Pub Date : 2021-01-29DOI: 10.51273/ESC20.25164-GUESTEDITORIAL
A. M. Chaudhary
The recent outbreak of COVID-19 has enor- mously affected every aspect of global arrange- ments with its fast and lethal reach. Originating from Wuhan, a Chinese city, this highly infectious virus has forced to impose nationwide closures in many countries impacting onsite educational systems to shut down. Considering the safety of students and following the steps taken by many infected countries, the Pakistan government initially closed all the edu- cational institutions and later allowed partial opening of schools where 30-50 % of students were allowed to attend classes in a cyclic manner. The direct and most immediate impact of this decision was an untimely break and loss of learning opportunities for all students. In order to continue with teaching and learning, Higher education commission, developed online tea- ching guidelines with the instructions to resume tea- ching, by following these guidelines. The guidelines included development and implementation of both online and hybrid curricula. Online teaching-learning is based on application of information technology tools to ensure access to learning resources for all students in the absence of face to face classes. It is conducted in the form of asynchronous or synchronous communication where-in asynchronous system tools like e-mail, discussion boards, learning newsgroups are used. For synchronous system webcasting, live chat and audio/video technologies are used for realtime class. Hybrid learning can be defined as a learning approach that combines both remote learning and inperson learning to improve student experience and ensure learning continuity.
{"title":"Teaching During Covid-19","authors":"A. M. Chaudhary","doi":"10.51273/ESC20.25164-GUESTEDITORIAL","DOIUrl":"https://doi.org/10.51273/ESC20.25164-GUESTEDITORIAL","url":null,"abstract":"The recent outbreak of COVID-19 has enor- mously affected every aspect of global arrange- ments with its fast and lethal reach. Originating from Wuhan, a Chinese city, this highly infectious virus has forced to impose nationwide closures in many countries impacting onsite educational systems to shut down. Considering the safety of students and following the steps taken by many infected countries, the Pakistan government initially closed all the edu- cational institutions and later allowed partial opening of schools where 30-50 % of students were allowed to attend classes in a cyclic manner. The direct and most immediate impact of this decision was an untimely break and loss of learning opportunities for all students. In order to continue with teaching and learning, Higher education commission, developed online tea- ching guidelines with the instructions to resume tea- ching, by following these guidelines. The guidelines included development and implementation of both online and hybrid curricula. Online teaching-learning is based on application of information technology tools to ensure access to learning resources for all students in the absence of face to face classes. It is conducted in the form of asynchronous or synchronous communication where-in asynchronous system tools like e-mail, discussion boards, learning newsgroups are used. For synchronous system webcasting, live chat and audio/video technologies are used for realtime class. Hybrid learning can be defined as a learning approach that combines both remote learning and inperson learning to improve student experience and ensure learning continuity.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44414957","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
F. R. Lodhi, Amjad Zafar, M. A. Khokhar, A. Goraya, S. Yaqub
Objective: Diffuse large B cell lymphoma (DLBCL) is a lymphoid B cells neoplasm with a diffuse pattern and high proliferation rate. Cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP) was considered effective as other complicated regimens with more toxicity profile. Rituximab is a monoclonal antibody directed against CD20 positive B cell. It has good activity therapeutically in patients of DLBCL. It increases response rates and survivals when added to CHOP chemotherapy. Although R-CHOP is more effective but due to high cost of Rituximab it is usually not incorporated with chemotherapy in most of our patients and CHOP is still used extensively. Due to heterogeneity of disease and difference in ethnicity, there may be difference in outcomes of two regimens. This study will help us in tailoring our management plan that will result in better outcome of patients. Methods: 70 patients aged between 20-65 years having DLBCL were taken in this study. We rando-mized patients by lottery method into two groups. Group I received CHOP with dose of Cyclophosphamide 750mg/m2, Doxorubicin 50mg/m2, Vincristine 1.4 mg/m2 and prednisolone 40mg/m2.Chemotherapy was given on Day-1 while prednisolone was given for 5 days from Day-1 of chemotherapy. Group II received RCHOP which includes same chemotherapy with same dosage. Rituximab was included in Group II with dose of Rituximab 375 mg /m2. Each cycle was given at three weeks interval. Response in terms of CR (Complete Response), PR (Partial Response), SD (Stable Disease) or PD (Progressive Disease) was evaluated as per leukemia network after 4 cycles of chemotherapy. The quantitative variables were calculated by taking mean and standard deviation. The response was assessed in percentage and frequencies and compared by applying chi square test. Results: Group I had 37.1% while Group II had 68.6% complete response with p value of 0.019. Partial response was 48.6% in Group I while 20.0% in Group II. 14.3% in Group I and 8.6% in Group II either had stable disease or progressive disease. Conclusions: R-CHOP has superior response rates as compared to CHOP, therefore, whenever possible Rituximab should be added as target therapy in chemotherapy.
