36 ± 83,141.91, p = 0.004), and neutrophil (9.99 ± 4.93 vs. 8.19 ± 3.27, p < 0.001). Similarly, the coagulation profile (d-dimer) was significantly high in mild-to-moderate patients (2,610.00 ± 3,607.04) compared with severe patients [2,213.67 ± 2,823.36 (mg L-1), p < 0.001]. Regarding the liver function test, total bilirubin was significantly high in severe patients (0.91 ± 1.41), while it was 0.54 ± 0.25 in mild-to-moderate patients (μmol L-1; p = 0.054). For renal function test, serum creatinine was significantly high in the mild-to-moderate group (1.22 ± 0.64), while it was 0.81 ± 0.25 mol L-1; p = 0.016) in severe patients. Lactate dehydrogenase (LDH) was significantly high in the mild-to-moderate group (619.00 ± 257.32) than in the severe group (587.58 ± 178.31, p < 0.001). Furthermore, severe patients had significantly high values of C-reactive protein (CRP) and ferritin (84.68 ± 57.25 and 996.81 ± 892.21 mcg/liter; p < 0.001), respectively, compared with the mild-to-moderate group of SARS-CoV-2-infected patients. From illness to discharge, the average length of hospital stay was longer in severe patients (10.79 ± 7.00 compared with the mild-to-moderate patients at 5.89 ± 3.41; p < 0.001). The detailed comparison of laboratory parameters is presented in Table 4. Furthermore, the laboratory parameters were also analyzed based on comorbidities in COVID-19 patients, and none of the above-reported laboratory parameters were significantly different in patients with and without comorbidities. However, Hb and ALT were significantly high in COVID-19 patients with hypertension (HTN). Similarly, PT was significantly high in COVID-19 patients with type 2 diabetes mellitus, and the urea-N/urea ratio was high in patients with IHD. It is worth mentioning that we have only analyzed the data of comorbidities with a significant number of patients i.e., HTN (42%), T2DM (34%), and IHD (14%). The rest of the comorbidities were not reported significantly in the study population to be included in the analysis (immunocompromised state, 2.2%), liver disease (0.7%), COPD (1.8), asthma (2.4%), and smoking (1.1%; Supplementary Data).
Table 4 Laboratory features of 452 symptomatic COVID-19 patients.
Medications Used in the Treatment
In Table 5, shown is a summary of the medication given to the SARS-CoV-2-infected patients. Almost all SARS-CoV-2-infected patients, spanning between mild-to-moderate and severe, had a combination of antiviral, antibacterial, and corticosteroid-based medication combined with oxygen therapy. The patients were treated for bacterial infection from the following sources: Pseudomonas spp., Klebsiella pneumoniae, Streptococcus pneumoniae, Acinetobacter spp., and Escherichia coli. Only two critically ill patients were on invasive ventilators, while others were managed with non-invasive ventilation. Compared with the mild-to-moderate patients, a significant percentage of severe patients were treated with dexamethasone (n = 211, 99 vs. 207; 86.6%, p < 0.001), remdesivir (n = 178; 83.5 vs. 136; 56.9%, p < 0.001), meropenem (n = 121; 56.8% vs. n = 76; 31.8%, p < 0.001), heparin (n = 112; 52.6% vs. n = 75; 31.4%; p <0.001), and tocilizumab (n = 14; 6.6% vs. n = 1; 0.42%; p < 0.001).
Table 5 Treatment of 452 symptomatic COVID-19 patients.
Correlation Between Laboratory Parameters
A significant correlation was assessed among laboratory parameters (the details of which are summarized in Table 6), namely:
i. A highly significant positive correlation was evaluated between ferritin and Hb, WBC, ALT/SGPT, total bilirubin, CRP, and LDH, while it had a highly negative correlation with lymphocytes.
ii. D-dimer had a highly significant positive correlation with WBC, INR, procalcitonin, and LDH.
iii. Hb had a highly significant positive correlation with ALT/SGPT and hematocrit. In contrast, it was negatively correlated with CRP and sodium.
iv. WBC had a highly significant positive correlation with neutrophil, LDH, CRP, and INR.
v. A highly significant positive correlation was assessed between hematocrit and ALT/SGPT.
vi. INR had a highly significant positive correlation with neutrophils.
vii. CRP had a highly significant positive correlation with procalcitonin, neutrophil, and LDH, whereas it was negatively correlated with potassium.
viii. LDH had a highly positive correlation with neutrophils.
ix. The platelets had a negative correlation with sodium and total bilirubin.
Table 6 Principal component analysis of the laboratory parameters.
Chest CT Scan Findings
The patients who underwent chest CT scans were also assessed in this study, and the details are summarized in Table 7 and Figure 2. The mean age of these patients was 57 ± 12.6 years, including 76.7% male patients and 23.3% females. The mean percentage of lung involvement in male patients was 51.3 ± 15.8), and it was 54.3 ± 14.3 in female patients. Only 20% of the patients had age ≤50 years (38.3 ± 7.7), while a high number of patients (80%) had age of >50 years (62.4 ± 8.1). The most common findings were ground glass opacity (GGO; n = 28, 93.3%), mixed pattern of consolidation (n = 12, 40%), and interlobular septal thickening (n = 6, 20%). A small percentage of patients had GGO and opacities (n = 2, 6.7%), infiltration (n = 2, 6.7%), consolidation (n = 1, 3.3%) and cavitation (n = 1, 3.3%). Seventeen (57.7%) had five affected lobes, 8 (26.7%) had four affected lobes, 2 (6.7%) had three affected lobes, 2 (6.7%) had two affected lobes, and 1 (3.3%) had one affected lobe Figure 2.
