Department of Surgery, Transplant Institute, NYU Langone Health, New York, New York, USA.
Department of Pediatrics, NYU Langone Health, New York, New York, USA.
Pediatr Transplant. 2024 Dec;28(8):e14874. doi: 10.1111/petr.14874.
Pretransplant functional, motor, cognitive, and academic deficits are common in pediatric patients requiring heart transplantation (HT); some persist post-HT. We assessed the association between these quality of life (QoL) deficits and post-HT outcomes.
Using SRTR data 2008-2023, we evaluated the functional, motor, cognitive, and academic status of pediatric HT recipients from listing to 15 years post-HT. We compared all-cause graft survival among patients with vs. without pre-HT deficits using Cox regressions. Among patients with a functioning graft at 1 year, we assessed the association between deficits at that time and subsequent graft failure.
In 6153 HT recipients, 85.3% had pre-HT functional status ≤ 80%, 53.1% of patients could not tolerate a full academic load; this decreased to 15.2% and 15.0% postoperatively, and was sustained. Definite or probable cognitive deficits were seen in 17.4% of patients and motor delays in 18.6%; both remained stable post-HT at 18.0% and 16.4%, respectively. Graft survival was worse in those with either pre- or post-HT deficits in functional status. Worse pre-HT functional status was associated with risk of graft failure (adjusted hazard ratio [aHR] per 10% decrease = 1.06 , p < 0.001); worse 1-year post-HT functional status was much more strongly associated with risk of graft failure (aHR = 1.18 , p < 0.001).
Pediatric HT recipients with decreased functional status are at higher risk for graft failure and mortality. These patients may benefit from early intervention aimed at improving functional status.
接受心脏移植(HT)的儿科患者在移植前存在功能、运动、认知和学业方面的缺陷,其中一些缺陷在移植后仍然存在。我们评估了这些生活质量(QoL)缺陷与移植后结局之间的关系。
利用 SRTR 数据(2008-2023 年),我们评估了从列入名单到移植后 15 年期间接受 HT 的儿科患者的功能、运动、认知和学业状况。我们使用 Cox 回归比较了移植前存在缺陷和不存在缺陷的患者之间的全因移植物存活率。在 1 年内具有功能移植物的患者中,我们评估了此时的缺陷与随后的移植物失败之间的关系。
在 6153 名 HT 受者中,85.3%的患者移植前功能状态≤80%,53.1%的患者不能耐受完整的学业负担;术后分别下降至 15.2%和 15.0%,并保持稳定。17.4%的患者存在明确或可能的认知缺陷,18.6%的患者存在运动迟缓;两者在 HT 后 1 年时分别稳定在 18.0%和 16.4%。无论是否存在移植前或移植后功能状态缺陷,移植物存活率均较差。移植前功能状态较差与移植物失败的风险相关(每降低 10%的调整风险比[aHR]为 1.06,p<0.001);而移植后 1 年功能状态较差与移植物失败的风险高度相关(aHR=1.18,p<0.001)。
功能状态下降的儿科 HT 受者发生移植物失败和死亡的风险较高。这些患者可能受益于旨在改善功能状态的早期干预。