CMR study materials
CMR study resources

CMR cheat sheet

CMR · Keep the key ideas within reach.

Quick reference

Medical Review Fundamentals and Regulatory Framework

  • Medicare coverage rests on two statutory pillars: a benefit category exists (Social Security Act) and the item or service is reasonable and necessary for diagnosis or treatment.

  • National Coverage Determinations (NCDs) bind all Medicare contractors; Local Coverage Determinations (LCDs) bind only the MAC jurisdiction that issued them.

  • An LCD may not restrict coverage more than an NCD; when they conflict, the NCD controls.

  • HIPAA Privacy Rule permits disclosure of protected health information for treatment, payment, and health care operations without patient authorization.

  • The minimum necessary standard applies to uses and disclosures except treatment and disclosures to the patient or authorized by the patient.

  • EMTALA requires a medical screening examination and stabilizing treatment for anyone presenting to an emergency department, regardless of insurance or ability to pay.

  • Conditions of Participation are the minimum health and safety standards a provider must meet to receive Medicare payment.

  • Recovery Audit Contractor (RAC) reviews target improper payments; MACs handle claims processing and medical review in their jurisdiction.

Quick reference

Clinical Documentation and Medical Record Analysis

  • The medical record must support the diagnosis, justify the treatment, and document the patient's response to care.

  • Documentation is considered late when not completed by the timeframe set in medical staff bylaws (commonly 14-30 days).

  • A valid history and physical is generally required within 30 days before admission or 24 hours after admission for inpatient stays.

  • Only the author of an entry may amend it; late entries must be clearly labeled, dated, and timed.

  • Authentication requires a legible identifier (written or electronic signature); a signature stamp is not acceptable.

  • Cloned documentation (identical text across records) is a compliance red flag and may support denial or fraud referral.

  • Missing documentation cannot be supplemented by verbal order or recollection after the fact for the date of service in question.

  • Objective elements such as vital signs, labs, and imaging must be documented to support the clinical impression.

Quick reference

Coding, Billing, and Claims Review

  • ICD-10-CM codes diagnoses; ICD-10-PCS codes inpatient procedures; CPT and HCPCS Level II code outpatient services and supplies.

  • Code the highest level of specificity documented; unspecified codes are used only when documentation lacks detail.

  • Principal diagnosis is the condition established after study to be chiefly responsible for admission.

  • Evaluation and management level is determined by documented medical decision making or time, per current CPT guidance.

  • Modifier 25 reports a significant, separately identifiable E/M service on the same day as a procedure.

  • Modifier 59 (or X{EPSU} subsets) identifies distinct procedural services not normally reported together.

  • The National Correct Coding Initiative (NCCI) edits define code pairs that are not separately payable; a modifier may bypass only when clinically appropriate.

  • Clean claim rate is the percentage of claims accepted on first submission without edits or rejection.

Quick reference

Utilization Management and Medical Necessity

  • Medical necessity is determined by matching documented clinical findings against coverage criteria (NCD, LCD, or InterQual/MCG).

  • InterQual and Milliman Care Guidelines are proprietary criteria sets; they inform but do not override Medicare coverage rules.

  • An observation stay is an outpatient status; it does not count toward the three-day inpatient prospective payment system (IPPS) stay requirement.

  • The two-midnight rule presumes inpatient status when a physician expects the stay to span two midnights.

  • Concurrent review occurs during the stay; retrospective review occurs after discharge and may result in denial and recoupment.

  • A condition code 44 allows a hospital to change inpatient to outpatient status before discharge when criteria are not met.

  • The admission review outcome options are certification, non-certification, or modification of the requested level of care.

  • Interrater reliability measures consistency of review determinations among reviewers using the same criteria.

Quick reference

Quality Assurance and Compliance Auditing

  • The seven elements of an effective compliance program include written policies, a compliance officer, training, communication, monitoring, enforcement, and corrective action.

  • Sampling in audits must be statistically valid to extrapolate findings; non-random samples cannot support extrapolation.

  • An error rate is calculated as the number of erroneous units divided by total units reviewed.

  • Root cause analysis identifies underlying system failures rather than individual blame for adverse events.

  • A Plan-Do-Study-Act (PDSA) cycle is a structured quality improvement method for testing changes.

  • The OIG Work Plan lists audit and enforcement priorities and signals areas of heightened scrutiny.

  • Audit findings should be tracked to closure with documented corrective action plans and re-audit to confirm effectiveness.

  • Benchmarking compares performance metrics against internal or external standards to identify variation.

Quick reference

Fraud, Waste, and Abuse Detection

  • Fraud is intentional deception for gain; waste is misuse of resources without intent; abuse is practices inconsistent with sound business or medical standards.

  • The False Claims Act imposes liability for knowingly submitting false claims, with treble damages and per-claim penalties.

  • The Anti-Kickback Statute prohibits remuneration to induce referrals for items or services payable by federal health programs.

  • The Stark Law prohibits physician self-referral for designated health services unless an exception applies.

  • The Civil Monetary Penalties Law prohibits offering inducements to Medicare or Medicaid beneficiaries.

  • The Physician Payments Sunshine Act requires reporting of transfers of value to physicians and teaching hospitals.

  • Red flags include upcoding, unbundling, duplicate billing, services not rendered, and billing for medically unnecessary services.

  • The OIG Self-Disclosure Protocol allows providers to voluntarily report potential fraud and negotiate resolution.

Quick reference

Appeals, Denials, and Peer Review

  • Medicare Part A and B redetermination (first level) is filed with the MAC, generally within 120 days of the initial determination.

  • The five Medicare appeal levels are redetermination, reconsideration, ALJ hearing, Medicare Appeals Council, and federal district court.

  • Reconsideration is performed by a Qualified Independent Contractor (QIC), not the MAC that issued the redetermination.

  • The amount in controversy threshold must be met for ALJ and judicial review levels and is updated annually.

  • Peer review is evaluation of a clinician's care by professional peers of comparable training and scope.

  • Peer review protections under the Health Care Quality Improvement Act (HCQIA) require due process and reporting to the National Practitioner Data Bank.

  • An appeal must include the denial notice, the appeal request, and supporting clinical documentation demonstrating medical necessity.

  • Timely filing deadlines are jurisdictional and cannot be waived for good cause.

Quick reference

Professional Ethics and Communication

  • Reviewers must make determinations based on the clinical record and coverage criteria, not on the payer's financial interest.

  • Conflicts of interest must be disclosed and managed; a reviewer should recuse when a personal or financial relationship exists.

  • Patient information should be shared only on a need-to-know basis consistent with HIPAA.

  • Communication with providers about denials should cite the specific criterion or policy not met.

  • Informed consent requires disclosure of risks, benefits, alternatives, and the patient's voluntary agreement.

  • Documentation should be factual, objective, and free of disparaging or speculative language.

  • Whistleblower protections exist under federal law for reporting suspected fraud or unsafe care.

  • Reviewers must not alter, fabricate, or backdate documentation; such actions are reportable compliance violations.