FINAL REPORT Evaluation of Healthcare Costs and Utilization

Total Page:16

File Type:pdf, Size:1020Kb

FINAL REPORT Evaluation of Healthcare Costs and Utilization University of Cincinnati Medical Center College of Pharmacy Health Economics & Outcomes Research FINAL REPORT Evaluation of Healthcare Costs and Utilization among Medicaid Recipients in Schools with School-Based Health Centers SUBMITTED TO THE HEALTH FOUNDATION OF GREATER CINCINNATI by Jeff J. Guo, B.Pharm., Ph.D.1,2 Raymond Jang, Ph.D. 1 Robert J. Cluxton, Pharm.D. 1,2 1 College of Pharmacy 2 Institute of Health Policy and Health Services Research University of Cincinnati Medical Center, Cincinnati, Ohio 3223 Eden Ave. Cincinnati, Ohio Tel. (513) 558-8613 Copyright © 2005 by The Health Foundation of Greater Cincinnati. All rights reserved. To cite this work, please follow this format: Health Foundation of Greater Cincinnati, The (2005). Evaluation of Healthcare Costs and Utilization among Medicaid Recipients in Schools with School-Based Health Centers. Cincinnati, OH: Author. Permission is granted to reproduce this publication provided that these reproductions are not used for a commercial purpose, that you do not collect any fees for the reproductions, that our materials are faithfully reproduced (without addition, alteration, or abbreviation), and that they include any copyright notice, attribution, or disclaimer appearing on the original. Final Report of SBHC Cost Study 2 Table of Contents I. INTRODUCTION ............................................................................................................. 12 Specific Aims and Hypotheses .............................................................................................. 13 Background and Significance ................................................................................................ 14 Significance of This Study .................................................................................................... 17 II. METHODOLOGY ............................................................................................................ 19 Study Design ........................................................................................................................ 19 Consent for Evaluation and IRB Approval ............................................................................ 19 Data Sources and Study Period ............................................................................................. 20 Target Population and Study Groups ................................................................................... 21 Theoretical Models ............................................................................................................... 22 Total Medicaid expenses: .................................................................................................. 22 Inflation Adjusted Discount Factor: .................................................................................. 25 Function of Medicaid Expenses per Recipient: .................................................................. 25 Theoretical Model of Cost-Benefit Analysis .......................................................................... 29 Questionnaire for Cost-Benefit Variables .......................................................................... 34 Study Subgroups: Cohort Study for Students with Chronic Diseases .................................... 35 Statistical Analyses ................................................................................................................ 37 III. RESULTS – Aim#1 ........................................................................................................... 41 Demographics ...................................................................................................................... 41 Trends for Medicaid Total Costs by SBHC .......................................................................... 42 Final Report of SBHC Cost Study 3 Total Medicaid Costs for Students before and after SBHC Program ..................................... 47 Hospitalization Costs Before and After SBHC Program ....................................................... 49 Costs of Emergency department Visits Before and After SBHC Program ............................. 49 Costs for Mental Health Services Before and After SBHC Program ...................................... 50 Prescription Drug Costs Before and After SBHC Program ................................................... 51 Dental Care Costs Before and After SBHC Program ............................................................ 52 Growth Curve Analysis (Hierarchical Linear/Nonlinear Modeling) for Total Medicaid Costs ................................................................................................. 54 Rates of Hospitalization Before and After SBHC Program ................................................... 60 Rates of Emergency department Visits Before and After SBHC Program .............................. 60 IV. RESULTS – Aim#2 ........................................................................................................... 62 Cohort Study for Students with Asthma ............................................................................... 62 Risk of Hospitalization and ED visits for Students with Asthma ........................................... 63 Costs of Hospitalization and ED visits for Students with Asthma ......................................... 65 Cohort Study for Students with Mental Health Problems .................................................... 66 Total Costs for Students with Mental Health Problems ........................................................ 68 V. RESULTS – Aim#3 ............................................................................................................ 