首页 > 最新文献

Lung India最新文献

英文 中文
RV in COPD - The complicated matters of the heart - Correlation of ECHO and biomarker with COPD severity and outcome. 慢性阻塞性肺病中的左心室--复杂的心脏问题--ECHO 和生物标志物与慢性阻塞性肺病严重程度和预后的相关性。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_351_23
Rajesh Bhat, Sindhu Kamath, Arpit Jain, Vishak Acharya, Thomas Antony, Ramesh Holla, Abhavya Jha

Background: Patients with chronic obstructive pulmonary disease (COPD) have an increased risk of cardiovascular involvement, which is among the leading causes of morbidity and mortality worldwide. Echocardiography (ECHO) could be a reliable, non-invasive tool for predicting the risk of cardiovascular modalities in patients with COPD. Combining the ECHO parameters with highly selective cardiac troponin could predict the severity and outcome of patients with COPD.

Methods: This prospective observational study was conducted at a tertiary care hospital in South India. All patients who met the criteria were included. Patients with other concomitant chronic lung diseases were excluded. An echocardiographic examination was performed, and blood samples for hs-Tnt were taken on admission for patients admitted with COPD. Categorical variables were analyzed using Pearson's Chi-square test, and the T-test was used to compare the means. One-way analysis of variance (ANOVA) followed by the Bonferroni multiple comparison tests was done to compare different echo parameters concerning COPD severity.

Results: The mean tricuspid annulus plane systolic excursion (TAPSE) and right ventricle (RV) fraction area change (FAC) values were lower with the increase in the disease severity (P < 0.001). There was a significant increase in the mean systolic pressures in the right atrium and ventricle in patients with severe COPD (P < 0.001). The mean hs-TnT values were significantly higher in patients with severe COPD (18.86 ± 18.12) and correlated well with the increase in the severity of the disease (P < 0.001). Changes in the echo parameters, such as mean TAPSE and RV FAC values, negatively correlated with COPD severity. There was an increase in systolic pressure in both atria and ventricles with the progression of COPD. Troponin helped predict mortality during hospitalization.

Conclusion: Comprehensive echocardiographic parameters, such as TAPSE and RV FAC, help assess the disease's severity, predict mortality, and evaluate whether the proper ventricular function is reliable. Troponin is a valuable adjunct that is an independent and strong predictor of overall mortality in patients with COPD.

