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Pulmonary Function and Respiratory Diseases in Different Genotypes of Alpha-1 Antitrypsin Deficiency. 不同基因型α -1抗胰蛋白酶缺乏症患者的肺功能与呼吸系统疾病
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22001
José María Hernández Pérez, Juan José Suárez Sánchez, Claudia Viviana López Charry, Yolanda Ramallo Fariña, José Antonio Pérez Pérez

Objective: Respiratory disease is the major cause of morbidity and mortality in patients with alpha-1 antitrypsin deficiency, mainly in homozygous PI*ZZ individuals. However, this association is uncertain in subjects with other deficiency genotypes. The objective of this study was to assess, in the context of alpha-1 antitrypsin deficiency, the existence of further risk factors that have been associated with respiratory diseases.

Material and methods: Lung function was assessed by spirometry in a sample of 1334 patients with a known genotype for the SERPINA1 gene whose serum alpha-1 antitrypsin levels had been previously determined. Patients with a normal genotype (PI*MM) were compared to 389 patients carrying a deficiency allele.

Results: Statistically significant associations were detected between (i) PI*ZZ genotype and abnormal FEV1 values (χ2 = 26.45; P <.0002), FEV1/FVC (χ2 = 14.8; P < .02) or forced mid-expiratory flow 25%-75% (χ2 =22.66; P < .0009); (ii) chronic obstructive pulmonary disease and PI*ZZ odds ratio: 26.5; 95% CI: (2.6-265.9); P <.005 and or PI*SS genotype odds ratio: 9; 95% CI: (2-40.1); P < .004; (iii) prevalence of COPD in PI*MZ subjects and smoking habit (P < .01), low body weight (P < .01) or older age (P < .0001).

Conclusion: The PI*ZZ and PI*SS genotypes seem to be associated with the prevalence of chronic obstructive pulmonary disease. Tobacco use, low body weight, and older age are risk factors that increase the probability of prevalence of chronic obstructive pulmonary disease by up to 70% in PI*MZ individuals.

目的:呼吸系统疾病是α -1抗胰蛋白酶缺乏症患者发病和死亡的主要原因,以纯合子PI*ZZ患者为主。然而,在其他基因型缺乏的受试者中,这种关联并不确定。本研究的目的是评估在α -1抗胰蛋白酶缺乏的情况下,是否存在与呼吸系统疾病相关的其他危险因素。材料和方法:在1334例已知SERPINA1基因型的患者样本中,通过肺活量测定法评估肺功能,这些患者的血清α -1抗胰蛋白酶水平先前已被确定。将正常基因型(PI*MM)患者与携带缺陷等位基因的389例患者进行比较。结果:(1)PI*ZZ基因型与FEV1异常值有统计学意义(χ2 = 26.45;结论:PI*ZZ和PI*SS基因型可能与慢性阻塞性肺疾病的患病率有关。烟草使用、体重过轻和年龄较大是使PI*MZ个体中慢性阻塞性肺病患病率增加高达70%的危险因素。
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引用次数: 0
Attitude and Practice Toward Use of Cigarettes and Electronic Cigarettes Among Pregnant Women: A Questionnaire-Based Survey. 孕妇使用香烟和电子烟的态度和行为:一项基于问卷的调查。
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22078
Elif Yıldırım, Serap Duru, Tülin Sevim, Füsun Topçu, Bilun Gemicioğlu, İpek Özmen, Birsen Ocaklı, Eylem Tuncay, Hilal Altınöz, Yaşam Kemal Akpak, Pınar Çelik, Yelda Varol, Gülru Polat, Serir Özkan, Neşe Dursunoğlu, Derya Kılıç, Pınar Yıldız Gülhan, Özlem Ercen Diken, Pelin Duru Çetinkaya, Arzu Yorgancıoğlu, Nursel Türkoğlu Selçuk, Füsun Yıldız, Tijen Atacağ, Elif Yelda Niksarlioğlu, Esra Uzaslan, Nurdan Köktürk

Objective: This study aimed to evaluate attitude and practice toward use of regular tobacco cigarettes and electronic cigarettes among pregnant women.

Material and methods: A total of 1123 pregnant women participated on a voluntary basis in this questionnaire survey. Maternal characteristics, cigarette consumption parameters, and personal opinions regarding the adverse effects of smoking during pregnancy were evaluated.

Results: Active smokers composed 12.4% (9.4%: regular tobacco cigarettes, 3.0%: electronic cigarettes) of the study population. Smoking during the current pregnancy, particularly via regular tobacco cigarettes, was more likely for women with smoking during previous pregnancies (56.0% vs. 7.8%, P < .001), previous history of low birth weight infant delivery (16.1% vs. 8.6%, P = .013), premature delivery (16.7% vs. 7.0%, P < .001), and stillbirth (22.8% vs. 11.7%, P = .002). The presence versus absence of smoking during pregnancy was associated with a lower likelihood of being a housewife (70.5% vs. 80.5%, P = .010) and a higher likelihood of having an actively smoking mother (25.9% vs. 11.2%, P < .001) or partner (65.7% vs. 46.9%, P < .001). Regular tobacco cigarette users considered electronic cigarettes to have a higher risk of adverse impacts (11.1% vs. 2.9%, P = .012), while electronic cigarette users considered regular cigarettes to have a higher risk of nicotine exposure (55.9% vs. 13.0%, P < .001).

