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1.
J Clin Anesth ; 89: 111186, 2023 10.
Article in English | MEDLINE | ID: mdl-37393856

ABSTRACT

STUDY OBJECTIVE: The current study tested the hypothesis that magnesium sulfate after reversal with sugammadex causes recurarization. DESIGN: A single-center, prospective, randomized, double-blind, controlled trial. SETTING: Terciary care hospital in Rio de Janeiro, Brazil. PATIENTS: Included 60 patients undergoing for elective otolaryngological surgery. INTERVENTIONS: All patients received total intravenous anesthesia and a single dose of rocuronium (0.6 mg/kg). In 30 patients, the neuromuscular blockade was reversed with sugammadex (4 mg/kg) at the reappearance of one or two posttetanic counts (deep-blockade series). In 30 other patients, sugammadex (2 mg/kg) was administered at the reappearance of the second twitch of the train-of-four (moderate-blockade series). After the normalized train-of-four ratio recovered to ≥0.9, the patients in each series were randomized to receive intravenous magnesium sulfate (60 mg/kg) or placebo for 10 min. Neuromuscular function was measured by acceleromyography. MEASUREMENTS: The primary outcome was the number of patients who exhibited recurarization (normalized train-of-four ratio < 0.9). The secondary outcome was rescue with an additional dose of sugammadex after 60 min. MAIN RESULTS: In the deep-blockade series, a normalized train-of-four ratio < 0.9 occurred in 9/14 (64%) patients receiving magnesium sulfate and 1/14 (7%) receiving placebo, RR 9.0 (95% CI: 62-1.30), and (p = 0.002), with four rescues with sugammadex. In the moderate-blockade series, neuromuscular blockade recurred in 11/15 (73%) patients receiving magnesium sulfate and in 0/14 (0%) receiving placebo (p < 0.001), with two rescues. The absolute differences in recurarization were 57% and 73% in the deep-blockade and moderate-blockade, respectively. CONCLUSIONS: Single-dose magnesium sulfate led to a normalized train-of-four ratio < 0.9, 2 min after recovery from rocuronium-induced deep and moderate neuromuscular blockade using sugammadex. Additional sugammadex reversed prolonged recurarization.


Subject(s)
Neuromuscular Blockade , Neuromuscular Nondepolarizing Agents , gamma-Cyclodextrins , Humans , Sugammadex , Rocuronium , gamma-Cyclodextrins/adverse effects , Magnesium Sulfate/adverse effects , Neuromuscular Nondepolarizing Agents/adverse effects , Prospective Studies , Androstanols/adverse effects , Brazil , Neuromuscular Blockade/adverse effects
2.
Braz J Anesthesiol ; 67(2): 147-152, 2017.
Article in English | MEDLINE | ID: mdl-28236862

ABSTRACT

BACKGROUND AND OBJECTIVES: The aim of our study is to compare the effects of sugammadex and neostigmine, used for neuromuscular blockage antagonism, on postoperative nausea and vomiting (PONV). METHODS: Our study was completed with 98 ASA I-II risk patients undergoing endotracheal intubation under general anesthesia. At the end of the surgery patients were randomly divided into two groups given 2mgkg-1 sugammadex (Group S) or 50µgkg-1 neostigmine plus 0.2mgkg-1 atropine (Group N). Monitoring and recording times were set as 1 hour postoperative and from 1-6, 6-12, and 12-24hours. The anti-emetic amounts administered were recorded. RESULTS: In the first hour postoperative 13 patients in Group N (27%) and 4 in Group S (8%) were observed to have nausea and/or vomiting and the difference was statistically significant (p=0.0016). During the 24 hours of monitoring there was no significant difference in the incidence and severity of PONV (p>0.05), however the number of patients given ondansetron for PONV treatment in Group N was statistically significantly higher than the number in Group S (16 in Group N, 6 in Group S, p<0.011). CONCLUSIONS: At the end of our study comparing neostigmine with sugammadex for neuromuscular blockage antagonism, we found use of sugammadex had lower incidence of PONV in the postoperative 1st hour and less anti-emetic use in 24 hours of monitoring.


Subject(s)
Antiemetics/therapeutic use , Neostigmine/administration & dosage , Postoperative Nausea and Vomiting/epidemiology , gamma-Cyclodextrins/administration & dosage , Adult , Anesthesia, General/methods , Antiemetics/administration & dosage , Atropine/administration & dosage , Drug Therapy, Combination , Female , Humans , Incidence , Intubation, Intratracheal , Male , Middle Aged , Neostigmine/adverse effects , Neuromuscular Blockade , Ondansetron/administration & dosage , Ondansetron/therapeutic use , Postoperative Nausea and Vomiting/chemically induced , Prospective Studies , Severity of Illness Index , Single-Blind Method , Sugammadex , gamma-Cyclodextrins/adverse effects
3.
Rev. bras. anestesiol ; Rev. bras. anestesiol;65(4): 240-243, July-Aug. 2015. tab, ilus
Article in English | LILACS | ID: lil-755140

ABSTRACT

OBJECTIVES:

A burn patient is a challenge for any anesthesiologist, undergoing several surgeries during admission, and requiring general anesthesia and muscle relaxation most of the times. The victim may have respiratory system impairment and a response to muscle relaxants that differs from the healthy patient, thus proper monitoring and reversal is crucial. We analyzed sugammadex effectiveness and safety in this population.