Table 7 Findings of the CT scan of 30 COVID-19 patients.
Figure 2 CT scan digital images of (A) mild-to-moderate and (B) severe SARS-CoV-2-infected patients. The percentage of lung involvement can be spotted significantly in both types of patient.
Discussion
Demography
The number of male patients was high compared with that of female patients, presumably due to men’s increased vulnerability to COVID 19 due to various reasons (Gargaglioni and Marques, 2020; Pradhan and Olsson, 2020). It has been attributed that female patients showed more resistance to COVID-19 infection than men due to differences in sex hormones and a lower expression of receptors (ACE-2) (Bwire, 2020). Others have reported that men show high mortality from heart disease and diabetes, contributing to sex-based severity from COVID-19 (Pradhan and Olsson, 2020; Tian et al., 2020). The older-age peoples are at a high risk to catch SARS-CoV-2 due to their weak immune system and a high prevalence of comorbidities, and this susceptibility has also been concluded in different studies (Al Mutair et al., 2020; Mueller et al., 2020; Yegorov et al., 2021). A high number of COVID-19 patients in the study belonged to the extended family type, presumably due to crowded living conditions that favored the spread of disease. The same has been concluded in different studies (Noreen et al., 2020; Ramadhana, 2020).
The source of infection was unknown for 60% of the COVID-19 cases. It has been reported in other studies that the prevalence of asymptomatic carriers is difficult to determine and requires comprehensive screening. This would provide essential information on hidden viral strains circulating in the community, and the rate of such carriers would be different in high-density urban areas (Ahmed et al., 2020; Cloutier et al., 2020). Similarly, it has also been reviewed that the majority of asymptomatic patients appear to have a milder clinical course during hospitalization, but the severity of the symptoms in asymptomatic patients among all confirmed cases varies widely (from 1.95 to 87.9%), according to the study setting and the populations studied (Han et al., 2020). It was concluded that patients with a travel history from abroad (11%) were positive for COVID-19 on the health authorities’ investigation. Since Pakistan has a high frequency of travel and trade with China and Iran, it has been reported that the risk of viral transmission across borders increases (Noreen et al., 2020; Javed et al., 2021).
Furthermore, an inclination to withhold information regarding travel history to high-risk epidemic regions also results in unpredictable outcomes (Wei et al., 2020). The susceptibility of getting infected while coming into contact with confirmed COVID-19 patients (27%) may be attributed to person-to-person transmission, as reported in several similar studies (Cloutier et al., 2020; Lechien et al., 2020; Martinez-Fierro et al., 2021). It was concluded that the average number of days spent in the hospital was significantly high among severe patients compared with mild/moderate patients (10 vs. 5 days, p < 0.001).
Clinical Features
Symptoms of illness, such as fever (80%), shortness of breath (75%), and cough (57%), are most common in patients, predominantly due to the reason that the disease is reported to affect the lower respiratory system (Petersen et al., 2020). Presumably, due to similar reasons, the symptoms of shortness of breath, pneumonia, and abnormal chest X-ray were significantly highly occurring in severe patients. The results coincide with those of other studies wherein it has been reported that fever, cough, fatigue, and shortness of breath are common symptoms in severe COVID-19 patients (Al Mutair et al., 2020; Durrani et al., 2020). The association of the lower respiratory system in affecting the severity of COVID-19 patients has also been reported in different studies (Marinari et al., 2019; Brosnahan et al., 2020; Hannawi et al., 2021).
Other symptoms of COVID-19 patients, including myalgia and generalized body aches, vomiting, headaches, etc., were presumably associated with symptoms of fever, cough, and shortness of breath. Similar findings were reported in various studies from different regions (Sun et al., 2020b; Weng et al., 2021). An alternative diagnosis should also be considered to prevent weak opinions—mainly other infectious diseases like pneumonia of bacterial etiology, bacteremia, respiratory infections such as exacerbation of COPD, and cardiovascular disorders like acute heart failure. Systematic evaluation of heart function should be done in COVID-19 suspected patients (Castiello et al., 2022). Ruling out other differences with similar clinical features prevents extended hospital stay in isolation wards and shortage of beds required for critical COVID-19 patients, thereby reducing the burden on the healthcare system.
Comorbidities
There was a predominance of patients who had a long-standing history of hypertension (48.8% vs. 35.9%), type 2 diabetes (38.5 vs. 31.4%), and ischemic heart disease (16.9 vs. 12.5%). In severe COVID-19 patients, these may be linked to multiple factors, among them as the significant ones were the aged patients, reduced systemic oxygenation intake due to pneumonia, concomitantly increased cardiac demand, and use of ACE inhibitors (Ejaz et al., 2020). The high percentage of hypertension and COPD in severe patients may also be linked to similar reasons, along with underlying poor lung reserves or the increased expression of ACE-2 receptors in small airways (Leung et al., 2020; Perrotta et al., 2020; Gómez Antúnez et al., 2021). Many studies found a high risk of infection in the cardiovascular, pulmonary, and renal patients (De Almeida-Pititto et al., 2020; Leung et al., 2020). Most importantly, studies revealed that the high mortality ratios in COVD-19 patients were associated with the cardiovascular and renal complications of diabetes and independently with glycemic control and body mass index (Holman et al., 2020; Richardson et al., 2020; Dyusupova et al., 2021).