69 Cost-Benefit Analysis for the SBHC Program ....................................................................... 69 Economic Outcomes from 3 years of SBHC Operations in Four School Districts ............. 70 Value of Additional Outside Sources of Funding .............................................................. 70 Estimation of the Value of Outcomes as Benefits .............................................................. 71 Net Social Benefit Estimation ........................................................................................... 77 Final Report of SBHC Cost Study 4 VI. Discussion .......................................................................................................................... 78 Total Costs and Effectiveness of SBHC Program .................................................................. 78 Effectiveness of SBHC Program on Hospitalization and ED Visits for Asthma Cohort Students ............................................................................................................................... 81 Effectiveness of SBHC Program on Primary Care for Students with Mental Health Problems ............................................................................................. 82 Cost-Benefit Analysis for the SBHC Program: Societal Perspective vs. Medicaid Perspective 84 Health Policy Implications ................................................................................................... 87 Limitations ........................................................................................................................... 88 Conclusions .......................................................................................................................... 89 ACKNOWLEDGMENTS ...................................................................................................... 91 VI. REFERENCES: ................................................................................................................. 92 Tables .............................................................................................................................................98 Figures ..........................................................................................................................................129 Appendix A: “Parent Survey Name” .............................................................................................. Appendix B: School-Based Health Center Coordinator’s Survey: Resource Use for SBHC Implementation 2000–2003 ................................................................................................. Appendix C: Brand-Names and Generic-Names of Medications for Asthma Treatment ............... Appendix D: International Classification of Disease (ICD-9) Codes of Mental Illnesses ............... Appendix E: Brand-Names and Generic-Names of Medications for Mental Health Therapy ........... Final Report of SBHC Cost Study 5 List of Tables Table 1. Summary of Published Major Studies on School-Based Health Centers (SBHCs) Table 2. Demographics and Medicaid Enrollment for Students in Intervention and Comparison Schools Table 3. Costs for All Students Enrolled in Medicaid and Schools from 9/1997 to 2/2003 (N=5,056) Table 4. Repeated Measures ANCOVA of Means of Total Costs for Students in Intervention and Comparison Schools (N =2,153) Table 5. Repeated Measures ANCOVA of Hospitalization Costs for Students in Intervention and Comparison Schools (N =2,153) Table 6. Repeated Measures ANCOVA of Emergency Department Costs for Students in Intervention and Comparison Schools (N =2,153) Table 7. Repeated Measures ANCOVA of Mental Health Service Costs for Students in Intervention and Comparison Schools (N =2,153) Table 8. Repeated Measures ANCOVA of EPSDT Costs for Students in Intervention and Comparison Schools (N=2,153)
Recommended publications
  • Guidelines for the Forensic Analysis of Drugs Facilitating Sexual Assault and Other Criminal Acts
    Vienna International Centre, PO Box 500, 1400 Vienna, Austria Tel.: (+43-1) 26060-0, Fax: (+43-1) 26060-5866, www.unodc.org Guidelines for the Forensic analysis of drugs facilitating sexual assault and other criminal acts United Nations publication Printed in Austria ST/NAR/45 *1186331*V.11-86331—December 2011 —300 Photo credits: UNODC Photo Library, iStock.com/Abel Mitja Varela Laboratory and Scientific Section UNITED NATIONS OFFICE ON DRUGS AND CRIME Vienna Guidelines for the forensic analysis of drugs facilitating sexual assault and other criminal acts UNITED NATIONS New York, 2011 ST/NAR/45 © United Nations, December 2011. All rights reserved. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Secretariat of the United Nations concerning the legal status of any country, territory, city or area, or of its authorities, or concerning the delimitation of its frontiers or boundaries. This publication has not been formally edited. Publishing production: English, Publishing and Library Section, United Nations Office at Vienna. List of abbreviations . v Acknowledgements .......................................... vii 1. Introduction............................................. 1 1.1. Background ........................................ 1 1.2. Purpose and scope of the manual ...................... 2 2. Investigative and analytical challenges ....................... 5 3 Evidence collection ...................................... 9 3.1. Evidence collection kits .............................. 9 3.2. Sample transfer and storage........................... 10 3.3. Biological samples and sampling ...................... 11 3.4. Other samples ...................................... 12 4. Analytical considerations .................................. 13 4.1. Substances encountered in DFSA and other DFC cases .... 13 4.2. Procedures and analytical strategy...................... 14 4.3. Analytical methodology .............................. 15 4.4.
