Journals / Genel Tıp Dergisi / 2016 / Cilt: 26 - Sayı: 1

Major özelliği yüz - ekstremite defektleri olan sendromlar ve anestezi yönetimi

Pages
28–33
DOI
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AI Summary & Key Takeaways

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⚡ TL;DR(Too Long; Didn't Read)

In this review we presented anesthetic managent with current knowledge and practice of craniofacial anomalies associated with extremity malformations in children.

📌 3 Key Takeaways

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Objective & Hypothesis:Syndromes with facial - extremity defects as major feature and anesthesia management Many of extremity defects could be part of a syndrome associated with congenital craniofacial abnormalities due to overlapp of embr- yological development period of upper limb and craniofacial skeleton and specific gene mutations which is effective in development of both systems.
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Key Findings & Data:The most common craniofacial syndromes coexistence of upper limb defects are Apert, Saethre -Chotzen, Pfeiffer and Carpenter syndrome.
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Conclusion & Impact:In this review we presented anesthetic managent with current knowledge and practice of craniofacial anomalies associated with extremity malformations in children.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Syndromes with facial - extremity defects as major feature and anesthesia management Many of extremity defects could be part of a syndrome associated with congenital craniofacial abnormalities due to overlapp of embr- yological development period of upper limb and craniofacial skeleton and specific gene mutations which is effective in development of both systems. The most common craniofacial syndromes coexistence of upper limb defects are Apert, Saethre -Chotzen, Pfeiffer and Carpenter syndrome. These syndroms can be a real challenge in terms of airway management, intravenous cannulation and hemodynamic control. The key to success is effective preparation, presence of personnel with expertise in difficult pediatric airway management and intravenous cannulation, regular training, and teamwork. In this review we presented anesthetic managent with current knowledge and practice of craniofacial anomalies associated with extremity malformations in children.

Özet

2Kadınhanı Refik Saime Koyuncu Devlet Hastanesi, Kadınhanı, Konya. Kraniyofasiyal iskelet ile üst ekstremitenin embriyolojik dönemde gelişim zamanlarının örtüşmesi ve belirli gen mutasyonlarının her iki sistemin gelişiminde de etkili olması sebebiyle bir çok ekstremite defekti, konjenital kraniyofasiyal anomaliler ile birlikte seyreden bir sendromun parçası olabilir. Apert, Saethre-Chotzen, Pfeiffer, and Carpenter sendromları üst ekstremite defektleri ile birliktelik gösteren en sık kraniyofasiyal sendromlardır. Bu sendromlar, hava yolu yönetimi, intravenöz damar yolu açılması ve hemodinamik kontrol açısından gerçek bir sorun olabilir. Başarının anahtarı etkin hazırlık, zor pediatrik havayolu yönetimi ve intravenöz kanü- lasyonda uzmanlığa sahip personel varlığı, düzenli eğitim ve takım çalışmasıdır. Bu derlemede kraniyofasiyal ve ekstremite gelişim anomalileri içeren çocuk hastalarda güncel bilgiler ve uygulamalar ışığında anestezik yaklaşım sunulmuştur.

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Cite This Article

KOZANHAN, B., SALTALI, A. Ö. (2016). Major özelliği yüz - ekstremite defektleri olan sendromlar ve anestezi yönetimi. Genel Tıp Dergisi, Cilt: 26 - Sayı: 1, 28–33. https://ajindex.com/articles/190609

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References (16)

  1. Zguricas J, Bakker W, Heus H, Lindhout D, Heutink P, Hovius SE. Genetics of limb development and congenital hand malformations. Plast Recontr Surg 1998;101:1126-35
  2. Daluiski A, Soyun EY, Lyons KM. The molecular control of upper extremity development: implications for congenital hand anomalies. J Hand Surg Am 2001; 26: 8-22
  3. Panthaki ZJ, Armstrong MB. Hand abnormalities associated with craniofacial syndromes. J Craniofac Surg 2003;14: 709-12
  4. Thomas K, Hughes C, Johnson D, Das S. Anesthesia for surgery related to craniosynostosis: A review part 1. Pediatric Anesthesia 2012; 22:1033-41
  5. Onal O, Apiliogullari S, Gunduz E, Celik JB, Senaran H. Spinal anaesthesia for orthopaedic surgery in children with cerebral palsy: Analysis of 36 patients.Pakistan Journal of Medical Sciences 2015;31:189-93. 6. de Beer D, Bingham R. The child with facial abnormalities. Curr Opin Anaesthesiol 2011;24:282-8
  6. Belanger J, Kossick M. Methods of identifying and managing the difficult airway in the pediatric population. AANA J 2015; 83:35-41
  7. Ng A, Vas L, Goel S. Difficult paediatric intubation when fibreoptic laryngoscopy fails. Paediatr Anaesth 2002;12:801-5
  8. Moore M. Upper airway obstruction in the syndromal craniosynotoses. Br J Plast Surg 1993;46:355-62
  9. Barnett S, Moloney C, Bingham R. Perioperative complications in children with Apert's syndrome; a review of 509 anaesthetics Pediatr Anesth 2011;21:72-7
  10. Pollard RJ, Mickle JP. Pediatric neuroanesthesia. In: Cucchiara RF, Black S, michenfelder JD, editors. Clinical Neuroanesthesia. Newyork: Churchil Livingstone; 1998. p. 497- 537 12. Goa KL, Noble S, Spencer CM. Sevoflurane in paediatric anaesthesia: a review. Paediatr Drugs 1999;1:127-53
  11. Szabo EZ, Luginbuehl I, Bissonnette B. Impact of anesthetic agents on cerebrovascular physiology in children. Pediatr Anesth 2009;19:108-18
  12. Morgan GE, Mikhail MS, Murray MJ. Paediatric Anesthesia. Clinical Anesthesiology. 4th ed. Newyork: Lange Medical Books/McGraw-Hill; 2008. p. 922-50
  13. Kocatürk Ö, Kayacan BN. Genel Anestezide Monitörizasyon. Türkiye Klinikleri J Anest Reanim. Special Topics 2013;6:18-27
  14. Kim P, Tahon T, Fetzer M, Tobias J. Perioperative hypothermia in the pediatric population: A quality improvement Project. Am J Med Qual 2013; 28:400-6
  15. Macario A, Dexter F. What are the most important risk factors for a patient's developing intraoperative hypothermia? Anesth Analg 2002;94:215-20
  16. Apiliogullari S, Oc B, Kara I, Celik