Original Launch Date: 03/01/23
Expiration Date: 03/01/25
ACCME PARS: 750
This activity is intended for healthcare providers delivering care to women and their families.
After completing this activity, the participant should be better able to:
1. Outline the frequency of repetitive quantitative HCG (qHCG) measurement and when it is necessary
2. Identify the discrimatory zone of qHCG and why it is important
Estimated time to complete activity: 0.25 hours
Susan J. Gross, MD, FRCSC, FACOG, FACMG
President and CEO, The ObG Project
Postgraduate Institute for Medicine (PIM) requires faculty, planners, and others in control of educational content to disclose all their financial relationships with ineligible companies. All identified conflicts of interest (COI) are thoroughly vetted and mitigated according to PIM policy. PIM is committed to providing its learners with high quality accredited continuing education activities and related materials that promote improvements or quality in healthcare and not a specific proprietary business interest of an ineligible company.
The PIM planners and others have nothing to disclose. The OBG Project planners and others have nothing to disclose.
Faculty: Susan J. Gross, MD, receives consulting fees from Cradle Genomics.
Planners and Managers: PIM Planners have nothing to disclose
Participants must read the learning objectives and faculty disclosures and study the educational activity.
If you wish to receive acknowledgment for completing this activity, please complete the test and evaluation. Upon registering and successfully completing the test with a score of 100% and the activity evaluation, your certificate will be made available immediately.
In support of improving patient care, this activity has been planned and implemented by the Postgraduate Institute for Medicine and The ObG Project. Postgraduate Institute for Medicine is jointly accredited by the Accreditation Council for Continuing Medical Education (ACCME), the Accreditation Council for Pharmacy Education (ACPE), and the American Nurses Credentialing Center (ANCC), to provide continuing education for the healthcare team.
Postgraduate Institute for Medicine designates this enduring material for a maximum of 0.25 AMA PRA Category 1 Credit(s)™. Physicians should claim only the credit commensurate with the extent of their participation in the activity.
The maximum number of hours awarded for this Continuing Nursing Education activity is 0.2 contact hours.
The goal of diagnosing an ectopic pregnancy is to make the determination before rupture, allowing conservative, medical treatment
If TVU definitively shows ectopic pregnancy (gestational sac with yolk sac and/or embryo in adnexa), or failed intrauterine pregnancy, treat accordingly
‘Discriminatory Level’
Trending hCG levels
NOTE: Obtain blood type and Rh status on all women suspected of ectopic pregnancy and all Rh-negative women with bleeding should receive RhO(D) immune globulin (RhoGam), regardless of the final outcome of the pregnancy
Over 90% of ectopic pregnancies are in the fallopian tube; the remainder can occur in the cervix, ovary, uterine cornua or abdomen. Risk factors for ectopic pregnancies include tubal surgery, PID, previous ectopic pregnancy (10% with one previous ectopic rising to 25% with ≥2), infertility, assisted reproductive technologies with multiple embryo transfer, previous pelvic/abdominal surgery, age >35 years and smoking. IUDs are associated with fewer ectopics compared to women not using contraception because IUDs are such an effective method of birth control. However, if a woman does become pregnant with an IUD, the risk of an ectopic is approximately 50%. Note that at least half of women with ectopic pregnancies have no risk factors.
Have a high index of suspicion for ectopic pregnancy in any premenopausal woman with abnormal uterine bleeding and pain
Role of Endometrial Aspiration
ACOG Practice Bulletin 193: Tubal Ectopic Pregnancy
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This educational activity may contain discussion of published and/or investigational uses of agents that are not indicated by the FDA. The planners of this activity do not recommend the use of any agent outside of the labeled indications.
The opinions expressed in the educational activity are those of the faculty and do not necessarily represent the views of the planners. Please refer to the official prescribing information for each product for discussion of approved indications, contraindications, and warnings.
Participants have an implied responsibility to use the newly acquired information to enhance patient outcomes and their own professional development. The information
presented in this activity is not meant to serve as a guideline for patient management. Any procedures, medications, or other courses of diagnosis or treatment discussed or suggested in this activity should not be used by clinicians without evaluation of their patient’s conditions and possible contraindications and/or dangers in use, review of any applicable manufacturer’s product information, and comparison with recommendations of other authorities.
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