Policy and Procedure Relating to Health Utilization Management Standards
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DC Health Systems Plan 2017
DISTRICT OF COLUMBIA HEALTH SYSTEMS PLAN 2017 NOTICE OF NON-DISCRIMINATION In accordance with the D.C. Human Rights Act of 1977, as amended, D.C. Code section 2.1401.01 et seq., the District of Columbia does not discriminate on the basis of race, color, religion, national origin, sex, age, marital status, personal appearance, sexual orientation, family responsibilities, matriculation, political affiliation, disability, source of income, or place of residence or business. Discrimination in violation of the Act will not be tolerated. Violators will be subject to disciplinary action. Published July, 2017 Dear Residents: Upon taking office in 2015, my Administration focused on improving health outcomes for all residents, recognizing that all government policies—from education and housing, to economic development and transportation—impact the health and wellness of our communities. Every Washingtonian, regardless of where they live, should have the ability to live a healthy and fulfilling life in our nation’s capital. This Health Systems Plan will serve as a guide for all stakeholders as they implement initiatives aimed at strengthening Washington DC’s health system to improve the overall health status of residents by ad- dressing social determinants of health and promoting health equity. Through this plan, we will ensure that public and private agencies throughout DC have the direction they need to make sound investments and implement initiatives that will improve the health and well-being of residents across all eight wards. I am proud of the work we have done thus far. In 2016, the number of newly diagnosed HIV cases in Washington, DC decreased by 52 percent to 347. -
Chapter 54 Manual of Requirements for Family Child Care Registration
CHAPTER 54 MANUAL OF REQUIREMENTS FOR FAMILY CHILD CARE REGISTRATION STATE OF NEW JERSEY DEPARTMENT OF CHILDREN AND FAMILIES EFFECTIVE - March 20, 2017 EXPIRES - February 21, 2024 DEPARTMENT OF CHILDREN AND FAMILIES OFFICE OF LICENSING PO BOX 717 TRENTON, NEW JERSEY 08625-0717 Toll - Free Telephone 1-877-667-9845 N.J.A.C. 3A:54 MANUAL OF REQUIREMENTS FOR FAMILY CHILD CARE REGISTRATION SUBCHAPTER 1. GENERAL PROVISIONS................................................................................ 1 3A:54-1.1 Legal authority ................................................................................................................ 1 3A:54-1.2 Definitions ....................................................................................................................... 2 3A:54-1.3 Approval requirements for sponsoring organizations ..................................................... 4 3A:54-1.4 Public access to records ................................................................................................... 6 SUBCHAPTER 2. ADMINISTRATION OF SPONSORING ORGANIZATIONS ................... 8 3A:54-2.1 Sponsoring organization eligibility ................................................................................. 8 3A:54-2.2 Administrative responsibility .......................................................................................... 8 3A:54-2.3 Reporting requirements ................................................................................................... 9 3A:54-2.4 Sponsoring organization records -
Medicaid Drug Utilization Review State Comparison/Summary Report FFY 2013 Annual Report Prescription Drug Fee for Service Programs
Medicaid Drug Utilization Review State Comparison/Summary Report FFY 2013 Annual Report Prescription Drug Fee For Service Programs December 2014 Executive Summary of 2013 State Medicaid DUR Annual Reports Each State Medicaid program under Section 1927 (g) (3) (D) of the Social Security Act (the Act) is required to submit an annual report on the operation of its Medicaid Drug Utilization Review (DUR) program. States are required to report on their state’s prescribing patterns, cost savings generated from their DUR programs and their programs’ operations, including adoption of new innovative DUR practices. DUR is a two-phase process that is conducted by the Medicaid state agencies. In the first phase (Prospective DUR - ProDUR) the state’s Medicaid agency’s electronic monitoring system screens prescription drug claims to identify problems such as therapeutic duplication, drug-disease contraindications, incorrect dosage or duration of treatment, drug allergy and clinical misuse or abuse. The second phase (Retrospective DUR -RetroDUR) involves ongoing and periodic examination of claims data to identify patterns of fraud, abuse, gross overuse, or medically unnecessary care and implements corrective action when needed. On May 19th, 2014 CMS sent the states the newly revised Medicaid DUR Annual Report Survey to complete. The new survey included a significantly-expanded Fraud, Waste and Abuse section, new questions about Prescription Drug Monitoring Programs (PDMP) section and inquiries regarding state Managed Care Organizations (MCOs). Below is a brief summary of the findings. I. Demographics – Page 1 All states and the District of Columbia submitted a 2013 Medicaid DUR Annual Report, with the exception of Arizona because almost all of its beneficiaries are enrolled in MCOs. -
