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Histochemical Study of Nasolabial Fold in Indian Cadavers 印度Cadavers鼻唇沟褶皱的组织化学研究
Pub Date : 2023-02-28 DOI: 10.14260/jemds.v12i2.344
Rahul Sharma, Pooja Bhadoria, Amarjyoti Chaturvedi
BACKGROUND A distinct change in human senescence occurs in the face and the most pioneering sign appears in the area surrounding the eyes and nasolabial fold. Each injector learns through experience, where to place the botulinum toxin for desired effects. Aims & Objectives Haematoxylin & Eosin study was performed to understand the histology of the Nasolabial fold (NLF). METHODS Nasolabial folds were identified in 5 formalin-fixed cadavers aged between 55-70 years. Tissue was obtained from three points: one from ala of the nose (A), second from the angle of the mouth (C), and third from the mid-centre of an imaginary line extending from point A to point C (B) bilaterally and then formalin-fixed, paraffin-installed, and stained with haematoxylin and eosin stain. RESULTS Macroscopically, several muscle fibres of different origins were observed to insert directly on the nasolabial fold. On microscopic investigation, muscular fibres were observed to extend from the subcutaneous layer to the dermis, at point A&C and few or no muscle fibres were observed at point B. CONCLUSIONS Microscopical investigation shows muscular fibres extending from the subcutaneous layer to the dermis, at point A&C and few or no muscle fibres were observed at point B. If botulism toxin is injected intradermally adjacent to the ala of nose and angle of mouth it gives a satisfactory result to reduce rhytids.
背景人类衰老的一个明显变化发生在面部,最具开创性的迹象出现在眼睛和鼻唇沟周围。每个注射器都通过经验来学习如何放置肉毒杆菌毒素以达到预期效果。目的:通过苏木精和曙红的研究,了解鼻唇襞(NLF)的组织学特征。方法对5具年龄在55-70岁之间的福尔马林固定尸体进行鼻唇折叠鉴定。从三个点获得组织:一个来自鼻子(A),第二个来自嘴角(C),第三个来自从A点延伸到C点(B)的假想线的中心,然后福尔马林固定,石蜡固定,并用苏木精和伊红染色。结果肉眼可见不同来源的几种肌纤维直接插入鼻唇沟。在显微镜检查中,在A和C点观察到肌肉纤维从皮下延伸到真皮,在B点观察到很少或没有肌肉纤维。如果肉毒杆菌毒素在靠近鼻翼和嘴角的皮内注射,可以达到令人满意的效果,减少皱纹。
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引用次数: 0
Prevalence of Influenza Virus in Patients with Severe Acute Respiratory Infections (SARI) 严重急性呼吸道感染(SARI)患者流感病毒流行情况
Pub Date : 2023-02-28 DOI: 10.14260/jemds.v12i2.340
Debadatta Dhar Chanda, Chhandasree Biswas, Supriya Upadhyay
BACKGROUND Influenza is viral fever with the main symptoms of the respiratory tract like cough, fever, breathlessness, nasal discharge, sore throat & myalgia. Pandemic 2009 H1N1 influenza A was the virus that presented a significant public health threat on a global scale. This prospective study was undertaken to analyse the prevalence of the influenza virus in patients with a severe acute respiratory infection (SARI) and also to determine the demographic characteristics and seasonal variations. METHODS This was a hospital-based prospective study done in the Department of Microbiology, Silchar Medical College & Hospital, Silchar for 1 year from June 2021 to May 2022. Respiratory specimens were tested for Influenza virus by one step real-time reverse transcription polymerase chain reaction (RT-PCR). RESULTS In real-time PCR, the influenza virus was detected in 6 out of 85 SARI patients (7%). Of 6 total positives, 4(67%) were influenza A and 2(33%) were influenza B. Among 4 influenza A positive cases, 3(75%) were influenza A (H1N1) pdm09 and 1(25%) was seasonal influenza A (H3N2). The highest percentage of positivity (50%) was detected in the age group of 15-29 years. The most common symptoms among the positive influenza cases were fever (100%), cough (88%), and breathlessness (56%). Other associated symptoms were sore throat (63%), nasal discharge (75%), and myalgia (75%). CONCLUSIONS This study clearly shows that influenza is an important cause of severe acute respiratory infection. It also suggests the need for continuous effective surveillance of influenza viruses to detect cases and control outbreaks. Early intervention and proper management of influenza virus cases are required to curb the disease burden.