MATERIALS AND METHODS:

It was a prospectively descriptive study, including 4 patients, and all of them were considered major burn patients, who underwent escharotomy with general anesthesia and neuromuscular relaxation. The main variable was the time for recovery of a TOF higher than 0.9 after the administration of sugammadex before extubation.

RESULTS:

Mean time of recovery from a TOF ratio higher than 0.9 following the administration of Sugammadex was of 4.95 min 95% CI (3.25-6.64, p= .53).

CONCLUSIONS:

The reversion of neuromuscular relaxation with sugammadex appears to be effective and safe in the burn patient. More analytical, comparative studies of larger populations would be necessary to confirm these data.

.

OBJETIVOS:

O paciente queimado representa um desafio para o anestesiologista, pois se submete a várias intervenções cirúrgicas durante sua hospitalização e necessita de anestesia geral e relaxamento muscular na maior parte delas. Apresenta sistema respiratório comprometido e uma resposta aos relaxantes musculares que difere do paciente sadio; portanto, um monitoramento correto e reversão tornam-se imprescindíveis. Avaliamos a eficácia e segurança do sugamadex nessa população.

MATERIAL E MÉTODOS:

Estudo descritivo com caráter prospectivo que inclui quatro pacientes, todos eles considerados grandes queimados, submetidos a escarectomia com anestesia geral e relaxamento neuromuscular. Como variável principal tomou-se o tempo de recuperação de TOF superior a 0,9 após a administração de sugamadex antes de extubação.

RESULTADOS:

O tempo médio de recuperação de uma razão TOF superior a 0,9 após a administração de sugamadex foi de 4,95 minutos (IC95% 3,25-6,64; p = 0,53).

CONCLUSÕES:

A reversão do relaxamento neuromuscular com sugamadex parece ser eficaz e segura no paciente queimado. Seriam necessários mais estudos analíticos, comparativos e de maior população para confirmar esses dados.

.

OBJETIVOS:

El paciente quemado supone un reto para el anestesista, pues se somete a varias intervenciones quirúrgicas durante su ingreso, requiriendo anestesia general y relajación muscular en la mayor parte de ellas. Presentan un sistema respiratorio comprometido y una respuesta a los relajantes musculares que difiere de la del paciente sano, por lo que se hace imprescindible una correcta monitorización y reversión. Valoramos la efectividad y seguridad del sugammadex en esta población.

MATERIAL Y MÉTODOS:

Estudio descriptivo con carácter prospectivo que incluyó a 4 pacientes, todos ellos considerados grandes quemados, sometidos a escarectomía con anestesia general y relajación neuromuscular. Como variable principal se tomó el tiempo de recuperación de un TOF superior a 0,9 tras la administración de sugammadex previa a extubación.

RESULTADOS:

El tiempo medio de recuperación de un TOF ratio superior a 0,9 tras la administración de sugammadex fue de 4,95 min, IC al 95% (3,25-6,64; p = 0,53).

CONCLUSIONES:

La reversión de la relajación neuromuscular con sugammadex parece ser efectiva y segura en el paciente quemado. Serían necesarios más estudios de índole analítica, comparativa y de mayor población para confirmar dichos datos.

.


Subject(s)
Humans , Male , Female , Aged , Burns/surgery , Neuromuscular Nondepolarizing Agents/administration & dosage , gamma-Cyclodextrins/administration & dosage , Anesthesia, General/methods , Burns/physiopathology , Prospective Studies , gamma-Cyclodextrins/adverse effects , Neuromuscular Monitoring/methods , Sugammadex
4.
Braz J Anesthesiol ; 65(4): 240-3, 2015.
Article in English | MEDLINE | ID: mdl-26123141

ABSTRACT

OBJECTIVES: A burn patient is a challenge for any anesthesiologist, undergoing several surgeries during admission, and requiring general anesthesia and muscle relaxation most of the times. The victim may have respiratory system impairment and a response to muscle relaxants that differs from the healthy patient, thus proper monitoring and reversal is crucial. We analyzed sugammadex effectiveness and safety in this population. MATERIALS AND METHODS: It was a prospectively descriptive study, including 4 patients, and all of them were considered major burn patients, who underwent escharotomy with general anesthesia and neuromuscular relaxation. The main variable was the time for recovery of a TOF higher than 0.9 after the administration of sugammadex before extubation. RESULTS: Mean time of recovery from a TOF ratio higher than 0.9 following the administration of Sugammadex was of 4.95min 95% CI (3.25-6.64, p=.53). CONCLUSIONS: The reversion of neuromuscular relaxation with sugammadex appears to be effective and safe in the burn patient. More analytical, comparative studies of larger populations would be necessary to confirm these data.


Subject(s)
Anesthesia, General/methods , Burns/surgery , Neuromuscular Nondepolarizing Agents/administration & dosage , gamma-Cyclodextrins/administration & dosage , Aged , Burns/physiopathology , Female , Humans , Male , Neuromuscular Monitoring/methods , Prospective Studies , Sugammadex , gamma-Cyclodextrins/adverse effects
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