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1.
J Obstet Gynaecol Can ; 42(1): 38-47.e5, 2020 Jan.
Article in English | MEDLINE | ID: mdl-31416705

ABSTRACT

OBJECTIVE: This study implemented a quality improvement program based on knowledge of medico-legal risk in obstetrics and sought to evaluate the impact of this program on workplace culture. METHODS: The study conducted needs assessments with front-line providers working in the obstetrical unit of the Queensway Carleton Hospital, an urban community hospital in Ottawa, Ontario, and included the safety, communication, operational reliability, and engagement (SCORE) survey. The study investigators delivered training in quality improvement science and co-developed three projects that were based on their alignment with local needs and aggregate medico-legal risk data: an organized team response to the need for an immediate cesarean section, a protocol for managing patients who present at term with pre-labour rupture of membranes, and regular morning team briefings. Outcome measures were determined for each project from a quality improvement indicator framework, and coaching was provided to project leads. Participants completed the SCORE survey and a program effectiveness tool after the intervention. RESULTS: The majority of participants (75.2% of 153 pre-intervention and 63.1% of 157 post-intervention participants) completed the SCORE surveys. Post-intervention improvements were found in teamwork, learning environment, and safety climate, whereas levels of provider burnout remained high. Program effectiveness was highly rated, and most projects showed qualitative improvements. CONCLUSION: This study showed positive workplace culture change associated with the quality improvement intervention. Lessons learned from the implementation of this program can inform future quality improvement initiatives.


Subject(s)
Fetal Membranes, Premature Rupture , Organizational Culture , Practice Patterns, Physicians'/standards , Workplace , Female , Hospitals, Community , Humans , Ontario , Practice Patterns, Physicians'/legislation & jurisprudence , Pregnancy , Program Evaluation , Quality Improvement , Surveys and Questionnaires
3.
CMAJ ; 180(6): 647, 2009 Mar 17.
Article in English | MEDLINE | ID: mdl-19289814
5.
Paediatr Child Health ; 13(6): 475, 2008 Jul.
Article in English | MEDLINE | ID: mdl-19436429
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8.
J Pediatr Adolesc Gynecol ; 18(6): 415-8, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16338608

ABSTRACT

BACKGROUND: Isolated absence of the clitoris is a rare entity with medical and sexual implications for patients. CASE: As part of an examination for alleged sexual abuse, a 13-year-old female was noted to have an apparent absence of the clitoris. Congenital absence of the clitoris was felt to be the most likely diagnosis. The differential diagnosis and medical implications are reviewed. CONCLUSION: Isolated absence of the clitoris is a rare entity. When faced with the finding, a detailed medical evaluation should be performed to clarify the nature of the finding, rule out other potential anomalies and help in the counseling of the patient.


Subject(s)
Clitoris/abnormalities , Adolescent , Child , Child Abuse, Sexual/psychology , Congenital Abnormalities/diagnosis , Diagnosis, Differential , Female , Humans , Physical Examination
10.
Paediatr Child Health ; 10(9): 539-41, 2005 Nov.
Article in English | MEDLINE | ID: mdl-19668685
11.
BMC Med ; 2: 11, 2004 Apr 15.
Article in English | MEDLINE | ID: mdl-15086953

ABSTRACT

BACKGROUND: Despite treatment recommendations from various organizations, oral rehydration therapy (ORT) continues to be underused, particularly by physicians in high-income countries. We conducted a systematic review of randomised controlled trials (RCTs) to compare ORT and intravenous therapy (IVT) for the treatment of dehydration secondary to acute gastroenteritis in children. METHODS: RCTs were identified through MEDLINE, EMBASE, CENTRAL, authors and references of included trials, pharmaceutical companies, and relevant organizations. Screening and inclusion were performed independently by two reviewers in order to identify randomised or quasi-randomised controlled trials comparing ORT and IVT in children with acute diarrhea and dehydration. Two reviewers independently assessed study quality using the Jadad scale and allocation concealment. Data were extracted by one reviewer and checked by a second. The primary outcome measure was failure of rehydration. We analyzed data using standard meta-analytic techniques. RESULTS: The quality of the 14 included trials ranged from 0 to 3 (Jadad score); allocation concealment was unclear in all but one study. Using a random effects model, there was no significant difference in treatment failures (risk difference [RD] 3%; 95% confidence intervals [CI]: 0, 6). The Mantel-Haenzsel fixed effects model gave a significant difference between treatment groups (RD 4%; 95% CI: 2, 5) favoring IVT. Based on the four studies that reported deaths, there were six in the IVT groups and two in ORT. There were no significant differences in total fluid intake at six and 24 hours, weight gain, duration of diarrhea, or hypo/hypernatremia. Length of stay was significantly shorter for the ORT group (weighted mean difference [WMD] -1.2 days; 95% CI: -2.4,-0.02). Phlebitis occurred significantly more often with IVT (number needed to treat [NNT] 33; 95% CI: 25,100); paralytic ileus occurred more often with ORT (NNT 33; 95% CI: 20,100). These results may not be generalizable to children with persistent vomiting. CONCLUSION: There were no clinically important differences between ORT and IVT in terms of efficacy and safety. For every 25 children (95% CI: 20, 50) treated with ORT, one would fail and require IVT. The results support existing practice guidelines recommending ORT as the first course of treatment in appropriate children with dehydration secondary to gastroenteritis.


Subject(s)
Dehydration/therapy , Diarrhea/complications , Fluid Therapy/methods , Gastroenteritis/complications , Rehydration Solutions/administration & dosage , Child , Dehydration/etiology , Fluid Therapy/adverse effects , Humans , Infusions, Intravenous , Publication Bias , Rehydration Solutions/adverse effects , Sensitivity and Specificity
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