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Oncology

Medication errors in chemotherapy

Medication error is defined as any preventable event that may cause or lead to inappropriate medication use or patient harm while the medication is under the control of the healthcare professional, patient, or consumer.1 Medication errors can be classified by considering the types of errors occurring, such as wrong patient dose, infusion rate, delivery route or medication. Medication errors may occur during any phase of the drug delivery process from prescription to drug administration and anywhere that medications are administered.2 Errors may occur with any medication, however, chemotherapy presents dangers due to narrow therapeutic indices, potential toxicity even at therapeutic dosages, complex regimens, and a vulnerable cancer patient population.3  

“It may be part of human nature to err, but it is also part of human nature to create solutions, find better alternatives and meet the challenges ahead.”

Linda T. Kohn et al, Committee on Quality of Health Care in America, Institute of Medicine
  • 0%

    involved over- and underdosing

  • 0%

    involved schedule and time errors

  • 0%

    involved wrong drugs

  • 0%

    involved chemotherapy given to the wrong patient

Did you know?

Of a total of 207 Infusion Bags: 8, 13

  • 0%

    were infused too slowly

  • 0%

    were infused too fast

  • 0%

    were correctly administered at the prescribed rate

Risk: Wrong delivery route for chemotherapy delivery 

Most of the chemotherapy regimes are given intravenously, i.e. directly into the venous system. Peripheral venous access may be suitable, however, given the high toxicity of the drugs, mostly central venous access is preferred.

Vascular Access

A vascular access port device consists of a catheter connected to a reservoir. It is implanted subcutaneously and namely used to deliver drugs into the blood stream.

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Intercepeted errors, that have not been discovered, lead to 216 additional days of hospitalisation.20

Hospital stays62.248 €
Additional drugs23.658 €
Total annual cost92.248 €

“First, do no harm.”

– Hippokrates

Product Measure

Standard concentrations pre-prepared by pharmacy or industry  , , ,  

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Product Measure

Standard concentrations pre-prepared by pharmacy or industry

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Product Measure

Label/Colour Code Concept 23, 24  and a Barcode/Data Matrix to handle preparation data and close the loop to patient 25

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Product Measure

 IV pumps with intuitive handling and integrated drug database 26,27,28  additionally, compatibility databases 29

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Organisational Measures

Comprehensive and interprofessional education and training of all involved staff 28,29,30,31as well as ward-based clinical pharmacists30,32

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Organisational Measures

Different storage areas for important drugs (e.g. concentrated potassium chloride) 33, 38 and introduction of separate medication preparation rooms on ward 34

Incident reporting system 30, 35, 36

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Risk: Wrong administration technique and exposure to hazardous medicinal products (HMP's)

Healthcare workers who prepare or administer HMP's, or who work in areas where these drugs are used can be exposed to these agents. These workplace exposures to HMP's have been associated with health effects such as skin disorders, adverse reproductive outcomes, and certain cancers 44

To improve healthcare workers safety and minimise the risk of exposure to HMP's all EU Member States are required to bring into force the laws, regulations and administrative provisions necessary to comply with the Carcinogens, Mutagens or Reprotoxic substances Directive (CMRD 2022) by 5 April 2024.

Where it is not technically possible to replace the carcinogen, mutagen or reprotoxic substance by a substance, mixture or process which, under its conditions of use, is not dangerous or is less dangerous to health or safety, the employer shall ensure that the carcinogen, mutagen or reprotoxic substance is, in so far as is technically possible, manufactured and used in a closed system 45

Wrong administration techniques may comprise multiple aspects of the infusion. One example is discussed in the following: 

„Paclitaxel is a chemotherapeutic drug frequently used for breast, ovarial and bronchial cancer. The drug is likely to form microbubbles and particulate matter. The suppliers recommend that an in-line IV filter should be used during the infusion of the agent (SmpC Paclitaxel). Not using the inline filter might result in particles being infused into the patient 37.“

 

Particles arising from infusion therapy may induce or aggravate inflammatory response syndromes. They have been shown to generate thrombosis, impair microcirculation, and modulate immune response. Sources of particles include components of infusion systems, incomplete reconstitution of solutions or drug incompatibility reactions. Up to one million particles may be infused per patient per day. In-line filters incorporated into infusion lines retain particles and thereby nearly entirely prevent their infusion.41

Others would be errors in assembling giving sets for secondary infusions with or without pumps, Luer access-devices unintentionally left open after use or needlestick injury due to needle-based manipulation44

Clara Pujol - hospital nurse

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[2] The Boston Globe, 2004 

[3] Ford et al (2006): Study of Medication Errors on a Community Hospital Oncology Ward. Journal of Oncology Practice, 2006, 2 (4), 149-154. available at: https://ascopubs.org/doi/full/10.1200/jop.2006.2.4.149; accessed 02-23-2023. 

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[12] Noble D. (2010): The quest to eliminate intrathecal vinchristine errors: a 40-year journey. BMJ Quality & Safety 2010, 19, 323-326. 

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[14] Arzneimittelkommission der deutschen Ärzteschaft (2005): Vincristin: Toedliche Zwischenfaelle nach versehentlicher intrathekaler Gabe. Deutsches Aerzteblatt 2005, 102,1615. 

[15] Dyer c (2001): Doctors suspended after injecting wrong drug into spine. BMJ 2001, 322 (7281). 257. 

[16] Kress R. et al. (2016): Unintentional Infusion of Phenylephrine into the Epidural Space. A&A Case Rep. 2016, 6(5),124-7. 

