Abstract | BACKGROUND: METHODS: RESULTS: Seven of the 14 children assessed for Tx were listed. Five were transplanted (lung Tx, n = 3; heart-lung Tx, n = 2) and two died on the waiting list. Mean age at diagnosis was 3.7 (0.4-9.5) years. Time from diagnosis to listing was 3.6 years (range 1.4-9.3). Children listed were in a worse functional class (WHO 3.5 vs. 2.5; P = 0.0006), had a lower SpO(2) on exercise (76.5% vs. 89%; P = 0.0001) and a shorter 6-min walk distance (154 m vs. 330 m; P < 0.01) than those not listed. Right ventricular function was worse in those listed (P = 0.03), as was pulmonary vascular resistance index (PVRI) on vasodilator testing (34 U m(2) vs. 14.6 U m(2); P = 0.03). Age at diagnosis and at assessment, weight, height, mean pulmonary artery pressure, baseline PVRI, B-type natriuretic peptide, spirometry and resting-SO(2) did not differ between the two groups. For the five children transplanted, median waiting time was 81 days. Age at Tx was 5.4 years. After 2.8 years all transplanted children are alive with a good functional outcome. Two patients died on the active waiting list. All children considered too well for listing are still alive and stable on treatment. CONCLUSIONS: Outcome after transplantation in children with IPAH has been encouraging. Defining listing criteria for these patients remains a challenge.
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Authors | Astrid E Lammers, Michael Burch, Christian Benden, Martin J Elliott, Philip Rees, Sheila G Haworth, Paul Aurora |
Journal | Pediatric pulmonology
(Pediatr Pulmonol)
Vol. 45
Issue 3
Pg. 263-9
(Mar 2010)
ISSN: 1099-0496 [Electronic] United States |
PMID | 20146397
(Publication Type: Journal Article)
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Topics |
- Adolescent
- Child
- Child, Preschool
- Female
- Follow-Up Studies
- Humans
- Hypertension, Pulmonary
(surgery)
- Infant
- Lung Transplantation
- Male
- Patient Selection
- Recovery of Function
- Retrospective Studies
- Survival Analysis
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