流感是病毒性发热,主要症状为呼吸道,如咳嗽、发烧、呼吸困难、流鼻水、喉咙痛及肌痛。2009年H1N1甲型流感大流行是在全球范围内对公共卫生构成重大威胁的病毒。这项前瞻性研究是为了分析流感病毒在严重急性呼吸道感染(SARI)患者中的流行情况,并确定人口统计学特征和季节变化。方法:这是一项以医院为基础的前瞻性研究,于2021年6月至2022年5月在锡尔查尔医学院和医院微生物学系进行,为期1年。采用实时反转录聚合酶链反应(RT-PCR)对呼吸道标本进行流感病毒检测。结果85例急性呼吸道感染患者中有6例(7%)检测到流感病毒。其中甲型流感4例(67%),乙型流感2例(33%)。其中甲型流感(H1N1) pdm09 3例(75%),季节性甲型流感(H3N2) 1例(25%)。15-29岁年龄组的阳性检出率最高(50%)。流感阳性病例中最常见的症状是发热(100%)、咳嗽(88%)和呼吸困难(56%)。其他相关症状为喉咙痛(63%)、鼻溢液(75%)和肌痛(75%)。结论流感是严重急性呼吸道感染的重要病因。它还表明,需要持续有效地监测流感病毒,以发现病例并控制疫情。需要对流感病毒病例进行早期干预和适当管理,以减轻疾病负担。
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引用次数: 0
Anaesthesia for Caesarean Section in a Patient with Large Ventricular Septal Defect with Pulmonary Hypertension with Single Ventricle Physiology 单心室生理下肺动脉高压大室间隔缺损患者剖宫产麻醉
Pub Date : 2023-02-28 DOI: 10.14260/jemds.v12i2.342
Anvar Sadath, Nisha Rajmohan, Vismaya Raj Mohan
Pregnancy in a patient with large ventricular septal defect (VSD) with severe pulmonary hypertension (PAH) increases the risk of mortality severalfold. This when combined with single ventricle physiology forms a rare and deadly combination. A 26-year-old female presented for elective LSCS at 35 weeks gestation. She had a large VSD with severe PAH with a single ventricle physiology. We report the successful conduct of a caesarean section in this patient under graded epidural anaesthesia.
妊娠合并严重肺动脉高压(PAH)的大面积室间隔缺损(VSD)患者的死亡风险增加数倍。当与单心室生理学相结合时,就会形成一种罕见而致命的组合。一名26岁女性在妊娠35周时接受选择性LSCS检查。她有一个巨大的室间隔缺损,伴有严重的PAH和单心室生理。我们报告了在分级硬膜外麻醉下对该患者成功进行剖腹产手术。
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引用次数: 0
Can We Use Our Dental Curing Lights to Polymerize Objects Produced with 3D Resin Printer? 我们可以使用牙科固化灯来聚合3D树脂打印机生产的物体吗?
Pub Date : 2023-02-28 DOI: 10.14260/jemds.v12i2.338
Türkay Kölüş, Mehmet Şahbaz, Uğur Köklü
BACKGROUND Dental treatment objects produced with 3D resin printers barely polymerize after fabrication. They need post-curing and an extra polymerization oven is required. Present study is aimed to determine the effectiveness of dental curing lights for post-curing of objects produced with a 3D resin printer. METHODS Samples were produced with Alias ​​Sharp & Rigid Model 3D Printing Resin in Photon Mono X 3D resin printer. The control set samples were cured with UV light for 2 min in Wash & Cure Plus device. T-20, T-40 and T-60 set samples were exposed to VALO Cordless curing light for 20, 40 and 60 seconds respectively. The hardness was measured with the Shore D Durometer. Then, the samples were subjected to compression. For statistical analysis, one way analysis of variance (ANOVA) and Tukey test was used. RESULTS The set cured with VALO Cordless for 20 seconds showed the highest strength. Compressive strength decreased with prolongation of the curing time. All experimental sets showed significantly higher hardness than the control set. Hardness increased gradually in the 20 and 40 second sets, but the difference between the 40 and 60 second sets was not significant. Also, color change was observed in the experimental sets samples. CONCLUSIONS Dental curing lights are effective in post-curing 3D printer resins.