{"title":"Comparison of R-CHOP with CHOP in Patients of Diffuse Large B Cell Lymphoma","authors":"F. R. Lodhi, Amjad Zafar, M. A. Khokhar, A. Goraya, S. Yaqub","doi":"10.51273/ESC20.2516417","DOIUrl":"https://doi.org/10.51273/ESC20.2516417","url":null,"abstract":"Objective: Diffuse large B cell lymphoma (DLBCL) is a lymphoid B cells neoplasm with a diffuse pattern and high proliferation rate. Cyclophosphamide, doxorubicin, vincristine and prednisolone (CHOP) was considered effective as other complicated regimens with more toxicity profile. Rituximab is a monoclonal antibody directed against CD20 positive B cell. It has good activity therapeutically in patients of DLBCL. It increases response rates and survivals when added to CHOP chemotherapy. Although R-CHOP is more effective but due to high cost of Rituximab it is usually not incorporated with chemotherapy in most of our patients and CHOP is still used extensively. Due to heterogeneity of disease and difference in ethnicity, there may be difference in outcomes of two regimens. This study will help us in tailoring our management plan that will result in better outcome of patients. Methods: 70 patients aged between 20-65 years having DLBCL were taken in this study. We rando-mized patients by lottery method into two groups. Group I received CHOP with dose of Cyclophosphamide 750mg/m2, Doxorubicin 50mg/m2, Vincristine 1.4 mg/m2 and prednisolone 40mg/m2.Chemotherapy was given on Day-1 while prednisolone was given for 5 days from Day-1 of chemotherapy. Group II received RCHOP which includes same chemotherapy with same dosage. Rituximab was included in Group II with dose of Rituximab 375 mg /m2. Each cycle was given at three weeks interval. Response in terms of CR (Complete Response), PR (Partial Response), SD (Stable Disease) or PD (Progressive Disease) was evaluated as per leukemia network after 4 cycles of chemotherapy. The quantitative variables were calculated by taking mean and standard deviation. The response was assessed in percentage and frequencies and compared by applying chi square test. Results: Group I had 37.1% while Group II had 68.6% complete response with p value of 0.019. Partial response was 48.6% in Group I while 20.0% in Group II. 14.3% in Group I and 8.6% in Group II either had stable disease or progressive disease. Conclusions: R-CHOP has superior response rates as compared to CHOP, therefore, whenever possible Rituximab should be added as target therapy in chemotherapy.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49630305","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Yunus, Bushra Bano, Ayesha Farooq, Amtullah Zarreen
Objective: To find out the frequency and to assess the degree of severity of premenstrual syndrome among undergraduate medical students Methods:Methods: It is a Cross-Sectional Study conducted in 161 female Students of Allama Iqbal Medical College of 1st year to final year who voluntarily consented for participation. PMS and its severity was diagnosed on the basis of a modified DRSP scale: mild if the score is 50-85, moderate if the score is 86120 and severe if the score is >120. Females having irregular periods or any organic pathology and those using hormonal contraception or any medication were excluded.Data was analyzed by SPSS version 23. Frequency, percentage charting was expressed for variables like presence of PMS and severity of PMS. Quantitative variables like age and BMI were expressed by Mean±S.D. Data was stratified for age, BMI, year of study, living status and marital status to deal with effect modifiers. Test of significance was applied i.e chisquare. A p-value ≤0.05 was considered significant. Results: Subjects ranged between 18-25 years with mean age of 19.9±2.1 years. Majority of the students were between 18-20 years. Mean BMI was 19.9±1.9 kg/m2. Mean year of study was 2.4±1.3 year. Out of 161 subjects, 53 (32.9%) were living with parents while remaining 108 (67.1%) were far from parents. Married students were 10 (6.2%). Premenstrual syndrome was found to be in 31 females (19.2%), mild 4.3%, moderate 8.1% and severe 6.8%,and severity was more in 4-5 years students, p-value was found significant with variable years of study (p-value= 0.095). Conclusion: PMS was found in 19.2% of undergraduate medical students. Early recognition and timely management can improve the quality of performance among undergraduates.