Balance Billing Protection for Out-Of-Network Services
Form 405-A (eff. 1/2021) BALANCE BILLING PROTECTION FOR OUT-OF-NETWORK SERVICES Starting January 1, 2021, Virginia state law may protect you from “balance billing” when you get: • EMERGENCY SERVICES from an out-of-network hospital, or an out-of-network doctor or other medical provider at a hospital; or • NON-EMERGENCY SURGICAL OR ANCILLARY SERVICES from an out-of-network lab or health care professional at an in-network hospital, ambulatory surgical center or other health care facility. What is balance billing? • An “IN-NETWORK” health care provider has signed a contract with your health insurance plan. Providers who haven’t signed a contract with your health plan are called “OUT-OF-NETWORK” providers. • In-network providers have agreed to accept the amounts paid by your health plan after you, the patient, has paid for all required cost sharing (copayments, coinsurance and deductibles for covered services). • But, if you get all or part of your care from out-of-network providers, you could be billed for the difference between what your plan pays to the provider and the amount the provider bills you. This is called “balance billing.” • The new Virginia law prevents certain balance billing, but it does not apply to all health plans. Applies May Apply Does Not Apply o Fully insured managed care plans, o Employer-based coverage o Health plans issued to an including those bought through o Health plans issued to an employer association outside Virginia HealthCare.gov outside Virginia o Health plans that do not use a o The state employee health plan o Short-term limited duration plans network of providers o Group health plans that opt-in o Limited benefit plans How can I find out if I am protected? Be sure to check your plan documents or contact your health plan to find out if you are protected by this law. -
The Power of TRU COMPLIANCETM
The Power of TRU COMPLIANCETM Compliant. Actionable. Ethical. THE The Gold Standard of GOLD Medication Reviews STANDARD CoPs-Compliant Med Reviews. Complete evaluation of medication history. EPCS Certified for controlled substances. Detailed clinical insights with actionable recommendations. Reduces lost and unfilled prescriptions. Less risk of adverse drug Drug Utilization Review shows cost-effective interactions and reactions. $ alternatives, recommends discontinuation of non-palliative medications. Fewer prescribing and dispensing errors. Covered vs. Non-covered medications: We provide industry-best practices for hospice and palliative medication coverage. CMS Reporting Recommendations on drug effectiveness, side effect CR-8358 and 10573 imported into your risks vs. drug benefits, interactions, duplicate EMR via SFTP. therapies, and drug therapy concurrently associated with laboratory monitoring. Opioid laxative report. Adverse Drug Reaction Reports. HCPCS coding. Alerts for inappropriate coverage The 5 Rights to a by Medicare Part D. Medication Pass The Best = Outcome The Right For the At the With the Right In the Right Drug Right Patient Right Time Route of Dosage Form Administration Introducing: Tru360TM Tru Partnership. Tru Customization. Tru Service.TM Tru360 is the most comprehensive, hospice-centered, patient-focused solution in the market today. Tru360 drives sustained cost reduction while improving patient satisfaction and outcomes. Tru360 is built on five key components that produce excellent end-of-life care in a cost-effective manner. PARTNERSHIP EFFICIENCY Real Collaboration. Powered by People. Intuitive Workflow. Proactive Intervention. Driven by Data. Real Results. We build a custom service model to fit your Our technology provides proactive intervention, workflow and your culture. Your Tru360 Team, streamlines pharmacy interaction and saves up including a dedicated pharmacist and account to $2,000 per nurse annually. -
Tool 1. Scenarios Guide
Tool 1. Scenarios Guide Tool 1. Scenarios Guide The following 18 scenarios were developed specifically for the privacy and security project to provide a standardized context for discussing organization-level business practices across all states and territories. The scenarios represent a wide range of purposes for the exchange of health information (eg, treatment, public health, biosurveillance, payment, research, marketing) across a broad array of organizations involved in health information exchange and actors within those organizations. The product of the “guided or focused” discussions will be a database of organization-level business practices that will form the basis for the assessment of variation upon which all other work will be based. Each scenario describes a health information exchange (HIE) within a given context to ensure that we cover most of the areas in which we expect to find barriers. Clearly, these scenarios do not cover the universe of exchanges. However, the purposes and conditions represented should be more than adequate to get the discussions of privacy and security policy moving forward. Exhibit 1 shows a mapping of stakeholder organizations identified in the HIE scenarios. A shaded box containing an “X” with some additional text indicates stakeholders that are explicitly identified in the scenario. A yellow box with no text indicates a stakeholder group that could conceivably weigh in on a scenario. For example, Scenario 1: Patient Care Scenario A, involves an exchange between the emergency room in Hospital A and an out-of- state hospital, Hospital B. Both the requesting and releasing organizations are hospitals, regardless of the actors that may be representing those organizations in the work group meetings, which may include physicians, nurses, health information management professionals, and others. -
