Section 1

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Questions to ask while evaluating reply

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Date created

Mar 1, 2020

Cards (138)

Section 1

(50 cards)

Questions to ask while evaluating reply

Front

1. does the response answer the question? 2. is the info clinically applicable? 3. is response organized? 4. follow-up

Back

Role of P and T committee?

Front

Develop: Formulary, policies, MUE, ADR, Med Safety

Back

Why is it critical to follow the systematic steps in a DI consult?

Front

legal implications

Back

Which steps do you follow during a DI consult?

Front

systematic process

Back

A BLANK is a summary of evidence, requiring you to interpret the information and synthesize a response

Front

literature review

Back

What is the secondary audience?

Front

other physicians, caregiver, nutrition/PT, pt (if access to medical records)

Back

What guidelines does research follow?

Front

clinical practice guidelines

Back

What are the 4 R's to the simplified process?

Front

receive, research, respond, record

Back

When answering a question, what should you always anticipate?

Front

secondary questions

Back

How should a DI consult be edited?

Front

for clarity, efficiency, directness, avoid excessive pronoun use

Back

What does research entail?

Front

develop strategy and conduct systematic search

Back

How to formulate a response?

Front

intro with background info, body with presentation of data, conclusion with recommendation, references

Back

The intro contains background info, which entails...

Front

PMH, SH, FH, physical/objective findings

Back

How to systematic search with DI resources?

Front

tertiary --> secondary --> primary --> internet

Back

Describe secondary resources

Front

ID pertinent review articles, ID primary literature with comparing listings of abstracts/full text

Back

How to analyze?

Front

critical assessment, objective review/critique, positive and negative findings

Back

What is a DI consult?

Front

when a provider consults the pharmacist (drug specialist) with regards to a medical question

Back

Why is background info important?

Front

communicate with requestor to learn question context, pertinent pt data, time need if requestor

Back

What does the conclusion entail?

Front

answer the question, no new info, references

Back

How many steps to the modified approach?

Front

7 steps

Back

What happens when you fail to obtain the ultimate question?

Front

correct answer to an incorrect question

Back

What are ad hoc committees?

Front

subcommittee (nutrition, ID, special working groups)

Back

How to keep track of data?

Front

use collection sheet/program

Back

Describe primary resources

Front

original data, needs critique, most current evidence

Back

Describe tertiary resources

Front

can help get the researcher up to speed, review disease states, may completely answer question with sufficient evidence summary

Back

Why does categorization matter?

Front

help determine rational search strategy

Back

Why is determining the ultimate question important?

Front

to ensure the pharmacist is giving the correct answer with appropriate background info

Back

What is a formulary committee?

Front

a subcomittee of P and T

Back

When do you do a DI consult?

Front

questions that are substantially involved

Back

Why is a formulaic approach not useful?

Front

no systematic approach applies to all situations

Back

How to reference?

Front

sequential numbering in text, superscripted, end notes

Back

Parts of a DI consult

Front

1. intro/purpose 2. assessment 3. lit review 4. conclusion

Back

Disadvantages of tertiary resources?

Front

may be outdated, inconsistent, biased, incomplete

Back

What is the purpose of a DI consult?

Front

To provide a solution, relate findings, voice concern, or convince audience of a treatment path

Back

Disadvantage of primary resource?

Front

time consuming to evaluate

Back

What is a P and T committee?

Front

Pharmacy and Therapeutics Committee

Back

How many steps to the systematic approach?

Front

5 steps

Back

What does record entail?

Front

verify response appropriateness (was recommendation accepted/questions or follow-up), systematic process, provide updates if new info becomes available

Back

What to do after response?

Front

evaluate reply

Back

What does background information entail?

Front

pt-specific questions, treatment's already tried, resources already consulted

Back

What is the primary audience?

Front

person who asks the question

Back

Which methods are used to assess quality of guidelines?

Front

GRADE and consensus based

Back

What information does receive entail?

Front

demographics, background info, ultimate question

Back

What does the membership committee entail?

Front

voting and non-voting, chair, secretary (usually pharmacist)

Back

What does a P and T committee do?

Front

oversees all aspects of drug therapy; safety, efficacy, cost effectiveness

Back

Disadvantages of secondary resources?

Front

need to know how to use it

Back

What is the best source for a foreign drug?

Front

Martindale or Index Nominum

Back

What does "respond" entail?

Front

analysis of evidence and synthesis

Back

GRADE

Front

Grading of Recommendations, Assessment, Development and Evaluations

Back

What does the assessment entail?

Front

evaluation of situation/pt by interview or reviewing medical records and lab data, descending order of importance, factual

Back

Section 2

(50 cards)

Which of the following attributes specific to a drug would be an appropriate rationale for conducting an MUE?

Front

significant side effect profile, narrow therapeutic index window, new drug

Back

What does MUE analysis entail?