目的:了解医学生经前综合征的发生频率及严重程度。方法:对161名自愿参加的阿拉马伊克巴尔医学院大一至大四女学生进行横断面调查。经前综合症及其严重程度根据改良DRSP量表进行诊断:50-85分为轻度，86120分为中度，bb0 - 120分为重度。有月经不规律或器质性病变的女性以及使用激素避孕或任何药物的女性被排除在外。数据采用SPSS version 23进行分析。频率，百分比图表表示变量如经前症候群的存在和严重程度。年龄、BMI等定量变量以Mean±sd表示根据年龄、BMI、研究年份、生活状况和婚姻状况对数据进行分层，处理影响因子。采用显著性检验，即凿方检验。A p值≤0.05被认为是显著的。结果:受试者年龄18 ~ 25岁，平均年龄19.9±2.1岁。大多数学生年龄在18-20岁之间。平均BMI为19.9±1.9 kg/m2。平均研究年为2.4±1.3年。161名受试者中，53名(32.9%)与父母同住，108名(67.1%)远离父母。已婚学生10名(6.2%)。经前综合征女性31人(19.2%)，轻度4.3%，中度8.1%，重度6.8%，其中4-5年级学生的严重程度更高，p值与学习年限差异有统计学意义(p值= 0.095)。结论:经前症候群发生率为19.2%。早期发现和及时管理可以提高大学生的绩效质量。
{"title":"Frequency and Severity of Premenstrual Syndrome among Undergraduate Medical Students","authors":"S. Yunus, Bushra Bano, Ayesha Farooq, Amtullah Zarreen","doi":"10.51273/ESC20.251646","DOIUrl":"https://doi.org/10.51273/ESC20.251646","url":null,"abstract":"Objective: To find out the frequency and to assess the degree of severity of premenstrual syndrome among undergraduate medical students Methods:Methods: It is a Cross-Sectional Study conducted in 161 female Students of Allama Iqbal Medical College of 1st year to final year who voluntarily consented for participation. PMS and its severity was diagnosed on the basis of a modified DRSP scale: mild if the score is 50-85, moderate if the score is 86120 and severe if the score is >120. Females having irregular periods or any organic pathology and those using hormonal contraception or any medication were excluded.Data was analyzed by SPSS version 23. Frequency, percentage charting was expressed for variables like presence of PMS and severity of PMS. Quantitative variables like age and BMI were expressed by Mean±S.D. Data was stratified for age, BMI, year of study, living status and marital status to deal with effect modifiers. Test of significance was applied i.e chisquare. A p-value ≤0.05 was considered significant. Results: Subjects ranged between 18-25 years with mean age of 19.9±2.1 years. Majority of the students were between 18-20 years. Mean BMI was 19.9±1.9 kg/m2. Mean year of study was 2.4±1.3 year. Out of 161 subjects, 53 (32.9%) were living with parents while remaining 108 (67.1%) were far from parents. Married students were 10 (6.2%). Premenstrual syndrome was found to be in 31 females (19.2%), mild 4.3%, moderate 8.1% and severe 6.8%,and severity was more in 4-5 years students, p-value was found significant with variable years of study (p-value= 0.095). Conclusion: PMS was found in 19.2% of undergraduate medical students. Early recognition and timely management can improve the quality of performance among undergraduates.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44204874","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: To evaluate the frequency of Paediatricians who have good knowledge for diagnosis of Autism Spectrum Disorder (ASD). Methods: It is cross-sectional study conducted in department of Paediatric Medicine, Children Hospital, Lahore, Jinnah Hospital and Services Hospital Lahore, in 6 months duration, spanning from June 27, 2016 till December 27, 2016. A total of 89 doctors fulfilling the inclusion criteria were registered after informed consent. Demographic data (including age, sex, qualification and duration of clinical experience) was taken. Doctors were given a questionnaire to assess their knowledge of ASD. The questionnaire was a nineteen-item self-administered questionnaire divided into four domains namely, social interaction (Domain 1), impairment in communication (Domain 2), repetitive behavior (Domain 3), characteristics of autism as a disorder and its comorbidities (Domain 4). The KCAHW sore ≥ 15 was considered as good. Data was entered and analyzed in (SPSS) version 22.0. Results: The mean age of subjects was 30.67±2.80 years with 31(31%) physicians male and 69(69%) were females. The mean KCAHW score was 15.07±3.54 with minimum and maximum score of 7 and 19. According to operational definition a total of 62(62%) subjects had good knowledge while 38(38%) physician had score < 15. Conclusion: Though 68% of paediatricians had good knowledge about childhood autism according to our study. The physicians who had poor knowledge, must be considered for different educational activities to enhance their knowledge regarding ASD, which may help in early diagnosis and improving prognosis of children with ASD. Key Words: Paediatricians, Autism spectrum disorder How to Cite: Zia F, Qamar H, Aslam I, Siddiqui MA. Assessment of knowledge about autism spectrum disorder among paediatricians. Esculapio.2020;16(04):83-86.
