| Literature DB >> 30841893 |
Aislinn Conway1,2, Maura Dowling3, Áine Binchy3,4, Jane Grosvenor4, Margaret Coohill5, Deirdre Naughton3,5, Jean James3,4, Declan Devane6,3.
Abstract
BACKGROUND: Evidence-informed practice is fundamental to the delivery of high quality health care. Delays and gaps in the translation of research into practice can impact negatively on patient care. Previous studies have reported that problems facing health care professionals such as information overload, underdeveloped critical appraisal skills, lack of time and other individual, organisational and system-level contextual factors are barriers to the uptake of evidence. Health services research in this area has been restricted largely to the evaluation of program outcomes. This paper aims to describe the implementation process of an educational initiative for health care professionals working in midwifery, neonatology or obstetrics aimed at disseminating evidence and enhancing evidence-informed clinical care.Entities:
Keywords: Adaptation; Context; Dissemination; Education; Evidence-informed practice; Health services research; Implementation; Knowledge translation; Sustainability; TIDieR
Mesh:
Year: 2019 PMID: 30841893 PMCID: PMC6402167 DOI: 10.1186/s12909-019-1489-y
Source DB: PubMed Journal: BMC Med Educ ISSN: 1472-6920 Impact factor: 2.463
Fig. 1Process-oriented logic model of the Evidence Rounds educational initiative
Evidence Rounds session details and follow-up
| Session number, topic and (number of attendees who signed in) | Specific questions/ issues explored | Potential resulting actions identified | Resulting actions and contextual factors |
|---|---|---|---|
| 1. Premedication for non-emergency neonatal intubations (17) | • What are the risks and benefits of using premedication for neonatal intubation? | • Develop a policy for premedication for non-emergency neonatal intubation. | Evidence Rounds identified as the ‘driving force’ for the policy. |
| 2. Timing of umbilical cord clamping (32) | • The impact on delayed resuscitation at delivery | • Change discharge sheet to include optimal timing of cord clamping. | Staff report a ‘concerted effort’ to offer DCC to preterm infants since Evidence Rounds educational initiative. |
| 3. Medical management of patent ductus arteriosus (PDA) in preterm infants (20) | • What are the risks and benefits of using medical treatments (specifically indomethacin, paracetamol, ibuprofen) for treating PDA in preterm infants? | Confirmation that best practice was currently in place which is | In December 2018, a doctor was writing this standard operating procedure using evidence presented during the educational session. |
| 4. Antenatal screening for group B Streptococcus (GBS) (32) | • What is the rate of recurrence of GBS? | The evidence presented at this educational session highlighted a) the increased risk of early-onset group B Streptococcus (EOGBS) in infants of women with risk factors and b) the existence of strategies (screening or intrapartum antibiotic prophylaxis (IAP)) that could reduce the risk. There was consensus amongst staff that there was a need for action because women with GBS in a previous pregnancy were not being offered either strategy. The recommendations from this session were to offer screening to all women who had GBS in a previous pregnancy and to change the local guideline accordingly. | After this educational session, the Royal College of Obstetricians and Gynaecologists (RCOG) published their Green-top Guideline no.36 Prevention of Early-onset Neonatal Group B Streptococcal Disease [ |
| 5. Antenatal steroid use for preterm deliveries less than 37 weeks gestational age (GA) (20) | • At what GA should the corticosteroid be administered? | The consultant dealing with the patient should consider antenatal steroids when there is a risk of preterm birth at a gestational age of 23 weeks + 0 days to 23 weeks + 6 days (previously 24 weeks + 0 days). | There was a gap in knowledge of the evidence prior to Evidence Rounds. After the educational session, awareness of the evidence increased and it was discussed at subsequent meetings. |
| 6. Fetal blood sampling (FBS) (27) | • The specificity and sensitivity of FBS. | The evidence presented in this session demonstrated that digital fetal scalp stimulation is effective as a first option in fetal monitoring if a cardiotocography (CTG) trace is pathological. If the fetal heart rate accelerates, the FBS should only be undertaken if the CTG trace is still pathological. This means that FBS procedures, which are more invasive for mother and fetus, will be reduced. Staff to update existing fetal monitoring guideline accordingly. | The local guideline was updated to reflect these recommendations. The implementation team reported an increased awareness of the evidence however, there has been no real practice change. Staff are questioning why, there are education sessions every month and this topic is frequently discussed at caesarean section meetings. |
Modes of delivery used in Evidence Rounds for promotional purposes, communication and dissemination
| Mode of delivery | Details and contextual influences |
|---|---|
| Group educational sessions and discussion forum | The presentations at all sessions had a similar structure with small differences if warranted by the topic eg. presenters carried out a retrospective local audit for 3 out of the 6 group sessions. Therefore, repeat attendees became familiar with the format and upcoming and potential presenters knew what to expect. |
| In-person meetings | One-to-one and group meetings were arranged with key informants (eg. practice development and front-line staff interested in research) for implementation planning. These interactions were important for gaining an understanding of the organizational context and choosing the implementation team. It was pivotal to our initiative to gain buy in, and collaborate and partner with HCPs to give them the opportunity to be involved in, contribute to and co-design and development of the initiative. Through recommendations from these meetings and additional contacts, we reached out to those who could be considered as potential opinion leaders and champions. A key intention was to identify people with different professional perspectives to identify their needs and bring them on board. |
| Website | Using a web hosting platform, we designed a logo for Evidence Rounds, purchased a suitable domain name and created a dedicated website. It was designed to present information in a minimalist and aesthetically-pleasing format. During the initiative, the site was updated regularly with current information. The website homepage contained six clickable links, each of which had a distinct core function: |
