Introduction: In patients undergoing surgery for mitral valve replacement (MVR) for valvular heart disease, pulmonary artery hypertension (PAH) has been considered a major risk factor. In this prospective study, we ha...Introduction: In patients undergoing surgery for mitral valve replacement (MVR) for valvular heart disease, pulmonary artery hypertension (PAH) has been considered a major risk factor. In this prospective study, we have studied the early hemodynamic changes and post-operative outcomes of MVR among patients with severe PAH. Methods: 68 consecutive patients who underwent mitral valve replacement for severe rheumatic mitral valve disease with severe PAH (pulmonary artery pressure (PAP) > 50 mmHg) were studied prospectively for immediate postoperative hemodynamics and outcomes. The mean age of the patients was 32.1 years. 32 (47.05%) patients had mitral stenosis, 13 (19.11%) had mitral regurgitation and 23 (33.82%) had mixed lesions. Patients were divided into two groups based on preoperative pulmonary artery pressures. In 56 patients (82.35%, group I) PAP was sub-systemic or systemic, with a mean of 58.4 mmHg. Twelve patients (17.65%, group II) had supra-systemic PAP with a mean of 82.4 mmHg. Results: After mitral valve replacement, the PAP and pulmonary vascular resistance (PVR) decreased significantly in group I to near normal levels. In group II also the PAP and PVR decreased significantly but significant residual PAH remained. Operative mortality was 3.5% in group I and 16.6% in group II. Conclusions: MVR is safe and effective at the presence of severe PAH as long as the PAP is below or equal to systemic pressures. With suprasystemic PAP, MVR carries a high risk of mortality and the patient continues to have severe PAH in the postoperative period.展开更多
Left main coronary compression syndrome(LMCS)may complicate pulmonary artery aneurysms(PAA),usually developed in the context of pulmonary arterial hypertension(PAH).We report the case of a 51-year-old female patient w...Left main coronary compression syndrome(LMCS)may complicate pulmonary artery aneurysms(PAA),usually developed in the context of pulmonary arterial hypertension(PAH).We report the case of a 51-year-old female patient with an atrial septal defect(unsuitable for device closure)complicated by a PAA generating a 90%left main stenosis.The significant PAH held us back from immediate surgery.After specific dual PAH-targeted therapy(sildenafil and bosentan),the atrial septal defect could be closed with a unidirectional valved patch;the PAAinduced LMCS was treated by reductive arterioplasty.The postoperative course was uneventful.Follow-up showed clinical improvement,but PAH treatment was still needed.After three months,coronary angiography showed only an insignificant residual left main stenosis,proving that reductive pulmonary arterioplasty was effective in treating LMCS.Any PAA requires further evaluation for LMCS,a dangerous but treatable complication.The“treat-repair-treat”strategy and shunt-closure with a unidirectional valved patch can both improve surgical prospects of LMCS with shunt-related PAH.展开更多
