Pub Date : 2025-07-21eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.27656
Selen Öztürk, Gözde Tekin, Hüseyin Uzandı, Mehmet Kızılay, İbrahim Öztürk
Background: In this review, we discuss the risk factors of intraabdominal hypertension developing after cardiac surgery.
Methods: We used records from electronic databases (PubMed, Scopus, Web of Science and Ovid) between 1980 and 2025. All studies in which possible pre- and intraoperative risk factors (age, sex, hypertension, diabetes mellitus, lung disease, coronary artery bypass grafting, body mass index and, cardiopulmonary bypass duration) were recorded were included in the analysis. The results of the studies were evaluated with a random or fixed effect model depending on the presence of heterogeneity (I2 >25%).
Results: A total of 4,286 articles were found from the database search. After analyzing the abstract and full texts, six articles which met the inclusion criteria and covered 696 patients were included in the analysis. The overall rate of intraabdominal hypertension was 44.68%. Age (standardized mean difference [SMD]: 0.303, 95% confidence interval [CI]: 0.123-0.484, p<0.001), hypertension (odds ratio [OR]=0.524, 95% CI: 0.087-0.960, p=0.019), body mass index (SMD: 0.532, 95% CI: 0.004-1.061, p=0.048), and cardiopulmonary bypass duration (SMD: 0.545, 95% CI: 0.184-0.907, p=0.003) were preoperative risk factors.
Conclusion: The patient's age, hypertension, body mass index, and duration of cardiopulmonary bypass are the risk factors for the development of intraabdominal hypertension after cardiac surgery. However, larger studies are needed to avoid heterogeneity of results.
背景:在这篇综述中,我们讨论了心脏手术后发生腹内高压的危险因素。方法:使用1980 - 2025年间PubMed、Scopus、Web of Science和Ovid等电子数据库的记录。所有记录可能的术前和术中危险因素(年龄、性别、高血压、糖尿病、肺病、冠状动脉旁路移植术、体重指数和体外循环时间)的研究均纳入分析。根据异质性(I2 bb0 25%)的存在,采用随机或固定效应模型对研究结果进行评估。结果:检索到文献4286篇。摘要和全文分析后,符合纳入标准的6篇文献纳入分析,共涉及696例患者。总腹内高压发生率为44.68%。年龄(标准化平均差[SMD]: 0.303, 95%可信区间[CI]: 0.123-0.484)结论:患者年龄、高血压、体重指数、体外循环时间是心脏手术后发生腹内高血压的危险因素。然而,需要更大规模的研究来避免结果的异质性。
{"title":"Risk factors of intraabdominal hypertension in cardiac surgery: A systematic review and meta-analysis.","authors":"Selen Öztürk, Gözde Tekin, Hüseyin Uzandı, Mehmet Kızılay, İbrahim Öztürk","doi":"10.5606/tgkdc.dergisi.2025.27656","DOIUrl":"10.5606/tgkdc.dergisi.2025.27656","url":null,"abstract":"<p><strong>Background: </strong>In this review, we discuss the risk factors of intraabdominal hypertension developing after cardiac surgery.</p><p><strong>Methods: </strong>We used records from electronic databases (PubMed, Scopus, Web of Science and Ovid) between 1980 and 2025. All studies in which possible pre- and intraoperative risk factors (age, sex, hypertension, diabetes mellitus, lung disease, coronary artery bypass grafting, body mass index and, cardiopulmonary bypass duration) were recorded were included in the analysis. The results of the studies were evaluated with a random or fixed effect model depending on the presence of heterogeneity (<i>I<sup>2</sup></i> >25%).</p><p><strong>Results: </strong>A total of 4,286 articles were found from the database search. After analyzing the abstract and full texts, six articles which met the inclusion criteria and covered 696 patients were included in the analysis. The overall rate of intraabdominal hypertension was 44.68%. Age (standardized mean difference [SMD]: 0.303, 95% confidence interval [CI]: 0.123-0.484, p<0.001), hypertension (odds ratio [OR]=0.524, 95% CI: 0.087-0.960, p=0.019), body mass index (SMD: 0.532, 95% CI: 0.004-1.061, p=0.048), and cardiopulmonary bypass duration (SMD: 0.545, 95% CI: 0.184-0.907, p=0.003) were preoperative risk factors.</p><p><strong>Conclusion: </strong>The patient's age, hypertension, body mass index, and duration of cardiopulmonary bypass are the risk factors for the development of intraabdominal hypertension after cardiac surgery. However, larger studies are needed to avoid heterogeneity of results.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"321-328"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421560/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041972","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-21eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.95364
