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Chapter 9. Protocols for High-Risk Drugs: Reducing Adverse Drug Events Related to Anticoagulants

Tejal K. Gandhi, M.D., M.P.H.
Harvard Medical School

Kaveh G. Shojania, M.D.
University of California, San Francisco School of Medicine

David W. Bates, M.D., M.Sc.
Harvard Medical School

Background

Published studies of adverse drug events and multiple case reports have consistently identified certain classes of medications as particularly serious threats to patient safety.1-3 These "high risk" medications include concentrated electrolyte solutions such as potassium chloride, intravenous insulin, chemotherapeutic agents, intravenous opiate analgesics, and anticoagulants such as heparin and warfarin. Analyses of some of the adverse events involving these mediations have led to important recommendations regarding their administration. Examples include the use of order templates for chemotherapeutic agents, removal of intravenous electrolyte solutions from general ward stock, and protocols for reviewing the settings of intravenous pumps delivering continuous or frequent doses of opiates.2,4,5 While these recommendations have high face validity, they have generally not been subject to formal evaluation regarding their impact in reducing the targeted adverse events. By contrast, several practices relating to the management of patients receiving anticoagulants have been evaluated quite extensively, and therefore constitute the focus of this chapter.

Heparin and warfarin are medications whose use or misuse carry significant potential for injury. Subtherapeutic levels can lead to thromboembolic complications in patients with atrial fibrillation or deep venous thrombosis (DVT), while supratherapeutic levels can lead to bleeding complications. These medications are commonly involved in ADEs for a variety of reasons, including the complexity of dosing and monitoring, patient compliance, numerous drug interactions, and dietary interactions that can affect drug levels. Strategies to improve both the dosing and monitoring of these high-risk drugs have potential to reduce the associated risks of bleeding or thromboembolic events.

Practice Description

The practices reviewed in this chapter are all intended to reduce dosing and/or monitoring errors for heparin and warfarin, as follows:

  • Heparin dosing protocols ("nomograms") typically involve a standard initial bolus and infusion rate, instructions for when to draw the first partial thromboplastin time (PTT), and orders for dosing adjustments in response to this and subsequent values (so nurses can adjust doses automatically). In some cases, the initial bolus and infusion rates are based on patient weight.
  • Inpatient anticoagulation services for both heparin and warfarin (with or without dosing nomograms) typically consist of pharmacist-run services that provide daily pharmacy input on dosing and monitoring for patients on heparin and/or warfarin (We excluded studies focusing solely on warfarin prophylaxis in orthopedic patients6).
  • Outpatient anticoagulation clinics provide coordinated services for managing outpatient warfarin therapy. Services typically include anticoagulation monitoring and follow-up, warfarin dose adjustment, and patient education. These clinics are usually run by pharmacists or nurses operating with physician back-up, and sometimes following specific dosing nomograms.
  • Patient self-monitoring using a home finger-stick device and self-adjustment of warfarin dosages using a nomogram (The accuracy of these devices and the comparability of patients' and professional readings have been extensively evaluated7-11).

Prevalence and Severity of the Target Safety Problem

Intravenous heparin and oral warfarin are commonly used medications for cardiac disease and thromboembolism in the inpatient and outpatient settings. While in the aggregate they are highly beneficial (see Chapter 31), these drugs can have significant morbidities unless they are dosed and monitored appropriately. For example, inadequate therapeutic dosing of heparin can lead to increased length of stay and the potential for clot formation and/or propagation.12 The risk of recurrent thromboembolism is reduced if the therapeutic effect of heparin is achieved quickly.12 In addition, Landefeld et al13 showed that the frequency of fatal, major, and minor bleeding during heparin therapy was twice that expected without heparin therapy. The effect with warfarin therapy was even more pronounced—approximately 5 times that expected without warfarin therapy. Consistent with this finding, anticoagulants accounted for 4% of preventable ADEs and 10% of potential ADEs in one large inpatient study.1 Finally, careful drug monitoring in hospitals can reduce ADEs, suggesting that some events are due to inadequate monitoring of therapies and doses.14 These studies highlight the clear need for safety-related interventions with respect to both the dosing and monitoring of these high-risk drugs in order to prevent thromboembolic and bleeding complications.

