(b) Protocol for Pharmacists Furnishing
Self-Administered Hormonal Contraception
(1)
Authority: Section
4052.3(a)(1)
of the California Business and Professions Code authorizes a pharmacist to
furnish self-administered hormonal contraceptives in accordance with a protocol
approved by the California State Board of Pharmacy and the Medical Board of
California. Use of the protocol in this section satisfies that
requirement.
(2) Purpose: To
provide timely access to self-administered hormonal contraception medication
and to ensure that the patient receives adequate information to successfully
comply with therapy.
(3) Definition
of Self-Administered Hormonal Contraception: Hormonal contraception products
with the following routes of administration are considered self-administered:
(A) Oral;
(B) Transdermal;
(C) Vaginal;
(D) Depot Injection.
(4) Procedure: When a patient requests
self-administered hormonal contraception, the pharmacist shall complete the
following steps:
(A) Ask the patient to use
and complete the self-screening tool;
(B) Review the self-screening answers and
clarify responses if needed;
(C)
Measure and record the patient's seated blood pressure if combined hormonal
contraceptives are requested or recommended;
(D) Before furnishing self-administered
hormonal contraception, the pharmacist shall ensure that the patient is
appropriately trained in administration of the requested or recommended
contraceptive medication.
(E) When
a self-administered hormonal contraceptive is furnished, the patient shall be
provided with appropriate counseling and information on the product furnished,
including:
1. Dosage;
2. Effectiveness;
3. Potential side effects;
4. Safety;
5. The importance of receiving recommended
preventative health screenings;
6.
That self-administered hormonal contraception does not protect against sexually
transmitted infections (STIs).
(5) Self-Screening Tool: The pharmacist shall
provide the patient with a self-screening tool containing the list of questions
specified in this protocol. The patient shall complete the self-screening tool,
and the pharmacist shall use the answers to screen for all Category 3 and 4
conditions and characteristics for self-administered hormonal contraception
from the current United States Medical Eligibility Criteria for Contraceptive
Use (USMEC) developed by the federal Centers for Disease Control and Prevention
(CDC). The patient shall complete the self-screening tool annually, or whenever
the patient indicates a major health change.
A copy of the most recently completed self-screening tool
shall be securely stored within the originating pharmacy or health care
facility for a period of at least three years from the date of dispense.
This self-screening tool should be made available in
alternate languages for patients whose primary language is not
English.
(6) Fact Sheets:
(A) The pharmacist should provide the patient
with a copy of a current, consumer-friendly, comprehensive birth control guide
such as that created by the Food and Drug Administration (FDA). Examples of
appropriate guides are available on the Board of Pharmacy's website.
(B) The pharmacist shall provide the patient
with the FDA-required patient product information leaflet included in all
self-administered hormonal contraception products, as required by Business and
Professions Code Section
4052.3(c).
The pharmacist shall answer any questions the patient may have regarding
self-administered hormonal contraception.
(C) The pharmacist should provide the patient
with a copy of an administration-specific factsheet. Examples of appropriate
factsheets are available on the Board of Pharmacy's
website.
(7) Follow-Up
Care: Upon furnishing a self-administered hormonal contraceptive, or if it is
determined that use of a self-administered hormonal contraceptive is not
recommended, the pharmacist shall refer the patient for appropriate follow-up
care to the patient's primary care provider or, if the patient does not have a
primary care provider, to nearby clinics. A patient who is determined not to be
an appropriate candidate for self-administered hormonal contraception shall be
advised of the potential risk and referred to an appropriate health care
provider for further evaluation.
(8) Notifications: The pharmacist shall
notify the patient's primary care provider of any drug(s) or device(s)
furnished to the patient, or enter the appropriate information in a patient
record system shared with the primary care provider, as permitted by that
primary care provider. If the patient does not have a primary care provider, or
is unable to provide contact information for his or her primary care provider,
the pharmacist shall provide the patient with a written record of the drug(s)
or device(s) furnished and advise the patient to consult an appropriate health
care professional of the patient's choice.
(9) Referrals and Supplies: If
self-administered hormonal contraception services are not immediately available
or the pharmacist declines to furnish pursuant to a conscience clause, the
pharmacist shall refer the patient to another appropriate health care provider.
The pharmacist shall comply with all state mandatory
reporting laws, including sexual abuse laws.