Conclusion: Our findings indicate being employed, having an actively smoking mother or partner, as well as smoking in previous pregnancies, to be the risk factors for increased likelihood of smoking during pregnancy.

目的:本研究旨在评估孕妇对使用常规卷烟和电子烟的态度和行为。材料与方法:在自愿的基础上,共1123名孕妇参与了本次问卷调查。评估了孕妇的特征、香烟消费参数和个人对怀孕期间吸烟不良影响的看法。结果:活跃吸烟者占研究人群的12.4%(9.4%:普通烟草,3.0%:电子烟)。在怀孕期间吸烟,特别是通过常规香烟吸烟,在以前怀孕期间吸烟的妇女更有可能吸烟(56.0%比7.8%,P < 0.001),以前有低出生体重婴儿分娩史(16.1%比8.6%,P = 0.013),早产(16.7%比7.0%,P < 0.001)和死产(22.8%比11.7%,P = 0.002)。怀孕期间是否吸烟与成为家庭主妇的可能性较低相关(70.5%对80.5%,P = 0.010),与母亲吸烟的可能性较高相关(25.9%对11.2%,P < 0.001)或伴侣吸烟的可能性较高(65.7%对46.9%,P < 0.001)。经常吸烟的人认为电子烟有更高的不良影响风险(11.1%比2.9%,P = 0.012),而电子烟的人认为普通香烟有更高的尼古丁暴露风险(55.9%比13.0%,P < 0.001)。结论:我们的研究结果表明,有工作,有一个吸烟的母亲或伴侣,以及以前怀孕时吸烟,是怀孕期间吸烟可能性增加的危险因素。
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引用次数: 0
Radiological Findings in the Case Exposed to Zirconium. 暴露于锆的病例的放射学表现。
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22109
Merve Demirci Atik, Abdullah Taylan, Eyüp Sabri Uçan

Pneumoconiosis is a lung disease that develops as a result of a tissue reaction that occurs with the accumulation of inorganic particles. Pathoclinical features may vary depending on the type of inhaled particle. Today, fibrotic and nonfibrotic tissue reactions are well defined in some substances. For example, it is known that exposures such as silica, asbestos, beryllium, and talc are associated with fibrosis in the lung, while exposures such as iron, tin, and barium sulfate cause non-fibrogenic changes. However, the pathoclinic and radiological findings of some rare exposures such as zirconium are not widely known. In a 52-year-old dental technician with a 26-year history of zirconium exposure, more prominent parenchymal emphysematous and fibrotic changes were detected in the upper zones of the thorax high-resolution computed tomography. Since zirconium exposure was clearly defined, radiological findings of this case may be useful to current literature.

尘肺病是一种肺部疾病,是由于无机颗粒积聚引起的组织反应而发展起来的。病理临床特征可能因吸入颗粒的类型而异。今天,在一些物质中,纤维化和非纤维化组织反应是明确的。例如,已知暴露于二氧化硅、石棉、铍和滑石粉与肺纤维化有关,而暴露于铁、锡和硫酸钡则引起非纤维化改变。然而,一些罕见的暴露如锆的病理、临床和放射学表现尚不为人所知。一位52岁的牙科技师,有26年的锆暴露史,在胸部高分辨率计算机断层扫描的上部区域检测到更突出的实质肺气肿和纤维化改变。由于锆暴露有明确的定义,本病例的放射学结果可能对当前文献有用。
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引用次数: 0
The Knowledge and Attitude about New Generation Tobacco Products among Physicians. 医师对新一代烟草产品的认知与态度。
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22072
Pınar Bostan, Aslı Görek Dilektaşlı

Objective: Health hazards of e-cigarettes including "e-cigarette or vaping product use-associated lung injury" are better understood today. Just as e-cigarettes, heated tobacco products release toxic emissions. We aimed to determine the knowledge and attitude about new generation tobacco products among physicians who were the members of an organization for health care professionals, the majority of whom are pulmonologists.

Material and methods: In this cross-sectional study, a self-administered online questionnaire-based survey was conducted among the physicians from April to October 2019. The survey included questions about demographics (gender, age, graduation date from medical institution, and academic title), their smoking status, their knowledge and attitudes toward new generation tobacco products, and additionally about whether new generation tobacco products can be used to aid in smoking cessation.

Results: Among the 506 members who responded to the survey, 56.7 % were female; the mean age was 42.4 ± 10.9 years (20-74). About 74.5% were pulmonologists, 5.5% were thoracic surgeons, and 20% were other physicians. Among the responders, the frequency of those who have not heard of new generation tobacco products before was determined as 9.5%, 24.5%, and 41.3%. At least 58.9% of participants lacked the knowledge necessary to discuss these products with their patients and the rate reached 76.7% for the heated tobacco product. To the question of whether new generation tobacco products can be used in smoking cessation, 68.4% responded "I never agree that they can be used." Non-current smokers (P = .003), elders (P = .001), those who had training on smoking cessation assistance (P = .001), and those who had experience in smoking cessation assistance (P = .009) were significantly more prevalent in the group who answered: "I never agree that they can be used."

Conclusion: Physicians must become considerably more knowledgeable about the new generation tobacco products and hazards. Otherwise, these new tobacco products may pose new threats to national and global tobacco control efforts.