背景用3D树脂打印机生产的牙科治疗对象在制造后几乎不聚合。它们需要后固化,需要额外的聚合炉。本研究旨在确定牙科固化灯对用3D树脂打印机生产的物体进行后固化的有效性。方法用Alias生产样品​​夏普&刚性模型三维打印树脂在光子单X三维树脂打印机。对照组样品在Wash&Cure Plus装置中用紫外线固化2分钟。将T-20、T-40和T-60组样品分别暴露于VALO无绳固化光20、40和60秒。硬度是用肖氏D硬度计测量的。然后,对样品进行压缩。统计分析采用单因素方差分析(ANOVA)和Tukey检验。结果VALO Cordless固化20秒的固化体强度最高。抗压强度随养护时间的延长而降低。所有实验组的硬度都明显高于对照组。硬度在20秒和40秒组中逐渐增加,但40秒和60秒组之间的差异不显著。此外,在实验组样品中观察到颜色变化。结论牙科固化灯在固化后的3D打印机树脂中是有效的。
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引用次数: 0
Study of Effect of Stress on Lactation in Postnatal Women 应激对产后妇女泌乳影响的研究
Pub Date : 2023-01-31 DOI: 10.14260/jemds.v12i1.323
Tatapudi Susmitha Madhuri, Moravineni Usha Rani, Paidi Sirisha
BACKGROUND Stress is a physiological response to psychological and physical demands. Cortisol is a stress hormone that is released in increasing quantities as pregnancy progresses. Stress is a cumulative effect of changing life events with failure of coping reflex that leads to chronic stress which repeatedly activates hypothalamic–pituitary-adrenal (HPA) axis without relaxation response, to release excess cortisol. Duration of stress and its sites of action lead to decrease in lactation. In this study, we wanted to determine the relationship between stress and levels of maternal serum cortisol before and after the delivery and assess the relation between stress and milk output in the first week of post-partum period. METHODS A cross-sectional study was carried out among 96 pregnant women, using HOLMES-RAHE STRESS SCALE: categorized into mild, moderate, and severe stressed. Serum cortisol levels are assessed using electrochemiluminescence immunoassay before and after delivery. Postnatal mothers were advised to breastfeed their newborns ten times a day after delivery and the baby's weight is measured using the baby-test weighing method using digital weighing machine at regular intervals for seven days. Mean serum cortisol levels were computed and compared with milk production. RESULTS 48.9 % pregnant women were mildly, 29.1 % were moderately and 21.8 % severely stressed. Serum cortisol levels were significantly high (p < 0.05) in moderately and severely stressed women with significant reduction in milk volume when compared to mildly stressed women. CONCLUSIONS Findings of this study indicates that moderate and severe stressful events reduce lactation in post-natal women. More research is needed to understand relationship between stress, other maternal factors, and their impact on breastfeeding outcomes.
应激是对心理和生理需求的生理反应。皮质醇是一种压力激素,随着怀孕的进展,它的释放量越来越大。压力是不断变化的生活事件与应对反射失败的累积效应,导致慢性压力,反复激活下丘脑-垂体-肾上腺(HPA)轴而没有放松反应,释放过量的皮质醇。应激持续时间及其作用部位导致泌乳减少。在这项研究中,我们想要确定分娩前后压力和母亲血清皮质醇水平之间的关系,并评估产后第一周压力和产奶量之间的关系。方法采用HOLMES-RAHE应激量表对96名孕妇进行横断面研究,量表分为轻度、中度和重度应激。在分娩前后使用电化学发光免疫分析法评估血清皮质醇水平。建议产后母亲在分娩后每天母乳喂养10次,并在7天内定期使用数字称重机使用婴儿测试称重法测量婴儿体重。计算平均血清皮质醇水平,并与产奶量进行比较。结果轻度应激占48.9%,中度应激占29.1%,重度应激占21.8%。与轻度压力妇女相比,中度和重度压力妇女的血清皮质醇水平显著高(p < 0.05),泌乳量显著减少。结论:本研究结果表明,中度和重度应激事件可减少产后妇女的泌乳。需要更多的研究来了解压力、其他母亲因素及其对母乳喂养结果的影响之间的关系。
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引用次数: 0
Tracheobronchomegaly (Mounier-Kuhn Syndrome) in Old Age - A Case Report 老年气管支气管扩张症(Mounier-Kuhn综合征)一例报告
Pub Date : 2023-01-31 DOI: 10.14260/jemds.v12i1.324
Khawaja Bilal Waheed, Jawad Nasser, Raghad Hamdi Alsaidalani, Zubair Ahmed
Tracheobronchomegaly or Mounier-Kuhn syndrome is a rare condition affecting the airways and is characterized by dilatation of the trachea and major bronchi secondary to atrophic or absent elastic fibres of the cartilage and thinning of the muscles.[1] The abnormally enlarged flaccid portions of the bronchial tree collapse and fail to maintain patency during expiration and coughing, predisposing the patient to stagnation of contents and recurrent lower respiratory tract infections, emphysema, bronchiectasis and chronic pulmonary suppuration.[2] The diagnosis is usually made on basis of specific radiographic features,[3] particularly on computed tomography (CT) scan. We report a case of a 69-year-old man who presented with recurrent lower respiratory tract infections and was found to have tracheobronchomegaly as an underlying primary airway abnormality on imaging and bronchoscopy that was initially undiagnosed.