背景:慢性阻塞性肺疾病(COPD)患者受心血管疾病影响的风险增加,而心血管疾病是全球发病率和死亡率的主要原因之一。超声心动图(ECHO)是预测慢性阻塞性肺病患者心血管疾病风险的可靠、无创工具。将超声心动图参数与高选择性心肌肌钙蛋白相结合,可以预测慢性阻塞性肺病患者的病情严重程度和预后:这项前瞻性观察研究在印度南部的一家三级医院进行。所有符合标准的患者均被纳入研究。排除了合并其他慢性肺部疾病的患者。对慢性阻塞性肺病患者进行超声心动图检查,并在入院时抽取血液样本检测 hs-Tnt。分类变量的分析采用皮尔逊卡方检验(Pearson's Chi-square test),平均值的比较采用T检验。采用单因素方差分析(ANOVA)和Bonferroni多重比较检验来比较有关慢性阻塞性肺病严重程度的不同回声参数:结果:三尖瓣环平面收缩期平均偏移(TAPSE)和右心室(RV)分数面积变化(FAC)值随病情严重程度的增加而降低(P < 0.001)。严重慢性阻塞性肺病患者右心房和右心室的平均收缩压明显升高(P < 0.001)。重度慢性阻塞性肺病患者的 hs-TnT 平均值明显更高(18.86 ± 18.12),且与病情严重程度的增加密切相关(P < 0.001)。平均 TAPSE 值和 RV FAC 值等回声参数的变化与慢性阻塞性肺病的严重程度呈负相关。随着慢性阻塞性肺病病情的发展,心房和心室的收缩压都会升高。肌钙蛋白有助于预测住院期间的死亡率:结论:综合超声心动图参数,如 TAPSE 和 RV FAC,有助于评估疾病的严重程度、预测死亡率以及评估适当的心室功能是否可靠。肌钙蛋白是一种有价值的辅助指标,可独立且有力地预测慢性阻塞性肺病患者的总体死亡率。
{"title":"RV in COPD - The complicated matters of the heart - Correlation of ECHO and biomarker with COPD severity and outcome.","authors":"Rajesh Bhat, Sindhu Kamath, Arpit Jain, Vishak Acharya, Thomas Antony, Ramesh Holla, Abhavya Jha","doi":"10.4103/lungindia.lungindia_351_23","DOIUrl":"10.4103/lungindia.lungindia_351_23","url":null,"abstract":"<p><strong>Background: </strong>Patients with chronic obstructive pulmonary disease (COPD) have an increased risk of cardiovascular involvement, which is among the leading causes of morbidity and mortality worldwide. Echocardiography (ECHO) could be a reliable, non-invasive tool for predicting the risk of cardiovascular modalities in patients with COPD. Combining the ECHO parameters with highly selective cardiac troponin could predict the severity and outcome of patients with COPD.</p><p><strong>Methods: </strong>This prospective observational study was conducted at a tertiary care hospital in South India. All patients who met the criteria were included. Patients with other concomitant chronic lung diseases were excluded. An echocardiographic examination was performed, and blood samples for hs-Tnt were taken on admission for patients admitted with COPD. Categorical variables were analyzed using Pearson's Chi-square test, and the T-test was used to compare the means. One-way analysis of variance (ANOVA) followed by the Bonferroni multiple comparison tests was done to compare different echo parameters concerning COPD severity.</p><p><strong>Results: </strong>The mean tricuspid annulus plane systolic excursion (TAPSE) and right ventricle (RV) fraction area change (FAC) values were lower with the increase in the disease severity (P < 0.001). There was a significant increase in the mean systolic pressures in the right atrium and ventricle in patients with severe COPD (P < 0.001). The mean hs-TnT values were significantly higher in patients with severe COPD (18.86 ± 18.12) and correlated well with the increase in the severity of the disease (P < 0.001). Changes in the echo parameters, such as mean TAPSE and RV FAC values, negatively correlated with COPD severity. There was an increase in systolic pressure in both atria and ventricles with the progression of COPD. Troponin helped predict mortality during hospitalization.</p><p><strong>Conclusion: </strong>Comprehensive echocardiographic parameters, such as TAPSE and RV FAC, help assess the disease's severity, predict mortality, and evaluate whether the proper ventricular function is reliable. Troponin is a valuable adjunct that is an independent and strong predictor of overall mortality in patients with COPD.</p>","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"192-199"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093146/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140858827","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comprehensive textbook of allergy - Striking the Right Balance. 过敏症综合教科书--《取得适当的平衡》。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_138_24
Rajesh Swarnakar
{"title":"Comprehensive textbook of allergy - Striking the Right Balance.","authors":"Rajesh Swarnakar","doi":"10.4103/lungindia.lungindia_138_24","DOIUrl":"10.4103/lungindia.lungindia_138_24","url":null,"abstract":"","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"229"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093135/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140867052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Prevalence of frailty among chronic respiratory disease patients. 慢性呼吸系统疾病患者体弱的普遍性。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_464_23
Rm Pl Ramanathan, Sivaguru Muthusamy, Krishna J Kumar, Anusuya Krishnan

Background: Although frailty is one of the aging syndromes, it can occur at a younger age and in individuals with organ diseases. Identifying frailty and pre-frailty in patients with chronic respiratory diseases (CRDs) is an emerging assessment in the field of pulmonary medicine and rehabilitation. The aim of this study was to find out the prevalence of frailty among chronic respiratory disease patients.

Methods: A single centre cross-sectional survey study with a total population of 381 patients, adults aged 18-90 years presenting to the pulmonology OPD was included based on the inclusion and exclusion criteria. Primary data collected were demographics, medical history, including comorbidities, use of long-term oxygen therapy (LTOT), BiPAP (Bilevel Positive Airway Pressure), previous hospital admissions, medication history and frailty assessment were done using the Fried frailty index.

Results: Univariate analysis showed that sex, ECHO abnormality, patients using LTOT, BiPAP, home nebulizers and patients who did not attend the pulmonary rehabilitation programme had a significant association with frailty. Multivariate analysis showed that female sex, LTOT use and older age were significantly associated with frailty.