Pharmacist's Role in Palliative and Hospice Care
456 Medication Therapy and Patient Care: Specific Practice Areas–Guidelines ASHP Guidelines on the Pharmacist’s Role in Palliative and Hospice Care Palliative care arose from the modern hospice movement and and in advanced clinical practice (medication therapy man- has evolved significantly over the past 50 years.1 Numerous agement services, pain and symptom management consulta- definitions exist to describe palliative care, all of which fo- tions, and interdisciplinary team participation). cus on aggressively addressing suffering. The World Health Organization and the U.S. Department of Health and Human Purpose Services both stipulate the tenets of palliative care to include a patient-centered and family-centered approach to care, In 2002, ASHP published the ASHP Statement on the with the goal of maximizing quality of life while minimiz- Pharmacist’s Role in Hospice and Palliative Care.28 These 2 ing suffering. In its clinical practice guidelines, the National guidelines extend beyond the scope of that statement and Consensus Project for Quality Palliative Care of the National are intended to define the role of the pharmacist engaged in Quality Forum (NQF) describes palliative care as “patient the practice of PHC. Role definition will include goals for and family-centered care that optimizes quality of life by an- providing services that establish general principles and best ticipating, preventing, and treating suffering . throughout practices in the care of this patient population. This docu- the continuum of illness . addressing the -
Kansas Department of Health and Environment
KANSAS DEPARTMENT OF HEALTH AND ENVIRONMENT KANSAS LAWS AND REGULATIONS FOR LICENSING DAY CARE HOMES AND GROUP DAY CARE HOMES FOR CHILDREN JANUARY 2020 Division of Public Health Bureau of Family Health Child Care Licensing Program 1000 SW Jackson, Suite 200, Topeka, KS 66612-1274 Phone: (785) 296-1270 Fax: (785) 559-4244 Website: http://www.kdheks.gov/bcclr/index.html E-mail: [email protected] TABLE OF CONTENTS I. Kansas Child Care Licensing Laws, Revised July 2018 Page K.S.A. 65-501 License or temporary permit required; exemptions ...........................1 K.S.A. 65-503 Definitions .........................................................................................1 K.S.A. 65-504 Licenses; contents; limitations; posting; inspections; temporary permits; access to premises; temporary licenses; denial or revocation of license; procedure ........................................................2 K.S.A. 65-505 License fees; maternity centers and child care licensing fee fund .....4 K.S.A. 65-506 Notice of issuance, limitation, modification, suspension or revocation of license; notice to parents or guardians of enrollees of limitation, modification, suspension, revocation or denial; unlicensed placements prohibited ......................................................5 K.S.A. 65-507 Records of maternity centers and child care facilities; confidentiality ....................................................................................6 K.S.A. 65-508 Equipment, supplies, accommodations; competent supervision and care of children; safe -
Part 2 Drug Utilization Review Board
Utah Code Part 2 Drug Utilization Review Board 26-18-101 Definitions. As used in this part: (1) "Appropriate and medically necessary" means, regarding drug prescribing, dispensing, and patient usage, that it is in conformity with the criteria and standards developed in accordance with this part. (2) "Board" means the Drug Utilization Review Board created in Section 26-18-102. (3) "Compendia" means resources widely accepted by the medical profession in the efficacious use of drugs, including "American Hospital Formulary Services Drug Information," "U.S. Pharmacopeia - Drug Information," "A.M.A. Drug Evaluations," peer-reviewed medical literature, and information provided by manufacturers of drug products. (4) "Counseling" means the activities conducted by a pharmacist to inform Medicaid recipients about the proper use of drugs, as required by the board under this part. (5) "Criteria" means those predetermined and explicitly accepted elements used to measure drug use on an ongoing basis in order to determine if the use is appropriate, medically necessary, and not likely to result in adverse medical outcomes. (6) "Drug-disease contraindications" means that the therapeutic effect of a drug is adversely altered by the presence of another disease condition. (7) "Drug-interactions" means that two or more drugs taken by a recipient lead to clinically significant toxicity that is characteristic of one or any of the drugs present, or that leads to interference with the effectiveness of one or any of the drugs. (8) "Drug Utilization Review" or "DUR" means the program designed to measure and assess, on a retrospective and prospective basis, the proper use of outpatient drugs in the Medicaid program. -
Pdf Examination Performances of U.S