Opportunities for Impact

The number of hospitals using weight-based heparin nomograms, or that have established anticoagulation clinics or services is unknown. Although common in some European countries,15 patient self-management of long-term anticoagulation with warfarin is unusual in the United States as many payers, including Medicare, do not currently cover the home testing technology.15

Study Designs

Heparin nomograms were evaluated in one randomized controlled trial (Level 1),16 one prospective cohort comparison (Level 2)17 and 4 controlled observational studies (Level 3).18-21 Two of these studies involved weight-based nomograms.16-21 A third study involving a weight-based nomogram22 was included with the studies of anticoagulation services (see below), as clinical pharmacists actively managed the dosing protocol. We excluded one retrospective before-after analysis of a weight-based heparin protocol for cardiac intensive care patients,23 because the method of selecting charts for review was never stated. Moreover, when the authors found an increase in the number of patients with excessive anticoagulation in the intervention group, they chose a second group of control patients (again with an unspecified selection method) for review, and in the end concluded that the difference was not significant.

All studies of outpatient anticoagulation clinics have been Level 3 studies, typically retrospective before-after analyses,22,24-28 although one study might more appropriately be regarded as a case-control study.29 A comprehensive review of the literature on various forms of anticoagulation management30 did not meet the criteria for a systematic review, but referenced all of the additional studies of anticoagulation clinics that we could identify31-36 and used quantitative methods to pool their results. We use the pooled results from this article30 in Table 9.2 in place of individual entries for each of these six Level 3 studies.

Two studies evaluated the impact of a coordinated inpatient anticoagulation service (with or without nomograms for dosing).22,37

Patient self-management of warfarin therapy has been evaluated in at least 3 randomized controlled trials38-40 (Level 1) and one non-randomized clinical trial. Because a number of higher-level studies exist, we did not include retrospective cohort analyses (Level 3) addressing this topic.42-45

Study Outcomes

Most studies did not evaluate bleeding complications or had insufficient numbers of patients to evaluate this outcome adequately. One recent study of an anticoagulation clinic's adverse events25 focused on anticoagulation as the primary outcome (Level 1), as did the review that pooled results from 6 observational studies of anticoagulation clinics.30 As shown in Tables 9.1-3, the rest of the studies reported Level 2 outcomes, consisting of various indicators of time to therapeutic anticoagulation and intensity or appropriateness of anticoagulation.

Evidence for Effectiveness of the Practice

  • Heparin nomograms: As shown in Table 9.1, all studies showed a significant decrease (i.e., improvement) in time to achievement of a therapeutic PTT and/or an increase in the proportion of patients in the therapeutic range.
  • Inpatient anticoagulation services: As shown in Table 9.2, both Level 3 studies evaluating this practice showed significant improvements in relevant measures of anticoagulation.22,37
  • Outpatient anticoagulation services for warfarin (with and without dosing nomograms): the multiple Level 3 studies of this practice showed improvements in relevant measures of anticoagulation, with one exception. This study took place in a semi-rural region of England, and the hospital-based anticoagulation clinic was staffed mainly by junior physician trainees rotating through the clinic. The one study that focused primarily on Level 1 outcomes25 showed significant reductions in adverse events related to under- or over-anticoagulation.
  • Patient self-management: Patient self-management achieved superior measures of anticoagulation on one Level 1 comparison with routine care.22,37 More impressive is that two Level 1 studies38,46 and one Level 2 study41 reported equivalent or superior measures of anticoagulation for self-management compared with anticoagulation clinics.