    [Show full text]
  • Forensic Toxicology Laboratory Office of Chief Medical Examiner City of New York
    FORENSIC TOXICOLOGY LABORATORY OFFICE OF CHIEF MEDICAL EXAMINER CITY OF NEW YORK CARISOPRODOL , MEPROBAMATE and TOPIRAMATE by SOLID PHASE EXTRACTION and GAS CHROMATOGRAPHY/MASS SPECTROMETRY (Selected Ion Monitoring) PRINCIPLE Carisoprodol is a carbamate derivative first synthesized in 1959. It is primarily used as a muscle relaxant. UncontrolledMeprobamate is also a carbamate derivative used as a muscle relaxant and the primary metabolite of carisoprodol. Topiramate is a sulfamate-substituted monosaccharide used as an anticonvulsant Carisoprodol, meprobamate and topiramate are quantitated by a selected ion monitoring (SIM) method using methapyrilene as the internal standard. Carisoprodol, meprobamate and topiramate are extracted from biological specimens by solid phase extraction. Drugs are temporarily bound to a sorbent in the solid phase cartridge as the prepared sample is poured through the column. The column is washed to remove interfering compounds, followed by elution of drugs from the column. The eluate is evaporated, reconstituted and injected in the GCMS. Quantitative analysis is performed by SIM GCMS using a six point calibration curve. SAFETY The handling of all biological specimens and reagents is performed within the guidelines which are detailed in the Safety and Health manual. Copy SPECIMEN PREPARATION The procedure is routinely applied to the following biological specimens and their aliquots unless otherwise specified: Blood 0.5 mL of the undiluted specimen Urine 0.5 mL for qualitative identification Brain 0.5 mL of a 1:3 homogenate Gastric Contents 0.5 mL of a 1:10 dilution Liver 0.5 mL of a 1:5 homogenate Vitreous Humor 0.5 mL of the undiluted specimen Bile 0.5 mL of the undiluted specimen Reviewed by: Date: Page 1 of 14 T:\FINALSOP\FINAL SOP PDF\G.
    [Show full text]
  • Assessment of Molecular Action of Direct Gating and Allosteric Modulatory Effects of Carisoprodol (Somartm) on GABA a Receptors
    Graduate Theses, Dissertations, and Problem Reports 2015 Assessment of molecular action of direct gating and allosteric modulatory effects of carisoprodol (SomaRTM) on GABA A receptors Manoj Kumar Follow this and additional works at: https://researchrepository.wvu.edu/etd Recommended Citation Kumar, Manoj, "Assessment of molecular action of direct gating and allosteric modulatory effects of carisoprodol (SomaRTM) on GABA A receptors" (2015). Graduate Theses, Dissertations, and Problem Reports. 6022. https://researchrepository.wvu.edu/etd/6022 This Dissertation is protected by copyright and/or related rights. It has been brought to you by the The Research Repository @ WVU with permission from the rights-holder(s). You are free to use this Dissertation in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you must obtain permission from the rights-holder(s) directly, unless additional rights are indicated by a Creative Commons license in the record and/ or on the work itself. This Dissertation has been accepted for inclusion in WVU Graduate Theses, Dissertations, and Problem Reports collection by an authorized administrator of The Research Repository @ WVU. For more information, please contact [email protected]. ASSESSMENT OF MOLECULAR ACTION OF DIRECT GATING AND ALLOSTERIC MODULATORY EFFECTS OF MEPROBAMATE (MILTOWN®) ON GABAA RECEPTORS Manish Kumar, MD, MS Dissertation submitted to the School of Pharmacy at West Virginia University in partial fulfillment of Requirements