U.S. Health Care Workforce By John J. Norcini, John R. Boulet, W. Dale Dauphinee, Amy Opalek, Ian D. Krantz, and Suzanne T. Anderson doi: 10.1377/hlthaff.2009.0222 HEALTH AFFAIRS 29, NO. 8 (2010): 1461–1468 ©2010 Project HOPE— Evaluating The Quality Of Care The People-to-People Health Foundation, Inc. Provided By Graduates Of International Medical Schools John J. Norcini (jnorcini@ ABSTRACT One-quarter of practicing physicians in the United States are FAIMER.org) is president and graduates of international medical schools. The quality of care provided chief executive officer of the Foundation for Advancement by doctors educated abroad has been the subject of ongoing concern. Our of International Medical Education and Research analysis of 244,153 hospitalizations in Pennsylvania found that patients (FAIMER), in Philadelphia, of doctors who graduated from international medical schools and were Pennsylvania. not U.S. citizens at the time they entered medical school had significantly John R. Boulet is associate lower mortality rates than patients cared for by doctors who graduated vice president for research and data resources at from U.S. medical schools or who were U.S. citizens and received their FAIMER. degrees abroad. The patient population consisted of those with congestive heart failure or acute myocardial infarction. We found no W. Dale Dauphinee is a senior scholar at FAIMER. significant mortality difference when comparing all international medical graduates with all U.S. medical school graduates. Amy Opalek is a data resource specialist at FAIMER. Ian D. Krantz is an associate professor of pediatrics at the Children’sHospitalof raduates of international medical We hope that the results will serve as a spring- Philadelphia and the Division schools make up approximately board for changes in medical education practices of Human Genetics and Molecular Biology at the one-quarter of U.S. -
Drug Utilization Review Drug Utilization Review (DUR) Board
Bruce Rauner, Governor Felicia F. Norwood, Director 201 South Grand Avenue East Telephone: (217) 782-1200 Springfield, Illinois 62763-0002 TTY: (800) 526-5812 Drug Utilization Review Drug Utilization Review (DUR) Board Federal regulations at 42 C.F.R. § 456.703 - 456.725 require that state Medicaid pharmacy programs establish and maintain a Drug Utilization Review (DUR) program that helps ensure appropriate drug utilization by conducting prospective and retrospective drug utilization review, and maintaining an educational program. Prospective Drug Utilization Review (DUR) Prospective Drug Utilization Review occurs at point-of-sale. Pharmacists review drug therapy at point-of-sale to screen for therapeutic duplication, drug-disease contraindication, adverse drug-drug interactions, incorrect drug doses or durations of therapy, drug allergy interactions, and clinical abuse/misuse. Pharmacists then counsel HFS clients regarding their medications according to state standards. Claims processing edits and prior authorization criteria for medications can impact this process. Prior approval status of a medication is searchable at http://ilpriorauth.com/. Retrospective Drug Utilization Review Retrospective DUR periodically evaluates drug claims data and other records to monitor for fraud, therapeutic appropriateness, overutilization and underutilization, appropriate use of generic products, therapeutic duplication, drug-disease contraindication, drug-drug interactions, incorrect drug dosage, incorrect duration of drug therapy, and clinical abuse -
Prescription Drug Benefit Manual Chapter 7 – Medication Therapy Management and Quality Improvement Program
Prescription Drug Benefit Manual Chapter 7 – Medication Therapy Management and Quality Improvement Program Table of Contents (Rev. 11, 02-19-10) Transmittals for Chapter 7 10 – Medication Therapy Management and Quality Improvement Program 10.1 Introduction 10.2 Definition of Terms 20 – Quality Assurance Requirements 20.1 – General Rule 20.2 – Compliance With State Standards 20.3 – Concurrent Drug Utilization Review (DUR) 20.4 – Retrospective Drug Utilization Review (RDUR) 20.5 – Medication Error Identification and Reduction (MEIR) 20.6 – Medwatch Reporting 20.7 – CMS Performance Measures 20.8 – Information for Quality Improvement Organizations (QIOs) 30 – Medication Therapy Management Program (MTMP) 30.1 – General Rule 30.2 – Targeted Beneficiaries 30.3 – MTM Services 30.4 – Use of Experts 30.5 – Considerations in MTMP Fees 30.6 – MTMP Application 30.7 – MTMP Approval Considerations 30.8 – Mid–Year MTMP Changes 30.9 – MTMP Reporting 30.10 - Claims Processing for MTM Services 40 – Consumer Satisfaction Surveys 40.1 – General Rule 40.2 – Part D Sponsor Follow-up Responsibilities 50 – Electronic Prescription Program (E-prescribing) 50.1 – General Rule 50.2 – State Law Preemption 50.3 – Standards for E-Prescribing 50.4 – Exemptions 50.5 – Promotion of Electronic Prescribing by MA-PD Plans 60 – Drug Utilization Management Program 60.1 – General Rule 60.2 – Over-the-Counter Drugs as Part of Utilization Management Programs 60.3 – Exception for Private Fee-for-Service MA Plans 60.4 – Drug Utilization Management Disclosure Requirements 60.5 – Web site Posting Requirements 60.6 – Revision of Utilization Management Criteria Requirements 70 - Part D Complaints Processing 70.1 – General Rule 70.2 – Timeframes for Complaints Processing Appendix A – Chapter 7 Related Web Sites 10 – Medication Therapy Management and Quality Improvement Program (Rev.