气管支气管肥大或Mounier-Kuhn综合征是一种影响气道的罕见疾病,其特征是继发于软骨弹性纤维萎缩或缺失和肌肉变薄的气管和主支气管扩张。[1] 支气管树异常增大的松弛部分在呼气和咳嗽时塌陷,无法保持通畅,使患者容易出现内容物停滞和反复出现下呼吸道感染、肺气肿、支气管扩张和慢性肺部化脓。[2] 诊断通常基于特定的放射学特征,[3]特别是计算机断层扫描(CT)。我们报告了一例69岁的男性患者,他出现反复的下呼吸道感染,并在成像和支气管镜检查中发现气管支气管扩张是一种潜在的原发性气道异常,最初未被诊断。
{"title":"Tracheobronchomegaly (Mounier-Kuhn Syndrome) in Old Age - A Case Report","authors":"Khawaja Bilal Waheed, Jawad Nasser, Raghad Hamdi Alsaidalani, Zubair Ahmed","doi":"10.14260/jemds.v12i1.324","DOIUrl":"https://doi.org/10.14260/jemds.v12i1.324","url":null,"abstract":"Tracheobronchomegaly or Mounier-Kuhn syndrome is a rare condition affecting the airways and is characterized by dilatation of the trachea and major bronchi secondary to atrophic or absent elastic fibres of the cartilage and thinning of the muscles.[1] The abnormally enlarged flaccid portions of the bronchial tree collapse and fail to maintain patency during expiration and coughing, predisposing the patient to stagnation of contents and recurrent lower respiratory tract infections, emphysema, bronchiectasis and chronic pulmonary suppuration.[2] The diagnosis is usually made on basis of specific radiographic features,[3] particularly on computed tomography (CT) scan. We report a case of a 69-year-old man who presented with recurrent lower respiratory tract infections and was found to have tracheobronchomegaly as an underlying primary airway abnormality on imaging and bronchoscopy that was initially undiagnosed.","PeriodicalId":47072,"journal":{"name":"Journal of Evolution of Medical and Dental Sciences-JEMDS","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"45848757","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}
引用次数: 0
Cytogenetic Analysis in Patients with Azoospermia 无精子症患者的细胞遗传学分析
Pub Date : 2023-01-31 DOI: 10.14260/jemds.v12i1.319
Asja Begovac, Mirela Mačkić-Đurović, Aganović-Mušinović
BACKGROUND Azoospermia (the absence of sperm in the semen) significantly amounts to infertility in men (15 % of infertile men). Since genetics plays a huge part in its origin, genetic testing needs to be considered as an important part of early diagnostics when evaluating azoospermic patients. The aim of our study was to determine the genetic cause of azoospermia, to analyze karyograms and the possible presence of Y chromosome microdeletion. METHODS The study included 20 men diagnosed with azoospermia. The oldest male was 50 and the youngest was 24 years old. They were sent for analysis of karyotype and microdeletions of the Y chromosome (AZF region) to the Center for Genetics of the Faculty of Medicine. RESULTS The results of the cytogenetic analysis showed 3/20 (15 %) of abnormal karyotypes. Three patients were identified with two different translocations that were not previously reported. Two brothers were identified with the same translocation between the short arm of chromosome 8 and the long arm of chromosome 17 [46, XY, t(8;17)(p23;q11)], after both of them had failed in-vitro fertilization (IVF). The third patient with chromosomal translocation between the short arm of chromosome 4 and the long arm of chromosome 11 [46, XY, t(4;11)(p16;q13)]. Molecular genetic analysis showed no Y chromosome microdeletion in any of these three cases. However, from the rest of the group, only one patient had Y chromosome microdeletion in the AZFc region (one of the most common causes of genetic azoospermia). His karyotype was normal. CONCLUSIONS Our study confirms that cytogenetic and molecular genetic analysis plays an important role in identifying the cause of azoospermia. Genetic counseling should be provided when these abnormalities are identified before making any future medical decisions.