Front

multidisciplinary group should oversee or review findings, compare actual performance with expected performance

Back

What is a concurrent claim?

Front

ongoing, monitoring of drug therapy during the course of treatment

Back

Why is prior authorization used?

Front

optimize pt outcomes, safety and efficacy, reduce waste, need approval from payer to dispense/administer, ensure med is medically necessary

Back

T/F: the monograph is not the package insert

Front

true

Back

What is an open formulary?

Front

All drugs are available on the formulary

Back

Goal of DUR?

Front

identify and decrease fraud, abuse, overuse, inappropriate/medically unnecessary care

Back

What is a formulary?

Front

Continually revised list of medications that are readily available for use within an institution or 3rd party that reflects the current clinical judgment of the medical staff or payer

Back

Minimum requirements for monograph?

Front

indication, effectiveness, risk, cost

Back

Impact of benefit management?

Front

ensures pt receives medication and benefits from it

Back

How to choose a drug?

Front

high volume, high risk, high alert (narrow index), new formulary conditions, new protocol policy/procedure, problem prone, high cost?

Back

What is a retrospective claim?

Front

review of drug therapy after the patient has received the medication

Back

Function of TJC?

Front

safe and effective medication management system, CQI required

Back

What is the treatment algorithm/step therapy based off of?

Front

national guidelines for agent safety and efficacy

Back

Why do we use drug monographs/class reviews?

Front

present information in an unbiased manner

Back

Is there a singular definition for specialty meds?

Front

no

Back

What is a positive formulary?

Front

Add drugs once they are approved

Back

there are 30 cases, how many should you review?

Front

all of them

Back

What is a MUE?

Front

medication use evaluation

Back

BLANK provide support for P and T committees

Front

Drug information centers

Back

What is a TJC?

Front

The Joint Commission

Back

What does MUE result entail?

Front

interventions, follow-up, repeat performance improvement process

Back

Why perform MUE?

Front

- evaluate effectiveness - improve patient safety - standardize therapy to decrease variation - optimize drug therapy - meet quality or regulatory standards - minimize costs

Back

Impact of cost savings on health system?

Front

less tax money on meds for government business, savings for ultimate payer/pts in terms of premium $

Back

there are 30-600 cases, how many should you review?

Front

at least 30

Back

What does MUE Plan entail?

Front

develop methodology based on performance improvement plan, standards of performance, evaluation time frame, pt selection/sampling, data collection, create data collection tool

Back

What is a negative formulary?

Front

Remove drugs that are deemed unsafe or inferior

Back

Is a package insert a primary source?

Front

yes, can reference

Back

Interventions/corrective actions entail...

Front

education, restriction, process change

Back

What does utilization management entail?

Front

1. prior authorization 2. step therapy "fail first" 3. quantity limits 4. generic substitution

Back

What is a DUR?

Front

drug utilization review

Back

Are dietary supplements proven for safety and efficacy?

Front

no

Back

What does a monograph entail?

Front

clinical indications, Pharmacology/MOA, kinetics, efficacy assessment, toxicity assessment, drug interactions, contraindications, special populations, dosage/admin, product availability, cost comparison, references

Back

there are >600 cases, how many should you review?

Front

5%

Back

What are the 9 concepts for effective prior authorization programs?

Front

1. pt safety and appropriate medication use 2. clinical decision making 3. evidence-based review criteria 4. automated decision support 5. transparency and advanced notice 6. emergency address 7. provider collaboration 8. need for timelines and avoiding disruptions in therapy 9. cost effectiveness and value

Back

How to perform MUE?

Front

Collaboration, responsibility, must adapt to practice setting w/ practice use guidelines

Back

What is a closed formulary?

Front

Has a specific list of drugs on the forumlary

Back

Goal of MUE?

Front

optimize pt outcomes (target drug program, drug use program)

Back

How does P and T committee agenda get determined?

Front

1. request for formulary change 2. change in 1 class 3. new entrant to market

Back

Purpose of MUE?

Front

evaluate medication use processes or tx response

Back

A formulary includes Nexium, this class (GERD) includes several more drugs not on the formulary - what type is it?

Front

closed

Back

Can a pt appeal prior authorization denials?

Front

yes, multiple times

Back

Function of DRR?

Front

drug review regimens in nursing facilities, required by HCFA and implemented in 1974 through medicare and medicaid

Back

What kinds of meds aren't considered medically necessary?

Front

cosmetic indication, sildenafil

Back

BLANK is an assortment of strategies/tools used by health plans and PBMs to administer the pharmaceutical benefit

Front

utilization management

Back

What is a DRR?

Front

drug regimen review

Back

What is a prospective claim?

Front

evaluation of a patient's drug therapy before medication is dispensed

Back

What goes into prior authorization criteria?

