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Torsade de pointes secondary to long QT syndrome after intragastric balloon placement. A rare but severe complication
García-Calonge, Marta; González-Sánchez, María Helena; Muíño-Domínguez, Daniel; Flórez-Díez, Pablo.
Afiliação
  • García-Calonge, Marta; Hospital Universitario Central de Asturias. Digestive Diseases Service. Oviedo. Spain
  • González-Sánchez, María Helena; Hospital Universitario Central de Asturias. Digestive Diseases Service. Oviedo. Spain
  • Muíño-Domínguez, Daniel; Hospital Universitario Central de Asturias. Digestive Diseases Service. Oviedo. Spain
  • Flórez-Díez, Pablo; Hospital Universitario Central de Asturias. Digestive Diseases Service. Oviedo. Spain
Rev. esp. enferm. dig ; 116(3): 169-170, 2024. ilus
Artigo em Inglês | IBECS | ID: ibc-231484
Biblioteca responsável: ES1.1
Localização: ES15.1 - BNCS
ABSTRACT
The obesity pandemic is becoming one of the most prevalent diseases nowadays. There is a wide spectrum of treatment, ranging from hygienic-dietary measures to bariatric surgery. Endoscopic intragastric balloon placement is becoming increasingly more frequent, due to its technical simplicity, safety and short-term success(1). Although complications are rare some can be severe, so pre-endoscopic evaluation must be carried out carefully. A 43-year-old woman with a history of grade I obesity (BMI 32.7) had an Orbera® intragastric balloon implanted successfully. After the procedure she presented frequent nausea and vomiting, partially controlled with antiemetics. She attended the Emergency Department(ED) with a persistent emetic syndrome - oral intolerance and short-term loss of consciousness(syncope), for which she was admitted. Lab tests showed metabolic alkalosis with severe hypokalemia(K+ 1.8mmol/L), so fluid therapy was initiated for hydroelectrolytic replacement. During the patient’s stay in the ED, two episodes of polymorphic ventricular tachychardia “Torsades de Pointes” (PVT-TDP) occurred, leading to cardiac arrest and requiring electrical cardioversion to restore sinus rhythm, in addition to a temporary pacemaker placement. Telemetry showed a corrected QT interval of >500ms, compatible with Long QT Syndrome(LQTS). Once the patient was hemodynamically stabilized a gastroscopy was performed. The intragastric balloon located in the fundus was removed using an extraction kit, puncturing and aspirating 500ml of saline solution, and extracting the collapsed balloon without any complications. The patient achieved an adequate oral intake afterwards, and no recurrence of emetic episodes were noticed. Previous ECGs revealed a prolonged QT interval and a genetic study confirmed a congenital type 1 LQTS. Treatment was initiated with beta-blockers and a bicameral automatic defibrillator was implanted in order to prevent recurrences. ... (AU)
Assuntos

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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Síndrome do QT Longo / Balão Gástrico / Torsades de Pointes Limite: Adulto / Feminino / Humanos Idioma: Inglês Revista: Rev. esp. enferm. dig Ano de publicação: 2024 Tipo de documento: Artigo Instituição/País de afiliação: Hospital Universitario Central de Asturias/Spain
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Coleções: Bases de dados nacionais / Espanha Base de dados: IBECS Assunto principal: Síndrome do QT Longo / Balão Gástrico / Torsades de Pointes Limite: Adulto / Feminino / Humanos Idioma: Inglês Revista: Rev. esp. enferm. dig Ano de publicação: 2024 Tipo de documento: Artigo Instituição/País de afiliação: Hospital Universitario Central de Asturias/Spain
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