Page Nav

HIDE

Grid

GRID_STYLE

DRUG UTILISATION REVIEW (DUR)

  By: Dr. Aqeel Nasim  (M.Phil Pharmacy Practice) INTRODUCTION OF DRUG UTILISATION REVIEW (DUR) Drug utilization review (DUR) is defined...

 


By: Dr. Aqeel Nasim  (M.Phil Pharmacy Practice)

INTRODUCTION OF DRUG UTILISATION REVIEW (DUR)

Drug utilization review (DUR) is defined as “an authorized, structured, ongoing review of prescribing, dispensing, and use of medication” and is the professional responsibility of the pharmacist entrusted to provide safe and effective care (Gupta, 2021).



Prescription medications are an essential part of health-care provision. Drugs, on the other hand, can only assist patients if they are administered correctly, which means that physicians must prescribe them based on evidence. Medication utilisation review (DUR) programmes are a popular technique of reviewing and addressing the appropriateness of drug prescriptions (Pharmacists, 1988). A DUR programme is a continuous technique of ensuring the quality of drug use by employing criteria and attempting to rectify drug usage that does not meet these standards; the efficacy of remedial measures is monitored (Stolar, 1978).

DUR gives health plans internal controls to guarantee that medication therapy is safe, medically required, and cost-effective. It also implements and supports DUR programmes for Medicaid managed care organisations and state Medicaid plans (Altman & Lewin, 2000).

Key Functions of DUR

Avoid negative drug responses.

Duplicate therapies should be avoided.

Check to see if there is a more cost-effective option. Make sure the medicine is effective and suitable.

If clinical recommendations have changed, make modifications to prescriptions.

Determine whether or if there is a problem with fraud or abuse.

Support the DUR and Pharmacy & Therapeutics (P&T) boards.

Management of the formulary

Use of generic drugs

Decisions on prior authorisation

Analyses of prescribing patterns and consequences

Statistics from clinical call centres

Results of prescriber education

 Classifications of DUR

DUR is divided into three groups:

Prospective

Prior to dispensing medicine, a patient's pharmacological treatment is evaluated prospectively.

 

Concurrent

Continuous monitoring of medication therapy throughout the duration of treatment is known as concurrent monitoring.

 

Retrospective

After the patient has received the medicine, the pharmacological therapy is reviewed.

 

 PROSPECTIVE DUR

Medicine orders are compared against criteria before the patient receives the drug in prospective DUR. This form of examination is beneficial for its prevention potential as well as the specific patient-centered therapy it provides.

The evaluation of pharmacotherapy before the patient takes the first dose of medicine is known as prospective DUR. During the prescription screening procedure, pharmacists may do a prospective assessment of the patient's drug regimen. Before the patient receives the medicine, the pharmacist is able to identify and fix issues. In their everyday practise, pharmacists conduct prospective evaluations by evaluating a prescription medication's dose and recommendations while checking patient information for potential drug interactions or duplication therapy (Schafermeyer, 2008). Although participation in prospective DUR has always been voluntary for pharmacists, when OBRA '90 went into force in January 1993, prospective DUR became a compulsory role (Chui, 2000).

Elements of Prospective DUR

1.       a correct and thorough prescription/medical order

2.       Allergies and unfavourable outcomes

3.       Choose the right medicine

4.       Recommended medication regimen - suitable dose, frequency, duration/length of therapy, formulation, and administration route

5.       Interactions between drugs

6.       Duplication of therapeutics

7.       Appropriate use and therapeutic results - new/refill prescriptions/med orders

8.       Misuse and Abuse

Example of Prospective DUR

A typical result of a prospective DUR is the discovery of drug-drug interactions. For example, a patient using warfarin to avoid blood clots may be recommended a new medicine to treat arthritis by a different doctor. If all of these factors are present, the patient may undergo internal bleeding. The pharmacist would note the probable medication interaction while checking the patient's prescriptions and call the physician to inform him or her of the concern (Peng et al., 2003).

CONCURRENT DUR

Concurrent DUR entails reviewing medication orders while on treatment. This form of assessment is helpful when medication therapy has to be adjusted based on continuing diagnostic and laboratory testing (Wertheimer, 1986).

Elements of Concurrent DUR

A concurrent DUR seeks to improve current prescription behaviours while also avoiding future incorrect prescribing (Lipton & Bird, 1993). Concurrent DUR monitoring compares drug usage to criteria set during treatment, similar to prospective monitoring. The fundamental distinction between the two is that treatments with contemporaneous monitoring are corrective.

1.       Interactions between drugs and diseases

2.       Interactions between drugs

3.       Modifications to drug dose

4.       Precautions for drug users (age, gender, pregnancy, etc.)

5.       Overutilization and underutilization

6.       Interchange of Therapeutics

Example of Concurrent DUR

In a hospital, for example, a rule may be set that gentamicin dosage should be determined using optimum body weight and modified depending on renal and hearing tests. The clinical pharmacologist or pharmacist would monitor these parameters on a daily basis, informing the prescribing physician if the dosage was calculated erroneously or if dosage modifications were not done (Peng et al., 2003).