目的:电子烟的健康危害,包括“与电子烟或电子烟产品使用相关的肺损伤”,今天得到了更好的了解。就像电子烟一样,加热后的烟草产品也会释放有毒物质。我们的目的是确定医疗保健专业人员组织成员中的医生对新一代烟草产品的知识和态度,其中大多数是肺科医生。材料与方法:在本横断面研究中,于2019年4月至10月对医生进行了自我管理的在线问卷调查。调查的问题包括人口统计学(性别、年龄、从医疗机构毕业的日期和学术头衔)、吸烟状况、对新一代烟草制品的了解和态度,以及新一代烟草制品是否可以用来帮助戒烟。结果:在参与调查的506名会员中,56.7%为女性;平均年龄42.4±10.9岁(20 ~ 74岁)。肺科医生占74.5%,胸外科医生占5.5%,其他医生占20%。在应答者中,未听说过新一代烟草制品的比例分别为9.5%、24.5%和41.3%。至少58.9%的参与者缺乏与患者讨论这些产品所需的知识,而加热烟草产品的比例达到76.7%。对于新一代烟草制品是否可以用于戒烟的问题,68.4%的人回答“我从不同意可以使用”。非吸烟者(P = 0.003)、老年人(P = 0.001)、接受过戒烟援助培训的人(P = 0.001)和有过戒烟援助经验的人(P = 0.009)在回答“我从不同意可以使用戒烟援助”的人群中明显更为普遍。结论:医生必须对新一代烟草制品及其危害有相当多的了解。否则,这些新的烟草制品可能对国家和全球烟草控制工作构成新的威胁。
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引用次数: 1
Clinical, Functional, and Prognostic Evaluation of Idiopathic Pulmonary Fibrosis, Connective Tissue Disease-Associated Interstitial Lung Disease, Interstitial Pneumonia with Autoimmune Features: A Single-Center Prospective Study. 特发性肺纤维化、结缔组织病相关间质性肺病、间质性肺炎伴自身免疫性特征的临床、功能和预后评价:一项单中心前瞻性研究
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22017
Miraç Öz, Serhat Erol, Orhan Küçükşahin, İrem Kar, Kayhan Çetin Atasoy, Özlem Özdemir Kumbasar

Objective: Our study aimed to evaluate clinical, functional, and prognostic features and to determine the prognosis of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung diseases, and interstitial pneumonia with autoimmune features.

Material and methods: Sixty-nine cases with interstitial lung diseases were recruited in this study prospectively. Demographic features, symptoms, radiological findings, functional measurements, and immunological markers were recorded twice (at the time of initial admission and in the 12th month). Twenty-four of 69 cases were idiopathic pulmonary fibrosis, 32 were connective tissue diseaseassociated interstitial lung diseases, and 13 were interstitial pneumonia with autoimmune features .

Results: Most of the patients with idiopathic pulmonary fibrosis were male, while there were more female patients in connective tissue disease-associated interstitial lung diseases and interstitial pneumonia with autoimmune features groups. Female patients (65.0%) predominated in connective tissue disease-associated interstitial lung diseases group (P <.001). There was no significant difference in the mean ages of the disease groups, yet connective tissue disease-associated interstitial lung diseases patients were generally younger (min- max: 34-82 years). In the idiopathic pulmonary fibrosis group, only low titers of antinuclear antibody positivity were found. Antinuclear antibody positivity in the connective tissue disease-associated interstitial lung diseases group and interstitial pneumonia with autoimmune features group was high (P = .001). The long-term survival of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung diseases, and interstitial pneumonia with autoimmune features patients were 37%, 40 months (median) (95% CI, 5.193- 74.807), 48.6%, 80 months (median) (95% CI, 57.032-102.968), 30.8%, 46 months (median) (95% CI, 26.624-65.376), respectively.

Conclusion: Although a consensus report describing interstitial lung diseases with autoimmune features has been published, diagnostic criteria for this group are still vague. Since the interstitial pneumonia with autoimmune features group had the worst results in terms of functional loss and survival rates, the follow-up parameters and follow-up algorithm should be established for this group. Clinical and immunological evaluation of the interstitial pneumonia with autoimmune features group should include detailed parameters because of follow-up and to estimate survival.