Adem İlkay Diken
{"title":"What the past echoes, the future dares to ask.","authors":"Adem İlkay Diken","doi":"10.5606/tgkdc.dergisi.2025.95364","DOIUrl":"10.5606/tgkdc.dergisi.2025.95364","url":null,"abstract":"","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"271"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421537/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041935","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-21eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.25878
İbrahim Kara, Fatih Toptan, Salih Salihi, Mustafa Tarık Ağaç, Yunus Emre Yazıcı
An aortic pseudoaneurysm is a rare, but serious condition which can result in life-threatening complications. It is usually caused by previous cardiac surgery, trauma, or infection. Due to the high likelihood of rupture with primary surgical intervention, endovascular closure may be performed as the standard of care in eligible cases. In this article, we present a case of a huge aortic pseudoaneurysm with a wide neck which could safely be closed using an atrial septal occluder.
{"title":"Use of an atrial septal defect occluder for the closure of an ascending aorta pseudoaneurysm after coronary artery bypass grafting.","authors":"İbrahim Kara, Fatih Toptan, Salih Salihi, Mustafa Tarık Ağaç, Yunus Emre Yazıcı","doi":"10.5606/tgkdc.dergisi.2025.25878","DOIUrl":"10.5606/tgkdc.dergisi.2025.25878","url":null,"abstract":"<p><p>An aortic pseudoaneurysm is a rare, but serious condition which can result in life-threatening complications. It is usually caused by previous cardiac surgery, trauma, or infection. Due to the high likelihood of rupture with primary surgical intervention, endovascular closure may be performed as the standard of care in eligible cases. In this article, we present a case of a huge aortic pseudoaneurysm with a wide neck which could safely be closed using an atrial septal occluder.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"397-400"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421551/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041941","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-21eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.27178
Gamze Vuran, Murat Muhtar Yılmazer, Mehmet Murat, Ceren Karahan, Mertkan Bilen, Mustafa Karaçelik, Timur Meşe
Background: This study aims to evaluate the mid-term outcomes of transcatheter ventricular septal defect closure with the Konar-MF™ device and to investigate the impact of an optimized device selection strategy using a retrograde approach.
Methods: Between January 2019 and November 2023, a total of 58 patients (32 males, 26 females; median age: 4.5 years; range, 8 months to 16 years) who underwent transcatheter closure of ventricular septal defects using the Konar-MF™ device were retrospectively analyzed. Patient demographics, procedural details, and follow-up data were recorded.
Results: Procedural success was achieved in 95% of cases, with a median procedure time of 60 min and fluoroscopy time of 12.6 min. Retrograde implantation was used in 79% of patients, significantly reducing procedural time and minimizing complications associated with an arteriovenous loop. Our refined strategy of selecting smaller devices when anatomically feasible played a crucial role in reducing interference with surrounding cardiac structures, substantially contributing to the absence of complete atrioventricular block in our cohort. Major complications included device embolization, moderate aortic regurgitation due to device dislocation, and right ventricular perforation (each in 1.8% of patients). The median follow-up was 34.5 months. Residual shunt rates were initially 42% on postoperative Day 1, reducing to 1.8% by the end of the follow-up period.
Conclusion: The Konar-MF™ occluder demonstrated high procedural success and acceptable complication rates for perimembranous ventricular septal defect closure. The use of a retrograde approach and a refined device selection strategy were key factors in achieving favorable outcomes, minimizing complications such as atrioventricular block and valve interference. The device offers significant advantages, making it a suitable alternative to surgical ventricular septal defect closure.