Conclusion: Frailty is frequent in CRD patients regardless of age. The prevalence of frailty has an association with female sex, patients using LTOT, and home BiPAP.

背景:虽然虚弱是衰老综合征之一,但它可以发生在更年轻的年龄和患有器官疾病的人身上。在慢性呼吸系统疾病(CRDs)患者中识别虚弱和虚弱前期是肺部医学和康复领域的一项新兴评估。本研究旨在了解慢性呼吸系统疾病患者体弱的发生率:根据纳入和排除标准,研究纳入了在肺科门诊就诊的 381 名 18-90 岁成人患者,这是一项单中心横断面调查研究。收集的主要数据包括人口统计学特征、病史(包括合并症)、长期氧疗(LTOT)和双水平气道正压(BiPAP)的使用情况、既往入院情况、用药史,并使用弗里德虚弱指数进行虚弱评估:单变量分析显示,性别、ECHO异常、使用LTOT、BiPAP、家用雾化器的患者以及未参加肺康复计划的患者与虚弱有显著关联。多变量分析表明,女性、使用LTOT和年龄较大与虚弱有显著相关性:结论:体弱在慢性阻塞性肺病患者中很常见,与年龄无关。结论:慢性阻塞性肺病患者无论年龄多大,都经常出现体弱的情况。体弱的发生率与女性、使用LTOT的患者和家用BiPAP有关。
{"title":"Prevalence of frailty among chronic respiratory disease patients.","authors":"Rm Pl Ramanathan, Sivaguru Muthusamy, Krishna J Kumar, Anusuya Krishnan","doi":"10.4103/lungindia.lungindia_464_23","DOIUrl":"10.4103/lungindia.lungindia_464_23","url":null,"abstract":"<p><strong>Background: </strong>Although frailty is one of the aging syndromes, it can occur at a younger age and in individuals with organ diseases. Identifying frailty and pre-frailty in patients with chronic respiratory diseases (CRDs) is an emerging assessment in the field of pulmonary medicine and rehabilitation. The aim of this study was to find out the prevalence of frailty among chronic respiratory disease patients.</p><p><strong>Methods: </strong>A single centre cross-sectional survey study with a total population of 381 patients, adults aged 18-90 years presenting to the pulmonology OPD was included based on the inclusion and exclusion criteria. Primary data collected were demographics, medical history, including comorbidities, use of long-term oxygen therapy (LTOT), BiPAP (Bilevel Positive Airway Pressure), previous hospital admissions, medication history and frailty assessment were done using the Fried frailty index.</p><p><strong>Results: </strong>Univariate analysis showed that sex, ECHO abnormality, patients using LTOT, BiPAP, home nebulizers and patients who did not attend the pulmonary rehabilitation programme had a significant association with frailty. Multivariate analysis showed that female sex, LTOT use and older age were significantly associated with frailty.</p><p><strong>Conclusion: </strong>Frailty is frequent in CRD patients regardless of age. The prevalence of frailty has an association with female sex, patients using LTOT, and home BiPAP.</p>","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"181-184"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093132/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140858299","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Gerhardt's syndrome misdiagnosed as asthma. 格哈特综合征被误诊为哮喘。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_521_23
Lili Hou, Ying Gong, Lei Zhu
{"title":"Gerhardt's syndrome misdiagnosed as asthma.","authors":"Lili Hou, Ying Gong, Lei Zhu","doi":"10.4103/lungindia.lungindia_521_23","DOIUrl":"10.4103/lungindia.lungindia_521_23","url":null,"abstract":"","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"218-220"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093141/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140869454","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Isolated tracheal mucormycosis in diabetes mellitus and bronchoscopic management. 糖尿病患者的孤立气管粘液瘤病及支气管镜治疗。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_45_24
Vikram Damaraju, Ritesh Agarwal, Nidhi Prabhakar, Amanjit Bal, Shivaprakash M Rudramurthy, Valliappan Muthu
{"title":"Isolated tracheal mucormycosis in diabetes mellitus and bronchoscopic management.","authors":"Vikram Damaraju, Ritesh Agarwal, Nidhi Prabhakar, Amanjit Bal, Shivaprakash M Rudramurthy, Valliappan Muthu","doi":"10.4103/lungindia.lungindia_45_24","DOIUrl":"10.4103/lungindia.lungindia_45_24","url":null,"abstract":"","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"226-227"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093139/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140872906","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Clinical behaviour and mortality in idiopathic vs secondary nonspecific interstitial pneumonia. 特发性与继发性非特异性间质性肺炎的临床表现和死亡率。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2023-08-01 DOI: 10.4103/lungindia.lungindia_64_23
Thisarana Wijayaratne, James Owen, Ahmed Fahim

