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A Surgical Model of Heart Failure with Preserved Ejection Fraction in Tibetan Minipigs
Published on: February 18, 2022
[Surgical heart failure treatment program - the experience of Kazakhstan]
Insights
Ventricular assist device (VAD) therapy offers a viable alternative to heart transplantation in Kazakhstan. This advanced heart failure treatment improved patient function and survival rates, demonstrating its effectiveness.
Area of Science:
- Cardiology
- Cardiovascular Surgery
- Medical Technology
Context:
- Kazakhstan faces geographical and cultural barriers to heart transplantation.
- A national healthcare system supports a specialized ventricular assist device (VAD) program.
- The program utilizes a central surgical center and regional outpatient follow-up infrastructure.
Purpose:
- To evaluate the feasibility and outcomes of a VAD program in Kazakhstan.
- To assess the impact of VAD therapy on advanced heart failure patients.
- To identify key components for a successful VAD program.
Summary:
- 95 patients received 100 left ventricular assist devices (LVADs) between 2011-2013.
- Significant improvements observed in NYHA class, 6-minute walk test, and NT-proBNP levels.
- One-year survival rate was 69%, with better outcomes for higher INTERMACS profiles.
Impact:
- LVAD therapy is a realistic alternative where heart transplantation is not feasible.
- Program success relies on a specialized multidisciplinary team, coordinated follow-up, and healthcare system support.
- Demonstrates the potential for VADs to manage advanced heart failure effectively in resource-limited settings.
Abstract:
In Kazakhstan, geographical and cultural reasons do not favor the development of heart transplant activity. Thus, a surgical program for treatment of advanced, refractory heart failure was implemented, focusing the efforts on ventricular assist device (VAD) therapy. The program, supported and funded by the national healthcare system, is based on a single, highly specialized surgical Center for the operation, and on a regional infrastructure for outpatient follow-up. Regional VAD coordinators are educated by the National Center. They are in charge of regular patient check, anticoagulant and antiplatelet treatment prescription, and continuing patients' and caregivers' education, mainly regarding driveline exit site dressing and driveline stabilization. From November 2011 to November 2013, 95 patients received 100 devices, mainly for left ventricular support (LVAD): HeartMate II, n=70, HeartWare, n=25. Mean age was 49.5 years, and 87.37% of the patients were males. Most patients had INTERMACS profile 4 (55%), followed by 3 and 2 (17% each). Symptomatic and functional improvement are testified by changes from baseline to month 3 of NYHA functional class (from III-IV to I-II), results of the 6-min walk test (from 152 to 440 m), and NT-proBNP levels (from 6997 to 1126 pg/ml). Overall 1-year survival was 69%, with a trend for outcome improvement over time and a relationship with preoperative INTERMACS profile (1-year survival of 60% in patients with INTERMACS profile 1-2 vs 75% in those with INTERMACS profile 3-4). In summary, where and when a heart transplant program cannot be implemented, LVAD represents a realistic therapeutic alternative. The key points for a successful VAD program are a dedicated, highly specialized multidisciplinary team at the Cardiac Surgery Center, an infrastructure throughout the country for coordinated outpatient follow-up, adequate reimbursement for this activity, and support by the healthcare system.
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