Cited by 238Craniofacial Disorders and TreatmentsReconstructive Facial Surgery TechniquesPectus Deformity Diagnosis and Treatment

The DOI matches its Crossref record; 450 of the 453 references it cites were found in a registry or an index.

Guideline for Care of Patients With the Diagnoses of Craniosynostosis: Working Group on Craniosynostosis

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Mathijssen, Irene M.J.·2015·Journal of Craniofacial Surgery

Abstract

Chaired by Irene M.J. Mathijssen, MD, PhD Participants: The Dutch National Cranial and Facial Deformities Patients and Parents Association (LAPOSA) The Netherlands Society for Ophthalmology The Netherlands Society for Anesthesiology The Netherlands Society for Otorhinolaryngology The Dutch Association for Pediatrics The Netherlands Society for Oral Medicine and Oral and Maxillofacial Surgery The Netherlands Society for Neurosurgery The Netherlands Society for Plastic Surgery The Society for Orthodontists The Netherlands Society for Clinical Genetics The Dutch Association of Psychologists The Netherlands Society for Relationship Counseling and Family Therapy Address correspondence and reprint requests to Irene M.J. Mathijssen, MD, PhD, Deptartment of Plastic and Reconstructive Surgery, and Hand Surgery, Room Sk-1202, Erasmus Medical Center-Sophia, Wytemaweg 80, 3015CN Rotterdam, The Netherlands. E-mail: [email protected] ABSTRACT This guideline for care of children with craniosynostosis was developed by a national working group with representatives of 11 matrix societies of specialties and the national patients’ society. All medical aspects of care for nonsyndromic and syndromic craniosynostosis are included, as well as the social and psychologic impact for the patient and their parents. Managerial aspects are incorporated as well, such as organizing a timely referral to the craniofacial center, requirements for a dedicated craniofacial center, and centralization of this specialized care. The conclusions and recommendations within this document are founded on the available literature, with a grading of the level of evidence, thereby highlighting the areas of care that are in need of high-quality research. The development of this guideline was made possible by an educational grant of the Dutch Order of Medical Specialists. The development of this guideline was supported by an educational grant of the Dutch Order of Medical Specialists. Contents Chapter 1. General introduction 1735 Chapter 2. Introduction to craniosynostosis 1736 Chapter 3. Referral and diagnostics 1737 Chapter 4. Perioperative care 1744 Chapter 5. Surgical treatment of nonsyndromic craniosynostosis 1747 Chapter 6. Surgical treatment of syndromic craniosynostosis—the cranial vault 1751 Chapter 7. Surgical treatment of syndromic craniosynostosis—the face 1753 Chapter 8. Increased intracranial pressure 1762 Chapter 9. Hydrocephalus 1768 Chapter 10. Chiari I malformation 1769 Chapter 11. Vision, refraction and motility abnormalities 1771 Chapter 12. Obstructive sleep apnea syndrome 1772 Chapter 13. Hearing impairments 1776 Chapter 14. Dentofacial deformities 1777 Chapter 15. Deformities of the extremities 1780 Chapter 16. Cognitive functioning and behavior 1783 Chapter 17. Patients’ and parents’ perspectives 1786 Chapter 18. Psychosocial functioning 1787 Chapter 19. Criteria for the craniofacial center and its team members 1790 Chapter 20. Summary 1794 1. GENERAL INTRODUCTION Objective This guideline provides recommendations for medical practice on suspicion of craniosynostosis and after confirmation of this diagnosis. It is based on the results of scientific research and subsequent forming of opinion by a multidisciplinary working group, composed of representatives of the medical specialties involved in the treatment of craniosynostosis, related professional disciplines, and other parties involved. The wishes of parents and health professionals regarding the organization of health care for craniosynostosis were inventoried. The guideline document addresses the important issues for the support of parents with a child with a craniosynostosis. Method Employed by the Working Group The content of this guideline is based on evidence from published scientific research. Relevant articles were identified using systematic searches in Medline, Embase, and the Cochrane Library. Existing guidelines were specifically searched for in online accessible international and national guideline clearinghouses. Searches were limited to the Dutch, English, and French languages. In addition, articles were extracted from reference lists of relevant literature. This resulted in additional articles for several basic questions. Care for children with craniosynostosis was introduced in the late 1960s and consequently the English literature from those years onwards was included. Searches were performed until December 1, 2009 and articles available as “Epub ahead of publication” at that date were included as well. The following search terms were used: craniofacial, craniosynostosis combined with: genetics, hydrocephalus, Chiari, cerebral pressure, otitis, hearing, vision, psychology, anesthesia, complications, infection, development, growth, maxilla, mandible, distraction, osteotomy, Fort, midface, RED, halo, monobloc, facial bipartition, median faciotomy, and hypertelorism. Relevant articles extracted from reference lists of retrieved literature and several relevant publicati

