SELF-ADMINISTRATION OF IN-PATIENT MEDICATIONS: A PILOT STUDY IN CHILDREN WITH CYSTIC FIBROSIS
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Khola Khan1, Aoife Harrington1, Rupinder Pannu1
1Royal Brompton & Harefield NHS Foundation Trust.
Insights
The Self-Administration Of Medicines Scheme (SAM) empowers children with Cystic Fibrosis (CF) and their families to manage medications, improving independence and reducing costs. This pilot program showed positive reception and significant cost savings, leading to its wider implementation.
Area of Science:
- Pediatric pulmonology
- Healthcare management
- Patient empowerment
Background:
- Children with Cystic Fibrosis (CF) require complex medication regimens.
- Parent/carer administration is typical until children are older.
- Hospitalization often shifts administration to nurses, potentially disempowering patients and families.
Purpose of the Study:
- To implement and evaluate the Self-Administration Of Medicines Scheme (SAM) for all pediatric CF admissions.
- To empower patients/parents/carers in medication administration.
- To reduce nursing workload, educate families, and achieve cost savings through Patients Own Medicines (PODs).
Main Methods:
- Developed and approved a policy and training program for SAM.
- Assessed all admitted CF families for participation over 10 months.
- Collected data via questionnaires for patient/parent/carer and nurse feedback, and POD re-use for cost analysis.
Main Results:
- 95 out of 159 (60%) CF admissions were assessed for SAM; 64 participated.
- Participants reported benefits including reduced waiting times for medication, increased independence, and routine maintenance.
- Nurses reported reduced administration time and pressure; significant cost savings of £1023 per patient over 3 months were observed with PODs.
Conclusions:
- The SAM pilot scheme was well-received by patients, parents/carers, and staff.
- The scheme facilitated greater engagement in medication administration and demonstrated cost-effectiveness.
- SAM will be extended to all patients on the ward due to its success.
Introduction:
Children with Cystic Fibrosis (CF) have complex medication regimens, where responsibility for administration usually lies with the parent/carer until the child is older and able to take over this role.1 On admission to hospital this role is usually undertaken by nurses, leaving patients/parents/carers feeling disempowered, and unprepared for discharge.
Aims:
All CF admissions to be offered the Self-Administration Of Medicines Scheme (SAM).▸ Empower patients/parents/carers with responsibility of administering their own medications▸ Reduce nursing time▸ Educate patients/parents/carers about their medications▸ Cost-saving by utilising Patients Own Medicines (PODs).
Method:
A policy and training programme was developed and approved by the Trust's Medicines Management Board. This provided a framework for staff to use so that they may:▸ Obtain consent▸ Evaluate and re-use PODs▸ Safely store and obtain supplies▸ Continuously negotiate accountability for administration with patient/parent/carer.The study was conducted over a 10 month period, where all families with CF admitted, were assessed for participation in SAM. The nursing teams acted as the primary assessors for SAM and any concerns were referred to the paediatric CF multidisciplinary team. To evaluate the pilot, families were given questionnaires to establish their views about the scheme. Nurses were asked to feedback if SAM decreased time for medication administration. To evaluate the associated cost-saving, data on PODs suitable for re-use was collected.
Results:
159 children with CF were admitted to the ward, 95 (60%) were assessed to participate in the scheme and 64 (40%) of these did not join. Reasons for not joining included 32 (50%) short admissions, 13 (20%) refused, 5 (8%) patients were seriously ill and 14 (22%) had 'other' reasons. Those who joined the scheme received questionnaires and 31 (33%) of these were completed. All welcomed the scheme and stated that they would take part again with the main benefits cited as not needing to wait for nurses to administer medications, greater independence and the ability to maintain the same routine as home. When asked what participants would change, 16 (52%) stated nothing, 10 (32%) wanted the assessment process to allow for faster progression through the levels of SAM, 4 (13%) asked for larger medication lockers and 1 (3%) wanted better communication about new medications. 30 nursing questionnaires were completed and highlighted that nursing staff spent less time on administering medicines. Nurses also stated that medication administration was less pressurised as double-checking of doses could be performed with the participant, rather than another nurse. Their main concern was the extra documentation required for SAM. Where PODs were used for patients, the average cost saving per patient over a 3 month period was £1023.
Conclusion:
The pilot scheme has been well received by staff and patients/parents/carers, allowing greater engagement in the administration of medicines and cost-savings. As a result of this, the SAM scheme will be extended to the remaining patients on the ward.
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