{"title":"Assessment of Knowledge About Autism Spectrum Disorder Among Paediatricians","authors":"Fatima Zia, Hafsa Qamar, I. Aslam, M. Siddiqui","doi":"10.51273/ESC20.2516418","DOIUrl":"https://doi.org/10.51273/ESC20.2516418","url":null,"abstract":"Objective: To evaluate the frequency of Paediatricians who have good knowledge for diagnosis of Autism Spectrum Disorder (ASD). Methods: It is cross-sectional study conducted in department of Paediatric Medicine, Children Hospital, Lahore, Jinnah Hospital and Services Hospital Lahore, in 6 months duration, spanning from June 27, 2016 till December 27, 2016. A total of 89 doctors fulfilling the inclusion criteria were registered after informed consent. Demographic data (including age, sex, qualification and duration of clinical experience) was taken. Doctors were given a questionnaire to assess their knowledge of ASD. The questionnaire was a nineteen-item self-administered questionnaire divided into four domains namely, social interaction (Domain 1), impairment in communication (Domain 2), repetitive behavior (Domain 3), characteristics of autism as a disorder and its comorbidities (Domain 4). The KCAHW sore ≥ 15 was considered as good. Data was entered and analyzed in (SPSS) version 22.0. Results: The mean age of subjects was 30.67±2.80 years with 31(31%) physicians male and 69(69%) were females. The mean KCAHW score was 15.07±3.54 with minimum and maximum score of 7 and 19. According to operational definition a total of 62(62%) subjects had good knowledge while 38(38%) physician had score < 15. Conclusion: Though 68% of paediatricians had good knowledge about childhood autism according to our study. The physicians who had poor knowledge, must be considered for different educational activities to enhance their knowledge regarding ASD, which may help in early diagnosis and improving prognosis of children with ASD. Key Words: Paediatricians, Autism spectrum disorder How to Cite: Zia F, Qamar H, Aslam I, Siddiqui MA. Assessment of knowledge about autism spectrum disorder among paediatricians. Esculapio.2020;16(04):83-86.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"49129344","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Fariha Khan, M. Z. Khan, A. M. Rehan, Zoobia Irum, F. Perveen, S. Chiragh
Objectives: This study was done to observe the effect of Enterococcus faecium SF68 and Saccharomyces boulardii in acute severe diarrhea in infants. Methods: It was a single blind, randomized controlled clinical trial done in Children Hospital, Lahore. The infants were selected between 6 months to 12 months of age. All the infants were suffering from acute diarrhea with severe dehydration. Total 105 infants were selected and randomly divided into three groups having 35 infants in each group. Infants in group A received standard treatment of diarrhea. Infants in group B and C received Enterococcus faecium SF68 and Saccharomyces boulardii respectively twice daily for five days along with standard treatment of diarrhea. All the infants were monitored for five days. The treatment response was observed in terms of frequency of diarrhea, duration of diarrhea, stool consistency and length of hospital stay. Results: The frequency of diarrhea, duration of diarrhea and length of hospital stay were significantly reduced in both group B and C as compared to group A. Conclusion: Enterococcus faecium SF68 and Saccharomyces boulardii helped to reduce the stool frequency, duration of diarrhea, length of hospital stay and also improved the stool consistency in acute severe diarrhea in infants.
