Extending medicare reimbursement in clinical trials / / Committee on Routine Patient Care Costs in Clinical Trials for Medicare Beneficiaries ; Henry J. Aaron and Hellen Gelband, editors

• Pubblicazione: Washington, D.C., : National Academy Press, c2000
• Edizione: 1st ed.
• Descrizione fisica: 1 online resource (86 p.)
• Disciplina: 338.4/33621/0973
• Soggetto topico: Medicare; Clinical trials - United States; Medical care, Cost of - United States
• Altri autori: AaronHenry J GelbandHellen
• Note generali: Description based upon print version of record.
• Nota di bibliografia: Includes bibliographical references (p. 65-66).
• Nota di contenuto: ""Front Matter""; ""Acknowledgments""; ""Contents""; ""Executive Summary""; ""1 Clinical Trials in the United States""; ""2 Paying for Patient Care in Clinical Trials""; ""3 Recommendations for Medicare Clinical Trial Reimbursement""; ""References""; ""APPENDIX A Glossary, Acronyms, and Abbreviations""; ""APPENDIX B Committee Biographies""
• Sommario/riassunto: Increasingly over the past five years, uncertainty about reimbursement for routine patient care has been suspected as contributing to problems enrolling people in clinical trials. Clinical trial investigators cannot guarantee that Medicare will pay for the care required, and they must disclose this uncertainty to potential participants during the informed consent process. Since Medicare does not routinely "preauthorize" care (as do many commercial insurers) the uncertainty cannot be dispelled in advance. Thus, patients considering whether to enter trials must assume that they may have to pay bills that Medicare rejects simply because they have enrolled in the trial. This report recommends an explicit policy for reimbursement of routine patient care costs in clinical trials. It further recommends that HCFA provide additional support for selected clinical trials, and that the government support the establishment of a national clinical trials registry. These policies (1) should assure that beneficiaries would not be denied coverage merely because they have volunteered to participate in a clinical trial; and (2) would not impose excessive administrative burdens on HCFA, its fiscal intermediaries and carriers, or investigators, providers, or participants in clinical trials. Explicit rules would have the added benefit of increasing the uniformity of reimbursement decisions made by Medicare fiscal intermediaries and carriers in different parts of the country. Greater uniformity would, in turn, decrease the uncertainty about reimbursement when providers and patients embark on a clinical trial.
• Titolo autorizzato: Extending medicare reimbursement in clinical trials
• ISBN: 9780309183888; 030918388X; 9780309558143; 030955814X; 9780309528542; 0309528542
• Formato: Materiale a stampa
• Livello bibliografico: Monografia
• Lingua di pubblicazione: Inglese
• Record Nr.: 9910970659603321
• Lo trovi qui: Univ. Federico II