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Antimicrobial Stewardship in Pediatric Surgery (AbxPS)

16 mars 2018 mis à jour par: Dr Anna Shawyer, Alberta Children's Hospital

An Antimicrobial Stewardship Intervention Program in Pediatric Surgery

Acute appendicitis is a common surgical emergency in children. Non-perforated appendicitis patients do not require antibiotics after appendectomy. Although guidelines and recommendations exist to decrease post-operative antibiotic mis-use after appendectomy, surgeons continue to prescribe unwarranted antibiotics.

The aim of this study is to determine if an Antimicrobial Stewardship Program in Pediatric Surgery will decrease the use of un-warranted antibiotics.

Aperçu de l'étude

Statut

Retiré

Les conditions

Description détaillée

Many surgeons continue to treat non-perforated or "borderline perforated" appendicitis with postoperative antibiotics despite an evidence-based definition of perforation (in the pediatric surgical literature) and many guidelines and recommendations that specify that no postoperative antibiotics are required. Children with perforated appendicitis are also often treated with longer-than-necessary courses of antibiotics. Although surgeons may feel that they only prescribe additional doses on occasion, evidence suggests that this behavior occurs in over 50% of children with non-perforated appendicitis.

These additional doses contribute to a longer length of stay, excess costs to the health care system, and disrupt patient flow. Additionally, the patients are exposed to more antibiotics and their potential for adverse effects (such as incorrect dose, incorrect medication, allergic reaction, antimicrobial resistance or c difficile infection).

Antimicrobial stewardship programs have been successful in pediatrics and adult general surgery in curbing unwarranted antibiotic use, but have never been evaluated in pediatric general surgery.

Type d'étude

Observationnel

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

Pas plus vieux que 18 ans (Enfant, Adulte)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

Méthode d'échantillonnage

Échantillon de probabilité

Population étudiée

The study population is the pediatric surgeons at our institution who will have their antibiotic prescribing audited.

La description

Inclusion Criteria:

  • Participant (surgeon) is a pediatric surgeon at McMaster Children's Hospital and takes care of patients under the age of 18 who undergo appendectomy.
  • Participant (surgeon) is able to read, write and understand English.
  • Participant (surgeon) is able to provide informed consent.

Exclusion Criteria:

  • Participant (surgeon) only has patients who undergo drain insertion, PICC line insertion or a secondary operation during the same admission
  • Participant (surgeon) only has patients who do not undergo operation (i.e. "conservative management with interval appendectomy)
  • Participant (surgeon) does not provide informed consent
  • Participant (surgeon) does not understand written and spoken English diagnosis other than appendicitis at time of operation

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

Cohortes et interventions

Groupe / Cohorte
Intervention / Traitement
NO Antimicrobial Stewardship Program
Prospective cohort of children who undergo appendectomy for acute appendicitis (perforated and non-perforated) BEFORE the implementation of the Antimicrobial Stewardship Program.
WITH Antimicrobial Stewardship Program
Prospective cohort of children who undergo appendectomy for acute appendicitis (perforated and non-perforated) WITH the implementation of the Antimicrobial Stewardship Program.
Twice weekly meeting with Infectious Disease and Pediatric Surgery team members to audit antibiotics prescribed and suggest role for discontinuation.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Compliance with American Pediatric Surgical Association recommendations for postoperative antibiotics for appendicitis
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Includes both intravenous and oral antibiotics prescribed, both during the time frame from admission until discharge, in addition to any prescription given for home, oral antibiotics. Measured as yes/no
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Postoperative intravenous antibiotics for non-perforated appendicitis
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
measured as number of days (ie number of doses divided by number of doses-per-day)
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Postoperative oral antibiotics for non-perforated appendicitis
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
measured as number of days (ie number of doses divided by number of doses-per-day)
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Postoperative fever
Délai: Length of admission
Rectal temperature above 100.4ºF (38ºC), measured as yes/no and on what postoperative day Oral temperature above 100ºF (37.8ºC) Axillary (armpit) temperature above 99ºF (37.2ºC) Ear (tympanic membrane) temperature above 100.4ºF (38ºC) in rectal mode or 99.5ºF (37.5ºC) in oral mode Forehead (temporal artery) temperature above 100.4ºF (38ºC)
Length of admission
Readmission within 30 days
Délai: Within 30 days of discharge
Need for readmission within 30 days of discharge, measured as yes/no
Within 30 days of discharge
Peripherally inserted intravenous catheter (PICC)
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Need for PICC insertion for long term antibiotics, intravenous fluids or parenteral nutrition, measured as yes/no
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Drain insertion
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Need for a drain insertion (by interventional radiology) for postoperative abscess, measured as yes/no
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Re-operation
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Need for re-operation on the same admission, measured as yes/no
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Length of Stay
Délai: Length of admission
Measured in days (from date of admission until date of discharge)
Length of admission
Adverse reaction to antibiotic
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Measured as yes/no in addition to description of reaction (eg hives, shortness of breath)
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Wrong medication/Wrong dose
Délai: From date of admission until date of first follow-up visit, typically within 4-6 weeks of discharge
Measured as yes/no in addition to description of problem (wrong dose, wrong medication)
From date of admission until date of first follow-up visit, typically within 4-6 weeks of discharge
C difficile infection
Délai: From date of admission until first follow-up visit, typically within 4-6 weeks of discharge
Measured as yes/no based on stool assay
From date of admission until first follow-up visit, typically within 4-6 weeks of discharge

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Anna Shawyer, MS, MSc, Alberta Children's Hospital

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude

1 janvier 2015

Achèvement primaire (Anticipé)

1 décembre 2015

Achèvement de l'étude (Anticipé)

1 décembre 2015

Dates d'inscription aux études

Première soumission

8 octobre 2014

Première soumission répondant aux critères de contrôle qualité

21 octobre 2014

Première publication (Estimation)

22 octobre 2014

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

20 mars 2018

Dernière mise à jour soumise répondant aux critères de contrôle qualité

16 mars 2018

Dernière vérification

1 mars 2018

Plus d'information

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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