{"title":"Optimized retrograde approach and device selection with Konar-MF™ for pediatric transcatheter ventricular septal defect closure.","authors":"Gamze Vuran, Murat Muhtar Yılmazer, Mehmet Murat, Ceren Karahan, Mertkan Bilen, Mustafa Karaçelik, Timur Meşe","doi":"10.5606/tgkdc.dergisi.2025.27178","DOIUrl":"10.5606/tgkdc.dergisi.2025.27178","url":null,"abstract":"<p><strong>Background: </strong>This study aims to evaluate the mid-term outcomes of transcatheter ventricular septal defect closure with the Konar-MF™ device and to investigate the impact of an optimized device selection strategy using a retrograde approach.</p><p><strong>Methods: </strong>Between January 2019 and November 2023, a total of 58 patients (32 males, 26 females; median age: 4.5 years; range, 8 months to 16 years) who underwent transcatheter closure of ventricular septal defects using the Konar-MF™ device were retrospectively analyzed. Patient demographics, procedural details, and follow-up data were recorded.</p><p><strong>Results: </strong>Procedural success was achieved in 95% of cases, with a median procedure time of 60 min and fluoroscopy time of 12.6 min. Retrograde implantation was used in 79% of patients, significantly reducing procedural time and minimizing complications associated with an arteriovenous loop. Our refined strategy of selecting smaller devices when anatomically feasible played a crucial role in reducing interference with surrounding cardiac structures, substantially contributing to the absence of complete atrioventricular block in our cohort. Major complications included device embolization, moderate aortic regurgitation due to device dislocation, and right ventricular perforation (each in 1.8% of patients). The median follow-up was 34.5 months. Residual shunt rates were initially 42% on postoperative Day 1, reducing to 1.8% by the end of the follow-up period.</p><p><strong>Conclusion: </strong>The Konar-MF™ occluder demonstrated high procedural success and acceptable complication rates for perimembranous ventricular septal defect closure. The use of a retrograde approach and a refined device selection strategy were key factors in achieving favorable outcomes, minimizing complications such as atrioventricular block and valve interference. The device offers significant advantages, making it a suitable alternative to surgical ventricular septal defect closure.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"301-311"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421569/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041921","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-21eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.27697
Hasan Cihan, Burak Toprak, Abdulkadir Bilgiç
Background: This study aims to investigate whether acute surgical manipulation of great saphenous vein grafts during coronary artery bypass grafting alters mammalian target of rapamycin (mTOR) activation and induces early histopathological damage.
Methods: Between September 2022 and September 2023, a total of 44 elective coronary artery bypass grafting patients (38 males, 6 females; mean age: 60.8±8.3 years; range, 36 to 70 years) were included in this prospective study. Saphenous vein segments were collected pre- and post-preparation. Light microscopy and enzyme-linked immunosorbent assay were used to assess structural changes and mTOR levels.
Results: Histopathological analyses revealed endothelial disruption and subendothelial inflammatory infiltration in post-preparation samples. However, mTOR protein levels showed no significant difference between pre- and post-manipulation tissues (p=0.41).
Conclusion: Mechanical stress during great saphenous vein graft preparation causes notable endothelial injury, but does not acutely activate the mTOR pathway. These findings suggest that mTOR may not participate in early responses, but could be implicated in long-term vascular remodeling.