    [Show full text]
  • Urine Drug Toxicology and Pain Management Testing
    Urine Drug Toxicology and Pain Management Testing Kara Lynch, PhD, DABCC University of California San Francisco San Francisco, CA Learning Objectives • Describe what chronic pain is, who is affected and how they are commonly treated • Explain the common methodologies used in pain management testing • Interpret urine drug testing results • Create protocols to minimize the occurrence of false positive or false negative results Pain – definition and types • Pain - an unpleasant sensory and emotional experience associated with actual or potential tissue damage • Chronic pain - pain that extends beyond the expected period of healing • Nociceptive Pain – Pain caused by tissue injury – Stimulus-evoked, high intensity – Opioid sensitive • Neuropathic Pain – Caused by nerve injury – Spontaneous activity – Develops in days or month – Opioid insensitive Chronic Pain Patients • Arthritis • Fibromyalgia – Osteoarthritis • Headaches – Rheumatoid arthritis – Migraine – Gout – Tension • Cancer – Cluster • Chronic non-cancer pain • Myofascial pain • Central pain syndrome • Neuropathic pain – CNS damage – Diabetic Peripheral – Multiple Sclerosis Neuropathy – Parkinson’s disease – Postherpetic neuralgia • Chronic abnominal pain • Neck and Back Pain – Intestinal obstructions Chronic Pain Medications • Opiates • Synthetic opioids – Codeine – Fentanyl – Morphine – Methadone • Semi-synthetic opioids – Meperidine – Oxymorphone – Tramadol – Oxycodone – Propoxyphene – Hydromorphone – Levorphanol – Hydrocodone – Tapentadol – Buprenorphine • Anticonvulsant • Muscle
    [Show full text]
  • 2021 Formulary List of Covered Prescription Drugs
    2021 Formulary List of covered prescription drugs This drug list applies to all Individual HMO products and the following Small Group HMO products: Sharp Platinum 90 Performance HMO, Sharp Platinum 90 Performance HMO AI-AN, Sharp Platinum 90 Premier HMO, Sharp Platinum 90 Premier HMO AI-AN, Sharp Gold 80 Performance HMO, Sharp Gold 80 Performance HMO AI-AN, Sharp Gold 80 Premier HMO, Sharp Gold 80 Premier HMO AI-AN, Sharp Silver 70 Performance HMO, Sharp Silver 70 Performance HMO AI-AN, Sharp Silver 70 Premier HMO, Sharp Silver 70 Premier HMO AI-AN, Sharp Silver 73 Performance HMO, Sharp Silver 73 Premier HMO, Sharp Silver 87 Performance HMO, Sharp Silver 87 Premier HMO, Sharp Silver 94 Performance HMO, Sharp Silver 94 Premier HMO, Sharp Bronze 60 Performance HMO, Sharp Bronze 60 Performance HMO AI-AN, Sharp Bronze 60 Premier HDHP HMO, Sharp Bronze 60 Premier HDHP HMO AI-AN, Sharp Minimum Coverage Performance HMO, Sharp $0 Cost Share Performance HMO AI-AN, Sharp $0 Cost Share Premier HMO AI-AN, Sharp Silver 70 Off Exchange Performance HMO, Sharp Silver 70 Off Exchange Premier HMO, Sharp Performance Platinum 90 HMO 0/15 + Child Dental, Sharp Premier Platinum 90 HMO 0/20 + Child Dental, Sharp Performance Gold 80 HMO 350 /25 + Child Dental, Sharp Premier Gold 80 HMO 250/35 + Child Dental, Sharp Performance Silver 70 HMO 2250/50 + Child Dental, Sharp Premier Silver 70 HMO 2250/55 + Child Dental, Sharp Premier Silver 70 HDHP HMO 2500/20% + Child Dental, Sharp Performance Bronze 60 HMO 6300/65 + Child Dental, Sharp Premier Bronze 60 HDHP HMO
    [Show full text]