Potential for Harm

Heparin nomograms are primarily intended to achieve PTT values within the therapeutic range as quickly as possible. Although none of the studies showed increased bleeding as a result of aggressive anticoagulation, it is important to note that 4 of the 6 studies showed a significant increase in the proportion of patients with PTTs above the target range.16,19-21

Anticoagulation clinics carry the usual theoretical risk that increased fragmentation of care will introduce new hazards, but no study showed any significant cause for concern.

Patient self-monitoring clearly carries with it risks relating to the possibilities of patient misunderstanding of, or non-compliance with dosing and monitoring protocols. No increases in adverse events were observed in the studies reviewed, but the patients evaluated in these studies, even if randomized, were still chosen from a group of relatively compliant and motivated patients.

Costs and Implementation

For anticoagulation clinics, one study showed reduced costs of $162,058 per 100 patients annually, primarily through reductions in warfarin-related hospitalizations and emergency room visits.25 Other studies indicate potential cost-savings due to reduced hospitalizations from anticoagulation-related adverse events, or show that the anticoagulation was revenue neutral.19,24,29 Considering without these offsetting potential savings, however, anticoagulant clinics often require institutional subsidy since professional fee or laboratory payments do not fully cover costs.

Heparin nomograms may increase lab costs due to more frequent monitoring, but one study calculated that lab costs were offset by the need for fewer heparin boluses.22

For patient self-management of warfarin, one study showed that the cost of self-monitoring was $11/international normalized ratio (INR) value and postulated that this would be cost-effective if it reduced the number of clinic visits.39 Other studies have suggested that the capillary blood testing devices themselves47 and the overall practice of patient self-management are cost-effective.48,49 In the United States, the home monitoring devices sell for approximately $1000. Factoring in the price of cartridges and assuming the devices operate without requiring repair for 5 years, one source estimated an annual cost of approximately $600.40

Implementation of a heparin nonogram appears feasible, and was well received by physicians and nurses.18 Physician/staff education about the protocols was important to its success.23,24 One study showed a high level of physician and patient satisfaction with an anticoagulation clinic.24 In addition, multiple studies reveal that patients who self-manage warfarin have significantly higher levels of satisfaction and experience less anxiety.9,10,38,39

Comment

The primary purpose of heparin nomograms is the timely achievement of therapeutic anticoagulation, and their superiority in this regard (compared with routine care) has been convincingly established. While none of the studies showed adverse consequences of this focus on timely anticoagulation, the trend toward increases in excessive anticoagulation presents safety concerns. Studies powered to detect significant differences in bleeding complications in patients being managed with heparin dosing protocols may be warranted.

The literature on anticoagulation clinics consists entirely of observational studies with important possible confounders. Nonetheless, with one exception they are consistently shown to achieve superior measures of anticoagulation, and in one study,25 superior clinical outcomes.

Among the practices reviewed in this chapter, the literature on patient self-management is perhaps the most impressive. Three randomized trials and one non-randomized clinical trial show that patient control of anticoagulation is at least equivalent, if not superior, to management by usual care or an anticoagulation clinic. Additional observational studies reach the same results.42-45 Thus, a relatively substantial literature supports patient self-management for outpatient warfarin therapy for motivated patients able to comply with the monitoring and dosing protocols. These studies clearly involved select groups of patients,9 so that a larger randomized trial with intention-to-treat analysis would be helpful.

Many insurance carriers in the United States, including Medicare, do not currently subsidize the home testing technology or provide only partial coverage. Despite the relatively high cost of the home testing devices, this practice may nonetheless be cost-effective due to reduced use of other clinical services.48,49 A larger US study or detailed cost-effectiveness analysis appears warranted, especially given the higher level of patient satisfaction with this approach as compared with outpatient anticoagulation.