{"title":"Acute histopathological and biochemical changes in saphenous vein grafts during coronary artery bypass grafting: A closer look at mTOR signaling.","authors":"Hasan Cihan, Burak Toprak, Abdulkadir Bilgiç","doi":"10.5606/tgkdc.dergisi.2025.27697","DOIUrl":"10.5606/tgkdc.dergisi.2025.27697","url":null,"abstract":"<p><strong>Background: </strong>This study aims to investigate whether acute surgical manipulation of great saphenous vein grafts during coronary artery bypass grafting alters mammalian target of rapamycin (mTOR) activation and induces early histopathological damage.</p><p><strong>Methods: </strong>Between September 2022 and September 2023, a total of 44 elective coronary artery bypass grafting patients (38 males, 6 females; mean age: 60.8±8.3 years; range, 36 to 70 years) were included in this prospective study. Saphenous vein segments were collected pre- and post-preparation. Light microscopy and enzyme-linked immunosorbent assay were used to assess structural changes and mTOR levels.</p><p><strong>Results: </strong>Histopathological analyses revealed endothelial disruption and subendothelial inflammatory infiltration in post-preparation samples. However, mTOR protein levels showed no significant difference between pre- and post-manipulation tissues (p=0.41).</p><p><strong>Conclusion: </strong>Mechanical stress during great saphenous vein graft preparation causes notable endothelial injury, but does not acutely activate the mTOR pathway. These findings suggest that mTOR may not participate in early responses, but could be implicated in long-term vascular remodeling.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"279-287"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421562/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041779","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: In this systematic review and meta-analysis, we discuss the estimated of global incidence, shunt related-mortality risk and factors associated with shunt blockage after modified Blalock-Taussig-Thomas (mBTT) procedure.
Methods: A systematic review and meta-analysis were conducted using PubMed, ScienceDirect, and EMBASE up to February 2024. The primary outcomes were the incidence and mortality risk associated with shunt blockage. Additional outcomes included study characteristics, surgical factors, and coagulation profiles. Single and two-group proportional meta-analyses were performed.
Results: A total of 25 studies involving 2,677 patients were included. The global incidence of shunt blockage was 7% (95% confidence interval [CI]: 0.05 to 0.10) with high heterogeneity (I2 =81%; p<0.01). In 15 studies eligible for mortality analysis, patients with shunt blockage had significantly higher odds of death (odds ratio [OR]=5.04; 95% CI: 2.69 to 9.44) with low heterogeneity (I2 =3%; p=0.41). Shunt size alone was not a significant predictor of blockage. However, patients with shunt blockage exhibited significantly lower partial thromboplastin time and activated partial thromboplastin time values, suggesting coagulation abnormalities. No significant difference was found in platelet counts.
Conclusion: Shunt blockage is a critical complication following mBTT shunt, significantly increasing mortality risk. While shunt size is not independently predictive, multiple factors, including patient weight, underlying pathology, coagulation profile, surgical factors, and shunt size-to-weight ratio, may contribute to thrombosis risk and warrant further investigation.
{"title":"Modified Blalock-Taussig-Thomas shunt blockage and mortality: A systematic review and meta-analysis.","authors":"Adli Daffa Ikhwani, Amar Rayhan, Suprayitno Wardoyo","doi":"10.5606/tgkdc.dergisi.2025.26521","DOIUrl":"10.5606/tgkdc.dergisi.2025.26521","url":null,"abstract":"<p><strong>Background: </strong>In this systematic review and meta-analysis, we discuss the estimated of global incidence, shunt related-mortality risk and factors associated with shunt blockage after modified Blalock-Taussig-Thomas (mBTT) procedure.</p><p><strong>Methods: </strong>A systematic review and meta-analysis were conducted using PubMed, ScienceDirect, and EMBASE up to February 2024. The primary outcomes were the incidence and mortality risk associated with shunt blockage. Additional outcomes included study characteristics, surgical factors, and coagulation profiles. Single and two-group proportional meta-analyses were performed.</p><p><strong>Results: </strong>A total of 25 studies involving 2,677 patients were included. The global incidence of shunt blockage was 7% (95% confidence interval [CI]: 0.05 to 0.10) with high heterogeneity (<i>I<sup>2</sup></i> =81%; p<0.01). In 15 studies eligible for mortality analysis, patients with shunt blockage had significantly higher odds of death (odds ratio [OR]=5.04; 95% CI: 2.69 to 9.44) with low heterogeneity (<i>I<sup>2</sup></i> =3%; p=0.41). Shunt size alone was not a significant predictor of blockage. However, patients with shunt blockage exhibited significantly lower partial thromboplastin time and activated partial thromboplastin time values, suggesting coagulation abnormalities. No significant difference was found in platelet counts.</p><p><strong>Conclusion: </strong>Shunt blockage is a critical complication following mBTT shunt, significantly increasing mortality risk. While shunt size is not independently predictive, multiple factors, including patient weight, underlying pathology, coagulation profile, surgical factors, and shunt size-to-weight ratio, may contribute to thrombosis risk and warrant further investigation.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"329-340"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421538/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041837","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-07-21eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.27159
Ensar Duras, Recep Siyar Balik, Perver Arslan, Erman Cilsal, Murat Sahin, Ibrahim Cansaran Tanidir, Yakup Ergul, Alper Guzeltas
Background: The aim of our study was to evaluate the hemodynamic effects and clinical outcomes of transcatheter fenestration in patients who developed Fontan failure.