目的:本研究旨在评估特发性肺纤维化、结缔组织病相关间质性肺疾病和具有自身免疫性特征的间质性肺炎的临床、功能和预后特征,并确定其预后。材料与方法:本研究前瞻性地招募了69例间质性肺疾病患者。人口统计学特征、症状、放射学表现、功能测量和免疫标志物记录两次(首次入院时和第12个月)。69例特发性肺纤维化24例,结缔组织病相关间质性肺疾病32例,具有自身免疫特征的间质性肺炎13例。结果:特发性肺纤维化患者以男性居多,结缔组织病相关间质性肺疾病组和具有自身免疫特征的间质性肺炎组以女性居多。结缔组织病相关间质性肺病组以女性患者为主(65.0%)。(P)结论:虽然有一致的报告描述了具有自身免疫性特征的间质性肺病,但该组的诊断标准仍不明确。由于间质性肺炎合并自身免疫性特征组在功能丧失和生存率方面的结果最差,因此需要建立该组的随访参数和随访算法。具有自身免疫性特征的间质性肺炎的临床和免疫学评估应包括详细的参数,因为随访和估计生存。
{"title":"Clinical, Functional, and Prognostic Evaluation of Idiopathic Pulmonary Fibrosis, Connective Tissue Disease-Associated Interstitial Lung Disease, Interstitial Pneumonia with Autoimmune Features: A Single-Center Prospective Study.","authors":"Miraç Öz,&nbsp;Serhat Erol,&nbsp;Orhan Küçükşahin,&nbsp;İrem Kar,&nbsp;Kayhan Çetin Atasoy,&nbsp;Özlem Özdemir Kumbasar","doi":"10.5152/TurkThoracJ.2022.22017","DOIUrl":"https://doi.org/10.5152/TurkThoracJ.2022.22017","url":null,"abstract":"<p><strong>Objective: </strong>Our study aimed to evaluate clinical, functional, and prognostic features and to determine the prognosis of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung diseases, and interstitial pneumonia with autoimmune features.</p><p><strong>Material and methods: </strong>Sixty-nine cases with interstitial lung diseases were recruited in this study prospectively. Demographic features, symptoms, radiological findings, functional measurements, and immunological markers were recorded twice (at the time of initial admission and in the 12th month). Twenty-four of 69 cases were idiopathic pulmonary fibrosis, 32 were connective tissue diseaseassociated interstitial lung diseases, and 13 were interstitial pneumonia with autoimmune features .</p><p><strong>Results: </strong>Most of the patients with idiopathic pulmonary fibrosis were male, while there were more female patients in connective tissue disease-associated interstitial lung diseases and interstitial pneumonia with autoimmune features groups. Female patients (65.0%) predominated in connective tissue disease-associated interstitial lung diseases group (P <.001). There was no significant difference in the mean ages of the disease groups, yet connective tissue disease-associated interstitial lung diseases patients were generally younger (min- max: 34-82 years). In the idiopathic pulmonary fibrosis group, only low titers of antinuclear antibody positivity were found. Antinuclear antibody positivity in the connective tissue disease-associated interstitial lung diseases group and interstitial pneumonia with autoimmune features group was high (P = .001). The long-term survival of idiopathic pulmonary fibrosis, connective tissue disease-associated interstitial lung diseases, and interstitial pneumonia with autoimmune features patients were 37%, 40 months (median) (95% CI, 5.193- 74.807), 48.6%, 80 months (median) (95% CI, 57.032-102.968), 30.8%, 46 months (median) (95% CI, 26.624-65.376), respectively.</p><p><strong>Conclusion: </strong>Although a consensus report describing interstitial lung diseases with autoimmune features has been published, diagnostic criteria for this group are still vague. Since the interstitial pneumonia with autoimmune features group had the worst results in terms of functional loss and survival rates, the follow-up parameters and follow-up algorithm should be established for this group. Clinical and immunological evaluation of the interstitial pneumonia with autoimmune features group should include detailed parameters because of follow-up and to estimate survival.</p>","PeriodicalId":37452,"journal":{"name":"Turkish Thoracic Journal","volume":" ","pages":"395-402"},"PeriodicalIF":0.9,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/2f/32/ttj-23-6-395.PMC9682965.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40356886","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 Spectrum of Nonalcoholic Fatty Liver Disease in Patients with Chronic Obstructive Pulmonary Disease. 慢性阻塞性肺疾病患者非酒精性脂肪性肝病的临床谱
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22002
Shaker Wagih Shaltout, Mohamed Abd El-Maksoud, Ashraf Abdel Rahman, Aida M Yousef, Walid El Sherbiny

Objective: The purpose of this study was to determine the prevalence of nonalcoholic fatty liver disease in a group of chronic obstructive pulmonary disease patients.

Material and methods: This study comprised 48 stable chronic obstructive pulmonary disease patients who were diagnosed and categorized using the Global Initiative for Chronic Obstructive Lung Disease 2017 criteria. The prevalence of nonalcoholic fatty liver disease in chronic obstructive pulmonary disease patients was determined using noninvasive biomarkers and imaging methods. Steatosis was detected using magnetic resonance mDIXON-Quant sequence imaging, while fibrosis was detected using the acoustic radiation force impulse and FIB-4 index.

Results: A total of 58.3% of the patients investigated had a fat level of 5%, and nearly a quarter of them had a fat content of 10% or more, and 45.8% of the patients studied had severe hepatic fibrosis. The Fibrosis-4 (FIB-4) index revealed advanced fibrosis in 18.75% of them. No statistically significant association was found between chronic obstructive pulmonary disease groups of studied patients and the presence of steatosis and fibrosis (≥F2) using acoustic radiation force impulse. The presence of fibrosis, however, was statistically significant linked with chronic obstructive pulmonary disease groups of examined patients using the FIB-4 index. γ-Glutamyl transferase and alkaline phosphatase levels were greater in Global Initiative for Chronic Obstructive Lung Disease 3/4 and C/D groups.

Conclusion: Nonalcoholic fatty liver disease is a common comorbidity in chronic obstructive pulmonary disease and should be included in the list of chronic obstructive pulmonary disease comorbidities.