Objective: To study early results of hand made fresh (autologous/homologous) pericardial valved conduit in achieving right ventricle to pulmonary artery continuity. Method: Between November 2014 and September 2015, 19...Objective: To study early results of hand made fresh (autologous/homologous) pericardial valved conduit in achieving right ventricle to pulmonary artery continuity. Method: Between November 2014 and September 2015, 19 cases, with diagnosis of Tetralogy of Fallot with Pulmonary stenosis (PS) or Pulmonary atresia (PA) underwent intracardiac repair and Right Ventricular Outflow Tract (RVOT) reconstruction with hand made fresh [autologous (n = 2)/ homologous (n = 17)] pericardial valved conduit. Mean age of the patients at time of surgery was 6.37 years (range 3 months to 18 years), mean weight was 18.52 kilograms (range 6 kg to 40 kg) and mean size of the conduit was 20.7 mm (range 16 mm to 24 mm). Results: All patients had a smooth post-operative course, with mean ICU (Intensive Care Unit) stay of 3.6 days (range 3 days to 6 days) and mean post-operative hospital stay 8.5 days (range 7 days to 16 days). Intra-operative and Post-operative echocardiography revealed moderate Pulmonary regurgitation (PR) in one patient, mild PR in 5 patients and no or trace PR in 13 patients. No patient has developed conduit stenosis or calcification till now. Conclusion: Autologous or homologous pericardial valved conduit provides good early results and is especially suitable for developing world because of zero cost. Long term usefulness of such option remains to be confirmed in terms of dilation, calcification and freedom from intervention.展开更多
Objective:The Pulmonary Arterial Denervation in Patients With Pulmonary Hypertension Associated With the Left Heart Failure(PADN-5)study proved that pulmonary artery denervation(PADN)is associated with significant imp...Objective:The Pulmonary Arterial Denervation in Patients With Pulmonary Hypertension Associated With the Left Heart Failure(PADN-5)study proved that pulmonary artery denervation(PADN)is associated with significant improvements in hemodynamic and clinical outcomes in patients with combined pre-and post-capillary pulmonary hypertension(CpcPH).This study aimed to assess the 3-year clinical results of PADN in patients who had heart failure with preserved ejection fraction(HFpEF)developing into CpcPH(HFpEF-CpcPH).Methods:In this post hoc analysis of the PADN-5 trial,38 patients with HFpEF were included in screening out of 98 patients with CpcPH who were randomly assigned to treatment with sildenafil and sham PADN(sham PADN(plus sildenafil)group,abbreviated as sham group)or PADN(PADN group).HFpEF in the PADN-5 trial was defined as a left ventricular ejection fraction≥50%,and CpcPH was defined as a mean pulmonary arterial pressure≥25 mmHg,a pulmonary arterial wedge pressure>15 mmHg,and a pulmonary vascular resistance>3.0 WU.The changes in the 6-minute walk distance(6-MWD)and the plasma concentration of N-terminal pro-brain natriuretic peptide(NT-proBNP)at 6-month and 3-year follow-up,as well as the clinical endpoint of the occurrence of clinical worsening,defined as cardiopulmonary-related death,rehospitalization,or heart or lung transplantation at 3-year follow-up were examined.Results:Thirty-eight patients with HFpEF-CpcPH were assigned to the PADN group(n=19)or the sham group(n=19).At the 6-month follow-up,6-MWD(433(275,580)m vs.342(161,552)m),and reductions in NT-proBNP(−47%(−99%,331%)vs.−12%(−82%,54%))were significantly improved in the PADN group(all P<0.05).Over the 3-year follow-up period,PADN treatment resulted in marked increases in 6-MWD(450(186,510)m vs.348(135,435)m)and reductions in NT-proBNP(−55%(−99%,38%)vs.−10%(−80%,95%))(all P<0.05).Clinical worsening was experienced by 12 patients(63%)in the sham group,but by only 5 patients(26%)in the PADN group(hazard ratio=0.149,95%confidence interval:0.038–0.584,P=0.006).The 6-MWD and PADN treatments were independent predictors of clinical deterioration in patients with HFpEF-CpcPH.Conclusions:PADN therapy is associated with improvements in exercise capacity and clinical outcomes.PADN therapy may have a potential role in patients with HFpEF-CpcPH for whom current treatment options are limited.展开更多
