Anesthesia for videolaparoscopic cholecystectomy in a patient with Steinert disease. Case report and review of the literature

Autor: Bisinotto, Flora Margarida Barra [UNESP], Fabri, Daniel Capucci, Calçado, Maida Silva, Perfeito, Paula Borela, Tostes, Lucas Vieira, Sousa, Gabriela Denardi
Přispěvatelé: Universidade Federal do Triângulo Mineiro (UFTM), Universidade Estadual Paulista (Unesp), Universidade Federal de São Paulo (UNIFESP)
Jazyk: Spanish; Castilian
Rok vydání: 2010
Předmět:
Male
blood pressure measurement
patient monitoring
blood oxygen tension
body temperature monitoring
rocuronium
Video-Assisted Surgery
cholecystectomy
heart repolarization
consciousness
endotracheal tube
ranitidine
respiratory function
adductor pollicis muscle
Myotonic Dystrophy
Anesthesia
sibling
intravenous anesthesia
endotracheal intubation
family history
adult
operation duration
artificial ventilation
respiratory failure [Complications
postoperative]

continuous infusion
heart left ventricle overload
pulse oximetry
myotonia
midazolam
muscle relaxation
Cholecystectomy
Laparoscopic

oxygenation
pneumoperitoneum
arterial gas
metoclopramide
remifentanil
tramadol
ketoprofen
extubation
myotonic dystrophy [Diseases
muscular]

atropine
electrocardiogram
cholecystectomy [Surgery
abdominal]

laryngeal mask
case report
Humans
dipyrone
human
myotonic dystrophy type 1
propofol
creatine kinase
cyanosis
neostigmine
hand muscle
respiratory failure
carbon dioxide
lung function
convalescence
scalpel
capnography
general anesthesia
clinical feature
anesthetic recovery
hemostasis
abdominal pressure
oxygen
cholelithiasis
Zdroj: Scopus
Repositório Institucional da UNESP
Universidade Estadual Paulista (UNESP)
instacron:UNESP
Popis: Submitted by Vitor Silverio Rodrigues (vitorsrodrigues@reitoria.unesp.br) on 2014-05-27T11:24:38Z No. of bitstreams: 0Bitstream added on 2014-05-27T14:35:44Z : No. of bitstreams: 1 2-s2.0-77953059475.pdf: 652790 bytes, checksum: cca240e80000ae3bc411a195a3a629a2 (MD5) Made available in DSpace on 2014-05-27T11:24:38Z (GMT). No. of bitstreams: 0 Previous issue date: 2010-03-01 BACKGROUND AND OBJECTIVES: Myotonic dystrophies are autosomal dominant neuromuscular diseases. Among them, myotonic dystrophy type 1 (MD1), or Steinert disease, is the most common in adults, and besides muscular involvement it also has important systemic manifestations. Myotonic dystrophy type 1 poses a challenge to the anesthesiologist. Those patients are more sensitive to anesthetics and prone to cardiac and pulmonary complications. Besides, the possibility of developing malignant hyperthermia and myotonic episodes is also present. CASE REPORT: This is a 39-year old patient with DM1 who underwent general anesthesia for videolaparoscopic cholecystectomy. Total intravenous anesthesia with propofol, remifentanil, and rocuronium was the technique chosen. Intercurrences were not observed in the 90-minute surgical procedure, but after extubation, the patient developed respiratory failure and myotonia, which made tracheal intubation impossible. A laryngeal mask was used, allowing adequate oxygenation, and mechanical ventilation was maintained until full recovery of the respiratory function. The patient did not develop further complications. CONCLUSIONS: Myotonic dystrophy type 1 presents several particularities to the anesthesiologist. Detailed knowledge of its systemic involvement along with the differentiated action of anesthetic drugs in those patients will provide safer anesthetic-surgical procedure. UFTM CET/SBA UFTM FMB-UNESP CET/SBA del Hospital Escuela UFTM Hospital São Paulo - UNIFESP Anestesióloga del Hospital Escuela UFTM FMB-UNESP
Databáze: OpenAIRE