Open Access

Pharmacotherapeutic friendly fire in the intensive care unit: high stakes seeking high calibre

Critical Care200812:137

https://doi.org/10.1186/cc6858

Published: 22 April 2008

Abstract

Increasing numbers of patients are surviving the intensive care unit. Concordant with our shifting focus to minimizing intensive care unit-acquired morbidity, in the present issue of Critical Care Moyen, Camire, and Stelfox describe the importance of quality pharmacotherapy. They describe challenges and potential solutions to this source of iatrogenic injury in our vulnerable patients. Their article reminds us not to understate the importance of medication error, to avoid overstating the benefits of incompletely proven methods to prevent medication error, and to distinguish harmful medication errors from other types of medication error.

Medication error is the most commonly observed threat to patient safety in the intensive care unit (ICU). In the present issue of Critical Care, Moyen, Camire, and Stelfox describe the importance of quality pharmacotherapy [1]. Their narrative review provides insight into medication errors in this complex, imperfect, multistakeholder process. They discuss vulnerability, error definition and measurement, and methods to improve the process and outcomes of pharmacotherapy in the ICU.

The ICU represents the meeting of the high-risk patient, polypharmacy, physiologic complexity, and an interventional environment that provides many opportunities for error [2]. Medication error is common [37]. Rothchild's direct observational, single-centre study in an adult ICU found a serious medication error occurred once every 8 patient-days. A harmful medication error occurred every 78 patient-days, a life-threatening medication error occurred every 300 patient-days, and a fatal medication error occurred once every 750 patient-days (95% confidence interval, 207 to 7,450) [4]. In a 20-bed ICU this conservatively translates to one preventable death due to a medication error every 6 to 8 weeks.

While sobering, these data remind us that all medication errors are not equal. Definitions are important. These definitions underscore our thinking and influence how measures are used. Moyen and colleagues define a medication error as 'any error in the medication process, whether there are adverse consequences or not' [8]. This definition includes both errors of commission and errors of omission. Errors involving omission of or delayed initiation of therapy may be difficult to detect but are clinically important. This definition includes near-miss errors and other errors that do not reach patients. This is consistent with a process-of-care approach to medication errors. An alternate, patient-centred philosophy defines a medication error as 'a failure in the medication process that results in a patient failing to receive the appropriate drug or drug dose' [9]. This definition excludes a near-miss error, and reflects our understanding of medication safety systems: drugs that are not administered cannot cause patient harm, and detecting and intercepting an error signals a functional safety system. The confusing heterogeneity introduced by use of these two valid definitions emphasizes the need for clarity when discussing medication errors, and the benefits of a standard, accepted nomenclature.

Clinical surveillance, like other forms of medication error research, can be used to improve future care. The benefits to the patient affected and to the providers involved in the error are less clear [10, 11]. Underreporting with voluntary methods is routine [6]. Our culture of silence may be understandable in environments where the one ubiquitous defence is frontline vigilance. Underreporting is unlikely to change while professional accountability is mediated through the administrators contributing to the implicated system-level errors.

Voluntary reporting is at best a qualitative tool to identify problems in a given system, and is suited to the inclusion of near-miss events as suggested by Moyen and colleagues [8]. The vigour of surveillance data collection should balance the workload, the merits of the collected data, and system-responsiveness to emerging signals [12]. Quantification of the effectiveness of error-reducing interventions requires more robust methods [6]. To date, only pharmacists attending multidisciplinary ICU ward rounds have been shown to reduce harmful medication errors [13].

Medication safety begins well before the ICU. Prelicensing evaluation, drug regulation practices, and drug manufacturers provide incomplete safety, dosing, and effectiveness data, that should be complimented by relevant clinical trials and postmarketing surveillance [14]. Drug preparation before ICU admission and within the ICU produces errors in up to 65% of prepared infusions [15]. Fatigue, practice, and the stock solutions produced by drug manufacturers are all contributors [16]. A preparation-associated error is more frequent than other types of medication error. The cascading effects of licensing an unsafe drug, making a diagnostic error leading to multiple erroneous therapies, or making a prescription error that is repeatedly administered, however, may be far greater than a preparation-associated error and might underscore the need for a standard, clinically relevant metric for assessing medication safety across these dimensions.

Reducing error is different to reducing harm. Moyen and colleagues [1] describe computerized physician order entry, bar-coding, smart infusion pumps, and infusion concentration standardization as methods to reduce medication error. As pointed out by Moyen and colleagues, none of these activities have been shown to reduce harmful medication errors [1]. In fact, new harmful errors may be uncovered and worse outcomes have been reported with computerized physician order entry in the ICU [17]. Improvement should mean fewer harmful errors or less risk-adjusted morbidity or mortality. Whichever metric is used, demonstration of improved patient outcomes should be a minimum requirement before implementation of any expensive system-level intervention.

Moyen and colleagues [1] remind us that pharmacotherapy in the ICU is a large-calibre weapon. Patients may be harmed by optimal pharmacotherapy. Attribution of harm is difficult; however, large epidemiologic studies suggest that up to one-half of adverse drug events in hospitalized patients are preventable, and 10% of medication errors in ICU patients result in harm [4]. This issue should not be understated. Quality pharmacotherapy is a core component of high-calibre ICU care. Thanks go to Moyen and colleagues for their insightful synthesis and for promoting ongoing discussion of this multifaceted, challenging and fundamental aspect of the practice of critical care medicine.

Abbreviations

ICU: 

intensive care unit.

Declarations

Acknowledgements

CSP is a Career Scientist of the Ministry of Health and Long Term Care.

