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2.
J Spinal Disord Tech ; 21(6): 451-4, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18679103

ABSTRACT

STUDY DESIGN: Case report. OBJECTIVE: We report a case of severe hypotension associated with prone positioning in a child with scoliosis and pectus excavatum. SUMMARY OF BACKGROUND DATA: Pectus excavatum is commonly associated with scoliosis and can impact cardiac function. METHODS: Retrospective case analysis. RESULTS: After a modified Ravitch procedure to repair the pectus excavatum, the patient was able to undergo posterior spinal fusion. CONCLUSIONS: Pediatric deformity surgery requires a multidisciplinary approach.


Subject(s)
Funnel Chest/complications , Hypotension/etiology , Scoliosis/complications , Scoliosis/surgery , Adolescent , Humans , Male , Prone Position , Spinal Fusion
3.
Anesth Analg ; 104(2): 265-70, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17242078

ABSTRACT

Two recent studies have identified copious secretions as an independent risk factor for perioperative adverse events in children who present for elective surgery in the presence of an upper respiratory tract infection (URI). We designed this study, therefore, to determine whether the administration of the anticholinergic drug, glycopyrrolate, to children with URIs would reduce the incidence of adverse perioperative respiratory events. One hundred thirty children (1 mo to 18 yr of age) who presented for elective surgery with a URI were randomized to receive either 0.01 mg/kg glycopyrrolate or placebo and were followed for the appearance and severity of any perioperative respiratory adverse events. The two groups were similar with respect to demographics, presenting URI symptoms, anesthetic management, and surgical procedure. In the intention-to-treat analysis, there were no statistical differences in the incidence or severity of perioperative respiratory adverse events between the glycopyrrolate and placebo groups (45.2% vs 37.5% respectively, P = NS). Furthermore, there were no differences in outcome between the two groups when children with congestion and secretions were analyzed separately (45.0% vs 37.0%, respectively). However, compared with the placebo group, children in the glycopyrrolate group had significantly shorter discharge times (83.9 min vs 111.4 min, P = 0.024), and significantly less postoperative nausea and vomiting (10.7% vs 33.3%, P = 0.005). These results suggest that glycopyrrolate, administered after induction of anesthesia to children with URIs, does not reduce the incidence of perioperative respiratory adverse events, and thus may not be clinically indicated for routine use in this population.


Subject(s)
Glycopyrrolate/therapeutic use , Intraoperative Complications/drug therapy , Intraoperative Complications/epidemiology , Respiratory Tract Infections/drug therapy , Respiratory Tract Infections/epidemiology , Adolescent , Child , Child, Preschool , Female , Humans , Incidence , Infant , Male , Respiratory Tract Infections/surgery
4.
Ther Clin Risk Manag ; 3(4): 691-4, 2007 Aug.
Article in English | MEDLINE | ID: mdl-18472992

ABSTRACT

Strabismus surgery in pediatric patients is associated with a high incidence of postoperative nausea and vomiting (PONV). Ondansetron disintegrating tablets (ODT), an oral freeze-dried formulation of the 5-HT(3) antagonist, are well-tolerated and have been shown to reduce chemotherapy-induced vomiting. The purpose of this study was to assess the efficacy of the ODT in preventing postoperative vomiting (POV) in children undergoing strabismus repair. Healthy children aged 4-12 years of age were administered a 4 mg ODT 30 minutes prior to the induction of general anesthesia. Induction and maintenance of anesthesia were standardized; each child received acetaminophen and ketorolac pre-emptively for analgesia. This study group was compared with a historical control group who received a placebo in previously conducted identical trials of POV. The 35 children included in this study were compared with 31 controls. The incidence and severity of POV and use of rescue antiemetics were significantly lower in children who received ODT compared with placebo (p

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