TY - JOUR
T1 - Family-Centered Care for Children and Families Impacted by Neonatal Seizures
T2 - Advice From Parents
AU - Neonatal Seizure Registry
AU - Lemmon, Monica E.
AU - Glass, Hannah C.
AU - Shellhaas, Renée A.
AU - Barks, Mary Carol
AU - Bansal, Simran
AU - Annis, Dana
AU - Guerriero, Jennifer L.
AU - Pilon, Betsy
AU - Wusthoff, Courtney J.
AU - Chang, Taeun
AU - Soul, Janet S.
AU - Chu, Catherine J.
AU - Thomas, Cameron
AU - Massey, Shavonne L.
AU - Abend, Nicholas S.
AU - Rau, Stephanie
AU - Rogers, Elizabeth E.
AU - Franck, Linda S.
N1 - Funding Information:
We are immensely grateful to the Neonatal Seizure Registry Parent Advisory Panel for their sustained engagement and guidance throughout the study: Martha E. Barnes, Lisa Grossbauer, Katie Grant, Jennifer Guerriero, Betsy Pilon, Dana Annis, Elizabeth Hill, Kamil Pawlowski, Katrina Moline and Ashley Hamlett. Funding source: Funded by PCORI, United States contract number CER-1507-31187. M.E.L. is supported by the National Institute of Neurological Disorders and Stroke of the National Institutes of Health under award number K23NS116453.
Funding Information:
Funding source: Funded by PCORI, United States contract number CER-1507-31187. M.E.L. is supported by the National Institute of Neurological Disorders and Stroke of the National Institutes of Health under award number K23NS116453.
Publisher Copyright:
© 2021 Elsevier Inc.
PY - 2021/11
Y1 - 2021/11
N2 - Background: Parents of neonates with seizures are at risk of mental health symptoms due to the impact of illness on family life, prognostic uncertainty, and the emotional toll of hospitalization. A family-centered approach is the preferred model to mitigate these challenges. We aimed to identify strategies to promote family-centered care through an analysis of parent-offered advice to clinicians caring for neonates with seizures. Methods: This prospective, observational, and multicenter (Neonatal Seizure Registry) study enrolled parents of neonates with acute symptomatic seizures. Parents completed surveys about family well-being at 12, 18, and 24 months corrected gestational age. Parents were asked open-ended questions eliciting their advice to clinicians caring for neonates with seizures. Responses were analyzed using a conventional content analysis approach. Results: Among the 310 parents who completed surveys, 118 (38%) shared advice for clinicians. These parents were predominantly mothers (n = 103, 87%). Three overarching themes were identified. (1) Communicate information effectively: parents appreciate when clinicians offer transparent and balanced information in an accessible way. (2) Understand and validate parent experience: parents value clinicians who display empathy, compassion, and a commitment to parent-partnered clinical care. (3) Provide support and resources: parents benefit from emotional support, education, connection with peers, and help navigating the health care system. Conclusions: Parents caring for neonates with seizures appreciate a family-centered approach in health care encounters, including skilled communication, understanding and validation of the parent experience, and provision of support and resources. Future interventions should focus on building structures to reinforce these priorities.
AB - Background: Parents of neonates with seizures are at risk of mental health symptoms due to the impact of illness on family life, prognostic uncertainty, and the emotional toll of hospitalization. A family-centered approach is the preferred model to mitigate these challenges. We aimed to identify strategies to promote family-centered care through an analysis of parent-offered advice to clinicians caring for neonates with seizures. Methods: This prospective, observational, and multicenter (Neonatal Seizure Registry) study enrolled parents of neonates with acute symptomatic seizures. Parents completed surveys about family well-being at 12, 18, and 24 months corrected gestational age. Parents were asked open-ended questions eliciting their advice to clinicians caring for neonates with seizures. Responses were analyzed using a conventional content analysis approach. Results: Among the 310 parents who completed surveys, 118 (38%) shared advice for clinicians. These parents were predominantly mothers (n = 103, 87%). Three overarching themes were identified. (1) Communicate information effectively: parents appreciate when clinicians offer transparent and balanced information in an accessible way. (2) Understand and validate parent experience: parents value clinicians who display empathy, compassion, and a commitment to parent-partnered clinical care. (3) Provide support and resources: parents benefit from emotional support, education, connection with peers, and help navigating the health care system. Conclusions: Parents caring for neonates with seizures appreciate a family-centered approach in health care encounters, including skilled communication, understanding and validation of the parent experience, and provision of support and resources. Future interventions should focus on building structures to reinforce these priorities.
KW - Communication
KW - Mental Health
KW - Neonate
KW - Neurology
UR - http://www.scopus.com/inward/record.url?scp=85114471963&partnerID=8YFLogxK
U2 - 10.1016/j.pediatrneurol.2021.07.013
DO - 10.1016/j.pediatrneurol.2021.07.013
M3 - Article
C2 - 34509000
AN - SCOPUS:85114471963
SN - 0887-8994
VL - 124
SP - 26
EP - 32
JO - Pediatric Neurology
JF - Pediatric Neurology
ER -