Authors’ Affiliations

(1)
Department of Critical Care Medicine, Hospital for Sick Children
(2)
Center for Safety Research, Hospital for Sick Children
(3)
Child Health and Evaluation Sciences Program, The Research Institute, Hospital for Sick Children
(4)
Department of Pediatrics, University of Toronto
(5)
Interdepartmental Division of Critical Care Medicine, University of Toronto

References

  1. Moyen E, Camire E, Stelfox HT: Clinical review: Medication errors in critical care. Crit Care. 2008, 12: 208-10.1186/cc6813.PubMedPubMed CentralView ArticleGoogle Scholar
  2. Donchin Y, Gopher D, Olin M, Badihi Y, Biesky M, Sprung CL, Pizov R, Cotev S: A look into the nature and causes of human errors in the intensive care unit. Crit Care Med. 1995, 23: 294-300. 10.1097/00003246-199502000-00015.PubMedView ArticleGoogle Scholar
  3. Cimino MA, Kirschbaum MS, Brodsky L, Shaha SH: Assessing medication prescribing errors in pediatric intensive care units. Pediatr Crit Care Med. 2004, 5: 124-132. 10.1097/01.PCC.0000112371.26138.E8.PubMedView ArticleGoogle Scholar
  4. Rothschild JM, Landrigan CP, Cronin JW, Kaushal R, Lockley SW, Burdick E, Stone PH, Lilly CM, Katz JT, Czeisler CA, Bates DW: The Critical Care Safety Study: the incidence and nature of adverse events and serious medical errors in intensive care. Crit Care Med. 2005, 33: 1694-1700. 10.1097/01.CCM.0000171609.91035.BD.PubMedView ArticleGoogle Scholar
  5. Sharek PJ, Horbar JD, Mason W, Bisarya H, Thurm CW, Suresh G, Gray JE, Edwards WH, Goldmann D, Classen D: Adverse events in the neonatal intensive care unit: development, testing, and findings of an NICU-focused trigger tool to identify harm in North American NICUs. Pediatrics. 2006, 118: 1332-1340. 10.1542/peds.2006-0565.PubMedView ArticleGoogle Scholar
  6. Krahenbuhl-Melcher A, Schlienger R, Lampert M, Haschke M, Drewe J, Krahenbuhl S: Drug-related problems in hospitals: a review of the recent literature. Drug Saf. 2007, 30: 379-407. 10.2165/00002018-200730050-00003.PubMedView ArticleGoogle Scholar
  7. Cullen DJ, Sweitzer BJ, Bates DW, Burdick E, Edmondson A, Leape LL: Preventable adverse drug events in hospitalized patients: a comparative study of intensive care and general care units. Crit Care Med. 1997, 25: 1289-1297. 10.1097/00003246-199708000-00014.PubMedView ArticleGoogle Scholar
  8. Leape LL: Preventing adverse drug events. Am J Health Syst Pharm. 1995, 52: 379-382.PubMedGoogle Scholar
  9. National Library of Medicine – Medical Subject headings. accessed 14 April 2008. Tree Number E02.319.529., [http://www.nlm.nih.gov/mesh/MBrowser.html]
  10. West CP, Huschka MM, Novotny PJ, Sloan JA, Kolars JC, Habermann TM, Shanafelt TD: Association of perceived medical errors with resident distress and empathy: a prospective longitudinal study. JAMA. 2006, 296: 1071-1078. 10.1001/jama.296.9.1071.PubMedView ArticleGoogle Scholar
  11. Wu AW: Medical error: the second victim. The doctor who makes the mistake needs help too. BMJ. 2000, 320: 726-727. 10.1136/bmj.320.7237.726.PubMedPubMed CentralView ArticleGoogle Scholar
  12. Frey B, Buettiker V, Hug MI, Waldvogel K, Gessler P, Ghelfi D, Hodler C, Baenziger O: Does critical incident reporting contribute to medication error prevention?. Eur J Pediatr. 2002, 161: 594-599. 10.1007/s00431-002-1055-0.PubMedView ArticleGoogle Scholar
  13. Leape LL, Cullen DJ, Clapp MD, Burdick E, Demonaco HJ, Erickson JI, Bates DW: Pharmacist participation on physician rounds and adverse drug events in the intensive care unit. JAMA. 1999, 282: 267-270. 10.1001/jama.282.3.267.PubMedView ArticleGoogle Scholar
  14. Bloomfield R, Noble DW: Etomidate, pharmacological adrenalectomy and the critically ill: a matter of vital importance. Crit Care. 2006, 10: 161-10.1186/cc5020.PubMedPubMed CentralView ArticleGoogle Scholar
  15. Parshuram CS, Ng GY, Ho TK, Klein J, Moore AM, Bohn D, Koren G: Discrepancies between ordered and delivered concentrations of opiate infusions in critical care. Crit Care Med. 2003, 31: 2483-2487. 10.1097/01.CCM.0000089638.83803.B2.PubMedView ArticleGoogle Scholar
  16. Parshuram CS, To T, Seto W, Trope A, Koren G, Laupacis A: Systematic evaluation of errors occurring during the preparation of intravenous medication. CMAJ. 2008, 178: 42-48.PubMedPubMed CentralView ArticleGoogle Scholar
  17. Han YY, Carcillo JA, Venkataraman ST, Clark RS, Watson RS, Nguyen TC, Bayir H, Orr RA: Unexpected increased mortality after implementation of a commercially sold computerized physician order entry system. Pediatrics. 2005, 116: 1506-1512. 10.1542/peds.2005-1287.PubMedView ArticleGoogle Scholar

Copyright

© BioMed Central Ltd 2008

Advertisement