{"title":"Protective Effect of Enterococcus faecium SF68 and Saccharomyces boulardii in Acute Severe Diarrhea in Infants: Randomized Controlled Trial","authors":"Fariha Khan, M. Z. Khan, A. M. Rehan, Zoobia Irum, F. Perveen, S. Chiragh","doi":"10.51273/ESC20.2516413","DOIUrl":"https://doi.org/10.51273/ESC20.2516413","url":null,"abstract":"Objectives: This study was done to observe the effect of Enterococcus faecium SF68 and Saccharomyces boulardii in acute severe diarrhea in infants. Methods: It was a single blind, randomized controlled clinical trial done in Children Hospital, Lahore. The infants were selected between 6 months to 12 months of age. All the infants were suffering from acute diarrhea with severe dehydration. Total 105 infants were selected and randomly divided into three groups having 35 infants in each group. Infants in group A received standard treatment of diarrhea. Infants in group B and C received Enterococcus faecium SF68 and Saccharomyces boulardii respectively twice daily for five days along with standard treatment of diarrhea. All the infants were monitored for five days. The treatment response was observed in terms of frequency of diarrhea, duration of diarrhea, stool consistency and length of hospital stay. Results: The frequency of diarrhea, duration of diarrhea and length of hospital stay were significantly reduced in both group B and C as compared to group A. Conclusion: Enterococcus faecium SF68 and Saccharomyces boulardii helped to reduce the stool frequency, duration of diarrhea, length of hospital stay and also improved the stool consistency in acute severe diarrhea in infants.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48297259","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jawariea Ali, Sheikh Sajjad Ali, M. Imran, T. Tariq, Umair Mahmood, J. Iqbal
Objective: To find association between antidiabetic treatment and the type of obesity in type 2 diabetic patients. Methods: The study was conducted in National Institute of Diabetes & Endocrinology (NIDE), Karachi, over a period of 6 months, ie. from January to June, 2018. It was an observational analytical study, for which 59 patients were selected via non-probability sampling, as per inclusion and exclusion criteria. Data was collected through detailed history, examination. A database was developed and analyzed on SPSS 17. A pvalue <0.05 was taken as statistically significant. Results: Fifty nine patients fulfilling the inclusion criteria were included in this study. While 30 (50.8%) had generalized obesity, 29 (49.2%) were not having generalized obesity. Further it was observed that 35 (59.3%) had abdominal obesity, while 24 (40.7%) were not having abdominal obesity. A total of 39 (66.1%) were on insulin, while 20 (43.9%) were not on insulin. Finally, 41 (69.5%) were on oral hypoglycemic drugs, while 18 (30.5%) were not on oral hypoglycemic drugs. P-values were not significant for the study parameters. Conclusion: There is no association between antidiabetic treatment and type of obesity in type 2 diabetic patients.
{"title":"Association of Antidiabetic Treatment with the Type of Obesity in Type 2 Diabetic Patients","authors":"Jawariea Ali, Sheikh Sajjad Ali, M. Imran, T. Tariq, Umair Mahmood, J. Iqbal","doi":"10.51273/ESC20.2516421","DOIUrl":"https://doi.org/10.51273/ESC20.2516421","url":null,"abstract":"Objective: To find association between antidiabetic treatment and the type of obesity in type 2 diabetic patients. Methods: The study was conducted in National Institute of Diabetes & Endocrinology (NIDE), Karachi, over a period of 6 months, ie. from January to June, 2018. It was an observational analytical study, for which 59 patients were selected via non-probability sampling, as per inclusion and exclusion criteria. Data was collected through detailed history, examination. A database was developed and analyzed on SPSS 17. A pvalue <0.05 was taken as statistically significant. Results: Fifty nine patients fulfilling the inclusion criteria were included in this study. While 30 (50.8%) had generalized obesity, 29 (49.2%) were not having generalized obesity. Further it was observed that 35 (59.3%) had abdominal obesity, while 24 (40.7%) were not having abdominal obesity. A total of 39 (66.1%) were on insulin, while 20 (43.9%) were not on insulin. Finally, 41 (69.5%) were on oral hypoglycemic drugs, while 18 (30.5%) were not on oral hypoglycemic drugs. P-values were not significant for the study parameters. Conclusion: There is no association between antidiabetic treatment and type of obesity in type 2 diabetic patients.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44076704","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Muhammad Ali, M. Azam, Maimoona Zaheer, Fahad Wali Shah Khagha, A. Shah, F. Masood
Objective: To compare the efficacy of Hyaluronic acid (HA) and Platelet rich plasma (PRP) for treatment of Knee osteoarthritis. Methods: A randomized controlled trial done at department of Orthopedics Unit-I, Mayo Hospital Lahore. 130 cases fulfilling inclusion criteria were enrolled. All patients were divided into two groups. In group-A, cases were treated with HA (1% sodium Hyaluronate mixed in a phosphate buffered saline). In group-B, cases were treated with 10ml of PRP extracted from 100ml of their blood. Before and after procedure pain and efficacy was recorded. Results: The frequency of pain reduction ≥ 50% was statistically higher in PRP group as compared to HA group, p-value < 0.05. Conclusion: Through the findings of this study we conclude that the efficacy of efficacy of PRP was high than HA for treatment of Knee osteoarthritis.
