98 research outputs found

    How learning style affects evidence-based medicine:a survey study

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    BACKGROUND: Learning styles determine how people manage new information. Evidence-based medicine (EBM) involves the management of information in clinical practice. As a consequence, the way in which a person uses EBM can be related to his or her learning style. In order to tailor EBM education to the individual learner, this study aims to determine whether there is a relationship between an individual's learning style and EBM competence (knowledge/skills, attitude, behaviour). METHODS: In 2008, we conducted a survey among 140 novice GP trainees in order to assess their EBM competence and learning styles (Accommodator, Diverger, Assimilator, Converger, or mixed learning style). RESULTS: The trainees' EBM knowledge/skills (scale 0-15; mean 6.8; 95%CI 6.4-7.2) were adequate and their attitudes towards EBM (scale 0-100; mean 63; 95%CI 61.3-64.3) were positive. We found no relationship between their knowledge/skills or attitudes and their learning styles (p = 0.21; p = 0.19). Of the trainees, 40% used guidelines to answer clinical questions and 55% agreed that the use of guidelines is the most appropriate way of applying EBM in general practice. Trainees preferred using evidence from summaries to using evidence from single studies. There were no differences in medical decision-making or in EBM use (p = 0.59) for the various learning styles. However, we did find a link between having an Accommodating or Converging learning style and making greater use of intuition. Moreover, trainees with different learning styles expressed different ideas about the optimal use of EBM in primary care. CONCLUSIONS: We found that EBM knowledge/skills and EBM attitudes did not differ with respect to the learning styles of GP trainees. However, we did find differences relating to the use of intuition and the trainees' ideas regarding the use of evidence in decision-making

    Abnormal vaginal bleeding in women of reproductive age: a descriptive study of initial management in general practice

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    <p>Abstract</p> <p>Background</p> <p>Abnormal vaginal bleeding (AVB) in women of reproductive age is a common reason for consulting a general practitioner. Nevertheless, how general practitioners (GPs) choose to initially manage AVB is largely unknown, as is the prevalence of underlying pathology of AVB in primary care.</p> <p>Methods</p> <p>To investigate the initial diagnostic procedures and treatment for AVB used in general practice, we performed a descriptive study based on computerised medical records. New consultations for AVB in 2000 and 2001 were selected. Patient characteristics, diagnostic procedures and treatment were analysed.</p> <p>Results</p> <p>In total, 270 new consultations were included. The majority of patients (75%) consulted the GP for AVB only once. GPs performed diagnostic procedures in 54% of all consultations. Overall, additional diagnostic procedures revealed abnormalities in 11% of women. However, the diagnostic procedures implemented by the GPs varied widely per bleeding type and contraceptive use. Anaemia was found in 36% of 45 women tested. Uterine fibroids were found in 41% of 27 women examined by ultrasound. Medication was prescribed in 34% of all consultations. A gynaecological referral was registered in 4% of all contacts.</p> <p>Conclusion</p> <p>Initially, GPs tend to follow a policy of expectant management in women of reproductive age with AVB. However, when additional diagnostic procedures were performed, anaemia and uterine fibroids were found in a considerable number of women.</p

    Does Random Treatment Assignment Cause Harm to Research Participants?

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    BACKGROUND: Some argue that by precluding individualized treatment, randomized clinical trials (RCTs) provide substandard medical care, while others claim that participation in clinical research is associated with improved patient outcomes. However, there are few data to assess the impact of random treatment assignment on RCT participants. We therefore performed a systematic review to quantify the differences in health outcomes between randomized trial participants and eligible non-participants. METHODS AND FINDINGS: Studies were identified by searching Medline, the Web of Science citation database, and manuscript references. Studies were eligible if they documented baseline characteristics and clinical outcomes of RCT participants and eligible non-participants, and allowed non-participants access to the same interventions available to trial participants. Primary study outcomes according to patient group (randomized trial participants versus eligible non-participants) were extracted from all eligible manuscripts. For 22 of the 25 studies (88%) meeting eligibility criteria, there were no significant differences in clinical outcomes between patients who received random assignment of treatment (RCT participants) and those who received individualized treatment assignment (eligible non-participants). In addition, there was no relation between random treatment assignment and clinical outcome in 15 of the 17 studies (88%) in which randomized and nonrandomized patients had similar health status at baseline. CONCLUSIONS: These findings suggest that randomized treatment assignment as part of a clinical trial does not harm research participants

    Dreigende miskraam in de eerste lijn - Antwoord (letter)

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    Bloedverlies en zwangerschap: 'Dokter, heb ik een miskraam?'

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    Wordt de patiënt er beter van? : Over huisartsopleiding, kwaliteit, evidence-based medicine en nog het een en ander

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    De patiënt van nu mag ervan uitgaan dat de huisarts een gedegen, academische opleiding achter de rug heeft. Een opleiding die zich voortdurend aanpast aan en vooruitloopt op de veranderingen in het beroep, zoals het werken in grotere samenwerkingsverbanden, en in de maatschappij (bijvoorbeeld de vergrijzing). Alle facetten van de huisartsopleiding nemen hiertoe deel aan een continu kwaliteitsproces. Niet alleen moet de kwaliteit van het opleidingsinstituut als organisatie optimaal zijn, maar ook dat van de opleidingspraktijken en de stage-instellingen, van de daar werkzame opleiders, de docenten van het opleidingsinstituut en van het cursorisch onderwijs. Dit alles gericht op het 'product': een competente huisarts. Een proces dat nooit 'af' is en dat wordt ondersteund door wetenschappelijk onderzoek om waar mogelijk en nodig evidence based de opleiding te verbeteren. Margrethe Wieringa-de Waard zoekt naar aanleiding hiervan in haar oratie antwoorden op de vragen: wat merkt de patiënt hiervan, hoe evidence based is de opleiding zelf, en voldoet het aloude model van opleiding nog wel of is het tijd voor een nieuwe aanpak
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