INTRODUCTION
Diabetes mellitus (DM) constitutes one of the major risk factors for developing cardiovascular diseases, most importantly, coronary artery disease (CAD)1. Patients burdened with DM are at increased risk of adverse cardiovascular events by two-fold to three-fold when compared to patients without DM2. Recent guidelines of the European Society of Cardiology/European Association for Cardio-Thoracic Surgery, or ESC/EACTS, on myocardial revascularization recommended coronary artery bypass grafting (CABG) as the method of choice in the treatment of patients with multivessel CAD and DM (Class I-a)3. Although CABG is the most effective revascularization therapy in these patients, a recent meta-analysis showed that pre-existing DM places patients at higher risk for inferior long-term postoperative outcomes4. This observation could be explained by several possible mechanisms including insulin resistance, release of fatty acids in addition to other metabolic phenomena that may in turn lead to a series of events such as endothelial dysfunction, oxidative stress, inflammation, and platelet hyper-reactivity, which affects the vascular wall and enhances the progress of atherosclerosis5. It is a well-established fact that aspirin due to its antiplatelet and anti-inflammatory function is beneficial for patients with CAD. The administration of aspirin within 48 hours following CABG is associated with a reduced incidence of major adverse cardiac and cerebral events (MACCE)6. Despite aspirin’s beneficial effect in patients following CABG, its continuation throughout the perioperative period or the time of its discontinuation prior to surgery remain ambiguous.
Current guidelines differ in their recommendations regarding the use of preoperative aspirin before CABG. While some recommend its continuation until the day of surgery7-8, others recommend its discontinuation at least a few days prior elective CABG to decrease the risk of bleeding9. On the other hand, a recent meta-analysis showed that the continuation of preoperative aspirin intake is associated with reduced early mortality as well as reduced incidence of perioperative myocardial infarction (MI) following cardiac surgery10. Studies have shown that platelet function gradually recovers within 72 hours reaching full recovery within 96 hours after aspirin cessation11-12. Therefore, withdrawal of aspirin a few days before CABG could potentially lead to a partial or complete recovery of platelet function which could in turn increase the risk of thrombo-occlusive events in patients with DM. Recent studies showed that the continuation of aspirin intake with its last dose within 24 hours before CABG is associated with improved postoperative outcomes in terms of mortality, MACCE, and acute kidney injury13-15. Despite abundant evidence generated by the recent studies or meta-analyses, none of them evaluated the impact of preoperative aspirin on postoperative outcomes following CABG in patients with DM. Therefore, we aimed to investigate the effect of preoperative aspirin administration on early and long-term clinical outcomes in patients suffering from DM and CAD undergoing CABG.
METHODS
This observational, retrospective study was designed according to the Strengthening the Reporting of Observational Studies in Epidemiology, or STROBE, guidelines16. Between January 2014 and April 2018, 1221 patients underwent isolated CABG at the Department of Cardiac Surgery, Medinet Heart Center Ltd, Nowa Sol, Poland. Of these, 388 patients were diagnosed with type 2 DM. After analyzing and reviewing the data, 315 patients were included in the study and were divided into groups according to the time interval between their last aspirin dose and the time of surgery. Patients who had been continued aspirin with last administered dose ≤ 24 hours before CABG (n=144) and those who had been given the last dose of aspirin between 24 to 48 hours before CABG (n=171). Seventy-three patients were excluded due to: missing or unclear preoperative medication history (n=12), aspirin administration for more than 48 hours before CABG but less than seven days (n=18), documented intolerance to aspirin or did not take aspirin for more than seven days (n=6), emergency CABG (n=1), minimally invasive CABG (n=9), enrollment to ongoing randomized controlled trial (RCT) testing antiplatelet therapy following CABG (n=15), and administration of > 75 mg of aspirin before CABG (n=12). Figure 1 represents the patients’ flowchart diagram. The study was approved by the institutional review board at Medinet Heart Center and by the Bioethics Committee of Wroclaw’s Medical University, Poland. An individual consent of the patient for anonymous data analysis was waived by the Committee.