Laboratory Parameters
Complete blood count, coagulation profile, biochemical parameters, and inflammatory mediators predict the disease severity and outcomes (Angioni et al., 2020; Zeng et al., 2020). Values of WBC, platelets, neutrophil, total bilirubin, CRP, and ferritin were significantly high in severe patients compared with those in mild/moderate cases. The study signifies the usefulness of biomarkers in assessing the severity of COVID-19 infection in patients, which may help to improve the treatment of the disease. The results of this study are in line with contrasting findings in similar studies (Yang et al., 2020; Hannawi et al., 2021; Yegorov et al., 2021). The increase of CRP and ferritin in critically ill COVID-19 patients has been measured in various findings (Al Mutair et al., 2020; Wang et al., 2020; Hannawi et al., 2021). The same tendency was observed for WBC, platelets, neutrophils, and bilirubin (Yin et al., 2020; Taj et al., 2021; Yegorov et al., 2021). A significantly positive correlation was observed between the ferritin and laboratory parameters, including Hb, WBC, ALT/SGP, total bilirubin, CRP, and LDH, while these were negatively correlated with lymphocytes. Low D-dimer, serum creatinine, and LDH were observed in severe patients compared with mild-to-moderate patients. This may be because the regular administration of anticoagulant drugs for treatment in severe patients decreased the levels of D-dimers in them presumably (Mouhat et al., 2020). Similar results were obtained in studies conducted to assess on-protocol COVID-19 patients (Kamel et al., 2021; Tassiopoulos et al., 2021). Apparently, due to similar reasons, the D-dimer had a highly significant positive correlation with WBC, INR, procalcitonin, and LDH. A retrospective study by Taj et al. (2021) on confirmed COVID-19 patients concluded that leukocytosis, neutrophilia, elevated neutrophil-to-lymphocyte ratio, activated partial thromboplastin time, D-dimer, lactate dehydrogenase, serum ferritin, and CRP are associated with the severity of the disease.
Procalcitonin (PCT) is a food and drug administration (FDA)-approved diagnostic marker for different diseases. As per FDA executive summary (Gaithersburg, 2016), the normal range of PCT is <0.05 to <0.1 ng/ml. Therefore, any elevation of PCT beyond <0.1 ng/ml as shown in the current study (mild/moderate = 0.21 ng/ml, severe/critical = 2.79 ng/ml, and normal range = 0.1 ng/ml) should be taken as clinically significant because it is linked with disease severity.
Medications Used in the Treatment
A significantly high percentage of severe patients were treated with steroid (dexamethasone), antiviral (remdesivir), antibiotic (meropenem), anticoagulant (heparin), and immunosuppressive (tocilizumab) compared with mild/moderate patients. Dexamethasone helps control the inflammation of the lower respiratory tract with its immunosuppressive role (Selvaraj et al., 2020). Similarly, the use of remdesivir had provided evidence of lowering the respiratory tract infection (Beigel et al., 2020). The controlled use of antibiotics is reported to have safely and effectively treated most bacterial cases of pneumonia. Antibiotics have played an effective role in treating superimposed bacterial infections, such as bacterial cases of pneumonia in COVID-19 patient settings (Beovic et al., 2020; Ginsburg and Klugman, 2020). Activation of the coagulation cascade leading to severe hypercoagulability has been detected in COVID-19 patients (Kichloo et al., 2020). Therefore, it has been recommended that early anticoagulation may reduce coagulopathy, micro-thrombus formation, and the risk of organ damages (Becker, 2020; Gozzo et al., 2020; Richardson et al., 2020). It has been reported that treatment with tocilizumab, whether administered intravenously or subcutaneously, might reduce the risk of invasive mechanical ventilation or death in patients with severe COVID-19 pneumonia (Guaraldi et al., 2020).
Radiological Findings
Chest X-ray
Chest X-ray is a valuable tool in assessing disease progression and severity (Borghesi and Maroldi, 2020). In COVID-19 patients, it may be normal initially but may later follow a characteristic pattern of progression from the bilateral lower predominant zones to the upper zones, vertically extending peripheral to diffuse in critical ICU patients, thus showing a picture of ARDS (Durrani et al., 2020). It has been concluded that, in the initial chest X-ray on admission, the involvement of >4 zones has been linked to increased severity and an unfavorable outcome.
Chest CT Scan
Non-enhanced chest CT is a vital component in the diagnosis of patients suspected of a COVID-19 infection (Korevaar et al., 2020; Pruis et al., 2020). The pattern of GGO, GGO, and consolidation and interlobular septal thickening was the most prominent finding among the infected patients of different age groups, gender, and severity. The pattern of the findings is somewhat similar to that described in related studies on severe acute respiratory syndrome (Bernheim et al., 2020; Pan et al., 2020; Wu et al., 2020). In critical patients, a honey-combing pattern, traction bronchiectasis, and interlobar pleural traction can be observed. A follow-up CT after 6 months may show fibrotic changes in such patients (Ginsburg and Klugman, 2020; Han et al., 2021). A combination RT-PCR analysis and chest CT scan increases the sensitivity and specificity of COVID-19 diagnosis to 88 and 100%, respectively (He et al., 2020b). The semi-quantitative CT Severity Score System helps in showing the extent of pulmonary involvement. These are as follows:
0 score = no involvement
1 score = <5% involvement
2 score = 5–25% involvement
3 score = 26–49% involvement
4 score = 50–75% involvement
5 score = >75% involvement
The total CT severity score is calculated by summing up the individual lobe score, with the cumulative score ranging from 0 to 25. A CT score >18 has been correlated with increased severity, mortality, and worse prognosis (Saeed et al., 2021). In another study, it has been reported that a CT score >7 has been linked to increased chances of developing the post-COVID syndrome (Ali and Ghonimy, 2021).