目的:本研究的目的是确定一组慢性阻塞性肺疾病患者中非酒精性脂肪性肝病的患病率。材料和方法:本研究纳入48名稳定型慢性阻塞性肺疾病患者,这些患者使用2017年全球慢性阻塞性肺疾病倡议标准进行诊断和分类。使用无创生物标志物和影像学方法确定慢性阻塞性肺疾病患者中非酒精性脂肪性肝病的患病率。采用磁共振mDIXON-Quant序列成像检测脂肪变性,采用声辐射力脉冲和FIB-4指数检测纤维化。结果:58.3%的患者脂肪含量为5%,近1 / 4的患者脂肪含量在10%及以上,45.8%的患者有严重的肝纤维化。纤维化-4 (FIB-4)指数显示18.75%的患者处于晚期纤维化状态。使用声辐射力脉冲检测慢性阻塞性肺疾病患者组与脂肪变性和纤维化(≥F2)之间无统计学意义的关联。然而,在使用FIB-4指数检查的患者中,纤维化的存在与慢性阻塞性肺疾病组有统计学意义。γ-谷氨酰转移酶和碱性磷酸酶水平在慢性阻塞性肺疾病全球倡议3/4组和C/D组较高。结论:非酒精性脂肪性肝病是慢性阻塞性肺疾病的常见合并症,应列入慢性阻塞性肺疾病合并症。
{"title":"Clinical Spectrum of Nonalcoholic Fatty Liver Disease in Patients with Chronic Obstructive Pulmonary Disease.","authors":"Shaker Wagih Shaltout,&nbsp;Mohamed Abd El-Maksoud,&nbsp;Ashraf Abdel Rahman,&nbsp;Aida M Yousef,&nbsp;Walid El Sherbiny","doi":"10.5152/TurkThoracJ.2022.22002","DOIUrl":"https://doi.org/10.5152/TurkThoracJ.2022.22002","url":null,"abstract":"<p><strong>Objective: </strong>The purpose of this study was to determine the prevalence of nonalcoholic fatty liver disease in a group of chronic obstructive pulmonary disease patients.</p><p><strong>Material and methods: </strong>This study comprised 48 stable chronic obstructive pulmonary disease patients who were diagnosed and categorized using the Global Initiative for Chronic Obstructive Lung Disease 2017 criteria. The prevalence of nonalcoholic fatty liver disease in chronic obstructive pulmonary disease patients was determined using noninvasive biomarkers and imaging methods. Steatosis was detected using magnetic resonance mDIXON-Quant sequence imaging, while fibrosis was detected using the acoustic radiation force impulse and FIB-4 index.</p><p><strong>Results: </strong>A total of 58.3% of the patients investigated had a fat level of 5%, and nearly a quarter of them had a fat content of 10% or more, and 45.8% of the patients studied had severe hepatic fibrosis. The Fibrosis-4 (FIB-4) index revealed advanced fibrosis in 18.75% of them. No statistically significant association was found between chronic obstructive pulmonary disease groups of studied patients and the presence of steatosis and fibrosis (≥F2) using acoustic radiation force impulse. The presence of fibrosis, however, was statistically significant linked with chronic obstructive pulmonary disease groups of examined patients using the FIB-4 index. γ-Glutamyl transferase and alkaline phosphatase levels were greater in Global Initiative for Chronic Obstructive Lung Disease 3/4 and C/D groups.</p><p><strong>Conclusion: </strong>Nonalcoholic fatty liver disease is a common comorbidity in chronic obstructive pulmonary disease and should be included in the list of chronic obstructive pulmonary disease comorbidities.</p>","PeriodicalId":37452,"journal":{"name":"Turkish Thoracic Journal","volume":" ","pages":"420-425"},"PeriodicalIF":0.9,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/d5/d4/ttj-23-6-420.PMC9682942.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40377248","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: 2
COP27 Climate Change Conference: urgent action needed for Africa and the world. COP27气候变化会议:非洲和世界需要采取紧急行动。
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.121022
Lukoye Atwoli, Gregory E Erhabor, Aiah A Gbakima, Abraham Haileamlak, Jean-Marie Kayembe Ntumba, James Kigera, Laurie Laybourn-Langton, Bob Mash, Joy Muhia, Fhumulani Mavis Mulaudzi, David Ofori-Adjei, Friday Okonofua, Arash Rashidian, Siaka Sidibé, Abdelmadjid Snouber, James Tumwine, Mohammad Sahar Yassien, Paul Yonga, Lilia Zakhama, Chris Zielinski
{"title":"COP27 Climate Change Conference: urgent action needed for Africa and the world.","authors":"Lukoye Atwoli,&nbsp;Gregory E Erhabor,&nbsp;Aiah A Gbakima,&nbsp;Abraham Haileamlak,&nbsp;Jean-Marie Kayembe Ntumba,&nbsp;James Kigera,&nbsp;Laurie Laybourn-Langton,&nbsp;Bob Mash,&nbsp;Joy Muhia,&nbsp;Fhumulani Mavis Mulaudzi,&nbsp;David Ofori-Adjei,&nbsp;Friday Okonofua,&nbsp;Arash Rashidian,&nbsp;Siaka Sidibé,&nbsp;Abdelmadjid Snouber,&nbsp;James Tumwine,&nbsp;Mohammad Sahar Yassien,&nbsp;Paul Yonga,&nbsp;Lilia Zakhama,&nbsp;Chris Zielinski","doi":"10.5152/TurkThoracJ.2022.121022","DOIUrl":"https://doi.org/10.5152/TurkThoracJ.2022.121022","url":null,"abstract":"","PeriodicalId":37452,"journal":{"name":"Turkish Thoracic Journal","volume":" ","pages":"366-368"},"PeriodicalIF":0.9,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9682936/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40659456","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
Investigating the Differences in Polysomnography Results Evaluated According to the Recommended and Alternative Hypopnea Criteria Utilized in the Evaluation of Polysomnography. 探讨多导睡眠图评价中使用推荐和替代低通气标准评价多导睡眠图结果的差异。
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.22069
Ayşegül Gencer, Buket Çalışkaner Öztürk, Benan Musellim