RETROSPECTIVE DUR

Retrospective DUR entails looking back on medication prescriptions and usage after they've happened. Although it is the simplest and least expensive method, retrospective DUR does not allow for the modification of therapy for the patients whose data was obtained (Fulda, Lyles, Pugh, & Christensen, 2004).

Retrospective DUR Monitoring is going over prescription medications with the patient after they've been given to them. Its main flaw is that it does not allow for measures to improve drug usage for the patients whose records were examined. It may be used to track the same features of drug usage as prospective DUR, as well as: determining the frequency with which a specific drug or class of pharmaceuticals is prescribed (Moore, Bykov, Savelli, & Zagorski, 1997).

1.       comparing how doctors prescribe drugs

2.       prescription in comparison to established treatment recommendations

3.       Keeping track of the therapeutic usage of high-priced medications

Elements of Retrospective DUR

1.       Use of a generic term that is appropriate

2.       Abuse/misuse in the clinic

3.       Contraindications to drugs and diseases

4.       Interactions between drugs

5.       Inadequate treatment duration Inadequate medication dose

6.       When possible, use drugs on the formulary.

7.       Overutilization and underutilization

8.       Duplication and/or therapeutic appropriateness

Example of Prospective DUR

The discovery of a group of patients whose therapy does not match authorised criteria is an example of a retrospective DUR. A pharmacist, for example, may identify a group of asthmatic patients who, based on their medical and pharmaceutical histories, should be on orally inhaled steroids. The pharmacist can then use this information to persuade prescribers to use the medications that have been recommended ("Drug Utilization Review," 2019).

STEP-BY-STEP GUIDE TO CREATING A BASIC HOSPITAL DRUG UTILISATION REVIEW (DUR) PROGRAM

(Moore et al., 1997)

PHASE 1: PLANNING

1.       Create a DUR Committee.

2.       Procedures and policies should be written.

3.       Define all hospital locations or departments where medications are used (e.g., emergency room, intensive care unit, radiology, surgical department, medical department).

4.       Determine which medications should be considered for inclusion in the programme.

5.       Assess the resources available for developing criteria, collecting data, and evaluating the programme, as well as the pharmaceuticals to be included.

6.       Select features of medication usage to monitor and analyse for each medicine (indications, dose, dosage form selected, etc.).

7.       Make a list of criteria and set performance goals.

8.       Create a timetable and a process for data gathering and assessment.

9.       Educate hospital personnel on the DUR programme and current eligibility requirements.

PHASE 2: Data Collection

10.   Gather information.

11.   Analyse the data to see if there are any drug-related issues.

PHASE 3: Intervention

12.   Inform the hospital personnel of the findings.

13.   Create and conduct interventions if a drug use issue is discovered.

14.   Collect new data on the problematic substance to see if usage has improved since the intervention.

15.   Re-evaluation results should be disseminated.

PHASE 4: Program evaluation  

16.   At the end of the evaluation year, evaluate all DUR programme activities and plan programme activities for the next year (Moore et al., 1997).

 

 

References

Altman, S., & Lewin, M. E. (2000). America's health care safety net: intact but endangered.

Chui, M. (2000). Evaluation of online prospective DUR programs in community pharmacy practice. Journal of Managed Care Pharmacy, 6(1), 27-32.

Drug Utilization Review. (2019). Concepts in Managed Care Pharmacy. 2021, from https://www.amcp.org/about/managed-care-pharmacy-101/concepts-managed-care-pharmacy/drug-utilization-review

Fulda, T. R., Lyles, A., Pugh, M. C., & Christensen, D. B. (2004). Current status of prospective drug utilization review. Journal of Managed Care Pharmacy, 10(5), 433-441.

Gupta, V. (2021). S4: Assessment of Drug Utilization Review Activities within US Colleges of Pharmacy.

Lipton, H. L., & Bird, J. A. (1993). Drug utilization review in ambulatory settings: state of the science and directions for outcomes research. Medical Care, 1069-1082.

Moore, T., Bykov, A., Savelli, T., & Zagorski, A. (1997). Guidelines for implementing drug utilization review programs in hospitals. Management Sciences for Health, Arlington.

Peng, C. C., Glassman, P. A., Marks, I. R., Fowler, C., Castiglione, B., & Good, C. B. (2003). Retrospective drug utilization review: incidence of clinically relevant potential drug-drug interactions in a large ambulatory population. Journal of Managed Care Pharmacy, 9(6), 513-522.

Pharmacists, A. S. o. H. (1988). ASHP guidelines on the pharmacist's role in drug-use evaluation. Am J Hosp Pharm, 45, 385-386.

Schafermeyer, K. W. (2008). Impact of managed care on pharmacy practice. Managed Care Pharmacy Practice, 387.

Stolar, M. H. (1978). Drug use review: operational definitions. American Journal of Health-System Pharmacy, 35(1), 76-78.

Wertheimer, A. (1986). The defined daily dose system (DDD) for drug utilization review. Hospital pharmacy, 21(3), 233-234, 239.

 

No comments