Methods: Between January 2014 and December 2022, among a total of 187 patients undergoing the Fontan operation, 10 (6 males, 4 females; median age: 10.9 years; range, 4.2 to 23 years) who underwent transcatheter creation or dilation of a Fontan fenestration due to the development of Fontan failure were retrospectively analyzed. Demographic data, laboratory results, echocardiographic findings, and catheterization parameters of the patients were recorded. The patients were classified into two groups based on the timing of Fontan failure: those who underwent fenestration before hospital discharge constituted the early-stage group, while those who underwent fenestration after discharge were assigned to the late-stage group. These two groups were compared in terms of hemodynamic parameters, changes in oxygen saturation, and complication rates.
Results: Transcatheter fenestration was performed in five patients due to Fontan failure in the early postoperative period, and in five patients in the late period. The median follow-up duration was 2.2 (range, 0.1 to 6) years. Following the procedure, pleural effusion regressed in four patients; median systemic venous pressure decreased by 3.4 (range, 2 to 9) mmHg, while median oxygen saturation dropped by 5.9% (range, 3 to 9%). Clinical improvement was observed in 70% of the patients within the first month. However, one patient died on postoperative Day 44 due to low cardiac output. Fenestration was performed in three patients with protein-losing enteropathy, and clinical improvement was achieved in all of them.
Conclusion: Transcatheter Fontan fenestration is a reliable therapeutic option for reducing systemic venous pressure and achieving hemodynamic improvement in symptomatic Fontan patients. Our study highlights the low complication rates and the potential of this procedure to yield favorable clinical outcomes. Transcatheter fenestration plays an important role in the management of high-risk Fontan patients.
{"title":"Transcatheter fenestration in Fontan failure: Our clinical experience.","authors":"Ensar Duras, Recep Siyar Balik, Perver Arslan, Erman Cilsal, Murat Sahin, Ibrahim Cansaran Tanidir, Yakup Ergul, Alper Guzeltas","doi":"10.5606/tgkdc.dergisi.2025.27159","DOIUrl":"10.5606/tgkdc.dergisi.2025.27159","url":null,"abstract":"<p><strong>Background: </strong>The aim of our study was to evaluate the hemodynamic effects and clinical outcomes of transcatheter fenestration in patients who developed Fontan failure.</p><p><strong>Methods: </strong>Between January 2014 and December 2022, among a total of 187 patients undergoing the Fontan operation, 10 (6 males, 4 females; median age: 10.9 years; range, 4.2 to 23 years) who underwent transcatheter creation or dilation of a Fontan fenestration due to the development of Fontan failure were retrospectively analyzed. Demographic data, laboratory results, echocardiographic findings, and catheterization parameters of the patients were recorded. The patients were classified into two groups based on the timing of Fontan failure: those who underwent fenestration before hospital discharge constituted the early-stage group, while those who underwent fenestration after discharge were assigned to the late-stage group. These two groups were compared in terms of hemodynamic parameters, changes in oxygen saturation, and complication rates.</p><p><strong>Results: </strong>Transcatheter fenestration was performed in five patients due to Fontan failure in the early postoperative period, and in five patients in the late period. The median follow-up duration was 2.2 (range, 0.1 to 6) years. Following the procedure, pleural effusion regressed in four patients; median systemic venous pressure decreased by 3.4 (range, 2 to 9) mmHg, while median oxygen saturation dropped by 5.9% (range, 3 to 9%). Clinical improvement was observed in 70% of the patients within the first month. However, one patient died on postoperative Day 44 due to low cardiac output. Fenestration was performed in three patients with protein-losing enteropathy, and clinical improvement was achieved in all of them.</p><p><strong>Conclusion: </strong>Transcatheter Fontan fenestration is a reliable therapeutic option for reducing systemic venous pressure and achieving hemodynamic improvement in symptomatic Fontan patients. Our study highlights the low complication rates and the potential of this procedure to yield favorable clinical outcomes. Transcatheter fenestration plays an important role in the management of high-risk Fontan patients.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"288-300"},"PeriodicalIF":0.5,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421547/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041975","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: This study aims to evaluate the effectiveness of application of physiotherapy via remote telerehabilitation in the early postoperative period following thoracic surgery.
