Pulmonary Institute, Schneider Children's Medical Center of Israel, Petah Tikva.
Pulmonary Institute, Schneider Children's Medical Center of Israel, Petah Tikva; Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv.
Chest. 2020 Aug;158(2):660-669. doi: 10.1016/j.chest.2020.02.075. Epub 2020 Apr 13.
Prematurity is a risk factor for impaired lung function. We sought to assess the long-term effect of palivizumab immunization and extreme prematurity (<29 weeks gestation) on respiratory symptoms and pulmonary function in adolescence.
What is the long-term effect of palivizumab immunization and extreme prematurity (<29 weeks) on respiratory symptoms and pulmonary function in adolescence?
We examined survivors of extreme prematurity (<29 weeks gestation) at 13 to 18 years of age (study group). Study group babies who were born immediately before palivizumab immunization (nonpalivizumab group [NPG]) were compared with those babies who were born just after implementation (PG) and with a control group. For study group patients, lung function in adolescence was further compared longitudinally with that at primary school age.
Sixty-four adolescents aged 15.76 ± 1.52 years were included: 46 in the study group (17 PG and 29 NPG) and 18 in the control group. For the study group, wheezing episodes, inhaler use, and hospitalizations were uncommon. For the study group compared with the control group, FEV percent predicted was 82.60% ± 13.54% vs 105.83% ± 13.12% (P < .001), and the lung clearance index was 7.67 ± 1.02 vs 7.46 ± 0.70 (P = .48), respectively. Study group adolescents with bronchopulmonary dysplasia had a higher lung clearance index than did adolescents with no bronchopulmonary dysplasia (7.94 ± 1.11 vs 7.20 ± 0.60; P = .002). PG and NPG adolescents were not significantly different. Comparing the study group in adolescence with primary school age, we found improvement in mean FEV percent predicted bronchodilator response (0.37% ± 9.98% vs 5.67% ± 9.87%; P = .036) and mean provocative concentration causing 20% decline in FEV (12.16 ± 4.71 mg/mL vs 4.14 ± 4.51 mg/mL, respectively; P < .001).
Palivizumab did not provide any discernable long-term protective effect. Nevertheless, adolescent survivors of extreme prematurity showed good clinical and physiologic outcomes, except for mildly raised lung clearance index in patients with bronchopulmonary dysplasia. Airway hyperreactivity detected at primary school age, decreased by adolescence.
早产是肺功能受损的一个危险因素。我们试图评估帕利珠单抗免疫接种和极早产(<29 周胎龄)对青少年呼吸症状和肺功能的长期影响。
帕利珠单抗免疫接种和极早产(<29 周)对青少年呼吸症状和肺功能的长期影响是什么?
我们检查了 13 至 18 岁极早产儿(<29 周胎龄)的幸存者(研究组)。与出生于帕利珠单抗免疫接种前(非帕利珠单抗组[NPG])的研究组婴儿相比,我们比较了出生于帕利珠单抗免疫接种后(PG)的婴儿和对照组婴儿。对于研究组患者,青少年期的肺功能与小学时的肺功能进行了进一步的纵向比较。
共纳入 64 名 15.76 ± 1.52 岁的青少年:46 名在研究组(17 名 PG 和 29 名 NPG)和 18 名在对照组。对于研究组,喘息发作、吸入器使用和住院治疗并不常见。与对照组相比,研究组的 FEV 预计百分比为 82.60%±13.54%与 105.83%±13.12%(P<0.001),肺清除指数分别为 7.67 ± 1.02 与 7.46 ± 0.70(P=0.48)。有支气管肺发育不良的研究组青少年的肺清除指数高于无支气管肺发育不良的青少年(7.94 ± 1.11 与 7.20 ± 0.60;P=0.002)。PG 和 NPG 青少年之间无显著差异。将研究组青少年与小学时的肺功能进行比较,我们发现支气管扩张剂反应的平均 FEV 预计百分比有改善(0.37%±9.98%与 5.67%±9.87%;P=0.036)和平均激发浓度导致 FEV 下降 20%(12.16 ± 4.71 mg/mL 与 4.14 ± 4.51 mg/mL,分别;P<0.001)。
帕利珠单抗并没有提供任何明显的长期保护作用。然而,极早产儿的青少年幸存者表现出良好的临床和生理结果,除了支气管肺发育不良患者的肺清除指数略有升高。在小学时检测到的气道高反应性,到了青春期有所下降。