{"title":"Comparing the Efficacy of Hyaluronic Acid and Platelet Rich Plasma Treatment by using Visual analogue Scale in the Patients of Knee Osteoarthritis","authors":"Muhammad Ali, M. Azam, Maimoona Zaheer, Fahad Wali Shah Khagha, A. Shah, F. Masood","doi":"10.51273/ESC20.251648","DOIUrl":"https://doi.org/10.51273/ESC20.251648","url":null,"abstract":"Objective: To compare the efficacy of Hyaluronic acid (HA) and Platelet rich plasma (PRP) for treatment of Knee osteoarthritis. Methods: A randomized controlled trial done at department of Orthopedics Unit-I, Mayo Hospital Lahore. 130 cases fulfilling inclusion criteria were enrolled. All patients were divided into two groups. In group-A, cases were treated with HA (1% sodium Hyaluronate mixed in a phosphate buffered saline). In group-B, cases were treated with 10ml of PRP extracted from 100ml of their blood. Before and after procedure pain and efficacy was recorded. Results: The frequency of pain reduction ≥ 50% was statistically higher in PRP group as compared to HA group, p-value < 0.05. Conclusion: Through the findings of this study we conclude that the efficacy of efficacy of PRP was high than HA for treatment of Knee osteoarthritis.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"42207685","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
S. Khaleeq, Azib Ali, Sahir Shafiq, M. M. Butt, M. Aslam, M. Jehangir
Objective: This study was designed to compare the mean pain score with bupivacaine versus tramadol plus bupivacaine in patients undergoing surgery under general anesthesia. Randomized Controlled Study. Anesthesia department of SIMS medical college/Services Hospital, Lahore. Duration is 13 months from 20th August2017 till 24th September 2018. Method: 80 patients aged 20-60 years of ASA I & II status, undergoing elective surgery were selected. Patients were randomly divided into two groups (Group A and B) of 40 each, using random numbers table. An epidural catheter was placed at L3-L4 intervertebral level. Group A was given 30 ml of 0.125% bupivacaine and Group B was given 25mg Tramadol plus 0.125% bupivacaine mixture in the same volume. General anesthesia was induced with IV Propofol 2mg/kg and atracurium 0.5mg/kg. After recovery from anesthesia, patients were shifted to HDU. Post-operative pain was assessed using the 10-point VAS score. Injection nalbuphine 0.1mg/kg was given as rescue analgesic when VAS score became more than 4. Results: The mean age of patient in Group A was 37.5 ± 9.1 years and 38.6 ± 7.0 years in Group B. Mean BMI in Group A was 33.2 ± 4.3 and 32.2 ± 4.2 in Group B. The mean pain score after 12 hours of surgery was 3.6 ± 0.8 in Group A and 1.5 ± 0.9 in Group B, p value was significant. Conclusion: Thus, the present study concludes that epidural administration of tramadol as adjuvant with bupivacaine is more effective in postoperative pain relief as compared to bupivacaine alone.