Methods: Between October 2020 and July 2024, a total of 40 patients (25 males, 15 females; mean age: 57.8±9.6 years; range, 42 to 77 years) who underwent thoracic surgery due to Stage 1A-3B non-small cell lung cancer were included in this randomized-controlled clinical study. The patients were divided into two groups: the telerehabilitation group (TG, n=20) and the control group (CG, n=20). Patients in the TG participated in a teleconference-based exercise program supervised by a physiotherapist, starting the day before surgery and continuing daily until discharge. Patients in the CG received a single preoperative exercise session and an educational brochure. All patients were assessed at five time points: preoperatively, immediately after surgery, prior to discharge, at one to three months post-discharge, and at six months post-discharge. Outcome measures included the duration of intensive care unit stay, total hospital stay, chest drain duration, postoperative complications, inflammatory biomarkers, pain, dyspnea, fatigue, spirometry, and State-Trait Anxiety Inventory (STAI) scores.
Results: Both groups had similar baseline characteristics including comorbidities and types of surgery (p>0.05). There were no significant differences in the intensive care unit stay duration (p=0.739), total hospital stay (p=0.311), or chest drain duration (p=0.431) between the groups. However, TG showed significantly lower pain and fatigue levels compared to CG (p<0.05).
Conclusion: Telerehabilitation effectively reduced pain and fatigue in patients after thoracic surgery. The lack of significant differences in other outcomes may be attributed to variations in patient compliance. These findings suggest that telerehabilitation can be a valuable alternative to traditional rehabilitation, particularly during pandemic or isolation.
{"title":"Telerehabilitation for thoracic surgery patients: An effective alternative during the pandemic.","authors":"Esra Pehlivan, Burcu Kılıç, Ayça Evkaya Acar, Yaman Khoraki, Sibel Gayretli Atan, Akif Turna","doi":"10.5606/tgkdc.dergisi.2025.27287","DOIUrl":"10.5606/tgkdc.dergisi.2025.27287","url":null,"abstract":"<p><strong>Background: </strong>This study aims to evaluate the effectiveness of application of physiotherapy via remote telerehabilitation in the early postoperative period following thoracic surgery.</p><p><strong>Methods: </strong>Between October 2020 and July 2024, a total of 40 patients (25 males, 15 females; mean age: 57.8±9.6 years; range, 42 to 77 years) who underwent thoracic surgery due to Stage 1A-3B non-small cell lung cancer were included in this randomized-controlled clinical study. The patients were divided into two groups: the telerehabilitation group (TG, n=20) and the control group (CG, n=20). Patients in the TG participated in a teleconference-based exercise program supervised by a physiotherapist, starting the day before surgery and continuing daily until discharge. Patients in the CG received a single preoperative exercise session and an educational brochure. All patients were assessed at five time points: preoperatively, immediately after surgery, prior to discharge, at one to three months post-discharge, and at six months post-discharge. Outcome measures included the duration of intensive care unit stay, total hospital stay, chest drain duration, postoperative complications, inflammatory biomarkers, pain, dyspnea, fatigue, spirometry, and State-Trait Anxiety Inventory (STAI) scores.</p><p><strong>Results: </strong>Both groups had similar baseline characteristics including comorbidities and types of surgery (p>0.05). There were no significant differences in the intensive care unit stay duration (p=0.739), total hospital stay (p=0.311), or chest drain duration (p=0.431) between the groups. However, TG showed significantly lower pain and fatigue levels compared to CG (p<0.05).</p><p><strong>Conclusion: </strong>Telerehabilitation effectively reduced pain and fatigue in patients after thoracic surgery. The lack of significant differences in other outcomes may be attributed to variations in patient compliance. These findings suggest that telerehabilitation can be a valuable alternative to traditional rehabilitation, particularly during pandemic or isolation.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"365-374"},"PeriodicalIF":0.5,"publicationDate":"2025-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421554/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041958","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-06-27eCollection Date: 2025-07-01DOI: 10.5606/tgkdc.dergisi.2025.27289
Selçuk Gürz, Ayşen Şengül
Background: This study aim to evaluate the feasibility of threedimensional (3D) modeling using open-source free software for preoperative planning and intraoperative guidance in uniportal video-assisted thoracoscopic segmentectomies.