Objective: The criteria of hypopnea recommended by the American Academy of Sleep Medicine until 2012 was 3% desaturation and 50% decline in the signal amplitude. The recommended and alternative criteria for hypopnea were determined as 3% desaturation accompanied by a 30% decline in the signal amplitude and 4% desaturation accompanied by a 30% decline in the amplitude by the 2013 update of the guideline was published by the American Academy of Sleep Medicine in 2012. The objective of our study was to investigate to what degree scoring of hypopneas has great importance in the diagnosis and severity grading of obstructive sleep apnea syndrome according to different criteria.

Material and methods: The present study was designed as a retrospective study in which the results of the polysomnography of 62 patients were recorded after evaluation according to 3 different hypopnea criteria. Criteria 1, criteria 2, and criteria 3 were accepted as a 3% drop in SaO2 accompanied by a 30% decline in the amplitude, as a 4% drop in SaO2 accompanied by a 30% decline in the amplitude, and as a 3% drop in SaO2 accompanied with a 50% decline in the amplitude, respectively.

Results: Statistically significant differences were determined between criteria 1 and criteria 2, criteria 1 and criteria 3, and criteria 2 and criteria 3 regarding the numbers of hypopneas.

Conclusion: For the same polysomnography, evaluations with different accepted hypopnea criteria cause different polysomnography results.

目的:截至2012年,美国睡眠医学会推荐的低通气标准为3%的去饱和度和50%的信号幅度下降。美国睡眠医学会(American Academy of Sleep Medicine)于2012年发布了2013年更新的指南,推荐和替代的低通气标准确定为3%的去饱和伴30%的信号幅度下降和4%的去饱和伴30%的幅度下降。本研究的目的是探讨根据不同的标准,低呼吸评分在阻塞性睡眠呼吸暂停综合征的诊断和严重程度分级中的重要程度。材料与方法:本研究为回顾性研究,根据3种不同的低通气标准评估62例患者的多导睡眠图结果。标准1、标准2和标准3分别被接受为SaO2下降3%伴随幅度下降30%,SaO2下降4%伴随幅度下降30%,SaO2下降3%伴随幅度下降50%。结果:诊断标准1与诊断标准2、诊断标准1与诊断标准3、诊断标准2与诊断标准3关于低呼吸次数的差异有统计学意义。结论:对于相同的多导睡眠图,采用不同公认的低通气标准评价会导致不同的多导睡眠图结果。
{"title":"Investigating the Differences in Polysomnography Results Evaluated According to the Recommended and Alternative Hypopnea Criteria Utilized in the Evaluation of Polysomnography.","authors":"Ayşegül Gencer,&nbsp;Buket Çalışkaner Öztürk,&nbsp;Benan Musellim","doi":"10.5152/TurkThoracJ.2022.22069","DOIUrl":"https://doi.org/10.5152/TurkThoracJ.2022.22069","url":null,"abstract":"<p><strong>Objective: </strong>The criteria of hypopnea recommended by the American Academy of Sleep Medicine until 2012 was 3% desaturation and 50% decline in the signal amplitude. The recommended and alternative criteria for hypopnea were determined as 3% desaturation accompanied by a 30% decline in the signal amplitude and 4% desaturation accompanied by a 30% decline in the amplitude by the 2013 update of the guideline was published by the American Academy of Sleep Medicine in 2012. The objective of our study was to investigate to what degree scoring of hypopneas has great importance in the diagnosis and severity grading of obstructive sleep apnea syndrome according to different criteria.</p><p><strong>Material and methods: </strong>The present study was designed as a retrospective study in which the results of the polysomnography of 62 patients were recorded after evaluation according to 3 different hypopnea criteria. Criteria 1, criteria 2, and criteria 3 were accepted as a 3% drop in SaO2 accompanied by a 30% decline in the amplitude, as a 4% drop in SaO2 accompanied by a 30% decline in the amplitude, and as a 3% drop in SaO2 accompanied with a 50% decline in the amplitude, respectively.</p><p><strong>Results: </strong>Statistically significant differences were determined between criteria 1 and criteria 2, criteria 1 and criteria 3, and criteria 2 and criteria 3 regarding the numbers of hypopneas.</p><p><strong>Conclusion: </strong>For the same polysomnography, evaluations with different accepted hypopnea criteria cause different polysomnography results.</p>","PeriodicalId":37452,"journal":{"name":"Turkish Thoracic Journal","volume":" ","pages":"383-386"},"PeriodicalIF":0.9,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/a7/5e/ttj-23-6-383.PMC9682957.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40622608","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
The Safety of Fiberoptic Bronchoscopy in Airway Pressure Release Ventilation Mode in Critically Ill Patients with Severe Acute Respiratory Distress Syndrome: A Preliminary Study. 纤维支气管镜对危重重症急性呼吸窘迫综合征患者气道压力释放通气模式安全性的初步研究。
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-11-01 DOI: 10.5152/TurkThoracJ.2022.21241
Mehmet Celal Öztürk, Murat Küçük, Yasin Levent Uğur, Bilgin Cömert, Ali Necati Gökmen, Begüm Ergan