Absent pulmonary valve is a rare congenital anomaly, characterized with a dysplastic or absent pulmonary valve tissue and severe pulmonary regurgitation. It is usually associated with tetralogy of Fallot (TOF). A 7-...Absent pulmonary valve is a rare congenital anomaly, characterized with a dysplastic or absent pulmonary valve tissue and severe pulmonary regurgitation. It is usually associated with tetralogy of Fallot (TOF). A 7-year-old girl with absent pulmonary valve, pulmonary artery aneurysm and tetralogy of Fallot without cyanosis was operated and 10 months followed up result was reported展开更多
目的:分析风湿性二尖瓣狭窄患者二尖瓣置换术后的早期临床转归。方法:回顾分析128例因风湿性二尖瓣狭窄行二尖瓣置换术患者的临床资料,根据心脏彩超估测的肺动脉收缩压(SPAP)结果分为A组(30 mm Hg≤SPAP<50 mm Hg,n=70)和B组(SPAP≥5...目的:分析风湿性二尖瓣狭窄患者二尖瓣置换术后的早期临床转归。方法:回顾分析128例因风湿性二尖瓣狭窄行二尖瓣置换术患者的临床资料,根据心脏彩超估测的肺动脉收缩压(SPAP)结果分为A组(30 mm Hg≤SPAP<50 mm Hg,n=70)和B组(SPAP≥50 mm Hg,n=58),比较2组一般资料、手术相关资料、围手术期结果及早期随访结果。结果:2组间除SPAP、肺功能及右心室内径外,其余术前指标差异均无统计学意义。围手术期死亡5例,A组2例,B组3例。术后机械通气时间及ICU治疗时间B组均大于A组(P均<0.05)。术后2组患者SPAP均较术前下降(P均<0.05)。术后6个月复查心脏彩超显示2组病例人工瓣膜功能良好;A组SPAP升高至术前水平或以上患者2例,B组11例,2组相比,差异有统计学意义(χ2=7.644,P=0.006)。结论:二尖瓣狭窄患者的术前肺动脉压高增加了术后复发肺动脉高压的风险,早期临床转归也相对较差。展开更多
目的平均肺动脉压(MPAP)是诊断和评价肺动脉高压的重要指标。本研究拟对比多普勒超声测量三尖瓣反流速度估测肺动脉收缩压(PASP)和三尖瓣反流速度诊断肺动脉高压2种方法,评价应用三尖瓣血流速度图对肺动脉高压的诊断效果。资料与方法收...目的平均肺动脉压(MPAP)是诊断和评价肺动脉高压的重要指标。本研究拟对比多普勒超声测量三尖瓣反流速度估测肺动脉收缩压(PASP)和三尖瓣反流速度诊断肺动脉高压2种方法,评价应用三尖瓣血流速度图对肺动脉高压的诊断效果。资料与方法收集2012年1月—2013年6月第四军医大学唐都医院以及沈阳军区总医院收治并拟行封堵术的先天性左向右分流心脏病患者80例。经心导管测量肺动脉压力,应用多普勒超声测量三尖瓣反流速度峰值。结果以导管测量的MPAP≥25 mm Hg为诊断标准,使用三尖瓣反流估算的PASP>30 mm Hg诊断肺动脉高压时,假阳性率为62.96%、假阴性率为0。使用三尖瓣反流速度诊断肺动脉高压具有较高的诊断一致性。分别以320 cm/s和340 cm/s为诊断界值时,假阳性率分别为14.81%和7.41%,假阴性率为15.91%和20.45%。结论对于左向右分流的先天性心脏病患者,采用超声心动图,并根据三尖瓣反流峰值速度直接诊断肺动脉高压可有效克服估算法存在较高假阳性率的问题,更适合基于MPAP为标准的肺动脉高压的诊断。展开更多
文摘Introduction: In patients undergoing surgery for mitral valve replacement (MVR) for valvular heart disease, pulmonary artery hypertension (PAH) has been considered a major risk factor. In this prospective study, we have studied the early hemodynamic changes and post-operative outcomes of MVR among patients with severe PAH. Methods: 68 consecutive patients who underwent mitral valve replacement for severe rheumatic mitral valve disease with severe PAH (pulmonary artery pressure (PAP) > 50 mmHg) were studied prospectively for immediate postoperative hemodynamics and outcomes. The mean age of the patients was 32.1 years. 32 (47.05%) patients had mitral stenosis, 13 (19.11%) had mitral regurgitation and 23 (33.82%) had mixed lesions. Patients were divided into two groups based on preoperative pulmonary artery pressures. In 56 patients (82.35%, group I) PAP was sub-systemic or systemic, with a mean of 58.4 mmHg. Twelve patients (17.65%, group II) had supra-systemic PAP with a mean of 82.4 mmHg. Results: After mitral valve replacement, the PAP and pulmonary vascular resistance (PVR) decreased significantly in group I to near normal levels. In group II also the PAP and PVR decreased significantly but significant residual PAH remained. Operative mortality was 3.5% in group I and 16.6% in group II. Conclusions: MVR is safe and effective at the presence of severe PAH as long as the PAP is below or equal to systemic pressures. With suprasystemic PAP, MVR carries a high risk of mortality and the patient continues to have severe PAH in the postoperative period.