Methods: Between October 2020 and November 2023, 50 patients (27 males, 23 females; mean age: 60±11.1 years; range, 34 to 78 years) who underwent uniportal video-assisted thoracoscopic pulmonary segmentectomy with preoperative 3D modeling were retrospectively analyzed. Preoperative 3D modeling was performed using computed tomography with an open-source 3D software program. The virtual models exported to the mobile device were compared with the anatomical structures of the patient intraoperatively. The patients were divided into two groups as simple and complex segmentectomy according to the characteristics of the surgical procedures.
Results: The overall matching success rate of the virtual 3D models with intraoperatively identified bronchovascular structures was 99.27%. The overall variation rate was 36% (n=18) among all patients. There was a significant difference between the two groups in terms of the bronchovascular variation. The bronchovascular variation rate was 11.1% (n=2) in Group 1 and 50% (n=16) in Group 2 (p=0.006).
Conclusion: Three-dimensional modeling using open-source software for preoperative planning and intraoperative guidance is a reliable method for detecting bronchovascular structures of the target segment with high accuracy in uniportal video-assisted thoracoscopic surgery segmentectomy.
{"title":"Three-dimensional modeling of bronchovascular anatomy for preoperative planning and intraoperative guidance in uniportal video-assisted thoracoscopic segmentectomy.","authors":"Selçuk Gürz, Ayşen Şengül","doi":"10.5606/tgkdc.dergisi.2025.27289","DOIUrl":"10.5606/tgkdc.dergisi.2025.27289","url":null,"abstract":"<p><strong>Background: </strong>This study aim to evaluate the feasibility of threedimensional (3D) modeling using open-source free software for preoperative planning and intraoperative guidance in uniportal video-assisted thoracoscopic segmentectomies.</p><p><strong>Methods: </strong>Between October 2020 and November 2023, 50 patients (27 males, 23 females; mean age: 60±11.1 years; range, 34 to 78 years) who underwent uniportal video-assisted thoracoscopic pulmonary segmentectomy with preoperative 3D modeling were retrospectively analyzed. Preoperative 3D modeling was performed using computed tomography with an open-source 3D software program. The virtual models exported to the mobile device were compared with the anatomical structures of the patient intraoperatively. The patients were divided into two groups as simple and complex segmentectomy according to the characteristics of the surgical procedures.</p><p><strong>Results: </strong>The overall matching success rate of the virtual 3D models with intraoperatively identified bronchovascular structures was 99.27%. The overall variation rate was 36% (n=18) among all patients. There was a significant difference between the two groups in terms of the bronchovascular variation. The bronchovascular variation rate was 11.1% (n=2) in Group 1 and 50% (n=16) in Group 2 (p=0.006).</p><p><strong>Conclusion: </strong>Three-dimensional modeling using open-source software for preoperative planning and intraoperative guidance is a reliable method for detecting bronchovascular structures of the target segment with high accuracy in uniportal video-assisted thoracoscopic surgery segmentectomy.</p>","PeriodicalId":49413,"journal":{"name":"Turk Gogus Kalp Damar Cerrahisi Dergisi-Turkish Journal of Thoracic and Cardiovascular Surgery","volume":"33 3","pages":"341-348"},"PeriodicalIF":0.5,"publicationDate":"2025-06-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12421563/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145041967","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}