{"title":"A Comparison between Bupivacaine Alone and Bupivacaine with Tramadol in Epidural Block for Postoperative Pain Management","authors":"S. Khaleeq, Azib Ali, Sahir Shafiq, M. M. Butt, M. Aslam, M. Jehangir","doi":"10.51273/ESC20.2516422","DOIUrl":"https://doi.org/10.51273/ESC20.2516422","url":null,"abstract":"Objective: This study was designed to compare the mean pain score with bupivacaine versus tramadol plus bupivacaine in patients undergoing surgery under general anesthesia. Randomized Controlled Study. Anesthesia department of SIMS medical college/Services Hospital, Lahore. Duration is 13 months from 20th August2017 till 24th September 2018. Method: 80 patients aged 20-60 years of ASA I & II status, undergoing elective surgery were selected. Patients were randomly divided into two groups (Group A and B) of 40 each, using random numbers table. An epidural catheter was placed at L3-L4 intervertebral level. Group A was given 30 ml of 0.125% bupivacaine and Group B was given 25mg Tramadol plus 0.125% bupivacaine mixture in the same volume. General anesthesia was induced with IV Propofol 2mg/kg and atracurium 0.5mg/kg. After recovery from anesthesia, patients were shifted to HDU. Post-operative pain was assessed using the 10-point VAS score. Injection nalbuphine 0.1mg/kg was given as rescue analgesic when VAS score became more than 4. Results: The mean age of patient in Group A was 37.5 ± 9.1 years and 38.6 ± 7.0 years in Group B. Mean BMI in Group A was 33.2 ± 4.3 and 32.2 ± 4.2 in Group B. The mean pain score after 12 hours of surgery was 3.6 ± 0.8 in Group A and 1.5 ± 0.9 in Group B, p value was significant. Conclusion: Thus, the present study concludes that epidural administration of tramadol as adjuvant with bupivacaine is more effective in postoperative pain relief as compared to bupivacaine alone.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"47214918","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Uswah Bokhari, Uswah Shoaib, S. Tariq, S. Khan, Fatima Syed, B. Amin, Farhat Ijaz, Rana Khurram Aftab
Objectives: The current lockdown in the country has led to a sedentary lifestyle because of a shift of daily activities online and a fear of contracting the illness leading to isolation inside homes; Hence an expected change in weight of the general population. This study aims to determine the frequency of weight gain and its impact in adults during the current lockdown of COVID-19. Methods: Participants selected from the ages of 18-25 from different universities of Pakistan were sent questionnaires via WhatsApp, posted online using Microsoft Forms. A total of 157 responses were attained. Results: Among the 157 participants the average weight before the lockdown was 61.95 kgs and after the lockdown was 64.99kgs so there was an increase of 3.016 kgs whereas 18.5% of the sample maintained their weight and 37.6% were reported to have lost weight. The results also depict a 1.6% increase in impairment of body image. Conclusion: We concluded that the Lockdown due to the COVID-19 pandemic has caused a gain in the weight and lowered self-esteem with regard to body image of most young adults in Pakistan due to many factors including higher food intake, lack of exercise and also emotional distress.
{"title":"Frequency of Weight Gain and its Impact in Adults during Lockdown: A Cross- Sectional Study","authors":"Uswah Bokhari, Uswah Shoaib, S. Tariq, S. Khan, Fatima Syed, B. Amin, Farhat Ijaz, Rana Khurram Aftab","doi":"10.51273/ESC20.2516424","DOIUrl":"https://doi.org/10.51273/ESC20.2516424","url":null,"abstract":"Objectives: The current lockdown in the country has led to a sedentary lifestyle because of a shift of daily activities online and a fear of contracting the illness leading to isolation inside homes; Hence an expected change in weight of the general population. This study aims to determine the frequency of weight gain and its impact in adults during the current lockdown of COVID-19. Methods: Participants selected from the ages of 18-25 from different universities of Pakistan were sent questionnaires via WhatsApp, posted online using Microsoft Forms. A total of 157 responses were attained. Results: Among the 157 participants the average weight before the lockdown was 61.95 kgs and after the lockdown was 64.99kgs so there was an increase of 3.016 kgs whereas 18.5% of the sample maintained their weight and 37.6% were reported to have lost weight. The results also depict a 1.6% increase in impairment of body image. Conclusion: We concluded that the Lockdown due to the COVID-19 pandemic has caused a gain in the weight and lowered self-esteem with regard to body image of most young adults in Pakistan due to many factors including higher food intake, lack of exercise and also emotional distress.","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":"16 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41988877","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: To compare the frequency of Ovulation Induction after administration of Letrozole with metformin versus Letrozole alone in females presenting with