Browsing by Author "Sibia, RPS"

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    Comparative Analysis of Efficacy and Safety of Gabapentin Vs Amitriptyline in Patients of Peripheral Neuropathic Pain in Case of Diabetes Mellitus
    (Dr. J.S. Sodhi Memorial Educational Society, 2019-07) Kaur, R; Sehgal, VK; Sibia, RPS; Kaur, A; Kumar, A
    Introduction: Diabetes mellitus frequently leads to development of peripheral neuropathies in almost 30-50% of patients and the most common type of neuropathy associated with this condition is Distal Symmetric Sensorimotor Polyneuropathy (DSPN). Gabapentin and Amitriptyline are two drugs frequently used for the treatment of neuropathic pain associated with type 2 diabetes. Aim of the study: The aim of this study was to compare efficacy and safety of Gabapentin and Amitriptyline in subjects of Type 2 diabetes mellitus with peripheral neuropathic pain. Material and Methods: A prospective, open, randomized, parallel group, comparative study was conducted in 60 patients coming to Department of Medicine, Rajindra Hospital attached to Government Medical College Patiala, to evaluate the efficacy and safety of Gabapentin and Amitriptyline in patients with diabetic peripheral neuropathic pain. The patients fulfilling the inclusion criteria were included in the study after taking written informed consent. The patients were divided into two groups of 30 cases each by simple randomization. Group I patients received Gabapentin 300 mg HS by oral route. Group II patients received Amitriptyline 25 mg HS by oral route. Therapeutic efficacy of both drugs, by using Michigan Neuropathy Screening Instrument (MNSI) was compared at the baseline and at the end of 4 months. Any adverse drug reactions of the respective drug observed in patient were also noted. All the observations thus made were statistically analysed using appropriate tests. Results: Baseline characteristics of the patients in two groups such as age, sex, duration of diabetes were similar (p>0.05). The mean age in group I and group II were 53.40±8.41 years and 57.17±8.55 years, respectively. There was statistically significant reduction in mean MNSI scores in questionnaire part and physical examination part in both the groups. Also, there was statistically significant difference between the two drugs in reducing mean MNSI score. Mean difference between two drugs in reducing MNSI score in history part (0.77±0.16, p<0.01) and physical examination part (0.75±0.19, p<0.01) favoured Gabapentin. No. of adverse drug reactions reported were significantly higher in Amitriptyline group, p value (<0.05) for the difference in ADRs between two drugs was statistically significant. Conclusion: In this study, we concluded that both drugs lead to improvement in signs and symptoms of diabetic neuropathy. Gabapentin was proved to be more efficacious than Amitriptyline. Gabapentin treated patient’s mean MNSI score at the study end point was significantly lower as compared to the Amitriptyline treated patient’s end-point score. Adverse drug reactions reported in our study were mild in both the groups and a significantly higher number of adverse effects were reported in the amitriptyline group. Dizziness and somnolence were two most commonly reported adverse drug reactions.
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    Hydroxychloroquine in Treatment of Asymptomatic and Mildly Symptomatic COVID-19: A Multi-Centre Cohort Study
    (Association of Physicians of India, 2022-01) Jain, Siddharth; Sharma, Shefali K; Suri, Vikas; Yaddanapudi, Narayana; Malhotra, Pankaj; Bhalla, Ashish; Singh, Mini P; Koushal, Vipin; Kajal, Kamal; Jakulla, Roopesh Sai; Marrapu, Sudheer; Guru, Rashmi Ranjan; Bora, Ishani; Chopra, Vishal; Sibia, RPS; Puri, Goverdhan Dutt
    Background: Although hydroxychloroquine (HCQ) lacks benefit in patients with moderate-to-severe COVID-19, its role in asymptomatic and mildly symptomatic disease needs better elucidation. Methods: This multi-centre cohort study included asymptomatic and mildly symptomatic, RT-PCR confirmed COVID-19 cases between 30 March and 20 May, 2020. Patients were categorized into two groups (HCQ-treated and untreated) based on exposure to HCQ. Dose of HCQ used was 400 mg twice daily (day one) followed by once daily for seven days. HCQ-untreated patients were managed supportively without any active antiviral or immunomodulatory therapy.h Nasopharyngeal SARS-CoV-2 clearance by RT-PCR (primary outcome) was compared between HCQ-treated and untreated patients using Kaplan-Meier analysis and Cox proportional-hazards regression. Clinical efficacy and safety profile of HCQ were assessed (secondary outcomes). Results:162 patients [84 (51·9%) males; mean age 38·2 (15·2) years] were included. Forty-four (27·2%) patients had mild disease, rest 118 (72·8%) were asymptomatic. Seventy-five (46·3%) patients received HCQ. Median time to virological negativity was lesser in HCQ-treated (13 days) versus untreated patients (15 days) (log- rank<0·001) in both asymptomatic and mildly symptomatic patients. Treatment with HCQ was the only independent predictor of virological negativity (hazard- ratio=2·24; adjusted p-value<0·001). Two (5·4%) mildly symptomatic patients progressed to severe disease within 24 hours (two doses) of HCQ initiation, compared to none in the HCQ-untreated group. Five HCQ-treated patients developed minor gastrointestinal side effects, not requiring drug discontinuation. Conclusion: HCQ reduced the time to virologic negativity (by 2 days) in asymptomatic and mildly symptomatic COVID-19, without any serious adverse events. However, no obvious clinical benefit was noted.
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    Spirometric Analysis in Post-COVID Patients
    (Ibn Sina Academy of Medieval Medicine & Sciences, 2023-04) Dua, Jasmeen Kaur; Sibia, RPS; Chander, Vikas; Gill, Harinder Singh
    Background: The spread of COVID-19 has taken on pandemic proportions, affecting almost 50 million people and causing more than 1 million deaths worldwide. The COVID-19 pandemic has gained global attention owing to its rapid transmission despite extensive measures to contain it. The majority of patients developing COVID-19 pneumonia have bilateral lung involvement leading to respiratory failure or acute respiratory distress syndrome. As a new infectious disease- carrying risk of severe course and ICU admissions, it is particularly important to explore its sequelae. There has been extensive research on the acute course of disease but enough studies are not available about the long term fibrotic sequelae and its effect on quality of life. Hence the present study. Aims and Objectives: 1. To study pulmonary function impairment in post covid patients. 2. To correlate spirometry changes with the severity of SARS-COV2 infection. Methods: A prospective study was conducted in the Medicine department at Rajindra Hospital/ Govt Medical College Patiala involving patients recovered from COVID-19. The study group included all patients above 18 yrs of age who were diagnosed as COVID-positive. So 100 post-COVID patients admitted at Rajindra hospital/Govt Medical College Patiala were followed up after discharge to study the spirometric changes and risk of development of chronic lung disease. It was a prospective study where patients were analysed spirometrically at regular intervals. Results: Abnormal spirometry was present in 16% patients after 6 months of COVID infection, thus necessitating longer follow-up in all post covid patients. Among the patients with abnormal spirometry, the majority of patients were had severe COVID-19.