背景无精子症(精液中没有精子)是男性不育的重要原因(占不育男性的15%)。由于遗传学在其起源中起着重要作用,在评估无精子症患者时,基因检测需要被视为早期诊断的重要组成部分。我们研究的目的是确定无精子症的遗传原因,分析核型和Y染色体微缺失的可能存在。方法本研究包括20名被诊断为无精子症的男性。年龄最大的男性50岁,最小的24岁。他们被送往医学院遗传学中心进行Y染色体(AZF区)的核型和微缺失分析。结果细胞遗传学分析结果显示3/20(15%)的异常核型。三名患者被发现有两种不同的易位,这两种易位以前没有报道过。两兄弟在8号染色体的短臂和17号染色体的长臂之间存在相同的易位[46,XY,t(8;17)(p23;q11)],因为他们都失败了体外受精(IVF)。第三例患者在4号染色体短臂和11号染色体长臂之间发生染色体易位[46,XY,t(4;11)(p16;q13)]。分子遗传学分析显示,这三个病例中的任何一个都没有Y染色体微缺失。然而,在该组的其他患者中,只有一名患者在AZFc区域有Y染色体微缺失(遗传性无精子症最常见的原因之一)。他的核型正常。结论我们的研究证实细胞遗传学和分子遗传学分析在确定无精子症的病因方面起着重要作用。在做出任何未来的医疗决定之前,当发现这些异常时,应该提供基因咨询。
{"title":"Cytogenetic Analysis in Patients with Azoospermia","authors":"Asja Begovac, Mirela Mačkić-Đurović, Aganović-Mušinović","doi":"10.14260/jemds.v12i1.319","DOIUrl":"https://doi.org/10.14260/jemds.v12i1.319","url":null,"abstract":"BACKGROUND \u0000Azoospermia (the absence of sperm in the semen) significantly amounts to infertility in men (15 % of infertile men). Since genetics plays a huge part in its origin, genetic testing needs to be considered as an important part of early diagnostics when evaluating azoospermic patients. The aim of our study was to determine the genetic cause of azoospermia, to analyze karyograms and the possible presence of Y chromosome microdeletion. \u0000METHODS \u0000The study included 20 men diagnosed with azoospermia. The oldest male was 50 and the youngest was 24 years old. They were sent for analysis of karyotype and microdeletions of the Y chromosome (AZF region) to the Center for Genetics of the Faculty of Medicine. \u0000RESULTS \u0000The results of the cytogenetic analysis showed 3/20 (15 %) of abnormal karyotypes. Three patients were identified with two different translocations that were not previously reported. Two brothers were identified with the same translocation between the short arm of chromosome 8 and the long arm of chromosome 17 [46, XY, t(8;17)(p23;q11)], after both of them had failed in-vitro fertilization (IVF). The third patient with chromosomal translocation between the short arm of chromosome 4 and the long arm of chromosome 11 [46, XY, t(4;11)(p16;q13)]. Molecular genetic analysis showed no Y chromosome microdeletion in any of these three cases. However, from the rest of the group, only one patient had Y chromosome microdeletion in the AZFc region (one of the most common causes of genetic azoospermia). His karyotype was normal. \u0000CONCLUSIONS \u0000Our study confirms that cytogenetic and molecular genetic analysis plays an important role in identifying the cause of azoospermia. Genetic counseling should be provided when these abnormalities are identified before making any future medical decisions.","PeriodicalId":47072,"journal":{"name":"Journal of Evolution of Medical and Dental Sciences-JEMDS","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"48893995","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}
引用次数: 0
Effect of Negative Pressure Wound Therapy on Diabetic Foot Ulcers 负压创伤治疗糖尿病足溃疡疗效观察
Pub Date : 2023-01-31 DOI: 10.14260/jemds.v12i1.318
Prerana Raju Gudimetla, Swarnadeepu Shabasu, Akshay Duppelly, Yadagiri Rao Jeripotula
BACKGROUND In this study, we wanted to evaluate the effect of negative pressure wound therapy on diabetic foot ulcers. METHODS This was a hospital based prospective comparative study, conducted among 40 patients who came for treatment of diabetic foot ulcers to the Department of General Surgery, Kamineni Academy of Medical Sciences and Research Centre, Hyderabad, Telangana, over a period of 2 years from September 2019 to September 2021, after obtaining clearance from Institutional Ethics Committee and written informed consent from the study participants. RESULTS The increase in amount of granulation tissue negative pressure wound therapy (NPWT) and saline-soaked gauzed dressing (SSGD groups were found to be statistically significant. Mean change (increase in granulation tissue in NPWT & SSGD groups) from day 0 to day 42 were 78.083 % and 66.103 % respectively. Whereas in NPWT and SSGD groups, the size of ulcer was decreased which was statistically significant. Mean decrease in ulcer size in NPWT & SSGD groups from day 0 to day 42 were 52 cm sq and 29.15 cm sq respectively. The mean duration of stay in hospital in NPWT & SSGD groups were 29.35 + 4.51 days and 32.75 + 4.75 days with p value of 0.02, which is statistically significant. Among patients with NPWT, response was present in 95 % (19) patients and among patients with SSGD, response was present in 85 % (17) patients. The association between the groups was found to be statistically not significant. CONCLUSIONS Length of stay was shorter in the NPWT group when compared with that of SSGD group. Rate of granulation tissue formation was faster in NPWT group when compared to SSGD group. Reduction in ulcer size was significantly better in the NPWT group. Patient compliance and satisfaction was better in NPWT group. Lesser number of changes of dressings were needed in the NPWT group. It could be concluded that negative pressure wound therapy helps in faster healing, better, safe, and convenient as compared to saline soaked gauzed dressing in the treatment of diabetic foot ulcers.
