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Published on: December 11, 2017
Single-dose del Nido Cardioplegia in Minimally Invasive Aortic Valve Surgery
Daniel Ziazadeh1, Regina Mater1, Ben Himelhoch1
1Michigan State University College of Human Medicine, Grand Rapids, Michigan.
Insights
Del Nido cardioplegia (DC) offers safe and effective cardiac protection in minimally invasive aortic valve surgery. This study found DC comparable to standard blood cardioplegia (BC), simplifying the regimen and reducing cross-clamp time.
Area of Science:
- Cardiovascular Surgery
- Cardiac Anesthesia
- Cardioplegia Solutions
Background:
- Del Nido cardioplegia (DC) is recognized for prolonged cardiac protection via single-dose administration and safety in adult CABG.
- Standard blood cardioplegia (BC) is commonly used, but its efficacy in minimally invasive procedures warrants comparison.
Purpose of the Study:
- To evaluate the efficacy of cardiac protection and clinical outcomes of DC compared to BC in minimally invasive aortic valve surgery (mini-AVR).
Main Methods:
- A retrospective analysis of 178 patients undergoing mini-AVR between August 2011 and May 2016.
- Patients received either BC (n=101) or DC (n=77) via ministernotomy or right minithoracotomy.
- Propensity score matching created 63 well-matched pairs to compare outcomes, controlling for baseline characteristics.
Main Results:
- DC was associated with significantly shorter cardiopulmonary bypass (108 vs 135 min) and aortic cross-clamp times (80 vs 102 min) (P<0.001).
- Maximal glucose levels during cardiopulmonary bypass were lower in the DC group (165 vs 202 mg/dL) (P<0.001).
- No significant differences were observed in troponin T levels or postoperative ejection fraction between the groups.
Conclusions:
- Del Nido cardioplegia provides equivalent myocardial protection and clinical outcomes to standard blood cardioplegia in minimally invasive aortic valve replacement.
- DC simplifies the cardioprotective regimen, reduces aortic cross-clamp time, and demonstrates the feasibility of single-dose administration.
Abstract:
del Nido cardioplegia (DC) offers prolonged cardiac protection with single-dose administration and has been shown to be safe in adult CABG surgery. We set out to evaluate the efficacy of cardiac protection and clinical outcomes of DC versus standard blood cardioplegia (BC) in minimally invasive aortic valve surgery. From August 2011 to May 2016, 178 patients underwent minimally invasive aortic valve replacement (mini-AVR) with BC (n = 101) or DC (n = 77). Ministernotomy or right minithoracotomy was utilized for surgical access. Clinical patient characteristics and data were extracted from our local Society of Thoracic Surgeons (STS) database and the electronic medical record. Patients were propensity matched for age, gender, body mass index, valve size and type, STS score, surgical access, preop creatinine, diabetes, and chronic obstructive pulmonary disease, yielding 63 well-matched pairs. There was no difference in patient age, preoperative creatinine, body mass index, diabetes, chronic obstructive pulmonary disease, or STS score between BC and DC before or after propensity matching. BC patients received both anterograde and retrograde cardioplegias in multiple doses, whereas DC was delivered almost entirely anterograde with 95% of the patients (73/77) receiving a single dose only. DC was associated with decreased cardiopulmonary bypass time (108 ± 24 vs 135 ± 43 minutes, P = 0.001) and aortic cross-clamp time (80 ± 16 vs 102 ± 30 min, P = 0.001) and maximal glucose levels during cardiopulmonary bypass (165 ± 39 vs 202 ± 49 mg/dL, P = 0.001), whereas troponin T level did not differ between DC and BC (0.3 ± 0.29 vs 0.44 ± 1.7 ng/mL, P = 0.7). Preoperative ejection fraction did not change in either BC (64% ± 12% vs 61% ± 10%, P = 0.09) or DC (58% ± 14% vs 57% ± 14%, P = 0.4) after AVR. In minimally invasive AVR surgery, DC provided equivalent myocardial protection and clinical outcomes to BC while simplifying cardioprotective regimen and reducing aortic cross-clamp time. DC was associated with lower cardiopulmonary bypass glucose levels and demonstrated the feasibility of a single-dose administration.
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