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[18] Institute for Safe Medication Practices (2014): ISMP List of High-Alert Medications in Acute Care Settings [online] available at: https://www.ismp.org/sites/default/files/attachments/2018-01/highalertmedications%281%29.pdf accessed 06-07-2019 

[19] Ranchon et al. (2011): Chemotherapeutic errors in hospitalised cancer patients: attributable damage and extra costs. BMC Cancer 2011, 11:478. 

[20] Sasse M. et al. (2015): In-line Filtration Decreases Systemic Inflammatory Response Syndrome, Renal and Hematologic Dysfunction in Pediatric Cardiac Intensive Care Patients. Pediatric Cardiology 2015, 36 (6),1270–1278. 

[21] Reason, James (2000-). Human error: models and management. BMJ, 320 (7237): 768–770. 

[22] Weingart SN (2018): Chemotherapy medication errors. Lancet Oncol 2018, 19 (4), 191–99. 

[23] Parshuram CS, To T, Seto W, Trope A, Koren G, Laupacis A (2008) Systematic evaluation of errors occurring during the preparation of intravenous medication. CMAJ; 178(1): 42-8. 

[24] Cousins DH, Sabatier B, Begue D, Schmitt C, Hoppe-Tichy T (2005) Medication errors in intravenous drug preparation and administration: a multicentre audit in the UK, Germany and France. Qual Saf Health Care; 14(3): 190-5. 

[25] Taxis K, Barber N,(2003) Etnographic study of incidence and serverity of intravenoius drug errors. BMJ 326:684 

[26] Dehmel C, Braune S, Keymann G, Baehr M, Langebrake C, Hilgarth H, Nierhaus A, Dartsch D, Kluge S (2011) Do centrallly pre-pared solutions achieve more reliable drug concentrations than solutions prepared on the ward? Intensive Care Med 2010-00231. R3 in press. 

[27] Tissot E. Cornette C, Limat S, Maourand J, Becker M, Etievent J et al. (2003) Observational study of potential risk factors of medication administration errors. J Qual Improve 25(6):264-68 

[28] Vogel Kahmann I, Bürki R et al. (2003) Incompatibility reactions in the intensive care unit. Five years after implementation of a simple "color code system". Anasthesist 52(5):409-12 

[29] Valentin A, Capuzzo M, Guidet B, Moreno R, Metnitz B, Bauer P et al. (2009). Errors in adminstration of parental drugs in intensive care units: multinational prospective study. BMJ 338:b814. doi:10.1136/bmj.b814 

[30] Langebrake C, Hilgarth H (2010) Clinical pharmacists' interventions in a German University Hospital. Pharm World Svi 32(2):194-99 

[31] Taxis K (2005) Who is responsible for the safety of infusion devices? It's high time for action! QSHC 14(2):76 

[32] Rothschild JM, Keohane CA, Thompson S, Bates DW (2003) Intelligent Intravenous Infusion Pumps to improve Medication Administration Safety. AMIA Symposium Proceedings, p.992 

[33] Trissel LA (2011). Handbook on Injectable Drugs. 16th ed. Bethesda: American Society of Pharmacist. 

[34] Brigss J (2005) Strategies to reduce medication errors with reference to older adults. Best practice 9(4):1-6 

[35] Irajpour A, Farzi S, Saghaei M, Ravaghi H. Effect of interprofessional education of medication safety program on the medication error of physicians and nurses in the intensive care units. J Educ Health Promot. 2019 Oct 24;8:196. 

[36] Kane-Gill SL, Jacobi J, Rothschild JM (2010)  Adverse drug events in intensive care units: Risk factors, impact and the role of team care. Crit Care Med 38(6): 83-89 

[37] Etchells E, Juurllink D, Levinson W (2008) Medication Errors: the human factor. CMAJ 178(1):63 

[38] Huckels-Baumgart S, Baumgart A, Buschmann U, Schüpfer G, Manser T. Separate Medication Preparation Rooms Reduce Interruptions and Medication Errors in the Hospital Setting: A Prospective Observational Study. J Patient Saf. 2021 Apr 1;17(3):e161-e168. 

[39] Smeulers M, Verweij L, Maaskant JM, de Boer M, Krediet CT, Nieveen van Dijkum EJ, Vermeulen H. (2015) Quality indicators for safe medication preparation and administration: a systematic review. PLoS One. 2015 Apr 17;10(4):e0122695. doi: 10.1371 

[40] Jones JH, Treiber L (2010) When 5 rights Go Wrong. J Nurs Care Qual 25:240-247 

[41] Schulmeister L (2007): Patient Misidentification in Oncology. Clinical Journal of Oncology Nursing 2007, 12 (3), 495-498. Available at: https://cjon.ons.org/cjon/12/3/patient-misidentification-oncology-care accessed: 02-23-2023 

[42] Schulmeister L (2002): Searching for Information for Presentations and Publications. Clinical Nurse Specialist, 2002, 16 (2); 79-84 

[43] Goldspiel B, Hoffman JM, Griffith NL, et al. ASHP guidelines on preventing medication errors with chemotherapy and biotherapy. Am J HealthSyst Pharm. 2015; 72:e6–35 

[44] https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4569003/pdf/nihms713303.pdf. Connor, T.H., Lawson, C.C., Polovich, M. and McDiarmid, M.A., (2014). Reproductive Health Risks Associated with Occupational Exposures to Antineoplastic Drugs in Health Care Settings: A Review of the Evidence. J Occup ENviron Med. 2014 September ; 56(9)

[45] https://echa.europa.eu/legislation-profile/-/legislationprofile/EU-WORKER_CARC_MUTA European Chemicals Agency (2004). CMD - Carcinogens and Mutagens Directive. [Online]. ECHA. Last Updated: March 2024. Available at: https://echa.europa.eu/legislation-profile/-/legislationprofile/EU-WORKER_CARC_MUTA [Accessed 21 June 2024]