Patients’ demographics, clinical characteristics, medications, and postoperative outcomes were retrieved from the database of Medinet Heart Center, Nowa Sol, Poland. Preoperative aspirin dosing as well as the time of its last administration were both obtained from patients’ medication chart. The data covering preoperative dosage and time of the last aspirin dose taken by patients admitted to the hospital the day before surgery were obtained from the preoperative medication questionnaire. As for patients transferred from other departments, preoperative aspirin dosage and timing were obtained from patients’ discharge letter. Postoperatively, all patients received aspirin between six and 24 hours following CABG and that was continued daily thereafter. Follow-up data were retrieved from the national health care registry of the Ministry of Health of the Republic of Poland, that stores and analyzes all health-related data.
Study endpoints included early (30-day) and long-term MACCE and the composite of mortality and MACCE. Safety endpoints included postoperative chest tube drainage at 24 hours, postoperative transfusion rate of packed red blood cells (pRBC), need for re-exploration of the chest for bleeding, and duration of hospital stay. MACCE was defined as the occurrence of MI or cerebral adverse events (CAEs). MI was defined according to the third international definition of MI17. CAEs were defined as the development of a new permanent or transient (lasting up to 72 hours) neurologic deficit as confirmed by stroke team member assessment of the patient and computed tomography of the central nervous system, magnetic resonance imaging, or at autopsy examination.
Statistical analyses were performed using statistical software STATISTICA (TIBCO Software Inc. 2017, data analysis software system, version-13, Palo Alto, United States of America). Continuous variables were expressed as means±standard deviation (SD), while categorical variables as number and percentages. For continuous data, Student’s t-test or Mann- Whitney’s U-test was used for between groups comparisons, while categorical variables were compared with Pearson’s χ2 test.
To identify independent predictors of 30-day MACCE and composite of 30-day mortality and MACCE, we built a multivariable logistic regression model for the whole cohort by using all preoperative variables presented in Table 1. In addition to the above, operative and postoperative outcomes such as the type of surgery, number of grafts performed, duration of surgery, inotropic support, total arterial revascularization, and pRBC transfusion were included into the model. Multivariable logistic regression analysis was performed using stepwise backward regression. Only relevant covariates identified during univariate analysis with a P-value ≤ 0.1 were included in the final computation of a multivariable logistic model.
[ Table Omitted - see PDF ]
RESULTS
Baseline and operative characteristics of the unadjusted and PS-adjusted populations are presented in Tables 1 and 2. In the unadjusted study groups, female patients were more likely to be found in the group where aspirin was discontinued between 24 and 48 hours before CABG, whereas patients in whom aspirin has been continued ≤ 24 hours before CABG were more likely to receive concurrent preoperative medication such as B-blockers and statins. There were no significant differences between both groups in terms of operative characteristics such as type of surgery, duration of surgery, number of grafts performed, and number of patients with total arterial revascularization (Table 2). After performing PS matching, the differences in baseline characteristics between both groups were eliminated (Table 1). PS matching selected 119 matched pairs for final comparison. The two matched groups were balanced (-0.1 < SMD < 0.1) (Table 1). Mirrored histogram showed adequate PS overlapping (Figure 2).
[ Table Omitted - see PDF ]
DISCUSSION
DM is one of the main risk factors for CAD and is known to be associated with an increased rate of cardiovascular events when compared to patients with normoglycemia1-2. Endothelial dysfunction caused by DM triggers inflammation, which is associated with cardiovascular events in these patients20. Hyperglycemia creates a disproportion between nitric oxide and reactive oxygen species as well as reactive nitrogen species resulting in endothelial dysfunction21-22. Therefore, DM leads to vascular wall damage which in addition to platelet hyperreactivity enhances the progress of atherosclerosis, which in turn may contribute to prothrombotic conditions5. On the other hand, studies have shown increased thromboembolic events in patients undergoing CABG due to the use of extracorporeal circulation. On-pump CABG is known to induce inflammation and promotes endothelial injury23. While, in patients undergoing offpump CABG, a hypercoagulable state and platelet hyper-reactivity are observed24-26. Patients with DM undergoing CABG could be, therefore, at even higher risk for thromboembolic events as this was recently proven by a meta-analysis showing that DM constitutes a risk factor for worse long-term outcomes after CABG4. Aspirin with its antiplatelet and anti-inflammatory effects could act as a preventive measure for early thromboembolic events following CABG, especially in patients with DM, in whom aspirin was shown to have a protective effect not only for secondary prevention but also for primary prevention of first cardiovascular events27. The pharmacological mechanism of aspirin action is well described. Duration of the antiplatelet effect is determined by cyclooxygenase re-synthesis, which in case of matured platelets, its full replacement is needed to recover cyclooxygenase. However, studies have shown that the function of the platelets could gradually recover within 72 hours after aspirin withdrawal and fully normalizing its function within 96 hours11-12. Therefore, a partial recovery of the platelet function could be observed as soon as 24 to 48 hours after aspirin discontinuation.