(10) Product Selection: The pharmacist, in
consultation with the patient, may select any hormonal contraceptive listed in
the current version of the USMEC for individuals identified as Category 1 or 2,
based on the information reported in the self-screening tool and the blood
pressure (if recorded by the pharmacist). The USMEC shall be kept current and
maintained in the pharmacy or health care facility, and shall be available on
the Board of Pharmacy's website.
Generic equivalent products may be
furnished.
(11)
Documentation: Each self-administered hormonal contraceptive furnished by a
pharmacist pursuant to this protocol shall be documented in a patient
medication record and securely stored within the originating pharmacy or health
care facility for a period of at least three years from the date of dispense. A
patient medication record shall be maintained in an automated data processing
or manual record mode such that the required information under title 16,
sections
1717 and
1707.1 of the California Code of
Regulations is readily retrievable during the pharmacy or facility's normal
operating hours.
(12) Training:
Prior to furnishing self-administered hormonal contraception, pharmacists who
participate in this protocol must have completed a minimum of one hour of a
board-approved continuing education program specific to self-administered
hormonal contraception, application of the USMEC, and other CDC guidance on
contraception. An equivalent, curriculum-based training program completed on or
after the year 2014 in an accredited California school of pharmacy is also
sufficient training to participate in this protocol.
(13) Patient Privacy: All pharmacists
furnishing self-administered hormonal contraception in a pharmacy or health
care facility shall operate under the pharmacy or facility's policies and
procedures to ensure that patient confidentiality and privacy are
maintained.
(14) Self-Screening
Tool Questions
HORMONAL CONTRACEPTION SELF-SCREENING TOOL
QUESTIONS
| 1 |
What was the first date of your last menstrual
period? |
/ / |
|
| 2a |
Have you ever taken birth control pills, or used a birth
control patch, ring, or shot/injection? (If no, go to question 3) |
Yes [] |
No [] |
| 2b |
Did you ever experience a bad reaction to using hormonal
birth control? |
Yes [] |
No [] |
| 2c |
Are you currently using birth control pills, or a birth
control patch, ring, or shot/injection? |
Yes [] |
No [] |
| 3 |
Have you ever been told by a medical professional not to
take hormones? |
Yes [] |
No [] |
| 4 |
Do you smoke cigarettes? |
Yes [] |
No [] |
| 5 |
Do you think you might be pregnant now? |
Yes [] |
No [] |
| 6 |
Have you given birth within the past 6 weeks? |
Yes [] |
No [] |
| 7 |
Are you currently breastfeeding an infant who is less
than 1 month of age? |
Yes [] |
No [] |
| 8 |
Do you have diabetes? |
Yes [] |
No [] |
| 9 |
Do you get migraine headaches, or headaches so bad that
you feel sick to your stomach, you lose the ability to see, it makes it hard to
be in light, or it involves numbness? |
Yes [] |
No [] |
| 10 |
Do you have high blood pressure, hypertension, or high
cholesterol? |
Yes [] |
No [] |
| 11 |
Have you ever had a heart attack or stroke, or been told
you had any heart disease? |
Yes [] |
No [] |
| 12 |
Have you ever had a blood clot in your leg or in your
lung? |
Yes [] |
No [] |
| 13 |
Have you ever been told by a medical professional that
you are at a high risk of developing a blood clot in your leg or in your
lung? |
Yes [] |
No [] |
| 14 |
Have you had bariatric surgery or stomach reduction
surgery? |
Yes [] |
No [] |
| 15 |
Have you had recent major surgery or are you planning to
have surgery in the next 4 weeks? |
Yes [] |
No [] |
| 16 |
Do you have or have you ever had breast cancer? |
Yes [] |
No [] |
| 17 |
Do you have or have you ever had hepatitis, liver
disease, liver cancer, or gall bladder disease, or do you have jaundice (yellow
skin or eyes)? |
Yes [] |
No [] |
| 18 |
Do you have lupus, rheumatoid arthritis, or any blood
disorders? |
Yes [] |
No [] |
| 19a |
Do you take medication for seizures, tuberculosis (TB),
fungal infections, or human immunodeficiency virus (HIV)? |
Yes [] |
No [] |
| 19b |
If yes, list them here: |
|
|
| 20a |
Do you have any other medical problems or take regular
medication? |
Yes [] |
No [] |
| 20b |
If yes, list them here: |
|
|