  • Sedation in Fmri : an Unsolved Challenge
    Sedation in fMRI : An unsolved challenge Byron Bernal *, MD Nolan Altman**, MD There are many medications that can be utilized to sedate children undergoing fMR examinations. The most frequently used drugs are chloral hydrate, thiopenthal, phenobarbital, propofol, and fentanyl. These medications have some secondary effects on the electrical and metabolic activity of the cortex, cerebral blood flow(CBF), cerebral blood volume(CBV), and tissue oxygen extraction. These effects are of no concern in regular MRI (Magnetic Resonance Imaging), however, may have a significant contribution in fMR performed in the sedated child. Since fMRI is based on the hemodynamic and metabolic response of the brain to a given stimulus the selection of the sedation medication seems crucial. The following reviews the current knowledge regarding the relation of these drugs to these physiological parameters. Chloral Hydrate.- Chloral hydrate (CH) does not reduce brain cortex activity. This is demonstrated on EEG where it is widely used. Thoresen M and Henriksen O (1997) did not find changes on the EEGs in 9 out of 13 children with epileptic seizures, before and after CH was administered. We do not know of any reported studies relating CBF, CBV, or cerebral regional metabolism changes, and CH in humans. Propofol.- Propofol has been used as a sedative in children undergoing EEGs. Low propofol doses (0.5- 1 mg/kg) show an increase in the number of beta-waves and a significant reduction of alpha- and theta- waves . Larger doses of propofol (total dose of 2-2.5 mg/kg), the number of beta-waves decreased and delta-waves appeared.
    [Show full text]
  • 2013 National Survey on Drug Use and Health
    140324 Table 1.88C Specific Hallucinogen, Inhalant, Needle, and Heroin Use in Lifetime, by Age Group: Standard Errors of Numbers in Thousands, 2012 and 2013 Total Total Aged 12-17 Aged 12-17 Aged 18-25 Aged 18-25 Aged 26+ Aged 26+ Drug or Method of Administration (2012) (2013) (2012) (2013) (2012) (2013) (2012) (2013) HALLUCINOGENS 674 707 39 35 131 133 641 678 PCP (Angel Dust, Phencyclidine) 311 346 13 8 30 30 309 342 LSD (Acid) 561 580 21 19 87 81 538 567 Peyote 338 328 10 9 31 33 331 327 Mescaline 362 378 7 6 30 35 359 375 Psilocybin (Mushrooms) 524 561 24 22 99 100 502 542 Ecstasy (MDMA) 405 464 30 24 117 114 374 442 INHALANTS 489 519 51 52 84 85 471 505 Amyl Nitrite, Poppers, Locker Room Odorizers, or Rush 311 364 21 18 40 40 306 357 Correction Fluid, Degreaser, or Cleaning Fluid 162 100 26 26 28 26 157 91 Gasoline or Lighter Fluid 184 164 31 28 40 29 174 156 Glue, Shoe Polish, or Toluene 182 175 31 31 32 30 175 168 Halothane, Ether, or Other Anesthetics 89 85 8 10 15 17 88 84 Lacquer Thinner or Other Paint Solvents 132 117 21 18 21 21 130 114 Lighter Gases (Butane, Propane) 91 80 18 15 16 17 89 77 Nitrous Oxide or Whippits 365 409 18 17 71 70 349 399 Spray Paints 123 121 34 24 28 28 115 115 Other Aerosol Sprays 154 130 24 21 33 39 149 121 NEEDLE USE1,2,3 225 265 10 10 38 40 222 261 Heroin Needle Use1,2 162 211 7 6 28 33 161 209 Cocaine Needle Use1,2 160 193 3 1 20 21 158 192 Stimulant Needle Use1,2,3 143 199 4 5 22 26 139 196 Methamphetamine Needle Use1,2,3 134 185 3 5 21 22 131 182 HEROIN 245 281 12 9 43 44 241 278 Smoke Heroin2 153 152 9 5 30 32 148 150 Sniff or Snort Heroin2 203 215 5 5 35 35 203 212 *Low precision; no estimate reported.