A recent meta-analysis showed that the continuation of preoperative aspirin intake is associated with reduced early mortality as well as reduced incidence of perioperative MI following cardiac surgery10. On the other hand, recent studies showed that the continuation of aspirin intake with the last aspirin dose administered within 24 hours before CABG is associated with reduced early mortality as well as reduced incidence of MACCE13-14. Deja et al.28 in a well-designed RCT showed that the administration of preoperative aspirin prior CABG is associated with a decreased long-term hazard of MI or repeated revascularization (HR: 0.58; 95% CI: 0.33-0.99; P=0.046), whereas Xiao et al.29 observed a trend toward decreased midterm hazard of angina recurrence in patients in whom aspirin was continued till surgery. However, none of the available metaanalyses nor studies described the effect of preoperative aspirin in patients with DM undergoing CABG. Therefore, in this study, we aimed on determining the effect of preoperative aspirin use on early and long-term outcomes according to time intervals in patients with DM following CABG. We showed a clear benefit in patients with DM who took aspirin 24 hours or less prior CABG without increasing the risk of bleeding.
Limitations
The present study has several limitations. Firstly, this was a single-center, retrospective study without randomization. To reduce the risk of bias, we used PS matching. However, despite its use, many factors may still affect outcomes. Secondly, we were unable to adjust for antifibrinolytic agents due to a systematic lack of its reporting. Thirdly, we had no influence on postoperative medication at follow-up and this factor could not be adjusted in long-term follow-up. Finally, we are aware that this study might be underpowered by the sample size. Therefore, large multi-center, randomized controlled studies are required in patients with DM undergoing CABG.
CONCLUSION
In conclusion, in patients with DM undergoing CABG, continuation of preoperative aspirin intake till the day of surgery with the last dose administered within 24 hours or less prior CABG is associated with reduced incidence of early MACCE, but without significant influence on long-term outcomes.
Authors' roles & responsibilities | |
---|---|
SSAH | Substantial contributions to the conception or design of the work; or the acquisition, analysis, or interpretation of data for the work; drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
TS | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
JM | Interpretation of data for the work; drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
MP | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
MN | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
RS | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
LM | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
AL | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
MPBOS | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
RC | Drafting the work or revising it critically for important intellectual content; final approval of the version to be published |
This study was carried out at the Department of Cardiac Surgery, Medinet Heart Center Ltd, Nowa Sol, Poland.
No financial support.
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Abstract
Recent guidelines of the European Society of Cardiology/European Association for Cardio-Thoracic Surgery, or ESC/EACTS, on myocardial revascularization recommended coronary artery bypass grafting (CABG) as the method of choice in the treatment of patients with multivessel CAD and DM (Class I-a)3. Studies have shown that platelet function gradually recovers within 72 hours reaching full recovery within 96 hours after aspirin cessation11-12. [...]withdrawal of aspirin a few days before CABG could potentially lead to a partial or complete recovery of platelet function which could in turn increase the risk of thrombo-occlusive events in patients with DM. Despite abundant evidence generated by the recent studies or meta-analyses, none of them evaluated the impact of preoperative aspirin on postoperative outcomes following CABG in patients with DM. [...]we aimed to investigate the effect of preoperative aspirin administration on early and long-term clinical outcomes in patients suffering from DM and CAD undergoing CABG. Hyperglycemia creates a disproportion between nitric oxide and reactive oxygen species as well as reactive nitrogen species resulting in endothelial dysfunction21-22. [...]DM leads to vascular wall damage which in addition to platelet hyperreactivity enhances the progress of atherosclerosis, which in turn may contribute to prothrombotic conditions5.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer