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1.
Aesthet Surg J ; 42(11): NP602-NP610, 2022 10 13.
Article in English | MEDLINE | ID: mdl-35512645

ABSTRACT

BACKGROUND: Patients undergoing facial rejuvenation surgery are at unique risk of perioperative complications from the anesthetic utilized during the procedure. The ideal anesthetic agent is one that is safe to use in the outpatient population, has analgesic, sedative, and anesthetic properties, yet does not cause respiratory depression or hemodynamic irregularities. OBJECTIVES: A retrospective analysis of a large outpatient facelift cohort was performed to determine if dexmedetomidine, an α 2-adrenergic receptor agonist, meets the criteria of an ideal adjunct for propofol in a total intravenous anesthesia protocol. METHODS: The charts of 791 patients who underwent rhytidectomy with total intravenous anesthesia were reviewed and data of patients' operative risk factors, perioperative management including medications administered, perioperative vital signs, and postoperative adverse events were recorded. Statistical univariate analyses were performed on the data. RESULTS: Dexmedetomidine resulted in a significant reduction and maintenance of blood pressure from onset of anesthesia until discharge from the postanesthetic recovery unit. The utilization of opioids and anxiolytics was significantly less than previously reported for other anesthetic types. The postoperative nausea/vomiting rate was 0.8% (6 patients). There were no postoperative admissions for inpatient management. Forty-three (5.3%) patients required a conversion to general endotracheal anesthesia and statistically significant risk factors include increased BMI, American Society of Anesthesiologists Class II or higher, preoperative hypertension, and multiple procedures performed. CONCLUSIONS: This study demonstrated the safety and efficacy of dexmedetomidine in a large cohort of outpatients undergoing facelift. Dexmedetomidine meets the requirements for an ideal adjunct anesthetic within a total intravenous anesthesia protocol.


Subject(s)
Anti-Anxiety Agents , Dexmedetomidine , Propofol , Surgery, Plastic , Adrenergic Agonists/pharmacology , Analgesics , Anesthesia, General , Anesthesia, Intravenous/methods , Anti-Anxiety Agents/pharmacology , Dexmedetomidine/adverse effects , Hemodynamics , Humans , Hypnotics and Sedatives/adverse effects , Propofol/adverse effects , Retrospective Studies
2.
J Infect Dis ; 188(9): 1336-44, 2003 Nov 01.
Article in English | MEDLINE | ID: mdl-14593591

ABSTRACT

The safety and immunogenecity of a booster dose of live attenuated varicella-zoster virus (VZV) vaccine was evaluated in 196 healthy subjects, >or=60 years old, who had already received a VZV vaccine >5 years before. This repeat booster dose was well tolerated. Cell-mediated immunity (CMI) to VZV was measured by an interferon-gamma (IFN-gamma) enzyme-linked immunosorbent spot-forming cell (ELISPOT) assay and a limiting dilution responder cell frequency (RCF) assay. Prevaccination responses decreased as a function of increasing age but were detectable in all subjects by use of the IFN-gamma ELISPOT assay. In most subjects, VZV-specific CMI was increased at 6 weeks postvaccination. The magnitude of the vaccine-induced IFN-gamma ELISPOT response was inversely related to prevaccination values. Although there was a significant correlation between the IFN-gamma ELISPOT and RCF assays, the ELISPOT assay had greater sensitivity and a wider dynamic range. A live attenuated VZV vaccine is safe and immunogenic in an elderly population, and the vaccine-induced immunity may be monitored by the IFN-gamma ELISPOT assay.


Subject(s)
Herpesvirus 3, Human/immunology , Viral Vaccines/immunology , Age Factors , Aged , Aged, 80 and over , Antigens, Viral/immunology , Cell Division/immunology , Female , Herpes Zoster/immunology , Herpes Zoster/prevention & control , Humans , Immunity, Cellular/immunology , Immunization, Secondary , Immunoenzyme Techniques , Interferon-gamma/immunology , Interferon-gamma/metabolism , Male , Middle Aged , Sex Factors , Th1 Cells/immunology , Vaccines, Attenuated/immunology
3.
AANA J ; 71(6): 431-9, 2003 Dec.
Article in English | MEDLINE | ID: mdl-15098530

ABSTRACT

Of the patients with end-stage cardiomyopathy on a heart transplant list, 95% do not receive a donor heart. Due to this severe shortage of donor organs, an artificial replacement heart has been pursued for several decades. To date, 10 patients have received an Abiocor artificial replacement heart (Abiomed, Inc, Danvers, Mass), the latest artificial heart device available. Anesthetic management often is complicated by the preoperative multisystem organ failure arising from the patient's advanced cardiomyopathy. Hemodynamic stabilization before cardiopulmonary bypass is extremely challenging, and the postbypass period creates a unique situation in which the only control the anesthesia provider has on the hemodynamics is management of the systemic vascular resistance. This article describes the anesthetic management of the recipient of the Abiocor artificial heart with the longest survival time.


Subject(s)
Anesthesia/methods , Cardiomyopathies/surgery , Heart, Artificial , Aged , Environmental Monitoring , Hemodynamics , Humans , Male
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