Therapeutics Hormonal Agents

Chapter 37: Role of Compounding Pharmacist

Hilgers TW, Reed-Kane D

The Medical and Surgical Practice of NaProTECHNOLOGY, 467-476, 2004

RRM Academy Synopsis

Compounding pharmacists prepare medications used in NaProTECHNOLOGY

The chapter says compounding pharmacists play a vital role in NaProTECHNOLOGY. The 2004 book chapter describes custom medicines, compounding law and bioidentical hormones. The chapter reports no patient results.

Key Findings

  • The chapter defines compounding as a pharmacist preparing a customized medication, to a doctor's specifications, for an individual patient need.
  • The chapter lists reasons to compound: medications that are not commercially available, medications that are not stable, and commercial medications modified for a specific patient need.
  • Section 503A of the 1997 Food and Drug Administration Modernization Act was struck down in its entirety after the Supreme Court ruled on April 29, 2002.
  • Bioidentical hormones have the exact molecular structure of hormones made in the human body, the chapter states, and no commercial or compounded product is both completely natural and bioidentical.
  • The chapter puts the average cash price of a compounding pharmacy prescription at about $35-$40 and says many compounding pharmacies do not accept insurance.

RRM Context

NaProTECHNOLOGY is one named method within restorative reproductive medicine, built on root-cause care before treatment. Other methods, such as Creighton or FEMM, use their own protocols and their own pharmacies. The chapter describes a care team of patient, doctor and pharmacist, working together on each prescription. The chapter notes that progestin is a man-made form of progesterone that drug makers can patent, while a bioidentical hormone cannot be patented. The field favors individual, root-cause care over one standard dose for everyone.

Abstract

This chapter describes the role of the compounding pharmacist in NaProTECHNOLOGY, noting that many of its protocols use compounded medications prepared to a physician's specifications for an individual patient. The chapter reviews the history, definition, reasons for and regulation of compounding, including the litigation that ended with Section 503A of the 1997 Food and Drug Administration Modernization Act struck down in its entirety. The authors list questions for judging a compounding pharmacy's training and quality control and discuss bioidentical hormones, which the chapter describes as having the exact molecular structure of hormones made in the human body. The chapter states that Women's Health Initiative results cannot be extrapolated to all forms of hormone replacement therapy, especially bioidentical hormone replacement therapy, and that most compounded prescriptions are not cost prohibitive.

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Topics

By this author

Related research

Therapeutics › Hormonal Agents › Progesterone and Progestins · Restorative Reproductive Medicine › NaProTechnology › Protocols and Framework · Clinical Practice Operations › Care Team and Roles › Allied Practitioner Role
Thomas W Hilgers
Tom Hilgers, T Hilgers
Hilgers et al. 2004, Hilgers 2004