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1.
Braz J Anesthesiol ; 74(4): 844524, 2024.
Article de Anglais | MEDLINE | ID: mdl-38848810

RÉSUMÉ

BACKGROUND: Prior research has established the effectiveness of magnesium in relieving postoperative pain. This article aims to evaluate magnesium sulfate for perioperative analgesia in adults undergoing general abdominal surgery under general anesthesia. OBJECTIVE: The primary aim was to assess pain scores at 6 and 24 hours postoperatively in patients receiving magnesium sulfate vs. the control group. Secondary outcomes were postoperative opioid consumption, perioperative complications, and time to rescue analgesia. METHODS: A comprehensive database search identified studies comparing magnesium sulfate with control in adults undergoing general anesthesia for general abdominal surgery. Using random-effects models, data were presented as mean ± Standard Deviation (SD) or Odds Ratios (OR) with corresponding 95% Confidence Intervals (95% CI). A two-sided p-value < 0.05 was considered statistically significant. RESULTS: In total, 31 studies involving 1762 participants met the inclusion criteria. The magnesium group showed significantly lower postoperative pain scores at both early (within six hours) and late (up to 24 hours) time points compared to the control group. The early mean score was 3.1 ± 1.4 vs. 4.2 ± 2.3, and the late mean score was 2.3 ± 1.1 vs. 2.7 ± 1.5, resulting in an overall Mean Difference (MD) of -0.72; 95% CI -0.99, -0.44; p < 0.00001. The magnesium group was associated with lower rates of postoperative opioid consumption and shivering and had a longer time to first analgesia administration compared to the saline control group. CONCLUSION: Magnesium sulfate administration was linked to reduced postoperative pain and opioid consumption following general abdominal surgery.


Sujet(s)
Abdomen , Analgésiques , Sulfate de magnésium , Douleur postopératoire , Essais contrôlés randomisés comme sujet , Humains , Douleur postopératoire/prévention et contrôle , Douleur postopératoire/traitement médicamenteux , Sulfate de magnésium/administration et posologie , Abdomen/chirurgie , Analgésiques/administration et posologie , Anesthésie générale/méthodes , Analgésiques morphiniques/administration et posologie , Analgésiques morphiniques/usage thérapeutique , Soins périopératoires/méthodes
2.
Cureus ; 16(3): e57057, 2024 Mar.
Article de Anglais | MEDLINE | ID: mdl-38681306

RÉSUMÉ

This systematic review was conducted to evaluate the optimal weight scalar to dose sugammadex in a morbidly obese (MO) patient population (BMI≥40 kg/m2). The primary outcome was recovery time from moderate neuromuscular blockade (NMB) or deep NMB. Secondary outcomes included time to extubation and incidence of postoperative residual curarization (PORC). Eight randomized controlled trials (RCTs) involving 645 participants were included. The different dose scalars included were total body weight (TBW), ideal body weight (IBW), 20% corrected body weight (CBW) and 40% CBW). A dose of 2 mg/kg of sugammadex based on 40% CBW and a 4 mg/kg dose of sugammadex based on 40% CBW provide a reliable and timely reversal of moderate and deep NMB respectively in the MO patients.

3.
Can J Microbiol ; 64(8): 551-558, 2018 Aug.
Article de Anglais | MEDLINE | ID: mdl-29658303

RÉSUMÉ

To study the mechanism by which human host cells respond to an infection of Toxoplasma gondii, we monitored the level of poly(A)-binding protein (PABP), an indicator of translation. Here, we report an observation of the relocalization of PABPs in human host cells upon T. gondii infection. Notably, the aggregates of PABPs formed upon infection are mainly found in the nucleus, which is a different response from that found after exposure to heat shock. Pyrimethamine treatment of the infected monolayers inhibits the multiplicity of the parasite and reverses the relocalization of PABP aggregates. This active interaction between the infected mammalian host cells and T. gondii appears to be different from that caused by viral infection.


Sujet(s)
Noyau de la cellule/composition chimique , Protéines de liaison au poly(A)/ultrastructure , Toxoplasma/physiologie , Toxoplasmose/anatomopathologie , Animaux , Transport biologique/effets des médicaments et des substances chimiques , Noyau de la cellule/métabolisme , Interactions hôte-parasite/effets des médicaments et des substances chimiques , Humains , Protéines de liaison au poly(A)/métabolisme , Pyriméthamine/pharmacologie , Toxoplasma/effets des médicaments et des substances chimiques , Toxoplasmose/parasitologie
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