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1.
J Perianesth Nurs ; 37(3): 369-373, 2022 06.
Artigo em Inglês | MEDLINE | ID: mdl-35177321

RESUMO

PURPOSE: To assess the knowledge of nursing staff regarding pediatric preoperative fasting in a tertiary pediatric center and a general hospital. DESIGN: Anonymous electronic survey with nine questions modified to each institution. METHODS: This was a prospective quantitative study. Nursing staff at a tertiary pediatric center and pediatric nursing staff at a general hospital with pediatric services were eligible for participation. An anonymous electronic survey with nine questions via Survey Monkey was used over a 2-month period. FINDINGS: There were 295 participants from the tertiary pediatric center and 24 from the general hospital which represented 10% of overall nursing staff at the tertiary pediatric center and approximately 50% of pediatric nursing staff at the general hospital. At both the tertiary pediatric center and the general hospital, 50 to 80% of participants correctly answered most questions. More participants were correct for the fasting times for infants less than 6 month of age than for those over 6 months old. For clear fluids, 61 (20.7%) and 13 (4.4%) considered jelly and breast milk as clear fluids respectively at the tertiary pediatric center. CONCLUSIONS: Preoperative fasting continues to be a core area of pediatric care that is not completely understood. Our survey showed that although the majority of staff claim to be able to access the hospital guidelines, knowledge of these guidelines can be improved. In light of ongoing changing evidence, it is clear that education is a key factor in reducing morbidity and improving patient experience related to preoperative fasting.


Assuntos
Jejum , Cuidados Pré-Operatórios , Criança , Humanos , Estudos Prospectivos , Inquéritos e Questionários
2.
Paediatr Anaesth ; 22(2): 136-43, 2012 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-22023485

RESUMO

OBJECTIVES: To provide parents of children with accurate information regarding postoperative pain, its management, and functioning following common surgical procedures. BACKGROUND: The increasing prevalence of pediatric day-case procedures demands a more thorough understanding of the recovery profiles associated with these operations. AIM: To document postdischarge pain profiles, analgesia requirements, and functional limitation in children following tonsillectomy, orchidopexy, or inguinal hernia repair (IHR). METHODS: Following hospital discharge, parents were asked to record their children's pain levels, analgesia consumption, and degree of functional limitation each day until complete recovery. Pain and functional limitation were measured using the Parents' Postoperative Pain Measurement (PPPM) scale and Functional Activity Score, respectively. Significant pain was defined as PPPM ≥ 6. RESULTS: One hundred and five patients (50, tonsillectomy; 24, orchidopexy; and 31, IHR) were recruited. Median PPPM was always <6 after IHR, ≥6 only on day 1 after orchidopexy and persisted through to day 8 after tonsillectomy. Mild or severe functional limitation was observed after all surgeries and persisted for 4, 5, and 4 days after median PPPM < 6 after IHR, orchidopexy, and tonsillectomy, respectively. Combination analgesia was commonly administered after orchidopexy and tonsillectomy but less so after IHR. The general practitioner consultation rate following tonsillectomy was 54%. CONCLUSIONS: After tonsillectomy, children experience significant pain and severe functional limitation for 7 days after surgery. For many children, pain and functional limitation persists throughout the second postoperative week. In children undergoing orchidopexy, paracetamol and ibuprofen provide adequate analgesia. Pain begins to subside after the first postoperative day, and normal activity resumes after 7 days. After IHR, children experience mild pain that can be treated with paracetamol and return to normal functioning after 4 days.


Assuntos
Analgésicos/administração & dosagem , Analgésicos/uso terapêutico , Hérnia Inguinal/cirurgia , Herniorrafia/efeitos adversos , Orquidopexia/efeitos adversos , Dor Pós-Operatória/diagnóstico , Dor Pós-Operatória/tratamento farmacológico , Tonsilectomia/efeitos adversos , Adenoidectomia/efeitos adversos , Criança , Pré-Escolar , Feminino , Seguimentos , Humanos , Masculino , Manejo da Dor , Medição da Dor/efeitos dos fármacos , Estudos Prospectivos , Recuperação de Função Fisiológica
3.
Anesth Analg ; 112(6): 1440-7, 2011 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-21543787