Rationale: Nonspecific interstitial pneumonia (NSIP) is a subtype of interstitial lung disease which can either be idiopathic or secondary to other conditions. Idiopathic NSIP is a relatively rare entity and diagnosis should be considered carefully as it is mainly a diagnosis of exclusion. The aim of this retrospective study was to evaluate a cohort of NSIP patients with a view to identifying any clinical and mortality differences between idiopathic and secondary varieties.

Methods: We screened 700 patients from our interstitial lung disease database and identified 44 cases of NSIP retrospectively. Statistical analysis was conducted to evaluate if there was a difference in demographics such as gender and ethnicity, physiological parameters including forced vital capacity, diffusing capacity, average oxygen saturations, and immunology profile between two groups. Furthermore, a difference in mortality was evaluated between idiopathic and secondary NSIP.

Results: The data analysis showed that 63.6% (28 of 44) of patients had idiopathic NSIP versus 36.4% (16 of 44) of patients had secondary NSIP. Majority of the secondary NSIP patients had an underlying connective tissue disease. In the idiopathic variety, there was a male preponderance (64.2%, P = .02) which was statistically different compared to relatively equal gender divide in secondary NSIP which was statistically insignificant (male vs. female: 43.8% vs. 56.3%, respectively, P = .42). The mean age of the idiopathic group was 74 years compared to 64 years in the secondary group which was statistically different (P = .01). In both groups (idiopathic and secondary NSIP), more than two-thirds (68%) were of White British ethnicity. Immunology profile was similar across both groups with no statistical difference in IgM, IgG, or IgA levels. At the time of analysis, there were 17.9% deaths (5 of 28) in the idiopathic NSIP group versus 6.3% (1 of 16) in the secondary NSIP group but this was not statistically significant (P = .14). Similarly, there was no statistically significant difference in the forced vital capacity (P = .59), diffusing capacity (P = .88), and resting oxygen saturations (P = .28) between idiopathic and secondary NSIP varieties.

Conclusion: Our analysis showed that there was a statistically significant difference in gender (male preponderance in idiopathic NSIP only) and mean age difference among both varieties. There were no statistically significant differences in the clinical features and outcomes including mortality, physiological, and immunological parameters between idiopathic and secondary NSIP. Idiopathic NSIP was more common than secondary NSIP and secondary NSIP is mostly due to underlying connective tissue disease.