Table 9.1. Studies focused primarily on heparin or warfarin nomograms*

StudyStudy Design, OutcomesResultsa

Raschke, 199316

Weight-based heparin nomogram for patients with venous thromboembolism or unstable angina

Randomized controlled trial (Level 1)

Various markers of adequate anticoagulation (Level 2)

PTT in therapeutic range within 24 hours: 97% vs. 77% (p<0.002)

Mean time to therapeutic PTT: 8.2 vs. 20.2 hours (p<0.001)

PTT exceeding the therapeutic range:
at 24 hours, 27% vs. 7% (p<0.001)
at 48 hours, 18% vs. 8% (p<0.001)

Elliott, 199417

Use of heparin nomogram for patients with acute proximal deep venous thrombosis

Non-randomized clinical trial (Level 2)

Time to therapeutic PTT (Level 2)

Time to therapeutic PTT: less with use of nomogram (values not given, p=0.025)

Brown, 199721

Weight-based heparin nomogram for ICU patients requiring acute anticoagulation with unfractionated heparin

Retrospective before-after analysis (Level 3)

Time to therapeutic PTT (Level 2)

Mean time to therapeutic PPT: 16 vs. 39 hours (p<0.05)

Supratherapeutic PTTs were more common after implementation of the nomogram, but there was no observed increase in bleeding

Cruickshank, 199118

Heparin nomogram for patients with acute venous thromboembolism

Retrospective before-after analysis (Level 3)

Time to first therapeutic PTT, time to correct subsequent PTTs, time outside the therapeutic range (Level 2)

PTT in therapeutic range at 24 hours, 66% vs. 37% (p<0.001)

PTT in therapeutic range at 48 hours, 81% vs. 58% (p<0.001)

Table 9.1. Studies focused primarily on heparin or warfarin nomograms* (cont.)
StudyStudy Design, OutcomesResultsa

Hollingsworth, 199519

Heparin nomogram for hospitalized patients with acute venous thromboembolism

Retrospective before-after analysis (Level 3)

Primary outcome of the study was length of hospital stay (Level 3) but time to therapeutic PTT was a secondary outcome (Level 2)

Time to therapeutic PTT: 17.9 vs. 48.8 hours (p<0.001)

PTTs were sub-therapeutic less often: 28% vs. 56% (p<0.001)

Proportion of patients with supra-therapeutic PTTs was significantly increased in the intervention group. There was no increase in bleeding complications associated with this finding, but the study was underpowered to detect such a difference.

Phillips, 199720

Inpatient heparin and warfarin nomograms and monitoring charts

Retrospective before-after analysis (Level 3)

Measures of under- and over-anticoagulation (Level 2)

Heparin nomogram

  • Time spent under-anticoagulated: 18.5% vs, 32.7% (p<0.0001)
  • Time spent above the therapeutic range: 35.6% vs. 24.4% (p<0.01)

Warfarin nomogram:

  • Time spent over-anticoagulated: 5.4% vs. 2.7% (p<0.001, but questionable clinical significance)

* PTT indicates partial thromboplastin time.

a Results reported as rates with intervention vs. control (Level 1 & 2 study designs) or after intervention vs. before intervention (Level 3 study designs).

Table 9.2. Inpatient anticoagulation services and outpatient anticoagulation clinics*

StudyStudy Design, OutcomesResults

Ansell, 199630

Pooled comparison of anticoagulation clinics and routine medical care

Pooled results from 6 Level 3 study designs comparing anticoagulation clinics with routine medical care (Level 3A)

Major bleeding and thromboembolic events (Level 1)

Major bleeding events per patient-year: anticoagulation clinic, 0.028 (95% CI: 0-0.069) vs. routine care, 0.109 (95% CI: 0.043-0.268)

Thromboembolic events per patient-year: anticoagulation clinic, 0.024 (95% CI: 0-0.08) vs. routine care, 0.162 (95% CI: 0.062-0.486)

Hamby, 200029

Analysis of adverse events related to outpatient warfarin therapy among 395 patients followed at a Veterans Affairs Hospital, with 306 enrolled in an anticoagulation clinic and 89 patients receiving usual care

Case-control study (Level 3)

Adverse events related to under- or over-anticoagulation (Level 1)

Among the 12 patients with preventable adverse events related to anticoagulation, 8 were not enrolled in the anticoagulation clinic

Patients receiving usual care had 20 times the relative risk (95% CI: 6-62) of an adverse event compared with patients in the anticoagulation clinic.