背景在本研究中,我们想评估负压伤口治疗糖尿病足溃疡的效果。方法这是一项基于医院的前瞻性比较研究,在2019年9月至2021年9月的2年时间里,对40名来特伦甘纳海得拉巴卡米尼医学科学院和研究中心普通外科治疗糖尿病足溃疡的患者进行了研究,在获得机构伦理委员会的批准和研究参与者的书面知情同意后。结果肉芽组织负压伤口治疗(NPWT)和生理盐水浸泡纱布敷料(SSGD组)的量增加具有统计学意义,从第0天到第42天的平均变化(NPWT和SSGD组肉芽组织增加)分别为78.083%和66.103%。而在NPWT和SSGD组中,溃疡的大小减小,这具有统计学意义。从第0天到第42天,NPWT和SSGD组溃疡面积的平均减少分别为52平方厘米和29.15平方厘米。NPWT和SSGD组的平均住院时间分别为29.35+4.51天和32.75+4.75天,p值为0.02,具有统计学意义。在NPWT患者中,95%(19)的患者存在应答,在SSGD患者中,85%(17)的患者出现应答。两组之间的关联在统计学上并不显著。结论与SSGD组相比,NPWT组的住院时间更短。与SSGD组相比,NPWT组的肉芽组织形成速率更快。NPWT组的溃疡缩小程度明显更好。NPWT组患者依从性和满意度较好。NPWT组需要较少次数的敷料更换。可以得出结论,与盐水浸泡的纱布敷料相比,负压伤口治疗有助于更快、更好、安全和方便地治疗糖尿病足溃疡。
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引用次数: 0
Thyroid Disorders in Pregnancy and Their Maternal and Foetal Outcome in Tertiary Care Centre 妊娠期甲状腺疾病及其在三级保健中心的母婴结局
Pub Date : 2023-01-31 DOI: 10.14260/jemds.v12i1.321
Vasani Asha Kuvarji, Tahseen Fathima, Susham S Shetty, Chandaa Vinodkumar Jakkannavar, Sangeetha K, Radha Nair, Nisarg Sutaria, Pramukh Hegde
BACKGROUND In pregnant women, thyroid disorders are common endocrine problems and due to non-specific symptoms and hyper-metabolic state of pregnancy they are often neglected. To know the prevalence of thyroid disorders in pregnant women and their maternal and foetal outcome was the purpose of this study. METHODS This was an observational study which was conducted from 15th November 2021 to 15th May 2022 in the Department of Obstetrics and Gynaecology, Srinivas Medical College, Mukka, (Mangalore). Registration of one fifty pregnant women attending antenatal clinic in first trimester was done. Detailed history and examination was done. Thyroid stimulating hormone (TSH), free triiodothyronine (FT3) and free thyroxine (FT4) level evaluation was done apart from routine antenatal investigations. RESULTS Among 150 pregnant women, the prevalence of thyroid disorders is 14 (9.31 %). Subclinical hypothyroidism 9 (6 %) was the most common thyroid disorder observed. Maternal anaemia and eclampsia was most common complication 3 each (33.33 %). 1 (11 %) was antepartum haemorrhage. Thyroid disorder occurred during the 2nd trimester 58.33 %; 25 % and 16.66 % in 1st and 3rd trimester. Most commonly observed foetal birth weight in this study were between 2 - 2.5 kgs 7 (77.77 %). Most common foetal complication observed were foetal growth restriction (five) with spontaneous abortion and intra uterine foetal demise (IUFD) (one each) was noted. Out of all thyroid disorders associated with pregnancy, subclinical hypothyroidism is the most frequently noted. Patients with subclinical hypothyroidism remain asymptomatic when not treated, but had bad obstetric and neonatal outcome, although less severe than overt hypothyroidism cases. CONCLUSIONS Timely screening of pregnant women is required during pregnancy for the prevention of pregnancy which helps in the early diagnosis and management of complications related to maternal and foetus due to thyroid disorders.