Polycystic Ovarian Syndrome Methods: This Randomized Controlled Trial was done in unit 5 of Lady Aitchison Hospital Lahore for 6 months. Total 200 females fulfilling the inclusion criteria were recruited from OPD. Lottery method was used for randomization of study subjects. Females in group A were given Letrozole 2.5mg once a day for five days (from third to seventh day)of the cycle for three consecutive months and metformin 1500mg (500mg 3 times a day) daily for three months, while females in group B were given Letrozole 2.5mg once a day for five days (from third to seventh day) le for three consecutive months. Then they were followed up in OPD for 3 cycles. In all 3 cycles TVS was done on day 12 to access the number of follicles and to measure the size of largest follicle, and on day 21 of cycle progesterone level will be assessed for confirmation of ovulation induction. The data was entered and analyzed through SPSS version 20. Mean and standard deviation was calculated for age and BMI. Frequency and percentage was calculated for Ovulation induction. Both groups were compared by using chi-square test taking p-value<0.05 as significant. Data was stratified for BMI (Normal, overweight and Obese).After stratification chi-square test was applied keeping a p value < 0.05 as significant. Results: In Group-A mean age of women was 28.18±6.58 years. In Group-B mean age of women was 27.08±5.15 years. In Group-A ovulation induction rate was much higher as compared to that of Group-B women. i.e. (89% vs. 60%). p-value=0.000. Ovulation induction rate was significantly higher with Letrozole+ Metformin in women who were having normal BMI, overweight & obese as compared to that of Letrozole alone. Conclusion: Letrozole with metformin is more effective for the ovulation Induction females presenting with polycystic ovarian Syndrome as compared to letrozole alone.()
目的:比较多囊卵巢综合征女性来曲唑联合二甲双胍与单独来曲唑诱导排卵的频率。方法:本随机对照试验在拉合尔艾奇逊夫人医院第五单元进行，为期6个月。从门诊部共招募了200名符合纳入标准的女性。采用抽签法对研究对象进行随机化。A组女性给予来曲唑2.5mg /天1次，连续3个月，连续5天(第3 ~ 7天)，二甲双胍1500mg (500mg /天3次)，连续3个月，B组女性给予来曲唑2.5mg /天1次，连续5天(第3 ~ 7天)，连续3个月。随访3个周期。在所有3个周期中，在第12天进行TVS以获取卵泡数量并测量最大卵泡的大小，在第21天评估黄体酮水平以确认促排卵。通过SPSS version 20录入数据并进行分析。计算年龄和BMI的平均值和标准差。计算促排卵次数和百分比。两组比较采用卡方检验，p值<0.05为差异有统计学意义。数据按BMI(正常、超重和肥胖)分层。分层后采用卡方检验，p < 0.05为显著性。结果:a组女性平均年龄28.18±6.58岁。b组女性平均年龄27.08±5.15岁。a组诱导排卵率明显高于b组。即(89% vs. 60%)。假定值= 0.000。在BMI正常、超重和肥胖的女性中，来曲唑+二甲双胍的促排卵率明显高于单独来曲唑。结论:来曲唑联合二甲双胍治疗多囊卵巢综合征的效果优于单独来曲唑。
{"title":"Comparison of Ovulation Induction with Letrozole with Metformin Versus Letrozole Alone in Females Presenting with Polycystic Ovarian Syndrome","authors":"Zubda Aiman, Amna Khanam, Mahliqa Maqsood, Mehwish Ayyaz, M. Alía, Tayyaba Kanwal","doi":"10.51273/ESC20.2516412","DOIUrl":"https://doi.org/10.51273/ESC20.2516412","url":null,"abstract":"Objective: To compare the frequency of Ovulation Induction after administration of Letrozole with metformin versus Letrozole alone in females presenting with Polycystic Ovarian Syndrome Methods: This Randomized Controlled Trial was done in unit 5 of Lady Aitchison Hospital Lahore for 6 months. Total 200 females fulfilling the inclusion criteria were recruited from OPD. Lottery method was used for randomization of study subjects. Females in group A were given Letrozole 2.5mg once a day for five days (from third to seventh day)of the cycle for three consecutive months and metformin 1500mg (500mg 3 times a day) daily for three months, while females in group B were given Letrozole 2.5mg once a day for five days (from third to seventh day) le for three consecutive months. Then they were followed up in OPD for 3 cycles. In all 3 cycles TVS was done on day 12 to access the number of follicles and to measure the size of largest follicle, and on day 21 of cycle progesterone level will be assessed for confirmation of ovulation induction. The data was entered and analyzed through SPSS version 20. Mean and standard deviation was calculated for age and BMI. Frequency and percentage was calculated for Ovulation induction. Both groups were compared by using chi-square test taking p-value<0.05 as significant. Data was stratified for BMI (Normal, overweight and Obese).After stratification chi-square test was applied keeping a p value < 0.05 as significant. Results: In Group-A mean age of women was 28.18±6.58 years. In Group-B mean age of women was 27.08±5.15 years. In Group-A ovulation induction rate was much higher as compared to that of Group-B women. i.e. (89% vs. 60%). p-value=0.000. Ovulation induction rate was significantly higher with Letrozole+ Metformin in women who were having normal BMI, overweight & obese as compared to that of Letrozole alone. Conclusion: Letrozole with metformin is more effective for the ovulation Induction females presenting with polycystic ovarian Syndrome as compared to letrozole alone.()","PeriodicalId":11923,"journal":{"name":"Esculapio","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2021-01-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"44481258","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
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