Lee, 199626

Comparison of pharmacist-managed anticoagulation clinic with patient receiving usual care

Retrospective cohort comparison (Level 3)

Hospital admissions related to under- or over-anticoagulation—i.e., thromboembolic or bleeding events (Level 1)a

Patients in anticoagulation clinic had non-significant reductions in hospital admissions related to thromboembolic or bleeding events compared with control groupb

Ellis, 199237

Pharmacy-managed inpatient anticoagulation service (flow sheet for monitoring, but no nomogram) for monitoring patients receiving warfarin for a variety of indications

Retrospective before-after analysis (Level 3)

Anticoagulation "stability" at discharge and odds of therapeutic anticoagulation at first outpatient visit (Level 2)

Patients receiving the intervention were more likely to have PT "stability" at discharge: 61.5% vs. 42.3% (p=0.02)

Odds of having therapeutic PT at first outpatient clinic visit with intervention: OR 5.4 (95% CI: 1.87-15.86)

Table 9.2. Inpatient anticoagulation services and outpatient anticoagulation clinics* (cont.)
StudyStudy Design, OutcomesResults

Gaughan, 200024

Anticoagulation clinic for outpatients receiving warfarin for atrial fibrillation (managed by nurse practitioner using warfarin dosing nomogram)

Retrospective before-after analysis (Level 3)

Percentage of patients in the desired range for anticoagulation (Level 2) was evaluated as a secondary outcome

Minor increase in percentage of patients with INR in desired range: 53.7% vs. 49.1% (p<0.05, but questionable clinical significance)

Radley, 199527

Performance of pharmacist-run hospital-based outpatient anticoagulation clinic in England compared with historical control (management by rotating physician trainees)

Retrospective before-after analysis (Level 3)

Proportions of INR measurements "in" or "out" of the therapeutic range

No significant difference for patients with stable INR in the baseline period, but patients with an INR result "out" of range were more likely to return to "in" range under anticoagulation clinic management compared with routine physician management

Rivey, 199322

Pharmacy-managed inpatient anticoagulation service (using weight-based heparin protocol) for medicine inpatients compared with older fixed-dose protocol without any active management by pharmacists

Before-after analysis (Level 3)

Time to therapeutic PTT (Level 2)

Time to therapeutic PTT was less with nomogram protocol: 40 vs. 20 hours (p<0.05)

Fewer supra-therapeutic PTTs with protocol: 1.7 vs. 5.5 (p<0.05)

Bleeding rates: no difference but numbers were small

* CI indicates confidence interval; INR, international normalized ratio; OR, odds ratio; PT, prothrombin time; and PTT, partial thromboplastin time.

a We counted this outcome as Level 1, but it is important to note that authors did not capture all of the designated clinical events, just those that resulted in admissions to the study hospital.

b Using the results reported in the study, we calculated the 95% CIs for admissions related to thromboembolic events (intervention, 0.2-18.5%; usual care, 12.7-42.5%) and bleeding events (intervention, 1.1-22.8%; usual care, 7-33.4%).

Table 9.3. Outpatient self-management using home testing devices and dosing nomograms*

< < < < 

StudyStudy Design, OutcomesResults

Cromheecke, 200038

Oral anticoagulation self-management with home monitoring and dose adjustment compared with anticoagulation clinic (Netherlands)

Randomized trial with crossover comparison (Level 1)

Adequacy of anticoagulation (Level 2)

Percent of self-managed measurements within 0.5 INR units of therapeutic target did not differ (55% vs. 49%, p=0.06). However, 29 patients (60%) during self-management spent >50% of time in target range, compared with 25 (52%) during clinic management (p<0.05).