文摘Left main coronary compression syndrome(LMCS)may complicate pulmonary artery aneurysms(PAA),usually developed in the context of pulmonary arterial hypertension(PAH).We report the case of a 51-year-old female patient with an atrial septal defect(unsuitable for device closure)complicated by a PAA generating a 90%left main stenosis.The significant PAH held us back from immediate surgery.After specific dual PAH-targeted therapy(sildenafil and bosentan),the atrial septal defect could be closed with a unidirectional valved patch;the PAAinduced LMCS was treated by reductive arterioplasty.The postoperative course was uneventful.Follow-up showed clinical improvement,but PAH treatment was still needed.After three months,coronary angiography showed only an insignificant residual left main stenosis,proving that reductive pulmonary arterioplasty was effective in treating LMCS.Any PAA requires further evaluation for LMCS,a dangerous but treatable complication.The“treat-repair-treat”strategy and shunt-closure with a unidirectional valved patch can both improve surgical prospects of LMCS with shunt-related PAH.
文摘Objective: To study early results of hand made fresh (autologous/homologous) pericardial valved conduit in achieving right ventricle to pulmonary artery continuity. Method: Between November 2014 and September 2015, 19 cases, with diagnosis of Tetralogy of Fallot with Pulmonary stenosis (PS) or Pulmonary atresia (PA) underwent intracardiac repair and Right Ventricular Outflow Tract (RVOT) reconstruction with hand made fresh [autologous (n = 2)/ homologous (n = 17)] pericardial valved conduit. Mean age of the patients at time of surgery was 6.37 years (range 3 months to 18 years), mean weight was 18.52 kilograms (range 6 kg to 40 kg) and mean size of the conduit was 20.7 mm (range 16 mm to 24 mm). Results: All patients had a smooth post-operative course, with mean ICU (Intensive Care Unit) stay of 3.6 days (range 3 days to 6 days) and mean post-operative hospital stay 8.5 days (range 7 days to 16 days). Intra-operative and Post-operative echocardiography revealed moderate Pulmonary regurgitation (PR) in one patient, mild PR in 5 patients and no or trace PR in 13 patients. No patient has developed conduit stenosis or calcification till now. Conclusion: Autologous or homologous pericardial valved conduit provides good early results and is especially suitable for developing world because of zero cost. Long term usefulness of such option remains to be confirmed in terms of dilation, calcification and freedom from intervention.
基金supported by the National Scientific Foundation of China(82100438,82270436,and 82121001).
文摘Objective:The Pulmonary Arterial Denervation in Patients With Pulmonary Hypertension Associated With the Left Heart Failure(PADN-5)study proved that pulmonary artery denervation(PADN)is associated with significant improvements in hemodynamic and clinical outcomes in patients with combined pre-and post-capillary pulmonary hypertension(CpcPH).This study aimed to assess the 3-year clinical results of PADN in patients who had heart failure with preserved ejection fraction(HFpEF)developing into CpcPH(HFpEF-CpcPH).Methods:In this post hoc analysis of the PADN-5 trial,38 patients with HFpEF were included in screening out of 98 patients with CpcPH who were randomly assigned to treatment with sildenafil and sham PADN(sham PADN(plus sildenafil)group,abbreviated as sham group)or PADN(PADN group).HFpEF in the PADN-5 trial was defined as a left ventricular ejection fraction≥50%,and CpcPH was defined as a mean pulmonary arterial pressure≥25 mmHg,a pulmonary arterial wedge pressure>15 mmHg,and a pulmonary vascular resistance>3.0 WU.The changes in the 6-minute walk distance(6-MWD)and the plasma concentration of N-terminal pro-brain natriuretic peptide(NT-proBNP)at 6-month and 3-year follow-up,as well as the clinical endpoint of the occurrence of clinical worsening,defined as cardiopulmonary-related death,rehospitalization,or heart or lung transplantation at 3-year follow-up were examined.Results:Thirty-eight patients with HFpEF-CpcPH were assigned to the PADN group(n=19)or the sham group(n=19).At the 6-month follow-up,6-MWD(433(275,580)m vs.342(161,552)m),and reductions in NT-proBNP(−47%(−99%,331%)vs.−12%(−82%,54%))were significantly improved in the PADN group(all P<0.05).Over the 3-year follow-up period,PADN treatment resulted in marked increases in 6-MWD(450(186,510)m vs.348(135,435)m)and reductions in NT-proBNP(−55%(−99%,38%)vs.−10%(−80%,95%))(all P<0.05).Clinical worsening was experienced by 12 patients(63%)in the sham group,but by only 5 patients(26%)in the PADN group(hazard ratio=0.149,95%confidence interval:0.038–0.584,P=0.006).The 6-MWD and PADN treatments were independent predictors of clinical deterioration in patients with HFpEF-CpcPH.Conclusions:PADN therapy is associated with improvements in exercise capacity and clinical outcomes.PADN therapy may have a potential role in patients with HFpEF-CpcPH for whom current treatment options are limited.
