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Published on: September 6, 2014
Pediatric Lung Transplantation in Israel: 29 Cases from a Single Center's Experience
Eyal Jacobi1, Moshe Heching2, Osnat Shtraichman2
1Pulmonary Institute, Schneider Children's Medical Center, Petah Tikva, Israel, Gray Faculty of Medical and Health Sciences, Tel Aviv University, Tel Aviv, Israel.
Insights
Pediatric lung transplants in Israel show survival rates consistent with international data, with cystic fibrosis being the most common reason for the procedure. Chronic lung allograft dysfunction was the leading cause of mortality.
Area of Science:
- Pediatric pulmonology
- Thoracic surgery
- Transplant medicine
Background:
- Lung transplantation is a critical intervention for end-stage lung disease.
- Pediatric lung transplantation is less common than in adults.
- Common indications include cystic fibrosis, pulmonary hypertension, and interstitial lung disease.
Purpose of the Study:
- To evaluate the experience and outcomes of pediatric lung transplantation at Israel's largest transplant center.
Main Methods:
- Retrospective review of pediatric lung and heart-lung transplantations performed since 1997.
- Data collected included demographics, indications, clinical parameters, complications, and survival rates.
- Analysis focused on patient characteristics and post-transplant outcomes.
Main Results:
- 29 pediatric lung/heart-lung transplants were performed (3.0% of total lung transplants).
- Primary indications were cystic fibrosis (44%), pulmonary hypertension (17%), and children's interstitial lung disease (10%).
- 1, 5, 10, and 15-year survival rates were 90%, 65%, 55%, and 20%, respectively; chronic lung allograft dysfunction was the main cause of death.
Conclusions:
- Outcomes from this pediatric lung transplant program align with international registry data.
- A centralized program with a multidisciplinary team likely contributes to favorable results.
- Survival rates were not associated with transplant indication or procedure type.
Background:
Lung transplantation is an advanced medical therapy reserved for patients with end-stage lung disease. Relative to other solid organ transplants, lung transplantation in children is infrequently performed. The most common etiologies for pediatric lung transplantation worldwide are cystic fibrosis, pulmonary hypertension, and children's interstitial lung disease.
Objectives:
To describe our experience in pediatric lung transplants at Israel's largest transplant center.
Methods:
We performed a retrospective review of all pediatric lung transplantations conducted in our center since 1997. We recorded demographic characteristics, indication for transplantation, clinical and laboratory parameters, post-transplant complications, and survival rates.
Results:
Of 965 lung transplants, 29 (3.0%) were pediatric patients who underwent lung or heart-lung transplants for end-stage lung disease. Age at transplantation ranged from 2 to 18 years, with a median of 14.0 years (IQR 11-15). Primary etiologies for transplantation were cystic fibrosis (44%), pulmonary hypertension (17%), and children's interstitial lung disease (10%). Survival at 1, 5, 10, and 15 years post-transplant were 90%, 65%, 55%, and 20%, respectively, which is consistent with data reported by pediatric lung transplantation registries. The primary cause of mortality post-transplant was chronic lung allograft dysfunction. Four patients (13.8%) underwent re-transplant. There was no association between survival and transplant indication, nor between survival and type of procedure (lung vs. heart-lung transplant).
Conclusions:
The short- and long-term outcomes from our program are consistent with published registry data. These outcomes may reflect the benefits of a centralized pediatric lung transplant program, supported by a multidisciplinary team trained in high-capacity international centers.
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