Objective: The most appropriate ventilatory mode during fiberoptic bronchoscopy is still not yet known clearly for patients with acute respiratory distress syndrome. Airway pressure release ventilation is used as a recovery treatment for patients with severe acute respiratory distress syndrome. In this study, the aim was to evaluate the safety of the fiberoptic bronchoscopy process in patients with severe acute respiratory distress syndrome ventilated with airway pressure release ventilation mode and its effect on gas exchange and respiratory mechanics.

Material and methods: Single-center retrospective observational study was performed in the intensive care unit of a tertiary referral center from September 2018 to November 2019. Patients with severe ARDS ventilated with APRV mode and undergoing FB were included. Fiberoptic bronchoscopy was performed by an expert intensivist-pulmonologist. All ventilator parameters set by the clinician were kept stable, and no change was made other than O2 concentration. The mechanical ventilation parameters and arterial blood gas values before and after the procedure and fiberoptic bronchoscopy-related complications were recorded for the first 24 hours.

Results: A total of 14 acute respiratory distress syndrome patients who were ventilated with airway pressure release ventilation were enrolled. No significant deteriorations were detected in gas exchange, pulmonary compliance, and airway resistance values in our case series. It was observed that a small reduction in PaO2 and an increase in PaCO2 were present after the 1st hour; however, both were returned to baseline values in the 24th hour. Only 1 patient developed fiberoptic bronchoscopy-induced hypoxemia (7.1%). Complications, such as fiberoptic bronchoscopy-induced barotrauma, pneumothorax, hemodynamic deterioration, and bleeding, were not detected.

Conclusion: According to our preliminary findings, performing fiberoptic bronchoscopy under airway pressure release ventilation mode by an experienced bronchoscopist does not bring additional complication risks in patients with severe acute respiratory distress syndrome.

目的:急性呼吸窘迫综合征患者纤维支气管镜检查时最适宜的通气方式尚不明确。气道压力释放通气是严重急性呼吸窘迫综合征患者的一种康复治疗方法。本研究旨在评价纤维支气管镜在气道压力释放通气模式下对严重急性呼吸窘迫综合征患者通气的安全性及其对气体交换和呼吸力学的影响。材料与方法:2018年9月至2019年11月在某三级转诊中心重症监护病房进行单中心回顾性观察研究。重症ARDS患者采用APRV模式通气并行FB。纤维支气管镜检查由肺病专家进行。保持临床医师设定的呼吸机各项参数稳定,除氧浓度外无变化。记录术前、术后24小时机械通气参数、动脉血气值及纤维支气管镜相关并发症。结果:共纳入14例急性呼吸窘迫综合征患者,均采用气道压力释放通气。在我们的病例系列中,没有发现气体交换、肺顺应性和气道阻力值的显著恶化。结果表明,1 h后PaO2略有降低,PaCO2略有升高;然而,两者在24小时内都恢复到基线值。仅有1例患者发生纤维支气管镜诱发的低氧血症(7.1%)。未发现纤维支气管镜引起的气压损伤、气胸、血流动力学恶化和出血等并发症。结论:根据我们的初步研究结果,由经验丰富的支气管镜医师在气道压力释放通气模式下进行纤维支气管镜检查不会给严重急性呼吸窘迫综合征患者带来额外的并发症风险。
{"title":"The Safety of Fiberoptic Bronchoscopy in Airway Pressure Release Ventilation Mode in Critically Ill Patients with Severe Acute Respiratory Distress Syndrome: A Preliminary Study.","authors":"Mehmet Celal Öztürk,&nbsp;Murat Küçük,&nbsp;Yasin Levent Uğur,&nbsp;Bilgin Cömert,&nbsp;Ali Necati Gökmen,&nbsp;Begüm Ergan","doi":"10.5152/TurkThoracJ.2022.21241","DOIUrl":"https://doi.org/10.5152/TurkThoracJ.2022.21241","url":null,"abstract":"<p><strong>Objective: </strong>The most appropriate ventilatory mode during fiberoptic bronchoscopy is still not yet known clearly for patients with acute respiratory distress syndrome. Airway pressure release ventilation is used as a recovery treatment for patients with severe acute respiratory distress syndrome. In this study, the aim was to evaluate the safety of the fiberoptic bronchoscopy process in patients with severe acute respiratory distress syndrome ventilated with airway pressure release ventilation mode and its effect on gas exchange and respiratory mechanics.</p><p><strong>Material and methods: </strong>Single-center retrospective observational study was performed in the intensive care unit of a tertiary referral center from September 2018 to November 2019. Patients with severe ARDS ventilated with APRV mode and undergoing FB were included. Fiberoptic bronchoscopy was performed by an expert intensivist-pulmonologist. All ventilator parameters set by the clinician were kept stable, and no change was made other than O2 concentration. The mechanical ventilation parameters and arterial blood gas values before and after the procedure and fiberoptic bronchoscopy-related complications were recorded for the first 24 hours.</p><p><strong>Results: </strong>A total of 14 acute respiratory distress syndrome patients who were ventilated with airway pressure release ventilation were enrolled. No significant deteriorations were detected in gas exchange, pulmonary compliance, and airway resistance values in our case series. It was observed that a small reduction in PaO2 and an increase in PaCO2 were present after the 1st hour; however, both were returned to baseline values in the 24th hour. Only 1 patient developed fiberoptic bronchoscopy-induced hypoxemia (7.1%). Complications, such as fiberoptic bronchoscopy-induced barotrauma, pneumothorax, hemodynamic deterioration, and bleeding, were not detected.</p><p><strong>Conclusion: </strong>According to our preliminary findings, performing fiberoptic bronchoscopy under airway pressure release ventilation mode by an experienced bronchoscopist does not bring additional complication risks in patients with severe acute respiratory distress syndrome.</p>","PeriodicalId":37452,"journal":{"name":"Turkish Thoracic Journal","volume":" ","pages":"403-408"},"PeriodicalIF":0.9,"publicationDate":"2022-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/b2/8b/ttj-23-6-403.PMC9682956.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"40356884","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: 1
Should Pneumothorax Developing During the Recovery Period After COVID-19 in Patients with Previously Healthy Lungs be Considered a Primary Spontaneous Pneumothorax or a Secondary Spontaneous Pneumothorax? 先前肺部健康的患者在COVID-19后恢复期发生气胸应被视为原发性自发性气胸还是继发性自发性气胸?
IF 0.9 Q4 RESPIRATORY SYSTEM Pub Date : 2022-09-01 DOI: 10.5152/TurkThoracJ.2022.22061
Selçuk Köse