理由:非特异性间质性肺炎(NSIP)是间质性肺病的一种亚型,可以是特发性的,也可以继发于其他疾病。特发性非特异性间质性肺炎是一种相对罕见的疾病,诊断时应慎重考虑,因为它主要是一种排除性诊断。这项回顾性研究的目的是对一组 NSIP 患者进行评估,以确定特发性和继发性之间在临床和死亡率方面的差异:我们从间质性肺病数据库中筛选出700名患者,并通过回顾性研究确定了44例NSIP患者。我们进行了统计分析,以评估两组患者在人口统计学(如性别和种族)、生理参数(包括强制生命容量、弥散容量、平均血氧饱和度和免疫学特征)方面是否存在差异。此外,还评估了特发性和继发性 NSIP 的死亡率差异:数据分析显示,特发性 NSIP 患者占 63.6%(44 人中有 28 人),而继发性 NSIP 患者占 36.4%(44 人中有 16 人)。大多数继发性 NSIP 患者有潜在的结缔组织疾病。在特发性NSIP患者中,男性占多数(64.2%,P = 0.02),这与继发性NSIP患者中相对平等的性别差异(男性对女性:分别为43.8%对56.3%,P = 0.42)有统计学差异。特发性组患者的平均年龄为 74 岁,而继发性组患者的平均年龄为 64 岁,两者之间存在统计学差异(P = .01)。两组患者(特发性和继发性 NSIP)中,超过三分之二(68%)为英国白人。两组患者的免疫学特征相似,IgM、IgG 或 IgA 水平无统计学差异。在分析时,特发性 NSIP 组的死亡人数为 17.9%(28 人中有 5 人死亡),而继发性 NSIP 组的死亡人数为 6.3%(16 人中有 1 人死亡),但两者没有统计学意义(P = .14)。同样,特发性和继发性NSIP品种之间的用力生命容量(P = .59)、弥散容量(P = .88)和静息氧饱和度(P = .28)差异也无统计学意义:我们的分析表明,特发性和继发性 NSIP 患者的性别和平均年龄差异具有统计学意义(特发性 NSIP 患者中男性居多)。特发性和继发性 NSIP 的临床特征和结果(包括死亡率、生理和免疫学参数)在统计学上没有明显差异。特发性 NSIP 比继发性 NSIP 更常见,而继发性 NSIP 主要是由于潜在的结缔组织疾病引起的。
{"title":"Clinical behaviour and mortality in idiopathic vs secondary nonspecific interstitial pneumonia.","authors":"Thisarana Wijayaratne, James Owen, Ahmed Fahim","doi":"10.4103/lungindia.lungindia_64_23","DOIUrl":"10.4103/lungindia.lungindia_64_23","url":null,"abstract":"<p><strong>Rationale: </strong>Nonspecific interstitial pneumonia (NSIP) is a subtype of interstitial lung disease which can either be idiopathic or secondary to other conditions. Idiopathic NSIP is a relatively rare entity and diagnosis should be considered carefully as it is mainly a diagnosis of exclusion. The aim of this retrospective study was to evaluate a cohort of NSIP patients with a view to identifying any clinical and mortality differences between idiopathic and secondary varieties.</p><p><strong>Methods: </strong>We screened 700 patients from our interstitial lung disease database and identified 44 cases of NSIP retrospectively. Statistical analysis was conducted to evaluate if there was a difference in demographics such as gender and ethnicity, physiological parameters including forced vital capacity, diffusing capacity, average oxygen saturations, and immunology profile between two groups. Furthermore, a difference in mortality was evaluated between idiopathic and secondary NSIP.</p><p><strong>Results: </strong>The data analysis showed that 63.6% (28 of 44) of patients had idiopathic NSIP versus 36.4% (16 of 44) of patients had secondary NSIP. Majority of the secondary NSIP patients had an underlying connective tissue disease. In the idiopathic variety, there was a male preponderance (64.2%, P = .02) which was statistically different compared to relatively equal gender divide in secondary NSIP which was statistically insignificant (male vs. female: 43.8% vs. 56.3%, respectively, P = .42). The mean age of the idiopathic group was 74 years compared to 64 years in the secondary group which was statistically different (P = .01). In both groups (idiopathic and secondary NSIP), more than two-thirds (68%) were of White British ethnicity. Immunology profile was similar across both groups with no statistical difference in IgM, IgG, or IgA levels. At the time of analysis, there were 17.9% deaths (5 of 28) in the idiopathic NSIP group versus 6.3% (1 of 16) in the secondary NSIP group but this was not statistically significant (P = .14). Similarly, there was no statistically significant difference in the forced vital capacity (P = .59), diffusing capacity (P = .88), and resting oxygen saturations (P = .28) between idiopathic and secondary NSIP varieties.</p><p><strong>Conclusion: </strong>Our analysis showed that there was a statistically significant difference in gender (male preponderance in idiopathic NSIP only) and mean age difference among both varieties. There were no statistically significant differences in the clinical features and outcomes including mortality, physiological, and immunological parameters between idiopathic and secondary NSIP. Idiopathic NSIP was more common than secondary NSIP and secondary NSIP is mostly due to underlying connective tissue disease.</p>","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"172-175"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093133/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140868571","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Computed tomography findings of COVID-19-associated pulmonary mucormycosis: Data from a multicenter retrospective study (Mucovi2), India. COVID-19 相关肺粘液瘤病的计算机断层扫描结果:印度一项多中心回顾性研究(Mucovi2)的数据。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_19_24
