Meta-analysis of phase-specific survival after transcatheter versus surgical aortic valve replacement from randomized control trials.

OBJECTIVE: Transcatheter aortic valve replacement (TAVR) is an established alternative to surgical aortic valve replacement (SAVR) for severe symptomatic aortic stenosis, although phase-specific survival and cause of death are implicated following these procedures. Herein, we conducted a phase-specific meta-analysis to compare outcomes after TAVR versus SAVR. METHODS: A systematic search of databases was performed from inception through December 2022 to identify randomized controlled trials that compared outcomes of TAVR and SAVR. For each trial, the hazard ratio (HR) with 95% confidence interval (CI) of outcomes of interest was extracted for the following each specific phase: the very short-term (0-1 years after the procedure), short-term (1-2 years), and mid-term (2-5 years). Phase-specific HRs were separately pooled using the random-effects model. RESULTS: Our analysis included 8 randomized controlled trials, which enrolled a total of 8885 patients with a mean age of 79 years. The survival after TAVR compared with SAVR was greater in the very short-term periods (HR, 0.85; 95% CI, 0.74-0.98; P = .02) but similar in the short-term periods. In contrast, lower survival was observed in the TAVR group compared with the SAVR group in the mid-term periods (HR, 1.15; 95% CI, 1.03-1.29; P = .02). Similar temporal trends favoring SAVR in the mid-term were present for cardiovascular mortality and rehospitalization rates. In contrast, the rates of aortic valve reinterventions and permanent pacemaker implantations were initially greater in the TAVR group, although SAVR's superiority eventually disappeared in the mid-term. CONCLUSIONS: Our analysis demonstrated phase-specific outcomes following TAVR and SAVR.

Role of CTA Surveillance for Management of Endovascular Repair of Aortic Dissection.

OBJECTIVES: The aim of this study was to evaluate the effect of timing for post-interventional CT imaging on the rate of re-intervention and all-cause mortality in patients with endovascular treatment of type B aortic dissections (TBAD). MATERIAL AND METHODS: Data on 70 patients with endovascular repair of aortic dissection during a three-year period from a single institution retrospectively were collected. Study participants were stratified based on those who had a postoperative CTA in the first 30 days after index intervention (early) vs. those who did not (late). The re-intervention and all-cause mortality rates between the two groups were investigated using Kaplan-Meier and Cox regression analysis. RESULTS: During a median follow-up time of 230 days, the primary endpoint (additional operation) was reached in 24/70 patients (34.3%) with no statistically significant difference between the early and late CTA group (log-rank-test: P = 0.886). All-cause mortality was present in 14/70 (20%) patients, with no statistically significant difference between both groups (log-rank-test: P = 0.440). Additionally, both groups had no significant differences in time to additional operation and death. Cox regression analysis revealed the presence of a chronic TBAD and underlying connective tissue disease as relevant risk factors for the need for an additional operation and obesity as a protective and renal failure as a negative factor for all-cause mortality. CONCLUSION: CTA surveillance within 30 days of the index operation did not significantly modify mortality or rate of re-intervention after endovascular treatment for TBAD. Surveillance recommendations should be tailored to individualized factors.

Prolonged Ischemia Times for Heart Transplantation: Impact of the 2018 Allocation Change.

BACKGROUND: In 2018, the United Network for Organ Sharing implemented a change in heart allocation policy resulting in increased organ ischemia times in early analyses. This study evaluated the effect of ischemia time on 1-year mortality in the context of allocation policy changes implemented in 2006 and 2018. METHODS: The United Network for Organ Sharing registry was used to identify adults undergoing heart transplantation from 2000 to 2020. Patients were stratified by the allocation policy era in which they received a transplant (2000-June 2006, July 2006-October 2018, October 2018-2020) and by ischemia time, defined as normal (≤4 hours) and prolonged (>4 hours). One-year survival was estimated using Kaplan-Meier analysis. Cox regression was used to determine risk-adjusted hazards for ischemia time on 1-year mortality. RESULTS: There were 40 052 patients included for analysis. Ischemia times were normal in 32 585 (81.36%) and prolonged in 7467 (18.64%) patients. The proportion of transplantations with prolonged ischemia times increased with each subsequent policy era. After the 2018 policy change, 1-year survival was 90.92% with normal ischemia times vs 87.52% with prolonged ischemia times (P < .001). Ischemia time independently predicted 1-year mortality in each era with a hazard ratio of 1.20 per hour (P = .004) in the current era. CONCLUSIONS: Prolonged ischemia times occur in a minority of cases but are increasing in frequency. The independent risk of prolonged ischemia time on 1-year mortality persists despite advances in storage technology and should remain a consideration in donor-recipient matching.

Pathophysiology and Pathogenesis of Marfan Syndrome.

Marfan syndrome (MFS) is a systemic connective tissue disorder that is inherited in an autosomal dominant pattern with variable penetrance. While clinically this disease manifests in many different ways, the most life-threatening manifestations are related to cardiovascular complications including mitral valve prolapse, aortic insufficiency, dilatation of the aortic root, and aortic dissection. In the past 30 years, research efforts have not only identified the genetic locus responsible but have begun to elucidate the molecular pathogenesis underlying this disorder, allowing for the development of seemingly rational therapeutic strategies for treating affected individuals. In spite of these advancements, the cardiovascular complications still remain as the most life-threatening clinical manifestations. The present chapter will focus on the pathophysiology and clinical treatment of Marfan syndrome, providing an updated overview of the recent advancements in molecular genetics research and clinical trials, with an emphasis on how this information can focus future efforts toward finding betters ways to detect, diagnose, and treat this devastating condition.