Conclusion
Older patients, predominantly male, were more in number in both groups with comorbidities, mainly hypertension, type 2 diabetes, and ischemic heart. The preventive measures against COVID-19 must be followed, and surveillance for asymptomatic carriers should be increased. The excessive use of antibacterial, antiviral, anticoagulant, and drugs for pain management was noted. Early detection based on laboratory-based biomarkers may prevent the severity of the illness.
Data Availability Statement
The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.
Ethics Statement
This project was conducted under approval number UHS/REG-20/ERC/1758 from the University of Health Sciences Lahore Ethical Review Committee. The patients/participants provided their written informed consent to participate in this study.
Author Contributions
All authors contributed to the article and approved the submitted version.
Funding
This study is part of the Rapid COVID Project (RRG# 211) funded by the Higher Education Commission and the World Bank. The funder was not involved in the study design, collection, analysis, and interpretation of data, the writing of this article or the decision to submit it for publication.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s Note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Acknowledgments
The authors duly acknowledge the hospital administration for their support as well as the patients and their families who participated in this study.
Supplementary Material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fcimb.2022.800511/full#supplementary-material
References
Ahmed, M. A. M., Colebunders, R., Siewe Fodjo, J. N. (2020). Evidence for Significant COVID-19 Community Transmission in Somalia Using a Clinical Case Definition. Int. J. Infect. Dis. 98, 206–207. doi: 10.1016/j.ijid.2020.06.068
Ali, R. M. M., Ghonimy, M. B. I. (2021). Post-COVID-19 Pneumonia Lung Fibrosis: A Worrisome Sequelae in Surviving Patients. Egypt J. Radiol. Nucl. Med. 52, 101. doi: 10.1186/s43055-021-00484-3
Al Mutair, A., Alhumaid, S., Alhuqbani, W. N., Zaidi, A. R. Z., Alkoraisi, S., Al-Subaie, M. F., et al. (2020). Clinical, Epidemiological, and Laboratory Characteristics of Mild-to-Moderate COVID-19 Patients in Saudi Arabia: An Observational Cohort Study. Eur. J. Med. Res. 25, 1–8. doi: 10.1186/s40001-020-00462-x
Angioni, R., Sánchez-Rodríguez, R., Munari, F., Bertoldi, N., Arcidiacono, D., Cavinato, S., et al. (2020). Age-Severity Matched Cytokine Profiling Reveals Specific Signatures in Covid-19 Patients. Cell Death Dis. 11, 957. doi: 10.1038/s41419-020-03151-z
Becker, R. C. (2020). COVID-19 Update: Covid-19-Associated Coagulopathy. J. Thromb. Thrombolysis 50, 54–67. doi: 10.1007/s11239-020-02134-3
Beigel, J. H., Tomashek, K. M., Dodd, L. E., Mehta, A. K., Zingman, B. S., Kalil, A. C., et al. (2020). Remdesivir for the Treatment of Covid-19 — Final Report. New Engl. J. Med. 383, 1813–1826. doi: 10.1056/nejmoa2007764
Beovic, B., Dousak, M., Ferreira-Coimbra, J., Nadrah, K., Rubulotta, F., Belliato, M., et al. (2020). Antibiotic Use in Patients With COVID-19: A “Snapshot” Infectious Diseases International Research Initiative (ID-IRI) Survey. J. Antimicrobial Chemotherapy 75, 3386–3390. doi: 10.1093/jac/dkaa326
Bernheim, A., Mei, X., Huang, M., Yang, Y., Fayad, Z. A., Zhang, N., et al. (2020). Chest CT Findings in Coronavirus Disease-19 (COVID-19): Relationship to Duration of Infection. Radiology 295, 200463. doi: 10.1148/radiol.2020200463
Bi, Q., Yongsheng, W., Shujiang, M., Ye, C., Zou, X., Zhang, Z., et al. (2020) "Epidemiology and Transmission of COVID-19 in 391 Cases and 1286 of their Close Contacts in Shenzhen, China: A Retrospective Cohort Study." Lancet Infect. Dis. 8, 911-919. doi: 10.1016/S1473-3099(20)30287-5
Borghesi, A., Maroldi, R. (2020). COVID-19 Outbreak in Italy: Experimental Chest X-Ray Scoring System for Quantifying and Monitoring Disease Progression. Radiol. Med. 125, 509–513. doi: 10.1007/s11547-020-01200-3
Brosnahan, S. B., Jonkman, A. H., Kugler, M. C., Munger, J. S., Kaufman, D. A. (2020). Covid-19 and Respiratory System Disorders Current Knowledge, Future Clinical and Translational Research Questions. Arteriosclerosis Thrombosis Vasc. Biol. 40, 2586–2597. doi: 10.1161/ATVBAHA.120.314515
Bwire, G. M. (2020). Coronavirus: Why Men are More Vulnerable to Covid-19 Than Women? SN Compr. Clin. Med. 2, 874–876. doi: 10.1007/s42399-020-00341-w
Castiello, T., Georgiopoulos, G., Finocchiaro, G., Claudia, M., Gianatti, A., Delialis, D., et al. (2022). COVID-19 and Myocarditis: A Systematic Review and Overview of Current Challenges. Heart Fail Rev. 27, 251–261. doi: 10.1007/s10741-021-10087-9
Cloutier, L., Merindol, N., Pépin, G., Marcoux-Huard, C., Vasil, P. A., Houle, C., et al. (2020). Asymptomatic Carriers of COVID-19 in a Confined Adult Community Population in Quebec: A Cross-Sectional Study. Am. J. Infection Control 49, 2020–2022. doi: 10.1016/j.ajic.2020.08.015
De Almeida-Pititto, B., Dualib, P. M., Zajdenverg, L., Dantas, J. R., De Souza, F. D., Rodacki, M., et al. (2020). Severity and Mortality of COVID 19 in Patients With Diabetes, Hypertension and Cardiovascular Disease: A Meta-Analysis. Diabetol. Metab. Syndrome 12, 1–12. doi: 10.1186/s13098-020-00586-4
Durrani, M., Haq, I. U., Kalsoom, U., Yousaf, A. (2020). Chest X-Rays Findings in Covid 19 Patients at a University Teaching Hospital-A Descriptive Study. Pakistan J. Med. Sci. 36, S22–S26. doi: 10.12669/pjms.36.COVID19-S4.2778
Dyusupova, A., Faizova, R., Yurkovskaya, O., Belyaeva, T., Terekhova, T., Khismetova, A., et al. (2021). Clinical Characteristics and Risk Factors for Disease Severity and Mortality of COVID-19 Patients With Diabetes Mellitus in Kazakhstan: A Nationwide Study. Heliyon 7, e06561. doi: 10.1016/j.heliyon.2021.e06561
Ejaz, H., Alsrhani, A., Zafar, A., Javed, H., Junaid, K., Abdalla, A. E., et al. (2020). COVID-19 and Comorbidities: Deleterious Impact on Infected Patients. J. Infect. Public Health 13, 1833–1839. doi: 10.1016/j.jiph.2020.07.014
Gaithersburg, M. (2016). “Discussion and Recommendations for the Application of Procalcitonin to the Evaluation and Management of Suspected Lower Respiratory Tract Infections and Sepsis,” in FDA Executive Summary. (Maryland) 1–49.