Valliappan Muthu, Ritesh Agarwal, Shivaprakash Mandya Rudramurthy, Deepak Thangaraju, Manoj Radhakishan Shevkani, Atul K Patel, Prakash Srinivas Shastri, Ashwini Tayade, Sudhir Bhandari, Vishwanath Gella, Jayanthi Savio, Surabhi Madan, Vinaykumar Hallur, Venkata Nagarjuna Maturu, Arjun Srinivasan, Nandini Sethuraman, Raminder Pal Singh Sibia, Sanjay Pujari, Ravindra Mehta, Tanu Singhal, Puneet Saxena, Varsha Gupta, Vasant Nagvekar, Parikshit Prayag, Dharmesh Patel, Immaculata Xess, Pratik Savaj, Inderpaul Singh Sehgal, Naresh Panda, Gayathri Devi Rajagopal, Riya Sandeep Parwani, Kamlesh Patel, Anuradha Deshmukh, Aruna Vyas, Raghava Rao Gandra, Srinivas Kishore Sistla, Priyadarshini A Padaki, Dharshni Ramar, Manoj Kumar Panigrahi, Saurav Sarkar, Bharani Rachagulla, Pattabhiraman Vallandaramam, Krishna Prabha Premachandran, Sunil Pawar, Piyush Gugale, Pradeep Hosamani, Sunil Narayan Dutt, Satish Nair, Hariprasad Kalpakkam, Sanjiv Badhwar, Kiran Kumar Kompella, Nidhi Singla, Amrita Prayag, Gagandeep Singh, Poorvesh Dhakecha, Arunaloke Chakrabarti
{"title":"Computed tomography findings of COVID-19-associated pulmonary mucormycosis: Data from a multicenter retrospective study (Mucovi2), India.","authors":"Valliappan Muthu, Ritesh Agarwal, Shivaprakash Mandya Rudramurthy, Deepak Thangaraju, Manoj Radhakishan Shevkani, Atul K Patel, Prakash Srinivas Shastri, Ashwini Tayade, Sudhir Bhandari, Vishwanath Gella, Jayanthi Savio, Surabhi Madan, Vinaykumar Hallur, Venkata Nagarjuna Maturu, Arjun Srinivasan, Nandini Sethuraman, Raminder Pal Singh Sibia, Sanjay Pujari, Ravindra Mehta, Tanu Singhal, Puneet Saxena, Varsha Gupta, Vasant Nagvekar, Parikshit Prayag, Dharmesh Patel, Immaculata Xess, Pratik Savaj, Inderpaul Singh Sehgal, Naresh Panda, Gayathri Devi Rajagopal, Riya Sandeep Parwani, Kamlesh Patel, Anuradha Deshmukh, Aruna Vyas, Raghava Rao Gandra, Srinivas Kishore Sistla, Priyadarshini A Padaki, Dharshni Ramar, Manoj Kumar Panigrahi, Saurav Sarkar, Bharani Rachagulla, Pattabhiraman Vallandaramam, Krishna Prabha Premachandran, Sunil Pawar, Piyush Gugale, Pradeep Hosamani, Sunil Narayan Dutt, Satish Nair, Hariprasad Kalpakkam, Sanjiv Badhwar, Kiran Kumar Kompella, Nidhi Singla, Amrita Prayag, Gagandeep Singh, Poorvesh Dhakecha, Arunaloke Chakrabarti","doi":"10.4103/lungindia.lungindia_19_24","DOIUrl":"10.4103/lungindia.lungindia_19_24","url":null,"abstract":"","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"221-224"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093136/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140872895","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Catamenial pneumothorax in thoracic endometriosis syndrome. 胸腔子宫内膜异位症综合征的卡他气胸
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-05-01 Epub Date: 2024-04-30 DOI: 10.4103/lungindia.lungindia_576_23
Surajit Chatterjee, Krishanu Mukhoti, Ankita Chakraborty
{"title":"Catamenial pneumothorax in thoracic endometriosis syndrome.","authors":"Surajit Chatterjee, Krishanu Mukhoti, Ankita Chakraborty","doi":"10.4103/lungindia.lungindia_576_23","DOIUrl":"10.4103/lungindia.lungindia_576_23","url":null,"abstract":"","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 3","pages":"217-218"},"PeriodicalIF":1.3,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11093147/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140861012","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Accuracy of endobronchial ultrasound (EBUS) in the staging of lung cancer - A comparison of staging EBUS with postoperative pathological nodal staging. 支气管内超声(EBUS)在肺癌分期中的准确性--EBUS分期与术后病理结节分期的比较。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-03-01 Epub Date: 2024-02-27 DOI: 10.4103/lungindia.lungindia_449_23
Eshita Shah, N Sankara Raman, Manish K Aggarwal, Amit Jain, Arushi Chokhani, Avinash Murugan, Rajiv Goyal, Laengmawia Darlong, Ullas Batra