    [Show full text]
  • 1,1,1 -Trichloroethane (M E T H Y L C H L O R O F O R M)
    criteria for a recommended standard occupational exposure to 1,1,1 -trichloroethane (m e t h y l c h l o r o f o r m) U.S. DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE Public Health Service Center for Disease Control National Institute for Occupational Safety and Health criteria for a recommended standard.. OCCUPATIONAL EXPOSURE TO 1,1,1 - TRICHLOROETHANE (Methyl Chloroform) U.S. DEPARTMENT OF HEALTH, EDUCATION, AND WELFARE Public Health Service Center for Disease Control National Institute for Occupational Safety and Health JULY 1976 HEW Publication No. (NIOSH) 76-184 PREFACE The Occupational Safety and Health Act of 1970 emphasizes the need for standards to protect the health and safety of workers exposed to an ever-increasing number of potential hazards at their workplace. The National Institute for Occupational Safety and Health has projected a formal system of research, with priorities determined on the basis of specified indices, to provide relevant data from which valid criteria for effective standards can be derived. Recommended standards for occupational exposure, which are the result of this work, are based on the health effects of exposure. The Secretary of Labor will weigh these recommen­ dations along with other considerations such as feasibility and means of implementation in developing regulatory standards. It is intended to present successive reports as research and epide­ miologic studies are completed and as sampling and analytical methods are developed. Criteria and standards will be reviewed periodically to ensure continuing protection of the worker. I am pleased to acknowledge the contributions to this report on 1,1,1-trichloroethane by members of my staff and the valuable, constructive comments by the Review Consultants on 1,1,1-Trichloroethane, by the ad hoc committees of the American Industrial Hygiene Association and the American Academy of Occupational Medicine, and by Robert B.
    [Show full text]
  • 17 Anesthesia for Nonobstetric Surgery During Pregnancy 
    17 Anesthesia for Nonobstetric Surgery During Pregnancy Maternal Safety ....................... 370 Fetal Well-Being ...................... 370 AcuteExposuretoAnesthetics.............. 371 ChronicExposuretoAnesthetics............ 371 EffectofAnestheticsontheFetus............ 372 Sedative and Hypnotic Agents ............ 372 Opioids ......................... 373 Muscle Relaxants ................... 373 Local Anesthetics ................... 373 Oxygen and Carbon Dioxide ............. 374 Inhalation Anesthetics ................. 374 Effects on the Fetal Brain: Behavioral Teratogenicity . 376 Continuation of the Pregnancy .............. 377 Recommendations for Minimizing Chances ofAbortionorPrematureLabor............377 Intrauterine Surgery .................... 379 It has been estimated that every year in the United States about 50,000 pregnant women (0.5–2.2%) will receive anesthesia for various surgical indications during their pregnancy. The purpose of this surgery may be (1) to prolong gestation, (2) unre- lated to the pregnancy, or (3) to correct fetal anomalies. Hence, an understanding of the effects of different anesthetic drugs and techniques on the mother and fetus is essential to the safe administration of anesthesia to pregnant women undergoing surgery. Recently, a question of preoperative pregnancy testing in adolescents has been raised. The authors observed retrospec- tively 412 adolescent women undergoing surgery. The overall incidence of a positive test was 1.2%. The authors concluded that mandatory pregnancy testing is advisable
    [Show full text]
  • Basic Analytical Toxicology
    The World Health Organization is a specialized agency of the United Nations with primary responsibility for international health matters and public health. Through this organization, which was created in 1948, the health professions of some 190 countries exchange their knowledge and experience with the aim of making possible the attainment by all citizens of the world by the year 2000 of a level of health that will permit them to lead a socially and economically productive life. By means of direct technical cooperation with its Member States, and by stimulating such coopera­ tion among them, WHO promotes the development of comprehensive health services, the prevention and control of diseases, the improvement of environmental conditions, the development of human resources for health, the coordination and development of biomedical and health services research, and the planning and implementation of health programmes. These broad fields of endeavour encompass a wide variety of activities, such as developing systems of primary health care that reach the whole population of Member countries; promoting the health of mothers and children; combating malnutrition, controlling malaria and other communicable diseases including tuberculosis and leprosy; coordinating the global strategy for the prevention and control of AIDS; having achieved the eradication of smallpox, promoting mass immunization against a number of other preventable diseases; improving mental health; providing safe water supplies; and training health personnel of all categories. Progress towards better health throughout the world also demands international cooperation in such matters as establishing international standards for biological substances, pesticides and pharma­ ceuticals; formulating environmental health criteria; recommending international nonproprietary names for drugs; administering the International Health Regulations; revising the International Statistical Classification of Diseases and Related Health Problems and collecting and disseminating healih statistical information.