Gao, J., Tian, Z., Yang, X. (2020). Breakthrough: Chloroquine Phosphate has Shown Apparent Efficacy in Treatment of COVID-19 Associated Pneumonia in Clinical Studies. Biosci. Trends 14, 72–73. doi: 10.5582/bst.2020.01047
Gargaglioni, L. H., Marques, D. A. (2020). Let’s Talk About Sex in the Context of COVID-19. J. Appl. Physiol. 128, 1533–1538. doi: 10.1152/japplphysiol.00335.2020
Ginsburg, A. S., Klugman, K. P. (2020). COVID-19 Pneumonia and the Appropriate Use of Antibiotics. Lancet Glob. Health 8, e1453–e1454. doi: 10.1016/S2214-109X(20)30444-7
Gómez Antúnez, M., Muiño Míguez, A., Bendala Estrada, A. D., Maestro de la Calle, G., Monge Monge, D., Boixeda, R., et al. (2021). Clinical Characteristics and Prognosis of COPD Patients Hospitalized With SARS-CoV-2. COPD 15, 3433–3445. doi: 10.2147/COPD.S276692
GOP. (2021). Pakistan Cases Details. (Punjab, Pakistan: Bureau of Statistics) Available at: https://covid.gov.pk/stats/pakistan (Accessed May 30, 2021).
Gozzo, L., Viale, P., Longo, L., Vitale, D. C., Drago, F. (2020). The Potential Role of Heparin in Patients With COVID-19: Beyond the Anticoagulant Effect. A Review. Front. Pharmacol. 11. doi: 10.3389/fphar.2020.01307
Grant, M. C., Geoghegan, L., Arbyn, M., Mohammed, Z., McGuinness, L., Clarke, E. L., et al. (2020). The Prevalence of Symptoms in 24,410 Adults Infected by the Novel Coronavirus (SARS-CoV-2; COVID-19): A Systematic Review and Meta-Analysis of 148 Studies From 9 Countries. PloS One 15(6), e0234765. doi: 10.1371/journal.pone.0234765
Guaraldi, G., Meschiari, M., Cozzi-Lepri, A., Milic, J., Tonelli, R., Menozzi, M., et al. (2020). Tocilizumab in Patients With Severe COVID-19: A Retrospective Cohort Study. Lancet Rheumatol. 2, e474–e484. doi: 10.1016/S2665-9913(20)30173-9
Gu, J., Korteweg, C. (2007). Pathology and Pathogenesis of Severe Acute Respiratory Syndrome. Am. J. Pathol. 170, 1136–1147. doi: 10.2353/ajpath.2007.061088
Han, X., Fan, Y., Alwalid, O., Li, N., Jia, X., Yuan, M., et al. (2021). Six-Month Follow-Up Chest CT Findings After Severe COVID-19 Pneumonia. Radiology 299, E177–E186. doi: 10.1148/radiol.2021203153
Han, D., Li, R., Han, Y., Zhang, R., Li, J. (2020). Covid-19: Insight Into the Asymptomatic Sars-Cov-2 Infection and Transmission. Int. J. Biol. Sci. 16, 2803–2811. doi: 10.7150/ijbs.48991
Hannawi, S., Hannawi, H., Naeem, K., Elemam, N. M., Hachim, M. Y., Hachim, I. Y., et al. (2021). Clinical and Laboratory Profile of Hospitalized Symptomatic COVID-19 Patients: Case Series Study From the First COVID-19 Center in the UAE. Front. Cell. Infection Microbiol. 11. doi: 10.3389/fcimb.2021.632965
He, J., Guo, Y., Mao, R., Zhang, J. (2021). Proportion of Asymptomatic Coronavirus Disease 2019: A Systematic Review and Meta-Analysis. J. Med. Virol. 93, 820–830. doi: 10.1002/jmv.26326
He, J.-L., Luo, L., Luo, Z.-D., Lyu, J.-X., Ng, M.-Y., Shen, X.-P., et al. (2020b). Diagnostic Performance Between CT and Initial Real-Time RT-PCR for Clinically Suspected 2019 Coronavirus Disease (COVID-19) Patients Outside Wuhan, China. Respir. Med. 168, 105980. doi: 10.1016/j.rmed.2020.105980
He, D., Zhao, S., Lin, Q., Zhuang, Z., Cao, P., Wang, M. H., et al. (2020a). The Relative Transmissibility of Asymptomatic COVID-19 Infections Among Close Contacts. Int. J. Infect. Dis. 94, 145–147. doi: 10.1016/j.ijid.2020.04.034
Holman, N., Knighton, P., Kar, P., O’Keefe, J., Curley, M., Weaver, A., et al. (2020). Risk Factors for COVID-19-Related Mortality in People With Type 1 and Type 2 Diabetes in England: A Population-Based Cohort Study. Lancet Diabetes Endocrinol. 8, 823–833. doi: 10.1016/S2213-8587(20)30271-0
Javed, A., Niazi, S. K., Ghani, E., Yamin, M., Saqib, M., Janjua, H. A., et al. (2021). Coding-Complete Genome Sequence of a SARS-CoV-2 Strain Isolated in Gilgit, Pakistan. Microbiol. Resour Announc 10(13), e01151–20. doi: 10.1128/MRA.01151-20
