When should myo‑inositol supplementation be stopped relative to the hCG (or GnRH‑agonist) trigger and egg retrieval in an IVF cycle?

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When to Stop Myo-Inositol Before Egg Retrieval

Continue myo-inositol supplementation throughout the entire ovarian stimulation period and stop it on the day of the hCG (or GnRH-agonist) trigger injection, approximately 35-37 hours before oocyte retrieval.

Evidence-Based Timing Protocol

The available research demonstrates that myo-inositol should be administered continuously during the stimulation phase to optimize outcomes:

  • Pre-treatment phase: Administer myo-inositol 2g twice daily (combined with 200 mcg folic acid) for 3 months before starting ovarian stimulation to improve insulin sensitivity, reduce androgen levels, and enhance oocyte quality 1, 2, 3.

  • During stimulation: Continue myo-inositol throughout the entire gonadotropin stimulation period (typically 10-14 days), as this is when it exerts its beneficial effects as a second messenger of FSH and facilitates glucose transport into developing follicles 1, 2.

  • Discontinuation timing: Stop myo-inositol on the day of trigger injection (when follicles reach ≥17-18mm diameter), which occurs 35-37 hours before scheduled oocyte retrieval 4, 5.

Rationale for This Timing

The mechanism of action supports continuation through stimulation:

  • Myo-inositol functions as a second messenger for FSH signaling, directly supporting follicular development and oocyte maturation throughout the stimulation phase 1.

  • Studies demonstrating benefit used protocols where myo-inositol was continued "during the stimulation itself" and "through treatment," indicating it should not be stopped prematurely 2, 3.

  • The trigger injection (hCG or GnRH-agonist) initiates final oocyte maturation over 35-40 hours, after which the oocytes are retrieved—at this point, myo-inositol's role in FSH signaling is complete 4, 5.

Expected Benefits When Used Correctly

When myo-inositol is continued appropriately through stimulation:

  • Reduced gonadotropin requirements: Significantly lower total rFSH doses needed to achieve follicular maturation 2.

  • Improved oocyte quality: Greater number of mature oocytes (>15mm follicles), higher-quality embryos (improved embryo scores), and reduced immature/degenerated oocytes 3.

  • Better pregnancy outcomes: Maintained or improved clinical pregnancy and implantation rates despite using less gonadotropin 1, 2.

Common Pitfalls to Avoid

  • Do not stop myo-inositol early in the stimulation cycle: The benefits on oocyte quality and FSH response require continuous supplementation throughout the entire stimulation period 2, 3.

  • Do not continue after trigger: There is no evidence supporting continuation beyond the trigger injection, and doing so provides no additional benefit once final oocyte maturation has been initiated 5.

  • Do not use myo-inositol as a substitute for evidence-based protocols: While myo-inositol is a useful adjunct, it does not replace appropriate monitoring (transvaginal ultrasound every 2-3 days plus estradiol levels) or proper trigger timing when ≥3 follicles reach ≥17mm 4.

Special Considerations

For patients with specific medical conditions requiring anticoagulation during ART (such as antiphospholipid syndrome):

  • Low-dose aspirin should be stopped 3 days before egg retrieval and resumed the following day 6.

  • LMWH should be stopped 12-24 hours prior to retrieval and resumed the same day if no bleeding 6.

  • These anticoagulation timing protocols are independent of myo-inositol discontinuation 6.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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