Sawicki, 199939

Oral anticoagulation self-management with home monitoring and dose adjustment compared with routine care (Germany)

Single blind, multicenter randomized controlled trial (Level 1)

Adequacy of anticoagulation (Level 2)

Intervention group more often had INRs within target range (p<0.01), and had significantly fewer deviations from target range and 6 months

White, 198940

Oral anticoagulation self-management with home monitoring and dose adjustment compared with anticoagulation clinic (United States)

Randomized prospective comparison (Level 1)

Adequacy of anticoagulation (Level 2)

Self-management group had significantly greater proportion of patients in target INR range (93% vs. 75%, p<0.01)

Watzke, 200041

Self-management compared with anticoagulation clinic (Austria)

Prospective cohort comparison (Level 2)

Various measures of adequacy of anticoagulation (Level 2)

Non-significant trends towards more INR values within the therapeutic range for self-management group compared with anticoagulation clinic, both for standard therapeutic range of INR 2.0-3.0 (82.2% vs. 68.9%) and for more intense anticoagulation targeted to INR range of 2.5-4.5 (86.2% vs. 80.1%)

* INR indicates international normalized ratio.

References

1. Bates DW, Cullen DJ, Laird N, Petersen LA, Small SD, Servi D, et al. Incidence of adverse drug events and potential adverse drug events. Implications for prevention. ADE Prevention Study Group. JAMA 1995;274:29-34.

2. Cohen MR, Anderson RW, Attilio RM, Green L, Muller RJ, Pruemer JM. Preventing medication errors in cancer chemotherapy. Am J Health Syst Pharm 1996;53:737-746.

3. Brennan TA, Leape LL, Laird NM, Hebert L, Localio AR, Lawthers AG, et al. Incidence of adverse events and negligence in hospitalized patients. Results of the Harvard Medical Practice Study I. N Engl J Med 1991;324:370-376.

4. Leape LL, Kabcenell AI, Berwick DM. Reducing Adverse Drug Events. Boston: Institute for Healthcare Improvement; 1998.

5. Massachusetts Coalition for the Prevention of Medical Errors. MHA best practice recommendations to reduce medication errors. Available at: www.mhalink.org/mcpme/mcpme_publications.htm. Accessed, 2001.

6. Rivey MP, Wood RD, Allington DR, Stratton TP, Erickson CC, Stenson TA. Pharmacy-managed protocol for warfarin use in orthopedic surgery patients. Am J Health Syst Pharm 1995;52:1310-1316.

7. Ansell J, Holden A, Knapic N. Patient self-management of oral anticoagulation guided by capillary (fingerstick) whole blood prothrombin times. Arch Intern Med 1989;149:2509-2511.

8. Hasenkam JM, Knudsen L, Kimose HH, Gronnesby H, Attermann J, Andersen NT, et al. Practicability of patient self-testing of oral anticoagulant therapy by the international normalized ratio (INR) using a portable whole blood monitor. A pilot investigation. Thromb Res 1997;85:77-82.

9. Sunderji R, Campbell L, Shalansky K, Fung A, Carter C, Gin K. Outpatient self-management of warfarin therapy: a pilot study. Pharmacotherapy 1999;19:787-793.

10. Point-of-care prothrombin time measurement for professional and patient self-testing use. A multicenter clinical experience. Oral Anticoagulation Monitoring Study Group. Am J Clin Pathol 2001;115:288-296.

11. Prothrombin measurement using a patient self-testing system. Oral Anticoagulation Monitoring Study Group. Am J Clin Pathol 2001;115:280-287.

12. Hull RD, Raskob GE, Hirsh J, Jay RM, Leclerc JR, Geerts WH, et al. Continuous intravenous heparin compared with intermittent subcutaneous heparin in the initial treatment of proximal-vein thrombosis. N Engl J Med 1986;315:1109-1114.

13. Landefeld CS, Beyth RJ. Anticoagulant-related bleeding: clinical epidemiology, prediction, and prevention. Am J Med 1993;95:315-328.