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Research works printed but not linked: 16

  1. Feijen, 2009, Zuigelingen met een scheef hoofd newborns with a moulded head., Ned Tijdschr Geneeskd, 153, A368
  2. 1993, American Cleft Palate-Craniofacial Association., Cleft Palate Craniofac J, 30, S1
  3. Lo, 1996, Orbital dysmorphology in unilateral coronal synostosis., Cleft-Palate Craniofac J, 33, 190, 10.1597/1545-1569_1996_033_0190_odiucs_2.3.co_2 · DOI
  4. Kreiborg, 1986, Pre- and postsurgical facial growth in patients with Crouzons and Aperts syndromes., Cleft Palate J, 23, 78
  5. Tessier, 1967, Total facial osteotomy. Crouzons syndrome, Aperts syndrome: oxycephaly, scaphocephaly, turricephaly., Ann Chir Plast, 12, 273
  6. Le, 2001, Intracranial migration of halo fixation pins: a complication of using an extraoral distraction device., Cleft Palate Craniofac J, 38, 401, 10.1597/1545-1569_2001_038_0401_imohfp_2.0.co_2 · DOI
  7. Bachmayer, 1986, Stability of Le Fort III advancement surgery in children with Crouzons, Aperts, and Pfeiffers syndromes., Cleft Palate J, 23, 69
  8. Latham, 1966, The postnatal pattern of growth at sutures of the human skull., Dent Pract, 17, 61
  9. Persson, 1973, Structure and growth of facial sutures., Odontol Rev, 24, 6
  10. Vallino-Napoli, 1996, Audiologic and otologic characteristics of Pfeiffer syndrome., Cleft Palate Craniofac J, 33, 524, 10.1597/1545-1569_1996_033_0524_aaocop_2.3.co_2 · DOI
  11. Carinci, 1994, Crouzon syndrome: cephalometric analysis and evaluation of pathogenesis., Cleft Palate Craniofac J, 31, 201, 10.1597/1545-1569_1994_031_0201_cscaae_2.3.co_2 · DOI
  12. Kaloust, 1997, Dental development in Apert syndrome., Cleft Palate Craniofac J, 34, 117, 10.1597/1545-1569_1997_034_0117_ddias_2.3.co_2 · DOI
  13. Speltz, 1997, Presurgical and postsurgical mental and psychomotor development of infants with sagittal synostosis., Cleft Palate Craniofac J, 34, 374, 10.1597/1545-1569_1997_034_0374_papmap_2.3.co_2 · DOI
  14. Kapp-Simon, 1998, Mental development and learning disorders in children with single suture craniosynostosis., Cleft Palate Craniofac J, 35, 197, 10.1597/1545-1569_1998_035_0197_mdaldi_2.3.co_2 · DOI
  15. Guzelcan, 2004, Posttraumatic stress disorder following physical illnesses or their treatment., Tijdschr Psychiatr, 46, 611
  16. Schaefer, 1986, The speech-language pathologists role on the craniofacial team., Ear Nose Throat J, 65, 346

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Metadata

Authors
Mathijssen, I. M. J.
Corresponding author
Mathijssen, Irene M.J.
Venue
Journal of Craniofacial Surgery
Published
2015-09
Volume
26
Issue
6
Pages
1735-1807
ISSN
1049-2275 (ISSN-L)
OpenAlex
W2409179428
Cited by
232
References
453
Citations by year
2026: 16 · 2025: 13 · 2024: 28 · 2023: 27 · 2022: 31 · 2021: 38 · 2020: 24 · 2019: 19 · 2018: 14 · 2017: 8 · 2016: 13
FWCI
8.02
Type
journal article
Language
en
Open access
Licence
cc-by-nc-nd
Locations
  • Journal of Craniofacial Surgery (publishedVersion, cc-by-nc-nd)
  • PubMed Central (publishedVersion, cc-by-nc-nd)
  • PubMed (publishedVersion)
  • EUR Research Repository (Erasmus University Rotterdam) (submittedVersion, other-oa)
  • RePub (Erasmus University Rotterdam) (submittedVersion, other-oa)
  • RePub (Erasmus University Rotterdam) (submittedVersion)
Topics
  • Health Sciences › Medicine › Surgery › Craniofacial Disorders and Treatments
  • Health Sciences › Medicine › Surgery › Reconstructive Facial Surgery Techniques
  • Health Sciences › Medicine › Surgery › Pectus Deformity Diagnosis and Treatment
Keywords
craniosynostosis, nonsyndromic craniosynostosis, syndromic craniosynostosis, multidisciplinary care, surgical treatment, perioperative care, cranial vault expansion, craniofacial deformities, intracranial hypertension, hydrocephalus, psychosocial impact, parental support

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