Front

indication, prescription by physician, initial criteria, continuing criteria, duration of approval, quantity limits

Back

Role of pharmacists on P and T committee?

Front

prepare agenda, prepare materials (monograph), present materials, answer questions, follow-up actions

Back

Common definition for specialty meds

Front

used in rare/orphan conditions, high touch agents (TPN), medicare >670/month

Back

Section 3

(38 cards)

Medicare Appeals Level 4

Front

review by medicare appeals council

Back

What are 2 legislative and regulatory efforts towards medication errors?

Front

1. pt safety and quality improvement act of 2005 2. inception of pt safety organizations

Back

Why do medication errors occur?

Front

Excessive task demand, personal characteristics, extra-organizational factors, work environment, intra-organizational factors, interpersonal factors, lack of comm, failure to comply w/ policy, lack of knowledge, lack of counseling

Back

Medicare Appeals Level 5

Front

judicial review by federal court

Back

T/F: Cause and effect relationships are difficult to prove

Front

true

Back

Mechanisms of ADR: pharmacologic

Front

respiratory depression with opioids, bleeding with warfarin

Back

ASHP definition of an ADR

Front

any undesirable or unexpected event that requires discontinuing a drug, modifying the dose, prolonging hospitalization, or providing supportive treatment

Back

Medicare Appeals Level 2

Front

review by an individual review entity (IRE)

Back

Who is responsible for public safety?

Front

board of pharmacy

Back

How do you report ADRs?

Front

MedWatch, VAERS

Back

What are ADRs usually reported through?

Front

P and T committee, Medication Safety/Pt safety

Back

Levels of appeal

Front

1. appeal to entity issuing denial 2. appeal to IRO 3. appeal (judicial review)

Back

List the 3 types of behavior that lead to medication errors

Front

1. human error 2. at-risk behavior 3. reckless behavior

Back

What is the IOMs position on pharmacy medication errors?

Front

not intentional acts, blame-free non-punitive environment with legal, confidential, non-discoverable protection

Back

How to prevent errors?

Front

1. standard procedures and enforced compliance 2. increased levels of automation/technology 3. use checklists and doublecheck systems 4. raise awareness for training and education 5. focus on entire system as well as ind. performers 6. report, analyze, and share error learning

Back

How to minimize human error?

Front

periodic changing of tasks/short break, light and magnification, high alert meds with shelftalkers and exaggerated shelf labels, tall man lettering, workload balance

Back

What is an ADR?

Front

adverse drug reaction

Back

Which remedial action should you do for at-risk behavior?

Front

coach the colleague and mange through removing incentives for engaging in at-risk behavior, create incentive for healthy behavior and increase situational awareness

Back

What is an at-risk behavior?

Front

intentional behavior that unknowingly increases risk of error

Back

List types of errors defined by ASHP

Front

prescribing, omission, wrong time, unauthorized drug, wrong dosage form, wrong preparation, administration, deteriorated, monitoring, compliance, wrong dose

Back

Mechanisms of ADR: drug interactions

Front

affect PK/PD of drugs

Back

T/F: An appeal may go to an independent review entity/organization before review by the pts PBM

Front

false

Back

Purpose of Naranjo algorithm?

Front

less time consuming method of determining causal relationship

Back

Medicare Appeals Level 3

Front

decision by the office of medicare hearings and appeals (OMHA)

Back

BLANK is a system of justice (investigatory and disciplinary) that reflects what we know of socio-technical system design, human free will, and our inescapable human faliability

Front

Just Culture

Back

BLANK behavior is when you recognize the risks associated with the chosen behavior

Front

reckless

Back

Which remedial action should you do for reckless behavior?

Front

punish the colleague and manage through remedial/disciplinary action

Back

Why report and ADR?

Front

to prevent recurrence

Back

Which remedial action should you do for human error?

Front

console colleague and mange through changes in processes, training, and drug design

Back

Mechanisms of ADR: intolerance

Front

could be any drug, depends on pt

Back

Medicare Appeals Level 1

Front

redetermination from your plan

Back

When do you report?

Front

life threatening, hospitalization

Back

Dietary supplements have a more BLANK response because of no guaranteed safety and efficacy from the FDA

Front

proactive

Back

How is human error medication mistakes managed?

Front

system design, technological steps (bar codes), focus on factors that impact human reliability

Back

Role of a pharmacist in ADR?

Front

- coordinate program: report to appropriate med staff committee, determine need for medwatch - ID and report - Decrease incidence

Back

How does the patient have a role in medication error reduction?

Front

ask questions, provide counseling, literacy awareness, educate caregivers, impact of noncompliance to tx

Back

Mechanisms of ADR: non-dose related

Front

idiosyncrasy = clozapine-induced agranulocytosis, sulfonamide- induced TEN hypersensitivity = allergic reaction

Back

BLANK is unintentional conduct

Front

human error

Back