Kamel, F. O., Magadmi, R. M., Alqutub, S. T., Badawi, M., Al-Sayes, F., Badawi, M., et al. (2021). Clinical and Hematologic Presentations of Adults With COVID-19 Patients in Jeddah: A Case Control Study. J. Infect. Public Health 14 (6), 709–716. doi: 10.1016/j.jiph.2021.03.007
Khalid, A., Ali, S. (2020). COVID-19 and Its Challenges for the Healthcare System in Pakistan. ABR 12, 551–564. doi: 10.1007/s41649-020-00139-x
Kichloo, A., Dettloff, K., Aljadah, M., Albosta, M., Jamal, S., Singh, J., et al. (2020). COVID-19 and Hypercoagulability: A Review. Clin. Appl. Thromb. Hemost 26, 107602962096285. doi: 10.1177/1076029620962853
Kirchberger, I., Berghaus, T. M., von Scheidt, W., Linseisen, J., Meisinger, C. (2021). COVID-19 Risk Perceptions, Worries and Preventive Behaviors in Patients With Previous Pulmonary Embolism. Thromb. Res. 202, 77–83. doi: 10.1016/j.thromres.2021.03.016
Korevaar, D. A., Kootte, R. S., Smits, L. P., van den Aardweg, J. G., Bonta, P. I., Schinkel, J., et al. (2020). Added Value of Chest Computed Tomography in Suspected COVID-19: An Analysis of 239 Patients. Eur. Respir. J. 56, 2001377. doi: 10.1183/13993003.01377-2020
Lechien, J. R., Chiesa-Estomba, C. M., Place, S., Van Laethem, Y., Cabaraux, P., Mat, Q., et al. (2020). Clinical and Epidemiological Characteristics of 1420 European Patients With Mild-to-Moderate Coronavirus Disease 2019. J. Internal Med. 288, 335–344. doi: 10.1111/joim.13089
Leung, J. M., Niikura, M., Yang, C. W. T., Sin, D. D. (2020). COVID-19 and COPD. Eur. Respir. J. 56, 1–9. doi: 10.1183/13993003.02108-2020
Lu, H., Stratton, C. W., Tang, Y. (2020). Outbreak of Pneumonia of Unknown Etiology in Wuhan, China: The Mystery and the Miracle. J. Med. Virol. 92, 401–402. doi: 10.1002/jmv.25678
Lvov, D. K., Alkhovsky, S. V. (2020). Source of the COVID-19 Pandemic: Ecology and Genetics of Coronaviruses (Betacoronavirus: Coronaviridae) SARS-CoV, SARS-CoV-2 (Subgenus Sarbecovirus), and MERS-CoV (Subgenus Merbecovirus). Vopr. Virusol. 65, 62–70. doi: 10.36233/0507-4088-2020-65-2-62-70
Marinari, L. A., Danny, M. A., Miller, W. T. (2019). Sporadic Coronavirus Lower Respiratory Tract Infection in Adults: Chest CT Imaging Features and Comparison With Other Viruses. Eur. Respir. J. 54, PA4547. doi: 10.1183/13993003.congress-2019.PA4547
Martinez-Fierro, M. L., Ríos-Jasso, J., Garza-Veloz, I., Reyes-Veyna, L., Cerda-Luna, R. M., Duque-Jara, I., et al. (2021). The Role of Close Contacts of COVID-19 Patients in the SARS-CoV-2 Transmission: An Emphasis on the Percentage of Nonevaluated Positivity in Mexico. Am. J. Infection Control 49, 15–20. doi: 10.1016/j.ajic.2020.10.002
Mehta, O. P., Bhandari, P., Raut, A., Kacimi, S. E. O., Huy, N. T. (2021). Coronavirus Disease (COVID-19): Comprehensive Review of Clinical Presentation. Front. Public Health 8. doi: 10.3389/fpubh.2020.582932
Mouhat, B., Besutti, M., Bouiller, K., Grillet, F., Monnin, C., Ecarnot, F., et al. (2020). Elevated D-Dimers and Lack of Anticoagulation Predict PE in Severe COVID-19 Patients. Eur. Respir. J. 56, 2001811. doi: 10.1183/13993003.01811-2020
Mueller, A. L., McNamara, M. S., Sinclair, D. A. (2020). Why Does COVID-19 Disproportionately Affect Older People? Aging 12, 9959–9981. doi: 10.18632/aging.103344
Mueller, A. L., McNamara, M. S., Sinclair, D. A. (2020). Why Does COVID-19 Disproportionately Affect Older People? Aging (Albany NY) 12, 9959–9981. doi: 10.18632/aging.103344
Mushtaq, A., Ikram, A., Chaudhry, A., Sandhu, M., Khalid, F., Hussain, S., et al. (2020). Evaluation of the COVID-19 Laboratory-Based Surveillance System in Islamabad-Pakistan 2020. Global Biosecur. 2(1). doi: 10.31646/gbio.73
Nawaz, A., Su, X., Barkat, M. Q., Asghar, S., Asad, A., Basit, F., et al. (2020). Epidemic Spread and Its Management Through Governance and Leadership Response Influencing the Arising Challenges Around COVID-19 in Pakistan—A Lesson Learnt for Low Income Countries With Limited Resource. Front. Public Health 8. doi: 10.3389/fpubh.2020.573431
NCOC (2021a). National Command and Operation Center, Goverment of Islamic Republic Pakistan Islamabad.