14. Evans RS, Pestotnik SL, Classen DC, Horn SD, Bass SB, Burke JP. Preventing adverse drug events in hospitalized patients. Ann Pharmacother 1994;28:523-527.

15. Becker D. Commentary on "Self-management of long-term oral anticoagulation was as effective as specialist anticoagulation clinic management." ACP Journal Club 2001;134:62.

16. Raschke RA, Reilly BM, Guidry JR, Fontana JR, Srinivas S. The weight-based heparin dosing nomogram compared with a "standard care" nomogram. A randomized controlled trial. Ann Intern Med 1993;119:874-881.

17. Elliott CG, Hiltunen SJ, Suchyta M, Hull RD, Raskob GE, Pineo GF, et al. Physician-guided treatment compared with a heparin protocol for deep vein thrombosis. Arch Intern Med 1994;154:999-1004.

18. Cruickshank MK, Levine MN, Hirsh J, Roberts R, Siguenza M. A standard heparin nomogram for the management of heparin therapy. Arch Intern Med 1991;151:333-337.

19. Hollingsworth JA, Rowe BH, Brisebois FJ, Thompson PR, Fabris LM. The successful application of a heparin nomogram in a community hospital. Arch Intern Med 1995;155:2095-2100.

20. Phillips WS, Smith J, Greaves M, Preston FE, Channer KS. An evaluation and improvement program for inpatient anticoagulant control. Thromb Haemost 1997;77:283-288.

21. Brown G, Dodek P. An evaluation of empiric vs. nomogram-based dosing of heparin in an intensive care unit. Crit Care Med 1997;25:1534-1538.

22. Rivey MP, Peterson JP. Pharmacy-managed, weight-based heparin protocol. Am J Hosp Pharm 1993;50:279-284.

23. Nemeth JS, Marxen TL, Piltz GW. Weight-based protocol for improving heparin therapy. Am J Health Syst Pharm 1996;53:1164-1166.

24. Gaughan GL, Dolan C, Wilk-Rivard E, Geary G, Libbey R, Gilman MA, et al. Improving management of atrial fibrillation and anticoagulation in a community hospital. Jt Comm J Qual Improv 2000;26:18-28.

25. Chiquette E, Amato MG, Bussey HI. Comparison of an anticoagulation clinic with usual medical care: anticoagulation control, patient outcomes, and health care costs. Arch Intern Med 1998;158:1641-1647.

26. Lee YP, Schommer JC. Effect of a pharmacist-managed anticoagulation clinic on warfarin-related hospital readmissions. Am J Health Syst Pharm 1996;53:1580-1583.

27. Radley AS, Hall J, Farrow M, Carey PJ. Evaluation of anticoagulant control in a pharmacist operated anticoagulant clinic. J Clin Pathol 1995;48:545-547.

28. Pell JP, McIver B, Stuart P, Malone DN, Alcock J. Comparison of anticoagulant control among patients attending general practice and a hospital anticoagulant clinic. Br J Gen Pract 1993;43:152-154.

29. Hamby L, Weeks WB, Malikowski C. Complications of warfarin therapy: causes, costs, and the role of the anticoagulation clinic. Eff Clin Pract 2000;3:179-184.

30. Ansell JE, Hughes R. Evolving models of warfarin management: anticoagulation clinics, patient self-monitoring, and patient self-management. Am Heart J 1996;132:1095-1100.

31. Bussey HI, Rospond RM, Quandt CM, Clark GM. The safety and effectiveness of long-term warfarin therapy in an anticoagulation clinic. Pharmacotherapy 1989;9:214-219.

32. Wilt VM, Gums JG, Ahmed OI, Moore LM. Outcome analysis of a pharmacist-managed anticoagulation service. Pharmacotherapy 1995;15:732-739.

33. Cortelazzo S, Finazzi G, Viero P, Galli M, Remuzzi A, Parenzan L, et al. Thrombotic and hemorrhagic complications in patients with mechanical heart valve prosthesis attending an anticoagulation clinic. Thromb Haemost 1993;69:316-320.

