Department of Surgery, Division of Vascular and Endovascular Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA; Department of Vascular Surgery, Erasmus University Medical Center, Rotterdam, The Netherlands.
Department of Surgery, Division of Vascular and Endovascular Surgery, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA; School of Medicine, Virginia Commonwealth University, Richmond, VA.
J Vasc Surg. 2024 Dec;80(6):1685-1696.e1. doi: 10.1016/j.jvs.2024.08.030. Epub 2024 Aug 23.
Current literature reports conflicting findings regarding the effect of diabetes mellitus (DM) on outcomes of abdominal aortic aneurysm (AAA) repair. In this study we examined the effect of DM and its management on outcomes after open AAA repair (OAR) and endovascular AAA repair (EVAR).
We identified all patients undergoing OAR or EVAR for infrarenal AAA between 2003 and 2018 in the Vascular Quality Initiative registry data linked with Medicare claims. We excluded patients with missing DM status. Patients were stratified by their preoperative DM status, and then further stratified by DM management: dietary, noninsulin antidiabetic medications (NIMs), or insulin. Outcomes of interest included 1-year aneurysm sac dynamics, 8-year aneurysm rupture, reintervention, and all-cause mortality. These outcomes were analyzed with the χ test, Kaplan-Meier methods, and multivariable Cox regression analyses.
We identified 34,021 EVAR patients and 4127 OAR patients, of whom 20% and 16% had DM, respectively. Of all DM patients, 22% were managed by dietary management, 59% by NIM, and 19% by insulin. After EVAR, DM patients were more likely to have stable sacs, whereas non-DM patients were more likely to have sac regression at 1 year. Compared with non-DM, DM was associated with a significantly lower risk for 8-year rupture in EVAR (EVAR hazard ratio [HR], 0.68; 95% confidence interval [CI], 0.51-0.92). Compared with non-DM, NIM was associated with lower risk of rupture within 8-years for both EVAR and OAR (EVAR HR, 0.64; 95% CI, 0.44-0.94; OAR HR, 0.29; 95% CI, 0.41-0.80), whereas dietary control and insulin had a similar rupture risk compared with non-DM. However, compared with non-DM, DM was associated with a higher risk of 8-year all-cause mortality after EVAR and OAR (DM vs non-DM: EVAR HR, 1.17; 95% CI, 1.11-1.23; OAR HR, 1.16; 95% CI, 1.00-1.36). After further DM management substratification, compared with non-DM, management with NIM and insulin were associated with a higher 8-year mortality in EVAR and OAR (EVAR: NIM HR, 1.12; 95% CI, 1.05-1.20; insulin: HR, 1.40; 95% CI, 1.26-1.55; OAR: NIM HR, 1.27; 95% CI, 1.06-1.54; and insulin: HR, 1.57; 95% CI, 1.15-2.13). Finally, there was a similar risk of reintervention across the DM and non-DM populations for EVAR and OAR.
DM was associated with a lower adjusted risk of rupture after EVAR as well as OAR in patients managed with NIM. Nevertheless, just as in patients without AAA, preoperative DM was associated with a higher adjusted risk of all-cause mortality. Further study is needed to evaluate for differences in aneurysm-related mortality between DM and non-DM patients, and studies are planned to evaluate the independent effect of NIM on aneurysm-related outcomes.
目前的文献报告了糖尿病(DM)对腹主动脉瘤(AAA)修复结果的影响存在矛盾。在这项研究中,我们检查了 DM 及其管理对开放 AAA 修复(OAR)和血管内 AAA 修复(EVAR)后结果的影响。
我们在 Vascular Quality Initiative 注册数据中确定了 2003 年至 2018 年间接受肾下 AAA 行 OAR 或 EVAR 的所有患者,并与 Medicare 索赔数据相关联。我们排除了 DM 状态缺失的患者。根据患者术前 DM 状态进行分层,然后根据 DM 管理方式进一步分层:饮食、非胰岛素抗糖尿病药物(NIMs)或胰岛素。感兴趣的结果包括 1 年瘤囊动力学、8 年瘤破裂、再次干预和全因死亡率。使用 χ2 检验、Kaplan-Meier 方法和多变量 Cox 回归分析来分析这些结果。
我们确定了 34021 例 EVAR 患者和 4127 例 OAR 患者,其中分别有 20%和 16%患有 DM。所有 DM 患者中,22%通过饮食管理,59%通过 NIM,19%通过胰岛素管理。在 EVAR 后,与非 DM 患者相比,DM 患者的瘤囊更可能稳定,而非 DM 患者在 1 年内瘤囊更可能缩小。与非 DM 患者相比,DM 患者在 EVAR 中 8 年破裂的风险显著降低(EVAR 风险比[HR],0.68;95%置信区间[CI],0.51-0.92)。与非 DM 患者相比,NIM 与 EVAR 和 OAR 8 年内的破裂风险降低相关(EVAR HR,0.64;95%CI,0.44-0.94;OAR HR,0.29;95%CI,0.41-0.80),而饮食控制和胰岛素与非 DM 患者的破裂风险相似。然而,与非 DM 患者相比,DM 与 EVAR 和 OAR 8 年内的全因死亡率升高相关(DM 与非 DM:EVAR HR,1.17;95%CI,1.11-1.23;OAR HR,1.16;95%CI,1.00-1.36)。进一步进行 DM 管理亚组分层后,与非 DM 患者相比,NIM 和胰岛素治疗与 EVAR 和 OAR 8 年内的死亡率升高相关(EVAR:NIM HR,1.12;95%CI,1.05-1.20;胰岛素:HR,1.40;95%CI,1.26-1.55;OAR:NIM HR,1.27;95%CI,1.06-1.54;胰岛素:HR,1.57;95%CI,1.15-2.13)。最后,在 EVAR 和 OAR 患者中,DM 和非 DM 患者的再干预风险相似。
在接受 NIM 治疗的患者中,DM 与 EVAR 和 OAR 后破裂风险降低相关。尽管如此,与没有 AAA 的患者一样,术前 DM 与全因死亡率升高相关。需要进一步研究评估 DM 和非 DM 患者之间与动脉瘤相关的死亡率差异,并计划开展研究评估 NIM 对与动脉瘤相关的结果的独立影响。