Objective: It is still unknown how to call the pneumothorax that develops during the recovery period after coronavirus disease 2019. Patients who developed pneumothorax during the recovery period after coronavirus disease 2019 were compared with those who had a primary or secondary spontaneous pneumothorax without a coronavirus disease 2019 history.

Material and methods: Between 2020 and 2021, 160 patients with pneumothorax were retrospectively analyzed. Twenty-three patients had a history of coronavirus disease 2019 (coronavirus disease recovery) confirmed by real-time reverse transcriptase-polyme rase chain reaction, whereas the remaining 137 patients did not have a history of coronavirus disease 2019 (18 of the patients with secondary spontaneous pneumothorax group and 119 patients with primary spontaneous pneumothorax group).

Results: The median time between discharge and readmission to the hospital because of pneumothorax was 9 days in the coronavirus disease recovery group. There were statistically significant differences in regards to age (P < .001), gender (P = .02), the presence of bullae (P = .02), and dystrophic severity lung score (P = .04) between the coronavirus disease recovery and primary spontaneous pneumothorax groups, whereas no difference was found between the coronavirus disease recovery and the secondary spontaneous pneumothorax groups (P > .05). The prolonged air leak was observed in 17.6% (n = 25). Patients who had prolonged air leak were statistically higher in the coronavirus disease recovery group than the primary spontaneous pneumothorax group (56.5% vs. 10.1%), although it was almost similar between the coronavirus disease recovery and secondary spontaneous pneumothorax groups (P = .951). On logistic regression analysis, the coronavirus disease recovery group was the independent factor for prolonged air leak (odds ratio = 9.900, 95% CI = 1.557- 62.500, P = .01).

Conclusion: Pneumothorax may be developed during the recovery period after coronavirus disease 2019 in patients with previously healthy lungs, and it should be called as secondary spontaneous pneumothorax.

目的:2019冠状病毒病后恢复期发生的气胸如何称呼尚不清楚。将2019冠状病毒病后恢复期发生气胸的患者与无2019冠状病毒病史的原发性或继发性自发性气胸患者进行比较。材料和方法:回顾性分析2020 - 2021年间160例气胸患者。实时逆转录酶-多聚酶链反应证实23例患者有2019冠状病毒病(冠状病毒病康复)病史,其余137例患者无2019冠状病毒病病史(继发性自发性气胸组18例,原发性自发性气胸组119例)。结果:冠状病毒病康复组因气胸出院至再入院的中位时间为9 d。冠状病毒病康复组与原发性自发性气胸组在年龄(P < 0.001)、性别(P = 0.02)、肺大泡存在情况(P = 0.02)、肺营养不良严重程度评分(P = 0.04)方面差异均有统计学意义,冠状病毒病康复组与继发性自发性气胸组间差异无统计学意义(P > 0.05)。17.6% (n = 25)出现长时间漏气。冠状病毒病康复组与继发性自发性气胸组相比,长时间漏气的发生率明显高于原发性自发性气胸组(56.5% vs. 10.1%),但冠状病毒病康复组与继发性自发性气胸组差异无统计学意义(P = .951)。经logistic回归分析,冠状病毒病恢复组是导致漏气时间延长的独立因素(优势比= 9.900,95% CI = 1.557 ~ 62.500, P = 0.01)。结论:原肺健康的患者在2019冠状病毒感染后恢复期可能发生气胸,应称为继发性自发性气胸。
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引用次数: 0
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Turkish Thoracic Journal
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