NCOC (2021b). Standard Operating Procedures (SOPs)/Guidelines (National Command and Operation Center) Islamic Republic of Pakistan Islamabad. Available at: https://ncoc.gov.pk/sop.php.
NCOC (2022). Pakistan Cases Details (National Command and Operation Center). Available at: https://covid.gov.pk/stats/pakistan.
Niazkar, H. R., Zibaee, B., Nasimi, A., Bahri, N. (2020). The Neurological Manifestations of COVID-19: A Review Article. Neurol. Sci. 41, 1667–1671. doi: 10.1007/s10072-020-04486-3
Noreen, N., Dil, S., Ullah, S., Niazi, K., Naveed, I., Khan, N. U., et al. (2020). (COVID-19) Pandemic and Pakistan; Limitations and Gaps. Limitations Gaps. Global Biosecur. 2(1). doi: 10.31646/gbio.63
Oberemok, V. V., Laikova, K. V., Yurchenko, K. A., Fomochkina, I. I., Kubyshkin, A. V. (2020). SARS-CoV-2 Will Continue to Circulate in the Human Population: An Opinion From the Point of View of the Virus-Host Relationship. Inflamm. Res. 69, 635–640. doi: 10.1007/s00011-020-01352-y
Pan, Y., Guan, H., Zhou, S., Wang, Y., Li, Q., Zhu, T., et al. (2020). Initial CT Findings and Temporal Changes in Patients With the Novel Coronavirus Pneumoni-Ncov): A Study of 63 Patients in Wuhan, China. Eur. Radiol. 30, 3306–3309. doi: 10.1007/s00330-020-06731-x
Perrotta, F., Matera, M. G., Cazzola, M., Bianco, A. (2020). Severe Respiratory SARS-CoV2 Infection: Does ACE2 Receptor Matter? Respir. Med. 168, 105996. doi: 10.1016/j.rmed.2020.105996
Petersen, E., Koopmans, M., Go, U., Hamer, D. H., Petrosillo, N., Castelli, F., et al. (2020). Comparing SARS-CoV-2 With SARS-CoV and Influenza Pandemics. Lancet Infect. Dis. 20, e238–e244. doi: 10.1016/S1473-3099(20)30484-9
Pradhan, A., Olsson, P. E. (2020). Sex Differences in Severity and Mortality From COVID-19: Are Males More Vulnerable? Biol. Sex Dif. 11, 1–11. doi: 10.1186/s13293-020-00330-7
Pruis, M. A., Hussain, B., Bakker, M., Hoek, R. A. S., Miedema, J. R., Dingemans, A.-M. C., et al. (2020). A Lung Cancer Patient With Dyspnea: Diagnostic Difficulties During the COVID-19 Pandemic. Cancer Cell 38, 611–612. doi: 10.1016/j.ccell.2020.10.005
Ramadhana, M. R. (2020). A Dataset for Emotional Reactions and Family Resilience During COVID-19 Isolation Period Among Indonesian Families. Data Brief 31, 105946. doi: 10.1016/j.dib.2020.105946
Richardson, S., Hirsch, J. S., Narasimhan, M., Crawford, J. M., McGinn, T., Davidson, K. W., et al. (2020). Presenting Characteristics, Comorbidities, and Outcomes Among 5700 Patients Hospitalized With COVID-19 in the New York City Area. JAMA - J. Am. Med. Assoc. 323, 2052–2059. doi: 10.1001/jama.2020.6775
Saeed, G. A., Gaba, W., Shah, A., Al Helali, A. A., Raidullah, E., Al Ali, A. B., et al. (2021). Correlation Between Chest CT Severity Scores and the Clinical Parameters of Adult Patients With COVID-19 Pneumonia. Radiol. Res. Pract. 2021, 1–7. doi: 10.1155/2021/6697677
Selvaraj, V., Dapaah-Afriyie, K., Finn, A., Flanigan, T. P. (2020). Short-Term Dexamethasone in Sars-CoV-2 Patients. Rhode Island Med. J. (2013) 103, 39–43.
