Walters Aurora, Grosse Jordan
Neonatal Intensive Care Unit, Children's Hospital Colorado, Aurora.
Adv Neonatal Care. 2020 Apr;20(2):127-135. doi: 10.1097/ANC.0000000000000697.
With advancements in neonatology, patients in the neonatal intensive care unit (NICU) are living in the hospital with complex life-limiting illnesses until their first birthday or beyond. As palliative care (PC) becomes a standard of care in neonatology, a level IV NICU developed an interdisciplinary PC team with the mission to ease the physical, mental, and moral distress of the patients, families, and staff. This case report highlights the teamwork and long-term palliative care and ultimately end-of-life care that an infant received by this dedicated NICU palliative care team.
This case discusses a premature ex-27-week gestation male infant who initially presented to the emergency department at 5 months of age with significant tachypnea, increased work of breathing, and poor appetite.
The primary diagnosis was severe pulmonary vein stenosis resulting in severe pulmonary hypertension.
The severity of the infant's pulmonary vein stenosis was incurable. He required substantial life-extending surgical procedures and daily intensive care interventions. In addition to his life-extending therapies, the infant and his family received palliative care support by the NICU PC team and the hospital-wide PC team (REACH team) throughout his admission. This was specialized care that focused on easing pain and suffering while also addressing any social/emotional needs in the infant, his family, and in the hospital staff. The PC teams also focused on protecting the families' goals of care, memory making, and providing a positive end-of-life experience for the infant and his family. The infant's end-of-life care involved providing adequate pain and symptom management, education, and communication to his family about the dying process and allowing unlimited family time before and after his death.
After 11 months in the NICU and despite aggressive therapies, he required more frequent trips to the cardiac catheterization laboratory for restenosis of his pulmonary veins. He was dependent on iNO to treat his pulmonary hypertension and he continued to require an ICU ventilator. His parents ultimately decided to pursue comfort care. He died peacefully in his mother's arms.
The American Academy of Pediatrics and the National Association of Neonatal Nurses both have statements recommending that palliative care be standard of care in NICUs. Establishing a NICU-dedicated interdisciplinary PC team can improve outcomes for infants and families living in the NICU with complex life-limiting illnesses.
随着新生儿学的进步,新生儿重症监护病房(NICU)的患者会带着复杂的、危及生命的疾病在医院里一直住到一岁生日或更久。随着姑息治疗(PC)成为新生儿学的一种标准治疗方式,一家四级NICU组建了一个跨学科的PC团队,其使命是缓解患者、家属和医护人员在身体、心理和精神上的痛苦。本病例报告重点介绍了这个专门的NICU姑息治疗团队为一名婴儿提供的团队协作、长期姑息治疗以及最终的临终关怀。
本病例讨论了一名孕27周早产的男婴,他在5个月大时因明显的呼吸急促、呼吸做功增加和食欲不佳首次被送往急诊科。
初步诊断为严重的肺静脉狭窄导致严重的肺动脉高压。
婴儿肺静脉狭窄的严重程度无法治愈。他需要进行大量延长生命的外科手术和每日的重症监护干预。除了延长生命的治疗外,婴儿及其家人在整个住院期间都得到了NICU PC团队和全院PC团队(REACH团队)的姑息治疗支持。这是一种专门的护理,重点是减轻疼痛和痛苦,同时满足婴儿、其家人以及医院工作人员的任何社会/情感需求。PC团队还专注于保护家庭的护理目标、留下记忆,并为婴儿及其家人提供积极的临终体验。婴儿的临终关怀包括提供充分的疼痛和症状管理、教育,以及与他的家人就死亡过程进行沟通,并在他去世前后给予家人无限制陪伴的时间。
在NICU住了11个月后,尽管接受了积极的治疗,但由于肺静脉再狭窄,他需要更频繁地前往心导管实验室。他依赖吸入一氧化氮来治疗肺动脉高压,并且仍然需要ICU呼吸机。他的父母最终决定采取舒适护理。他在母亲的怀抱中平静地去世。
美国儿科学会和全国新生儿护士协会都发表声明,建议姑息治疗成为NICU的标准治疗方式。建立一个专门的NICU跨学科PC团队可以改善患有复杂、危及生命疾病且住在NICU的婴儿及其家庭的治疗效果。