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1.
Am J Emerg Med ; 29(8): 890-3, 2011 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-20627213

RESUMO

INTRODUCTION: Appendicitis is the most common emergency operation in children. The rate of perforation may be related to duration from symptom onset to treatment. A recent adult study suggests that the perforation risk is minimal in the first 36 hours and remains at 5% thereafter. We studied a pediatric population to assess symptom duration as a risk factor for perforation. METHODS: We prospectively studied all children older than 3 years who underwent an appendectomy over a 22-month period. RESULTS: Of 202 patients undergoing appendectomies, 197 had appendicitis. Median age was significantly lower in the perforated group, but temperature and leukocytosis were not. As expected, length of hospital stay was longer in the perforated group (4-13 vs 2-6 days). The incidence of perforation was 10% if symptoms were present for less than 18 hours. This incidence rose in a linear fashion to 44% by 36 hours. Prehospital delays were greater in patients with perforated appendicitis. However, in-hospital delay (from presentation to surgery) was less than 5 hours in the perforated group and 9 hours in the nonperforated group. DISCUSSION: Appendiceal perforation in children is more common than in adults and correlates directly with duration of symptoms before surgery. Perforation is more common in younger children. Unlike in adults, the risk of perforation within 24 hours of onset is substantial (7.7%), and it increases in a linear fashion with duration of symptoms. In our experience, however, perforation correlates more with prehospital delay than with in-hospital delay.


Assuntos
Apendicite/epidemiologia , Diagnóstico Tardio/estatística & dados numéricos , Adolescente , Fatores Etários , Apendicectomia/estatística & dados numéricos , Apendicite/etiologia , Criança , Pré-Escolar , Serviço Hospitalar de Emergência/estatística & dados numéricos , Feminino , Humanos , Tempo de Internação , Masculino , Estudos Prospectivos , Fatores de Risco
2.
Ann Emerg Med ; 43(2): 256-62, 2004 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-14747817

RESUMO

STUDY OBJECTIVE: We compare the effectiveness of intravenous ketorolac and intravenous prochlorperazine in the treatment of pediatric migraine headaches. METHODS: We performed a prospective, randomized, double-blind clinical trial in 2 pediatric emergency departments (EDs) within children's hospitals. Children aged 5 to 18 years presenting to the ED with migraine headaches were eligible for the study. Contraindications to either medication or the inability to complete the pain score resulted in exclusion. Children were randomized to receive intravenous ketorolac (0.5 mg/kg; maximum 30 mg) or intravenous prochlorperazine (0.15 mg/kg; maximum 10 mg). All children also received a normal saline solution bolus. Successful treatment was defined as a 50% or greater reduction in the Nine Faces Pain Scale score at 60 minutes. If a less than 50% improvement occurred by 60 minutes, the child received the other medication. Forty-eight-hour follow-up telephone calls were made to each family to assess recurrence and late side effects. RESULTS: Sixty-two children were enrolled: 33 initially received prochlorperazine, and 29 initially received ketorolac. By 60 minutes, 16 (55.2%) of 29 of those who received ketorolac and 28 (84.8%) of 33 of those who received prochlorperazine were successfully treated (difference=30%; 95% confidence interval [CI] 8% to 52%). Fifty-six (93.3%) of the 60 children who completed the study were successfully treated by the study's conclusion. Approximately 30% of each group had a recurrence of some headache symptoms. Only 2 children reported side effects, both mild and self-limited. CONCLUSION: In children, intravenous prochlorperazine is superior to intravenous ketorolac in the acute treatment of migraine headaches.


Assuntos
Anti-Inflamatórios não Esteroides/uso terapêutico , Cetorolaco/uso terapêutico , Transtornos de Enxaqueca/tratamento farmacológico , Proclorperazina/uso terapêutico , Adolescente , Anti-Inflamatórios não Esteroides/efeitos adversos , Antieméticos/efeitos adversos , Antieméticos/uso terapêutico , Criança , Método Duplo-Cego , Feminino , Humanos , Cetorolaco/efeitos adversos , Masculino , Dor/tratamento farmacológico , Medição da Dor , Proclorperazina/efeitos adversos , Resultado do Tratamento
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