| Social media | Dedicated accounts on Twitter, Facebook and LinkedIn were set up. After discussion with staff regarding what they and their colleagues were finding useful, it was decided to discontinue updating each of these platforms and concentrate on modes of delivery preferred by staff such as email, word-of-mouth and the website. Staff were keen to manage work-life boundaries when it came to online technologies. |
| Reminders to attend group sessions were mostly sent via email to staff mailing lists by HCPs from the implementation team. Email was used commonly for communication by the implementation team and presenters and was used to recruit participants for focus groups and interviews. Personalised certificates of attendance or participation (for presenters) were emailed to attendees on an opt-in basis (see Additional file | |
| Posters | Staff reported that posters, although a more passive mode of delivery, were effective at reminding them about upcoming group sessions when strategically located. They were designed using an online graphic design service called Canva. |
| Word of mouth | Word-of-mouth played a vital role in the delivery of information during the implementation process and was deemed a very effective means of engaging our target audience by the implementation team. Some HCPs started attending group sessions based on recommendations from their colleagues and we were told that discussion about evidence covered in group sessions and its implications for practice continued from the classroom to the wards. |
TIDieR checklist
| Item number | Item | Description |
|---|---|---|
| Brief name | ||
| 1. | Provide the name or a phrase that describes the intervention. | Evidence Rounds |
| Why | ||
| 2. | Describe any rationale, theory, or goal of the elements essential to the intervention. | This information is provided in the Background section of this paper. |
| What | ||
| 3. | Materials: Describe any physical or informational materials used in the intervention, including those provided to participants or used in intervention delivery or in training of intervention providers. Provide information on where the materials can be accessed (e.g. online appendix, URL). | Physical materials: |
| 4. | Procedures: Describe each of the procedures, activities, and/or processes used in the intervention, including any enabling or support activities. | 1. |
| Who provided | ||
| 5. | For each category of intervention provider (e.g. psychologist, nursing assistant), describe their expertise, background and any specific training given. | Presenters and other members of the implementation team were qualified physicians, nurses or midwives. The initiative was led by a knowledge translation specialist who has experience of collaborating with HCPs to promote evidence-informed practice in women and children’s divisions at hospitals and had the following training: |
| How | ||
| 6. | Describe the modes of delivery (e.g. face-to-face or by some other mechanism, such as internet or telephone) of the intervention and whether it was provided individually or in a group. | The modes of delivery are described in Table |
| Where | ||
| 7. | Describe the type(s) of location(s) where the intervention occurred, including any necessary infrastructure or relevant features. | Each educational session was delivered in a classroom located adjacent to wards for the convenience of staff who could be bleeped or called away at any moment. After the second session, we discussed the possibility of changing to a larger venue but decided against this as the location worked well and the capacity it held was viewed as ideal for promoting discussion, had adequate seating capacity and audio-visual technology to display presentation slides. |
| When and How much | ||
| 8. | Describe the number of times the intervention was delivered and over what period of time including the number of sessions, their schedule, and their duration, intensity or dose. | Six educational sessions were delivered over nine months. We took a flexible approach to scheduling by avoided exam times, holidays, training or other educational sessions and meetings in order to maximise attendance figures. As requested by staff, Evidence Rounds group sessions were scheduled during lunchtimes. Each session lasted approximately 1 h because the implementation team identified this as a realistic duration of attendance for most HCPs. Immediately after each educational presentation, a facilitated discussion forum took place which lasted for up to 30 min. They were timetabled on Fridays at lunchtimes (excluding the final session which took place on a Wednesday). Before each session email reminders were sent to potential attendees by HCP members of the implementation team and in some cases they delivered in-person reminders on the hospital wards. |
| Tailoring | ||
| 9. | If the intervention was planned to be personalised, titrated or adapted, then describe what, why, when, and how. | Evidence Rounds was adapted throughout its duration in response to the needs and expressed preferences of the audience and the local context, as was planned. All feedback from attendees was considered and acted upon if appropriate and possible, at the earliest opportunity so that subsequent delivery was improved. |
| Modifications | ||
| 10. | If the intervention was modified during the course of the study, describe the changes (what, why, when, and how). | The initiative was modified throughout the course of the study in accordance with feedback from users and observations. For example: |
| How well | ||
| 11. | Planned: If intervention adherence or fidelity was assessed, describe how and by whom, and if any strategies were used to maintain or improve fidelity, describe them. | We did not assess adherence or fidelity. However, core components of the initiative were identified before the first session and adhered to throughout the duration. Those components were: |
| 12.a | Actual: If intervention adherence or fidelity was assessed, describe the extent to which the intervention was delivered as planned. | N/A |
aThis item is not applicable for the intervention being described
Fig. 2Website analytics data showing number of unique visitors to the website, visits (number of browsing sessions) and number of page views (requests on the website which were fully loaded), by month and year