34. Garabedian-Ruffalo SM, Gray DR, Sax MJ, Ruffalo RL. Retrospective evaluation of a pharmacist-managed warfarin anticoagulation clinic. Am J Hosp Pharm 1985;42:304-308.

35. Hamilton GM, Childers RW, Silverstein MD. Does clinic management of anticoagulation improve the outcome of prosthetic valve patients? Clin Res 1985;33:832A.

36. Cohen IA, Hutchison TA, Kirking DM, Shue ME. Evaluation of a pharmacist-managed anticoagulation clinic. J Clin Hosp Pharm 1985;10:167-175.

37. Ellis RF, Stephens MA, Sharp GB. Evaluation of a pharmacy-managed warfarin-monitoring service to coordinate inpatient and outpatient therapy. Am J Hosp Pharm 1992;49:387-394.

38. Cromheecke ME, Levi M, Colly LP, de Mol BJ, Prins MH, Hutten BA, et al. Oral anticoagulation self-management and management by a specialist anticoagulation clinic: a randomised cross-over comparison. Lancet 2000;356:97-102.

39. Sawicki PT. A structured teaching and self-management program for patients receiving oral anticoagulation: a randomized controlled trial. Working Group for the Study of Patient Self-Management of Oral Anticoagulation. JAMA 1999; 281:145-150.

40. White RH, Becker DM, Gunther-Maher MG. Outpatient use of a portable international normalized ratio/prothrombin time monitor. South Med J 1994;87:206-210.

41. Watzke HH, Forberg E, Svolba G, Jimenez-Boj E, Krinninger B. A prospective controlled trial comparing weekly self-testing and self-dosing with the standard management of patients on stable oral anticoagulation. Thromb Haemost 2000;83:661-665.

42. Christensen TD, Attermann J, Pilegaard HK, Andersen NT, Maegaard M, Hasenkam JM. Self-management of oral anticoagulant therapy for mechanical heart valve patients. Scand Cardiovasc J 2001;35:107-113.

43. Heidinger KS, Bernardo A, Taborski U, Muller-Berghaus G. Clinical outcome of self-management of oral anticoagulation in patients with atrial fibrillation or deep vein thrombosis. Thromb Res 2000;98:287-293.

44. Hasenkam JM, Kimose HH, Knudsen L, Gronnesby H, Halborg J, Christensen TD, et al. Self management of oral anticoagulant therapy after heart valve replacement. Eur J Cardiothorac Surg 1997;11:935-942.

45. Ansell JE, Patel N, Ostrovsky D, Nozzolillo E, Peterson AM, Fish L. Long-term patient self-management of oral anticoagulation. Arch Intern Med 1995;155:2185-2189.

46. White RH, McCurdy SA, von Marensdorff H, Woodruff DE, Jr., Leftgoff L. Home prothrombin time monitoring after the initiation of warfarin therapy. A randomized, prospective study. Ann Intern Med 1989;111:730-737.

47. Ansell JE, Hamke AK, Holden A, Knapic N. Cost effectiveness of monitoring warfarin therapy using standard versus capillary prothrombin times. Am J Clin Pathol 1989;91:587-589.

48. Taborski U, Wittstamm FJ, Bernardo A. Cost-effectiveness of self-managed anticoagulant therapy in Germany. Semin Thromb Hemost 1999;25:103-107.

49. Lafata JE, Martin SA, Kaatz S, Ward RE. Anticoagulation clinics and patient self-testing for patients on chronic warfarin therapy: A cost-effectiveness analysis. J Thromb Thrombolysis 2000;9(Suppl 1):S13-S19.

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Current as of July 2001
Internet Citation: Chapter 9. Protocols for High-Risk Drugs: Reducing Adverse Drug Events Related to Anticoagulants. July 2001. Agency for Healthcare Research and Quality, Rockville, MD. http://www.ahrq.gov/research/findings/evidence-based-reports/services/quality/er43/ptsafety/chapter9.html