Background: Endobronchial ultrasound-guided transbronchial fine-needle aspiration (EBUS-TBNA) has replaced mediastinoscopy as the preferred investigation for evaluating mediastinum in staging lung cancer. There is little evidence of mediastinal staging by EBUS-TBNA from India.

Objectives: To study endobronchial ultrasound's diagnostic accuracy in staging lung cancer.

Methodology: We retrospectively analysed patients operated on for lung cancer where EBUS was performed preoperatively for mediastinal staging. We compared the histological findings obtained from different mediastinal lymph nodes (LNs) by EBUS-TBNA with the pathology of the same LNs obtained after surgical dissection as the reference standard.

Results: Seventy-six patients underwent curative surgery for lung cancer. The diagnostic accuracy, sensitivity, specificity, positive predictive value and negative predictive value of EBUS-TBNA in predicting mediastinal metastasis were 93.9%, 40%, 99%, 80% and 94.6%, respectively. Of the 115 LNs sampled, EBUS-TBNA was false negative in six nodes, resulting in an up-staging of six patients.

Conclusions: EBUS-TBNA has a high diagnostic accuracy for lung cancer staging.

背景:支气管内超声引导下经支气管细针穿刺术(EBUS-TBNA)已取代纵隔镜检查,成为评估肺癌纵隔分期的首选检查方法。在印度,通过 EBUS-TBNA 进行纵隔分期的证据很少:研究支气管内超声对肺癌分期的诊断准确性:我们回顾性地分析了接受肺癌手术的患者,这些患者在术前进行了EBUS纵隔分期。我们将通过 EBUS-TBNA 获得的不同纵隔淋巴结(LN)的组织学结果与手术切除后获得的相同 LN 的病理学结果作为参考标准进行了比较:76名肺癌患者接受了根治性手术。EBUS-TBNA 预测纵隔转移的诊断准确率、敏感性、特异性、阳性预测值和阴性预测值分别为 93.9%、40%、99%、80% 和 94.6%。在取样的115个纵隔中,EBUS-TBNA对6个结节的预测为假阴性,导致6名患者向上分期:结论:EBUS-TBNA 对肺癌分期的诊断准确率很高。
{"title":"Accuracy of endobronchial ultrasound (EBUS) in the staging of lung cancer - A comparison of staging EBUS with postoperative pathological nodal staging.","authors":"Eshita Shah, N Sankara Raman, Manish K Aggarwal, Amit Jain, Arushi Chokhani, Avinash Murugan, Rajiv Goyal, Laengmawia Darlong, Ullas Batra","doi":"10.4103/lungindia.lungindia_449_23","DOIUrl":"10.4103/lungindia.lungindia_449_23","url":null,"abstract":"<p><strong>Background: </strong>Endobronchial ultrasound-guided transbronchial fine-needle aspiration (EBUS-TBNA) has replaced mediastinoscopy as the preferred investigation for evaluating mediastinum in staging lung cancer. There is little evidence of mediastinal staging by EBUS-TBNA from India.</p><p><strong>Objectives: </strong>To study endobronchial ultrasound's diagnostic accuracy in staging lung cancer.</p><p><strong>Methodology: </strong>We retrospectively analysed patients operated on for lung cancer where EBUS was performed preoperatively for mediastinal staging. We compared the histological findings obtained from different mediastinal lymph nodes (LNs) by EBUS-TBNA with the pathology of the same LNs obtained after surgical dissection as the reference standard.</p><p><strong>Results: </strong>Seventy-six patients underwent curative surgery for lung cancer. The diagnostic accuracy, sensitivity, specificity, positive predictive value and negative predictive value of EBUS-TBNA in predicting mediastinal metastasis were 93.9%, 40%, 99%, 80% and 94.6%, respectively. Of the 115 LNs sampled, EBUS-TBNA was false negative in six nodes, resulting in an up-staging of six patients.</p><p><strong>Conclusions: </strong>EBUS-TBNA has a high diagnostic accuracy for lung cancer staging.</p>","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 2","pages":"93-97"},"PeriodicalIF":1.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10959321/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140874928","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
A rare case of isoniazid mono-resistant tuberculosis presenting as cardiac tamponade along with an anterior mediastinal mass in a 15-year-old immunocompetent patient. 一例罕见的单耐药异烟肼结核病病例,患者 15 岁,免疫功能正常,表现为心脏填塞和前纵隔肿块。
IF 1.3 Q4 RESPIRATORY SYSTEM Pub Date : 2024-03-01 Epub Date: 2024-02-27 DOI: 10.4103/lungindia.lungindia_221_23
Richa Mishra, Ashima Jamwal, Bishal Gupta, Sudeep Kumar, Abhijeet Bharali, Parijat Das, Alok Nath, Manoj Jain, Zafar Neyaz

