Application of Failure Mode and Effects Analysis in risk management of drug therapy in an intensive care unit

Authors

  • Kamila Maria Maranhão Sidney Federal University of Ceará, Faculty of pharmacy, dentistry and nursing Pharmacy Department, Fortaleza, Brazil. https://orcid.org/0000-0001-7505-620X
  • Elana Figueiredo Chaves Walter Cantídio University Hospital, Multiprofessional Integrated Residency Program in Hospital Health Care, Fortaleza, Brazil. https://orcid.org/0000-0002-5817-0999
  • Jeanine Morais Pereira Maternity School Assis Chateaubriand, Multiprofessional Integrated Residency Program in Hospital Health Care, Fortaleza, Brazil. https://orcid.org/0000-0003-1340-8753
  • Henrique Jorge Maia Costa Messejana Hospital Dr. Carlos Alberto Studart Gomes, Fortaleza, Brazil.
  • Marta Maria de França Fonteles Federal University of Ceará, Faculty of pharmacy, dentistry and nursing Pharmacy Department, Fortaleza, Brazil.

DOI:

https://doi.org/10.30827/ars.v65i3.29973

Keywords:

Risk Assessment, Patient Safety, Quality of Health Care, Critical Care

Abstract

Objective: To utilize Failure Mode and Effects Analysis (FMEA) to manage risks in prescribed drug therapy within an Intensive Care Unit (ICU).

Methodology: This action research, integrating qualitative and quantitative methods, assesses medical prescriptions in a Coronary ICU (CECOR) in Fortaleza, Brazil, using FMEA. This study involves defining the process, forming a multidisciplinary team, conducting a situational diagnosis, evaluating failure modes (FMs) with Severity (S) and Detection (D) indices, monitoring FM Prevalence (P), and calculating the Prioritization Coefficient (PC). Each FM is accompanied by pharmaceutical recommendations (RF). Continuing education activities are designed based on the PC for CECOR professionals.

Results: In the situational diagnosis, 170 prescriptions and 60 FMs were assessed, with primary categories being drug interactions (39.7 %) and incompatibilities (30.0 %). Causes are multifactorial. Regarding the team’s response to an FM, it was determined that 36,7 % of the FMs would be accepted with monitoring. During prevalence monitoring, 63.3 % of FM types occurred 837 times, with high severity (50.0 %) and low detection (55.3 %). Most frequent FMs were absence of pharmaceutical form (29.4 %) and dose (8.8 %).

Conclusion: FMEA facilitates identifying, classifying, and prioritizing risks in drug therapy at CECOR, underlining its effectiveness as a quality tool for enhancing patient safety.

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References

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Published

2024-06-20

How to Cite

1.
Maranhão Sidney KM, Figueiredo Chaves E, Morais Pereira J, Jorge Maia Costa H, de França Fonteles MM. Application of Failure Mode and Effects Analysis in risk management of drug therapy in an intensive care unit. Ars Pharm [Internet]. 2024 Jun. 20 [cited 2024 Jun. 30];65(3):185-201. Available from: https://revistaseug.ugr.es/index.php/ars/article/view/29973

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