背景在孕妇中,甲状腺疾病是常见的内分泌问题,由于妊娠期的非特异性症状和高代谢状态,它们往往被忽视。了解孕妇甲状腺疾病的患病率及其母婴结局是本研究的目的。方法这是一项观察性研究,于2021年11月15日至2022年5月15日在芒格洛尔穆卡斯里尼瓦斯医学院妇产科进行。对妊娠早期到产前诊所就诊的150名孕妇进行了登记。做了详细的病史和检查。除常规产前检查外,还对促甲状腺激素(TSH)、游离三碘甲状腺原氨酸(FT3)和游离甲状腺素(FT4)水平进行了评估。结果150例孕妇甲状腺疾病患病率为14例(9.31%)。亚临床甲状腺功能减退9例(6%)是观察到的最常见的甲状腺疾病。母亲贫血和子痫是最常见的并发症,各有3例(33.33%)。产前出血1例(11%)。甲状腺疾病发生在妊娠中期58.33%;妊娠早期和晚期分别为25%和16.66%。在这项研究中,最常见的胎儿出生体重在2-2.5公斤7之间(77.77%)。观察到的最常见的胎儿并发症是胎儿生长受限(5例)、自然流产和宫内胎儿死亡(IUFD)(各1例)。在所有与妊娠相关的甲状腺疾病中,亚临床甲状腺功能减退症是最常见的。亚临床甲状腺功能减退症患者在未接受治疗时仍无症状,但产科和新生儿预后较差,尽管其严重程度低于显性甲状腺功能减退病例。结论在妊娠期间需要及时对孕妇进行筛查以预防妊娠,这有助于早期诊断和管理与母体和胎儿有关的甲状腺疾病并发症。
{"title":"Thyroid Disorders in Pregnancy and Their Maternal and Foetal Outcome in Tertiary Care Centre","authors":"Vasani Asha Kuvarji, Tahseen Fathima, Susham S Shetty, Chandaa Vinodkumar Jakkannavar, Sangeetha K, Radha Nair, Nisarg Sutaria, Pramukh Hegde","doi":"10.14260/jemds.v12i1.321","DOIUrl":"https://doi.org/10.14260/jemds.v12i1.321","url":null,"abstract":"BACKGROUND \u0000In pregnant women, thyroid disorders are common endocrine problems and due to non-specific symptoms and hyper-metabolic state of pregnancy they are often neglected. To know the prevalence of thyroid disorders in pregnant women and their maternal and foetal outcome was the purpose of this study. \u0000METHODS \u0000This was an observational study which was conducted from 15th November 2021 to 15th May 2022 in the Department of Obstetrics and Gynaecology, Srinivas Medical College, Mukka, (Mangalore). Registration of one fifty pregnant women attending antenatal clinic in first trimester was done. Detailed history and examination was done. Thyroid stimulating hormone (TSH), free triiodothyronine (FT3) and free thyroxine (FT4) level evaluation was done apart from routine antenatal investigations. \u0000RESULTS \u0000Among 150 pregnant women, the prevalence of thyroid disorders is 14 (9.31 %). Subclinical hypothyroidism 9 (6 %) was the most common thyroid disorder observed. Maternal anaemia and eclampsia was most common complication 3 each (33.33 %). 1 (11 %) was antepartum haemorrhage. Thyroid disorder occurred during the 2nd trimester 58.33 %; 25 % and 16.66 % in 1st and 3rd trimester. Most commonly observed foetal birth weight in this study were between 2 - 2.5 kgs 7 (77.77 %). Most common foetal complication observed were foetal growth restriction (five) with spontaneous abortion and intra uterine foetal demise (IUFD) (one each) was noted. Out of all thyroid disorders associated with pregnancy, subclinical hypothyroidism is the most frequently noted. Patients with subclinical hypothyroidism remain asymptomatic when not treated, but had bad obstetric and neonatal outcome, although less severe than overt hypothyroidism cases. \u0000CONCLUSIONS \u0000Timely screening of pregnant women is required during pregnancy for the prevention of pregnancy which helps in the early diagnosis and management of complications related to maternal and foetus due to thyroid disorders.","PeriodicalId":47072,"journal":{"name":"Journal of Evolution of Medical and Dental Sciences-JEMDS","volume":"1 1","pages":""},"PeriodicalIF":0.0,"publicationDate":"2023-01-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41379232","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}
引用次数: 0
Outcome of Concurrent Chemoradiation after Induction Chemotherapy in Locally Advanced Head and Neck Squamous Cell Carcinoma - A Prospective Study among Patients Attending a Tertiary Care Center in Kerala, India 局部晚期头颈部鳞状细胞癌诱导化疗后同步放化疗的结果-印度喀拉拉邦三级保健中心患者的前瞻性研究