Abstract: A 15-year-old boy presented with a sudden onset of breathlessness for 7 days, gradual loss of weight of 17.6 lbs over the last month and progressive hoarseness of voice for 7 months. The contrast-enhanced computed tomography (CECT) scan revealed a heterogeneously enhancing lesion in the anterior mediastinum with multiple discrete lymph nodes in the cervical and mediastinal locations. The GeneXpert MTB/RIF assay performed on the CT-guided biopsy of the mass was negative, but the culture for Mycobacterium tuberculosis was positive at 7 weeks of incubation. There was a suboptimal radiological response after 6 months of treatment. First-line drug susceptibility testing (DST) performed by line probe assay (LPA) on the positive culture detected high-level resistance to isoniazid. The treatment was modified as per DST results to which the patient responded well.

摘要:一名15岁男孩突然出现呼吸困难7天,近一个月来体重逐渐减轻17.6磅,声音逐渐嘶哑7个月。造影剂增强计算机断层扫描(CECT)显示,前纵隔有异质性增强病灶,颈部和纵隔位置有多个离散淋巴结。在CT引导下对肿块进行活检时,基因Xpert MTB/RIF检测结果为阴性,但经7周培养后,结核分枝杆菌培养结果呈阳性。治疗 6 个月后,放射学反应不理想。用线探针检测法(LPA)对阳性培养物进行了一线药敏试验(DST),检测出了对异烟肼的高度耐药性。根据 DST 结果对治疗进行了调整,患者反应良好。
{"title":"A rare case of isoniazid mono-resistant tuberculosis presenting as cardiac tamponade along with an anterior mediastinal mass in a 15-year-old immunocompetent patient.","authors":"Richa Mishra, Ashima Jamwal, Bishal Gupta, Sudeep Kumar, Abhijeet Bharali, Parijat Das, Alok Nath, Manoj Jain, Zafar Neyaz","doi":"10.4103/lungindia.lungindia_221_23","DOIUrl":"10.4103/lungindia.lungindia_221_23","url":null,"abstract":"<p><strong>Abstract: </strong>A 15-year-old boy presented with a sudden onset of breathlessness for 7 days, gradual loss of weight of 17.6 lbs over the last month and progressive hoarseness of voice for 7 months. The contrast-enhanced computed tomography (CECT) scan revealed a heterogeneously enhancing lesion in the anterior mediastinum with multiple discrete lymph nodes in the cervical and mediastinal locations. The GeneXpert MTB/RIF assay performed on the CT-guided biopsy of the mass was negative, but the culture for Mycobacterium tuberculosis was positive at 7 weeks of incubation. There was a suboptimal radiological response after 6 months of treatment. First-line drug susceptibility testing (DST) performed by line probe assay (LPA) on the positive culture detected high-level resistance to isoniazid. The treatment was modified as per DST results to which the patient responded well.</p>","PeriodicalId":47462,"journal":{"name":"Lung India","volume":"41 2","pages":"130-134"},"PeriodicalIF":1.3,"publicationDate":"2024-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10959313/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140861011","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Lung India
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1