Sun, J., He, W.-T., Wang, L., Lai, A., Ji, X., Zhai, X., et al. (2020a). COVID-19: Epidemiology, Evolution, and Cross-Disciplinary Perspectives. Trends Mol. Med. 26, 483–495. doi: 10.1016/j.molmed.2020.02.008
Sun, P., Qie, S., Liu, Z., Ren, J., Li, K., Xi, J. (2020b). Clinical Characteristics of Hospitalized Patients With SARS-CoV-2 Infection: A Single Arm Meta-Analysis. J. Med. Virol. 92, 612–617. doi: 10.1002/jmv.25735
Taj, S., Kashif, A., Arzinda Fatima, S., Imran, S., Lone, A., Ahmed, Q. (2021). Role of Hematological Parameters in the Stratification of COVID-19 Disease Severity. Ann. Med. Surg 62:68–72. doi: 10.1016/j.amsu.2020.12.035
Tassiopoulos, A. K., Mofakham, S., Rubano, J. A., Labropoulos, N., Bannazadeh, M., Drakos, P., et al. (2021). D-Dimer-Driven Anticoagulation Reduces Mortality in Intubated COVID-19 Patients: A Cohort Study With a Propensity-Matched Analysis. Front. Med. 8. doi: 10.3389/fmed.2021.631335
Tian, J., Yuan, X., Xiao, J., Zhong, Q., Yang, C., Liu, B., et al. (2020). Clinical Characteristics and Risk Factors Associated With COVID-19 Disease Severity in Patients With Cancer in Wuhan, China: A Multicentre, Retrospective, Cohort Study. Lancet Oncol. 21, 893–903. doi: 10.1016/S1470-2045(20)30309-0
Vohora, D., Jain, S., Tripathi, M., Potschka, H. (2020). COVID-19 and Seizures: Is There a Link? Epilepsia 61, 1840–1853. doi: 10.1111/epi.16656
Wang, G., Wu, C., Zhang, Q., Wu, F., Yu, B., Lv, J., et al. (2020). C-Reactive Protein Level may Predict the Risk of COVID-19 Aggravation. Open Forum Infect. Dis. 7, 1–5. doi: 10.1093/ofid/ofaa153
Wei, L., Sha, Z., Wang, Y., Zhang, G., Jia, H., Zhou, S., et al. (2020). Willingness and Beliefs Associated With Reporting Travel History to High-Risk Coronavirus Disease 2019 Epidemic Regions Among the Chinese Public: A Cross-Sectional Study. BMC Public Health 20, 1–9. doi: 10.1186/s12889-020-09282-4
Weng, L. M., Su, X., Wang, X. Q. (2021). Pain Symptoms in Patients With Coronavirus Disease (COVID-19): A Literature Review. J. Pain Res. 14, 147–159. doi: 10.2147/JPR.S269206
WHO. (2020). Naming the Coronavirus Disease (COVID-19) and the Virus That Causes itWorld Health Organization. Available at: https://www.who.int/emergencies/diseases/novel-coronavirus-2019/technical-guidance/naming-the-coronavirus-disease-(covid-2019)-and-the-virus-that-causes-it.
WHO. (2021). WHO Coronavirus (COVID-19) Dashboard (World Health Organization). Available at: https://covid19.who.int/.
WHO. (2022). WHO Coronavirus (COVID-19) Dashboard (World Health Organization). Available at: https://covid19.who.int/.
Wu, J., Wu, X., Zeng, W., Guo, D., Fang, Z., Chen, L., et al. (2020). Chest CT Findings in Patients With Coronavirus Disease 2019 and Its Relationship With Clinical Features. Invest. Radiol. 55, 257–261. doi: 10.1097/RLI.0000000000000670
Yang, L., Liu, J., Zhang, R., Li, M., Li, Z., Zhou, X., et al. (2020). Epidemiological and Clinical Features of 200 Hospitalized Patients With Corona Virus Disease 2019 Outside Wuhan, China: A Descriptive Study. J. Clin. Virol. 129, 104475. doi: 10.1016/j.jcv.2020.104475
Yegorov, S., Goremykina, M., Ivanova, R., Good, S. V., Babenko, D., Shevtsov, A., et al. (2021). Epidemiology, Clinical Characteristics, and Virologic Features of COVID-19 Patients in Kazakhstan: A Nation-Wide Retrospective Cohort Study. Lancet Regional Health - Europe 4, 100096. doi: 10.1016/j.lanepe.2021.100096
Yin, S., Huang, M., Li, D., Tang, N. (2021). Difference of Coagulation Features Between Severe Pneumonia Induced by SARS-CoV2 and non-SARS-Cov2. J. Thromb. Thrombolysis 51 (4), 1107–10. doi: 10.1007/s11239-020-02105-8
Zeng, Z., Yu, H., Chen, H., Qi, W., Chen, L., Chen, G., et al. (2020). Longitudinal Changes of Inflammatory Parameters and Their Correlation With Disease Severity and Outcomes in Patients With COVID-19 From Wuhan, China. Crit. Care 24, 525. doi: 10.1186/s13054-020-03255-0
Keywords: SARS-CoV-2, COVID-19, Acute Respiratory Distress Syndrome (ARDS), clinic-pathological characteristics, comorbidities, medication, ICU vs. non-ICU, Lungs-CT-scan
Citation: Omer S, Gondal MF, Usman M, Sarwar MB, Roman M, Khan A, Afzal N, Qaiser TA, Yasir M, Shahzad F, Tahir R, Ayub S, Akram J, Faizan RM, Naveed MA and Jahan S (2022) Epidemiology, Clinico-Pathological Characteristics, and Comorbidities of SARS-CoV-2-Infected Pakistani Patients. Front. Cell. Infect. Microbiol. 12:800511. doi: 10.3389/fcimb.2022.800511
Received: 23 October 2021; Accepted: 15 April 2022;
Published: 26 May 2022.
Edited by:
Nahed Ismail, University of Illinois at Chicago, United StatesReviewed by:
Firzan Nainu, Hasanuddin University, IndonesiaCarlo Contini, University of Ferrara, Italy
Copyright © 2022 Omer, Gondal, Usman, Sarwar, Roman, Khan, Afzal, Qaiser, Yasir, Shahzad, Tahir, Ayub, Akram, Faizan, Naveed and Jahan. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Shah Jahan, shahjahan@uhs.edu.pk
†These authors have contributed equally to this work