{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,2,26]],"date-time":"2026-02-26T12:33:11Z","timestamp":1772109191139,"version":"3.50.1"},"reference-count":40,"publisher":"AACN Publishing","issue":"4","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2013,8,1]]},"abstract":"<jats:p>Craniosynostosis is a developmental anomaly with premature closure of the cranial sutures causing an abnormally shaped skull in an infant. Recommended surgical treatment involves cranial vault reconstruction to open the closed suture, increase intracranial volume, and allow the brain to grow normally. Parents work with a multidisciplinary team during the evaluation process and face various preoperative and postoperative stressors. Critical care nurses can improve the care of the infants and their families by being knowledgeable about the anatomy, assessment, and surgical and nursing management of infants with this anomaly and its impact on the patients\u2019 families. This article discusses the definitions, diagnosis, and treatment of craniosynostosis and support for parents of infants with this malformation.<\/jats:p>","DOI":"10.4037\/ccn2013678","type":"journal-article","created":{"date-parts":[[2013,8,1]],"date-time":"2013-08-01T07:24:58Z","timestamp":1375341898000},"page":"39-50","source":"Crossref","is-referenced-by-count":20,"title":["Craniosynostosis: Caring for Infants and Their Families"],"prefix":"10.4037","volume":"33","author":[{"given":"Laura","family":"Burokas","sequence":"first","affiliation":[{"name":"Laura Burokas is the advanced practice nurse for pediatric neurosurgery at Advocate Children\u2019s Hospital, Oak Lawn Campus, Oak Lawn, Illinois."}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"2471","reference":[{"issue":"9","key":"2019112601255416200_b1-0330039","doi-asserted-by":"crossref","first-page":"1185","DOI":"10.1111\/j.1651-2227.2011.02299.x","article-title":"Evaluation and management of non-syndromic craniosynostosis","volume":"100","author":"Ursitti","year":"2011","journal-title":"Acta Paediatr"},{"issue":"suppl","key":"2019112601255416200_b2-0330039","doi-asserted-by":"crossref","first-page":"1S","DOI":"10.1597\/11-138","article-title":"Parameters of care for craniosynostosis","volume":"49","author":"McCarthy","year":"2012","journal-title":"Cleft Palate Craniofac J"},{"key":"2019112601255416200_b3-0330039","unstructured":"Robin NH , FalkMJ, Haldeman-EnglertCR. FGFR-related craniosynostosis syndromes. Gene Rev. http:\/\/www.ncbi.nlm.nih.gov\/books\/NBK1455\/. Published October 20, 1998. Last updated June 7, 2011. 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