    [Show full text]
  • August 2021 California Signaturevalue 4 Tier HMO Formulary
    Pharmacy | Formulary | California 2021 California SignatureValue 4-Tier HMO Formulary Please note: This Formulary is accurate as of August 1, 2021 and is subject to change after this date. All previous versions of this Formulary are no longer in effect. Your estimated coverage and copay/coinsurance may vary based on the benefit plan you choose and the effective date of the plan. This Formulary can also be accessed online at myuhc.com > Pharmacy Information > Prescription Drug Lists > California plans > SignatureValue HMO plans. Plan-specific coverage documents may be accessed online at uhc.com/statedruglists > Small Group Plans > California. If you are a UnitedHealthcare member, please register or log on to myuhc.com, or call the toll-free number on your health plan ID card to find pharmacy information specific to your benefit plan. This Formulary is applicable to the following health insurance products offered by UnitedHealthcare: • SignatureValue • SignatureValue Advantage • SignatureValue Alliance • SignatureValue Flex • SignatureValue Focus • SignatureValue Harmony • SignatureValue Performance Updated 6/17/2021 6/21 © 2021 United HealthCare Services, Inc. All Rights Reserved. WF3890815-N Contents At UnitedHealthcare, we want to help you better understand your medication options. ..................................................... 3 How do I use my Formulary? ............................................. 4 What are tiers? ........................................................ 5 When does the Formulary change? ........................................ 5 Utilization Management Programs ......................................... 6 Your Right to Request Access to a Non-formulary Drug ....................... 6 Requesting a Prior Authorization or Step Therapy Exception ................... 7 How do I locate and fill a prescription through a retail network pharmacy? . 7 How do I locate and fill a prescription through the mail order pharmacy? . 7 How do I locate and fill a prescription at a specialty pharmacy? ...............
    [Show full text]
  • Drug-Facilitated Sexual Assault in the U.S
    The author(s) shown below used Federal funds provided by the U.S. Department of Justice and prepared the following final report: Document Title: Estimate of the Incidence of Drug-Facilitated Sexual Assault in the U.S. Document No.: 212000 Date Received: November 2005 Award Number: 2000-RB-CX-K003 This report has not been published by the U.S. Department of Justice. To provide better customer service, NCJRS has made this Federally- funded grant final report available electronically in addition to traditional paper copies. Opinions or points of view expressed are those of the author(s) and do not necessarily reflect the official position or policies of the U.S. Department of Justice. AWARD NUMBER 2000-RB-CX-K003 ESTIMATE OF THE INCIDENCE OF DRUG-FACILITATED SEXUAL ASSAULT IN THE U.S. FINAL REPORT Report prepared by: Adam Negrusz, Ph.D. Matthew Juhascik, Ph.D. R.E. Gaensslen, Ph.D. Draft report: March 23, 2005 Final report: June 2, 2005 Forensic Sciences Department of Biopharmaceutical Sciences (M/C 865) College of Pharmacy University of Illinois at Chicago 833 South Wood Street Chicago, IL 60612 ABSTRACT The term drug-facilitated sexual assault (DFSA) has been recently coined to describe victims who were given a drug by an assailant and subsequently sexually assaulted. Previous studies that have attempted to determine the prevalence of drugs in sexual assault complainants have had serious biases. This research was designed to better estimate the rate of DFSA and to examine the social aspects surrounding it. Four clinics were provided with sexual assault kits and asked to enroll sexual assault complainants.
    [Show full text]