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1.
Anesth Analg ; 138(5): 955-966, 2024 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-38621283

RESUMO

In this Pro-Con commentary article, we discuss use of continuous physiologic monitoring for clinical deterioration, specifically respiratory depression in the postoperative population. The Pro position advocates for 24/7 continuous surveillance monitoring of all patients starting in the postanesthesia care unit until discharge from the hospital. The strongest arguments for universal monitoring relate to inadequate assessment and algorithms for patient risk. We argue that the need for hospitalization in and of itself is a sufficient predictor of an individual's risk for unexpected respiratory deterioration. In addition, general care units carry the added risk that even the most severe respiratory events will not be recognized in a timely fashion, largely due to higher patient to nurse staffing ratios and limited intermittent vital signs assessments (e.g., every 4 hours). Continuous monitoring configured properly using a "surveillance model" can adequately detect patients' respiratory deterioration while minimizing alarm fatigue and the costs of the surveillance systems. The Con position advocates for a mixed approach of time-limited continuous pulse oximetry monitoring for all patients receiving opioids, with additional remote pulse oximetry monitoring for patients identified as having a high risk of respiratory depression. Alarm fatigue, clinical resource limitations, and cost are the strongest arguments for selective monitoring, which is a more targeted approach. The proponents of the con position acknowledge that postoperative respiratory monitoring is certainly indicated for all patients, but not all patients need the same level of monitoring. The analysis and discussion of each point of view describes who, when, where, and how continuous monitoring should be implemented. Consideration of various system-level factors are addressed, including clinical resource availability, alarm design, system costs, patient and staff acceptance, risk-assessment algorithms, and respiratory event detection. Literature is reviewed, findings are described, and recommendations for design of monitoring systems and implementation of monitoring are described for the pro and con positions.


Assuntos
Fadiga de Alarmes do Pessoal de Saúde , Insuficiência Respiratória , Humanos , Oximetria , Monitorização Fisiológica , Exame Físico , Insuficiência Respiratória/diagnóstico
2.
Biomol Biomed ; 24(2): 395-400, 2024 Mar 11.
Artigo em Inglês | MEDLINE | ID: mdl-37715536

RESUMO

Postoperative urinary retention (POUR) is a well-known complication after gynecologic surgery. Our objective was to investigate whether the choice of pharmacologic agent for reversing neuromuscular blockade at the end of a hysterectomy is a risk factor for POUR. Among adult patients undergoing hysterectomy with general anesthesia from 2012 to 2017, those who received aminosteroid nondepolarizing neuromuscular agents followed by pharmacologic reversal were identified, and electronic health records were reviewed. The cohort was dichotomized into two groups by reversal agent: 1) sugammadex and 2) neostigmine with glycopyrrolate. The primary outcome, POUR, was defined as unplanned postoperative bladder recatheterization. A propensity-adjusted analysis was performed to investigate the association between POUR and reversal agent by using inverse probability of treatment weighting to adjust for potential confounders. We identified 1,974 patients, of whom 1,586 (80.3%) received neostigmine-glycopyrrolate and 388 (19.7%) received sugammadex for reversal of neuromuscular blockade. The frequency of POUR was 24.8% (393/1,586) after reversal with neostigmine-glycopyrrolate and 18.3% (71/388) with sugammadex. Results from the propensity-adjusted analysis showed that sugammadex was associated with a lower POUR risk than neostigmine-glycopyrrolate (odds ratio 0.53, 95% confidence interval [CI] 0.37 - 0.76, P < 0.001). A post hoc analysis of sugammadex recipients who received glycopyrrolate for another indication showed a higher POUR risk than among those who did not receive glycopyrrolate (odds ratio 1.86, 95% CI 1.07 - 3.22, P = 0.03). Use of sugammadex to reverse aminosteroid neuromuscular blocking agents is associated with decreased risk of POUR after hysterectomy. A potential mechanism is the omission of glycopyrrolate, which is coadministered with neostigmine to mitigate unwanted cholinergic effects.


Assuntos
Fármacos Neuromusculares não Despolarizantes , Retenção Urinária , Adulto , Humanos , Feminino , Sugammadex/uso terapêutico , Neostigmina/efeitos adversos , Glicopirrolato/farmacologia , Estudos de Coortes , Retenção Urinária/induzido quimicamente , Fármacos Neuromusculares não Despolarizantes/efeitos adversos , Complicações Pós-Operatórias/induzido quimicamente , Histerectomia
3.
AANA J ; 89(1): 19-25, 2021 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-33501905

RESUMO

Ketamine is a well-known anesthetic that has been used since the 1970s. Despite its ubiquitous use as a postoperative analgesic, no studies have described dosing differences between opioid-tolerant (OT) and nonopioid-tolerant (NOT) patients or determined optimal dosing. The primary aim of this study was to assess whether OT and NOT patients had significant differences in ketamine infusion dosing requirements. We also aimed to measure the overall incidence of psychotomimetic adverse effects associated with low-dose ketamine infusions. We hypothesized that NOT patients would have lower ketamine infusion dosing requirements and a higher incidence of psychotomimetic adverse effects compared with OT patients. We performed a retrospective chart review and showed that the percentages of OT and NOT patients experiencing psychotomimetic adverse effects were similar (15.5% vs 15.3%; P=.93) and that increasing age was the only factor associated with increased odds of experiencing a psychotomimetic adverse effect potentially associated with ketamine (odds ratio, 1.29 [95% CI, 1.11-1.50]; P=.001). Optimal subanesthetic ketamine infusion dosing could not be established, and further research in this area may be warranted.


Assuntos
Analgésicos não Narcóticos , Ketamina , Analgésicos/uso terapêutico , Analgésicos não Narcóticos/uso terapêutico , Analgésicos Opioides/efeitos adversos , Humanos , Infusões Intravenosas , Ketamina/efeitos adversos , Dor Pós-Operatória/tratamento farmacológico , Dor Pós-Operatória/prevenção & controle , Estudos Retrospectivos
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