基金supported by grants National Distinguished Youth Science Fund (No.30525020)
文摘Absent pulmonary valve is a rare congenital anomaly, characterized with a dysplastic or absent pulmonary valve tissue and severe pulmonary regurgitation. It is usually associated with tetralogy of Fallot (TOF). A 7-year-old girl with absent pulmonary valve, pulmonary artery aneurysm and tetralogy of Fallot without cyanosis was operated and 10 months followed up result was reported
文摘目的:分析风湿性二尖瓣狭窄患者二尖瓣置换术后的早期临床转归。方法:回顾分析128例因风湿性二尖瓣狭窄行二尖瓣置换术患者的临床资料,根据心脏彩超估测的肺动脉收缩压(SPAP)结果分为A组(30 mm Hg≤SPAP<50 mm Hg,n=70)和B组(SPAP≥50 mm Hg,n=58),比较2组一般资料、手术相关资料、围手术期结果及早期随访结果。结果:2组间除SPAP、肺功能及右心室内径外,其余术前指标差异均无统计学意义。围手术期死亡5例,A组2例,B组3例。术后机械通气时间及ICU治疗时间B组均大于A组(P均<0.05)。术后2组患者SPAP均较术前下降(P均<0.05)。术后6个月复查心脏彩超显示2组病例人工瓣膜功能良好;A组SPAP升高至术前水平或以上患者2例,B组11例,2组相比,差异有统计学意义(χ2=7.644,P=0.006)。结论:二尖瓣狭窄患者的术前肺动脉压高增加了术后复发肺动脉高压的风险,早期临床转归也相对较差。
文摘目的平均肺动脉压(MPAP)是诊断和评价肺动脉高压的重要指标。本研究拟对比多普勒超声测量三尖瓣反流速度估测肺动脉收缩压(PASP)和三尖瓣反流速度诊断肺动脉高压2种方法,评价应用三尖瓣血流速度图对肺动脉高压的诊断效果。资料与方法收集2012年1月—2013年6月第四军医大学唐都医院以及沈阳军区总医院收治并拟行封堵术的先天性左向右分流心脏病患者80例。经心导管测量肺动脉压力,应用多普勒超声测量三尖瓣反流速度峰值。结果以导管测量的MPAP≥25 mm Hg为诊断标准,使用三尖瓣反流估算的PASP>30 mm Hg诊断肺动脉高压时,假阳性率为62.96%、假阴性率为0。使用三尖瓣反流速度诊断肺动脉高压具有较高的诊断一致性。分别以320 cm/s和340 cm/s为诊断界值时,假阳性率分别为14.81%和7.41%,假阴性率为15.91%和20.45%。结论对于左向右分流的先天性心脏病患者,采用超声心动图,并根据三尖瓣反流峰值速度直接诊断肺动脉高压可有效克服估算法存在较高假阳性率的问题,更适合基于MPAP为标准的肺动脉高压的诊断。