Pub Date : 2023-01-31 DOI: 10.14260/jemds.v12i1.322
Preeya Vasanthakumary, Binitha Tresa Thomas, Devi Mohan
BACKGROUND Concurrent chemoradiation (CCRT) is the standard of care for locally advanced head and neck squamous cell carcinoma (LAHNSCC). In settings with considerable waiting period for radiation, institutional protocols advocate induction chemotherapy before CCRT. This study aimed to assess the outcome of concurrent chemoradiation after induction of chemotherapy among patients with LAHNSCC attending a tertiary care radiotherapy center in Kerala, India. METHODS Patients with non-metastatic LAHNSCC (stage 111 and 1V) with good performance score of 0-1 who received induction chemotherapy (with docetaxel 75mg/m2and cisplatin 75 mg/m2, day 1 and 5-fluorouracil 750 mg/m2, day 1 and 2 as infusion every 3 weeks for 3 cycles) followed by CCRT (with concurrent cisplatin 40 mg/m2 weekly) were selected for the study. CCRT was administered only to those patients who showed more than 30 % response to induction chemotherapy. They were followed up for 24 months. The primary end point was the clinical response assessed by ENT evaluation 8 weeks after the completion of CCRT. RESULTS 117 patients with LAHNSCC were enrolled. Four patients (3.4 %) dropped out after induction therapy. Out of 113 patients who initiated concurrent chemo radiation, two patients (1.7 %) dropped out while on CCRT, two patients (1.7 %) were intolerant to CCRT and two patients (1.7 %) left soon after CCRT. 107 patients were available for follow up after treatment completion. Acute toxicities were noticed in 9 (7.7 %) while on induction treatment. Mucositis occurred in 1 (0.9 %), haematological toxicities in 4 (3.4 %), gastrointestinal toxicities in 2 (1.7 %) and fatigue and malaise in 2 (1.7 %). In patients who underwent concurrent chemo radiation, 53 (49.03 %) had acute mucosal, skin, GIT and haematological toxicities. On treatment completion, 82 patients (70.1 %) had complete response, 24 (20.5 %) had partial response and one (0.9 %) had stable disease. During the follow up period of 24 months, locoregional failure (relapse) was noted in 15 patients (12.8 %) while 61 patients (52.1 %) remained disease free. Organ preservation rate was 53.4 % for laryngeal primaries. 4 patients (3.4 %) developed distant metastases during the follow up. CONCLUSIONS Induction chemotherapy with docetaxel containing regime followed by concurrent chemoradiation was associated with good clinical response and acceptable toxicity profile.
背景:同步放化疗(CCRT)是局部晚期头颈部鳞状细胞癌(LAHNSCC)的标准治疗方法。在放疗等待时间较长的情况下,机构方案提倡在CCRT前进行诱导化疗。本研究旨在评估在印度喀拉拉邦三级护理放疗中心接受LAHNSCC患者诱导化疗后同步放化疗的结果。方法选择表现评分为0-1分的非转移性LAHNSCC(111期和1V期)患者,接受诱导化疗(多西他赛75mg/m2 +顺铂75mg/m2,第1天,5-氟尿嘧啶750 mg/m2,第1天和第2天输注,每3周,共3个周期),然后进行CCRT(同时顺铂40mg /m2,每周)。CCRT仅用于对诱导化疗反应超过30%的患者。他们被随访了24个月。主要终点是完成CCRT后8周通过耳鼻喉科评估评估的临床反应。结果入选117例LAHNSCC患者。4例患者(3.4%)在诱导治疗后退出。在113名开始同步放化疗的患者中,2名患者(1.7%)在CCRT期间退出,2名患者(1.7%)对CCRT不耐受,2名患者(1.7%)在CCRT后不久离开。107例患者治疗完成后可随访。诱导治疗时出现急性毒性9例(7.7%)。粘膜炎1例(0.9%),血液学毒性4例(3.4%),胃肠道毒性2例(1.7%),疲劳和不适2例(1.7%)。在接受同步放化疗的患者中,53例(49.03%)出现急性粘膜、皮肤、胃肠道和血液学毒性。治疗结束时,82例患者(70.1%)完全缓解,24例(20.5%)部分缓解,1例(0.9%)病情稳定。在24个月的随访期间,15例(12.8%)患者出现局部失败(复发),61例(52.1%)患者无病。喉部原发病变的器官保存率为53.4%。4例(3.4%)患者在随访期间发生远处转移。结论:多西紫杉醇诱导化疗后同步放化疗具有良好的临床疗效和可接受的毒性特征。
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Journal of Evolution of Medical and Dental Sciences-JEMDS
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