RESUMO

BACKGROUND: Mortality is a basic measure for quality and safety in anesthesia. There are few anesthesia-related mortality data available for pediatric practice. Our objective for this study was to determine the incidence of 24-hour and 30-day mortality after anesthesia and to determine the incidence and nature of anesthesia-related mortality in pediatric practice at a large tertiary institution. METHODS: Children ≤ 18 years old who had an anesthetic between January 1, 2003, and August 30, 2008, at the Royal Children's Hospital, Melbourne, Australia, were included for this study. Data were analyzed by merging a database for every anesthetic performed with an accurate electronic record of mortality of children who had ever been a Royal Children's Hospital patient. Cases of children dying within 30 days and 24 hours of an anesthetic were identified and the patient history and anesthetic record examined. Anesthesia-related death was defined as those cases whereby a panel of 3 senior anesthesiologists all agreed that anesthesia or factors under the control of the anesthesiologist more likely than not influenced the timing of death. RESULTS: During this 68-month period, 101,885 anesthetics were administered to 56,263 children. The overall 24-hour mortality from any cause after anesthesia was 13.4 per 10,000 anesthetics delivered and 30-day mortality was 34.5 per 10,000 anesthetics delivered. The incidence of death was highest in children ≤ 30 days old. Patients undergoing cardiac surgery had a higher incidence of 24-hour and 30-day mortality than did those undergoing noncardiac surgery. From 101,885 anesthetics there were 10 anesthesia-related deaths. The incidence of anesthesia-related death was 1 in 10,188 or 0.98 cases per 10,000 anesthetics performed (95%confidence interval, 0.5 to 1.8). In all 10 cases, preexisting medical conditions were identified as being a significant factor in the patient's death. Five of these cases (50%) involved children with pulmonary hypertension. CONCLUSIONS: Anesthesia-related mortality is higher in children with heart disease and in particular those with pulmonary hypertension. The lack of anesthetic-related deaths in children who did not have major comorbidities reinforces the safety of pediatric anesthesia in healthy children.


Assuntos
Anestesia/efeitos adversos , Anestesia/mortalidade , Pediatria/métodos , Adolescente , Anestesiologia/métodos , Anestésicos/efeitos adversos , Austrália , Criança , Pré-Escolar , Bases de Dados Factuais , Feminino , Cardiopatias/complicações , Hospitais Pediátricos , Humanos , Hipertensão Pulmonar/complicações , Incidência , Lactente , Recém-Nascido , Masculino , Complicações Pós-Operatórias , Resultado do Tratamento
4.
Pediatr Crit Care Med ; 11(2): e26-7, 2010 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-20216174

RESUMO

OBJECTIVE: To describe the inadvertent creation of a connection between lumens of a multilumen catheter by use of an in-line intravenous hand pressure pump. DESIGN: Case report. SETTING: Operating theater. PATIENT: All lumens of a 4F triple lumen catheter were verified patent by irrigation with saline before insertion into an internal jugular vein of an 18-mo-old child undergoing cardiac surgery. During surgery, the flushing of saline into one lumen of the catheter by means of an in-line hand pressure pump caused registration of >300 mm Hg pressure recorded from another lumen. The connections to these two lumens were then reversed. Repeated flushing also caused registration of pressure >300 mm Hg. On removal of the catheter at the end of surgery, flushing of one lumen caused fluid to emerge from the wrong exit hole as the appropriate exit hole was blocked with blood clot. INTERVENTIONS: None. MEASUREMENTS AND MAIN RESULTS: Pressure measurement in intravenous catheter lumens. Greater than 300 mm Hg was recorded during flushing with an inline hand pressure pump. CONCLUSIONS: High pressure created by use of an in-line intravenous hand pressure pump may cause creation of a communication between lumens of multilumen catheters.


Assuntos
Pressão do Ar , Cateterismo Venoso Central/instrumentação , Falha de Equipamento , Descontaminação/métodos , Contaminação de Equipamentos/prevenção & controle , Humanos , Lactente , Procedimentos Cirúrgicos Torácicos
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