| Literature DB >> 35461276 |
Mais Iflaifel1, Rosemary Lim2, Clare Crowley1, Francesca Greco1, Rick Iedema3.
Abstract
BACKGROUND: The use of variable rate intravenous insulin infusion (VRIII) is a complex process that has consistently been implicated in reports of error and consequent harm. Investment in patient safety has focused mainly on learning from errors, though this has yet to be proved to reduce error rates. The Resilient Health Care approach advocates learning from everyday practices. Video reflexive ethnography (VRE) is an innovative methodology used to capture everyday practices, reflect on and thereby improve these. This study set out to explore the use of VRIIIs by utilising the VRE methodology.Entities:
Keywords: Hyperglycaemia; Resilient health care; Safety; Variable rate intravenous insulin infusions; Video reflexive ethnography; Work as done
Mesh:
Substances:
Year: 2022 PMID: 35461276 PMCID: PMC9034771 DOI: 10.1186/s12913-022-07883-w
Source DB: PubMed Journal: BMC Health Serv Res ISSN: 1472-6963 Impact factor: 2.908
Eligibility criteria and recruitment process
| Healthcare practitioners who are: | |
| 1. Willing to be observed by video recording. | |
| 2. Working in the Vascular Surgery Unit. | |
| 3. Managing/dealing with patients on VRIII. | |
| Patients who are: | |
| 1. Aged ≥18 years old. | |
| 2. Receiving VRIII for at least 24 h to treat elevated BG. | |
| 3. Under the care of a healthcare practitioners who have consented to participate in this study. | |
| 4. Able to provide informed consent. | |
| Healthcare practitioners who are: | |
| 1. Not willing to be observed by video recording. | |
| 2. Not working in the Vascular Surgery Unit. | |
| 3. Not involved in the use of VRIII. | |
| Patients who are: | |
| 1. Not willing to be observed by video recording. | |
| 2. Not prescribed VRIII. | |
| 3. On IV insulin and glucose infusion for hyperkalaemia (potassium levels > 5.5 mmol/L). | |
| 4. Unable to provide informed consent. | |
| 5. Non-English speakers. | |
| To recruit potential healthcare practitioners, an invitation letter and participant information sheet outlining the purpose of the study, the methodology, and the design was first sent by the Unit clinical and managerial lead to all potential healthcare practitioners. Then the researcher (MI) met the healthcare practitioners working in the Unit in two ward meetings and explained the study aims and process. Informed consent was then taken from interested healthcare practitioners. A poster with details about the study was also placed in the staff room until the completion of data collection. | |
| The study site collaborator with a pharmacist team identified potential patient participants. The researcher confirmed with the senior nurse the appropriateness of the patient before recruiting them. This is in addition to whether the patient had the capacity to consent. Once agreed, the researcher provided an invitation letter and participant information sheet to the patient and explained the purpose and objectives of the study and that as part of filming the work of healthcare practitioners, some parts of their body might appear in the video recordings (arm, leg, etc.). The researcher asked the patient if they had any questions about the study before taking written informed consent. |
Criteria used to choose the video clips for use in the reflexive meeting
| 1. The video clips were chosen on the basis that they could be used to address the research question with the healthcare practitioners, enabling them to describe and scrutinise how VRIII is used in everyday clinical work. The guiding principles of VRE are: | |
| • Does the footage reveal a range of tasks or a range of different people doing similar things in previously un (der) appreciated ways (reflexivity)? | |
| • Can the clips show different perspectives on a task and create the possibility for more appropriate understandings, perspectives or solutions (exnovation)? | |
| • Do the chosen clips and the feedback discussion maintain the psychological safety of the participants (care)? | |
| • Could the chosen clips help engage healthcare practitioners in collectively identifying safety interventions in the in situ, taken-for-granted everyday work (collaboration)? | |
| 2. The time available for the reflexive session | |
| • The video clips were chosen in such a way that they could be discussed in 30–45 min. |
Fig. 1Study flow diagram
Summary of the main tasks observed to treat elevated CBG using VRIIIs
| The treatment of elevated CBG using VRIIIs started with confirming the potential need for VRIII in the ward round/board meeting. Each morning between 8 am and 10 am there was a ward round during which consultants, registrars, foundation year one doctors, and a senior nurse checked each patient’s status, examined each patient and reviewed their progress, laboratory results, and medications. After the ward round finished at around 10.30 am there was a board meeting attended by various healthcare practitioners including nurses, consultants, registrars, foundation year one doctors, medical students, receptionists, pharmacists, and occupational therapists. The staff discussed patients’ cases and approved their treatment plans. Nurses came to check the confirmed plans for their patients, with a senior nurse documenting the plans on a yellow paper. | |
| Ensuring the right medications were prescribed, based on CBG readings, was conducted by doctors who were required to prescribe VRIII, IV fluids, and IV glucose, stop all diabetes medicines, except long-acting insulin analogues which were to be continued. | |
| Before assembling the components of VRIII | |
| Nurses then recorded on the ePMA the medications to be administered (VRIII and IV fluids). Independent verification of the VRIII/IV fluids was conducted before administering insulin/IV fluids by checking the label on the insulin/IV fluid syringe (name, dose, expiry date), confirming this by signing the details on the EPR. | |
| Ensuring CBG and blood ketones were within the normal range was conducted by bedside monitoring of CBG and blood ketones every 1–7 h. Nurses were required to regularly monitor cannula, patient complaints, and site of injection, based on the patient’s clinical status. | |
| Nursing handovers were conducted three times a day for each patient, sometimes during lunch breaks. | |
| It was clear that electronic documentation of CBG/ketone readings, VRIII rate, insulin/fluids administration, and VIP score was a crucial step by which healthcare practitioners made sure each task they accomplished using the EPR system was documented. |
Demographics and CBG monitoring data from two patients’ medical records
| Patient 1 | Patient 2 | |
|---|---|---|
| 87 | 84 | |
| Male | Male | |
| 4.5 h; 2–7 h | 2 h; 1–3 h | |
Day 1: 4% of 24 h Day 2: 25% of 24 h | 17% of 24 h | |
Day 1: 90% of CBG readings > 12 mmol/L Day 2: 0% | 0% | |
Day 1: persistent hyperglycaemia over 24 h Note: there was no DKA associated with the persistent hyperglycaemia | 0 | |
| No episode reported | 3 episodes | |
| 0 | 2 |
Prescribing IV fluids