TY - JOUR T1 - How can we optimise the pharmaceutical analysis of radiopharmaceutical pediatric prescriptions? JF - European Journal of Hospital Pharmacy JO - Eur J Hosp Pharm SP - 29 LP - 34 DO - 10.1136/ejhpharm-2020-002473 VL - 30 IS - 1 AU - Pauline Leclerc AU - Solène Marie AU - Julien Fouque AU - Madar Olivier AU - Sandy Blondeel-Gomes Y1 - 2023/01/01 UR - http://ejhp.bmj.com/content/30/1/29.abstract N2 - Objectives In France, dispensation is defined by the validation of a prescription associated with a pharmaceutical analysis, preparation of medication and provision of information necessary for proper use. There are very few data available in the literature that describe prescription analysis modality in radiopharmacy. The aim was to secure a place for paediatric prescription analysis in radiopharmacy by designing a flow chart validated by experts.Methods Experts from different disciplines and health setups (ie, public, private) were selected to represent the various paediatric patient care processes. A review of the literature on pharmaceutical analysis and paediatric prescription in radiopharmacy was conducted. A Delphi approach comprising two rounds (Google Form survey) was used to validate the flow chart. Answers were graded according to a nine-point Likert scale for agreement. Open-ended questions allowed experts to comment on the propositions. A consensus between experts was reached if more than 70% of the experts agreed on an item and fewer than 30% disagreed.Results Sixty-five experts were solicited: two oncopaediatricians, three nuclear medicine physicians, 46 radiopharmacists, three residents in radiopharmacy, one hospital pharmacist, five medical physicists, one pharmacy technician, two X-ray technicians and two patients who are pharmacists. The first round survey included a draft of the flow chart: 31 experts answered (48%). All professional disciplines were represented except pharmacy technician. The second round survey was sent with a new flow chart that had been improved by the experts' comments. After 3 weeks, 18 answers were obtained (28%). After the first round, consensus was obtained for each item. Experts gave a total of 97 comments. The second flow chart had three steps: regulatory aspects, patient data, and radiopharmaceutical data, and it was accompanied by descriptive text explaining the field of application.Conclusion The resulting flow chart will secure the pharmaceutical analysis step for this special patient population.Data are available upon reasonable request. ER -