Sedation and general anesthesia for patients with Cornelia De Lange syndrome: A case series. Issue 2 (4th May 2016)
- Record Type:
- Journal Article
- Title:
- Sedation and general anesthesia for patients with Cornelia De Lange syndrome: A case series. Issue 2 (4th May 2016)
- Main Title:
- Sedation and general anesthesia for patients with Cornelia De Lange syndrome: A case series
- Authors:
- Moretto, Alessandra
Scaravilli, Vittorio
Ciceri, Valentina
Bosatra, Mariagrazia
Giannatelli, Federica
Ateniese, Bianca
Mariani, Milena
Cereda, Anna
Sosio, Simone
Zanella, Alberto
Pesenti, Antonio
Selicorni, Angelo - Other Names:
- Noon Sarah E. guestEditor.
Deardorff Matthew A. guestEditor.
Krantz Ian D. guestEditor. - Abstract:
- Abstract : Cornelia De Lange syndrome (CdLS) is a rare congenital disease characterized by typical facial dysmorphism, developmental disability, and limb deficiency defects. Various congenital malformations and medical complications have been described with gastroesophageal reflux as the major one. CdLS patients often require multiple high‐risk anesthetic procedures. At San Gerardo Hospital (Monza, Italy) the management of CdLS patients is routinely organized through a standard protocol and a dedicated pediatric anesthesia team has been implemented. We report on a retrospective descriptive analysis of the anesthetic records of the CdLS patients admitted to San Gerardo Hospital from January 2010 to December 2015. We retrieved: demographics, genetic profiles, type of procedures, anesthetic approaches, anesthetics usage and complications. Data are reported as median (interquartile range) values. Twenty‐seven patients (11 female), with age 12 (7–15) years old, weight 24 (14–35) kg, and severity score of 25 (18–32) were included. NIBPL mutations were the most frequently represented. We analyzed 58 procedures (30 esophagogastroduodenoscopies, 8 evoked auditory potential tests, 5 radiodiagnostics, 5 catheters positioning, 4 bronchoscopies) managed by sedation (36) and general anesthesia (6). Each patient underwent one (1–2) anesthetic procedure. Propofol (59%), sevoflurane (31%), fentanyl (24%), and ketamine (10%) were used. Three out of six endotracheal intubations were difficult.Abstract : Cornelia De Lange syndrome (CdLS) is a rare congenital disease characterized by typical facial dysmorphism, developmental disability, and limb deficiency defects. Various congenital malformations and medical complications have been described with gastroesophageal reflux as the major one. CdLS patients often require multiple high‐risk anesthetic procedures. At San Gerardo Hospital (Monza, Italy) the management of CdLS patients is routinely organized through a standard protocol and a dedicated pediatric anesthesia team has been implemented. We report on a retrospective descriptive analysis of the anesthetic records of the CdLS patients admitted to San Gerardo Hospital from January 2010 to December 2015. We retrieved: demographics, genetic profiles, type of procedures, anesthetic approaches, anesthetics usage and complications. Data are reported as median (interquartile range) values. Twenty‐seven patients (11 female), with age 12 (7–15) years old, weight 24 (14–35) kg, and severity score of 25 (18–32) were included. NIBPL mutations were the most frequently represented. We analyzed 58 procedures (30 esophagogastroduodenoscopies, 8 evoked auditory potential tests, 5 radiodiagnostics, 5 catheters positioning, 4 bronchoscopies) managed by sedation (36) and general anesthesia (6). Each patient underwent one (1–2) anesthetic procedure. Propofol (59%), sevoflurane (31%), fentanyl (24%), and ketamine (10%) were used. Three out of six endotracheal intubations were difficult. The only documented intraoperative complications were three episodes of desaturation (oxygen saturation <90%) occurring during sedations and were managed without the need for an invasive control of the airways. Implementation of a specific management protocol and a dedicated allowed to provide anesthesia to CdLS patients without the occurrence of major complications. © 2016 Wiley Periodicals, Inc. … (more)
- Is Part Of:
- American journal of medical genetics. Volume 172:Issue 2(2016)
- Journal:
- American journal of medical genetics
- Issue:
- Volume 172:Issue 2(2016)
- Issue Display:
- Volume 172, Issue 2 (2016)
- Year:
- 2016
- Volume:
- 172
- Issue:
- 2
- Issue Sort Value:
- 2016-0172-0002-0000
- Page Start:
- 222
- Page End:
- 228
- Publication Date:
- 2016-05-04
- Subjects:
- De Lange syndrome -- retrospective study -- deep sedation -- general anesthesia -- intraoperative complications
Medical genetics -- Periodicals
616.04205 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
- DOI:
- 10.1002/ajmg.c.31493 ↗
- Languages:
- English
- ISSNs:
- 1552-4868
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 0827.940000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1767.xml