What are the medical eligibility criteria and pre‑treatment assessments required to deem a reproductive‑age (18‑45 years) patient medically fit for an in‑vitro fertilisation (IVF) cycle?

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Medical Fitness for IVF Procedure

Pre-Treatment Medical Assessment

All reproductive-age patients (18-45 years) must undergo comprehensive medical screening before IVF initiation to identify conditions that could compromise maternal or fetal outcomes, with particular attention to age-related factors, chronic diseases, and infectious disease status. 1, 2

Essential Baseline Evaluations

Infectious Disease Screening:

  • Rubella immunity status must be documented; approximately 6% of women lack immunity and require vaccination with a 1-month delay before IVF 3
  • Hepatitis B surface antigen screening is mandatory, as 5% of previously unscreened patients are carriers 3
  • Chlamydia trachomatis and mycoplasma cultures should be obtained, as 14-16% of patients harbor these organisms which can compromise outcomes 3
  • Cervical cytology (Pap smear) must be current, as 5% of newly referred patients have cervical intraepithelial dysplasia requiring treatment before IVF 3

Uterine Cavity Assessment:

  • Hysterosalpingography or sonohysterography is required to identify intrauterine pathology, which occurs in 11% of cases 3
  • Diagnostic hysteroscopy with treatment of identified pathology (adhesions, polyps) should precede IVF, as some patients conceive spontaneously after correction 3

Age-Specific Considerations

Women ≥35 Years:

  • Ovarian reserve testing (anti-Müllerian hormone, antral follicle count, day 3 FSH) is essential, as female fecundity declines significantly with age 2
  • Immediate IVF may be considered first-line in women 38-40 years or older rather than pursuing ovulation induction cycles, given time-sensitive fertility decline 2
  • More aggressive evaluation timelines are warranted; assessment after 6 months of unprotected intercourse rather than 12 months is justified 4

Chronic Disease Management

Cardiovascular and Metabolic Conditions:

  • Hypertension and diabetes must be optimally controlled before IVF, as these conditions significantly impact pregnancy outcomes 1
  • Body mass index (BMI) assessment is mandatory; obesity adversely affects fertility and IVF success rates 1, 2
  • Thrombophilia screening should be performed in patients with personal or family history of thrombotic events 1

Autoimmune Conditions:

  • Patients with systemic lupus erythematosus (SLE) or antiphospholipid syndrome (APS) require disease quiescence for at least 6 months before IVF 4
  • Antiphospholipid antibody testing is essential in patients with APS, as antithrombotic prophylaxis protocols must be implemented during ovarian stimulation 4
  • Low-dose aspirin and/or low molecular weight heparin should be initiated based on individual thrombotic risk profile 4

Male Partner Evaluation

Concurrent Male Assessment:

  • Male partner evaluation must begin simultaneously with female assessment, not sequentially 4
  • Semen analysis is required, with at least 2 samples obtained one month apart due to high biological variability 4
  • Reproductive history including duration of infertility, prior fertility, sexual dysfunction, and gonadotoxin exposures must be documented 4
  • Physical examination focusing on testicular size, varicocele, and penile abnormalities is mandatory 4

Lifestyle and Environmental Factors

Modifiable Risk Factors:

  • Smoking cessation is essential; tobacco use adversely affects fertility in both partners 4, 1, 2
  • Alcohol consumption should be minimized or eliminated 4
  • Nutritional adequacy must be assessed and optimized 1
  • Illicit drug use must be addressed and discontinued 1
  • Occupational and environmental exposures to gonadotoxins require evaluation and mitigation 4

Special Populations Requiring Additional Evaluation

Cancer Survivors:

  • Patients with prior gonadotoxic chemotherapy (alkylating agents, anthracyclines) or pelvic radiation require ovarian reserve assessment regardless of age 4
  • Cumulative cyclophosphamide equivalent dose >5 g/m² or pelvic radiation >6 Gy confers high risk of ovarian dysfunction 4
  • Karyotype analysis may be warranted in patients with recurrent pregnancy loss or failed IVF cycles 4

Patients on Immunosuppressive Therapy:

  • Cyclophosphamide and other alkylating agents cause dose- and age-dependent ovarian failure; less gonadotoxic regimens should be considered before IVF 4
  • GnRH analogs for ovarian protection during chemotherapy have demonstrated efficacy (RR 0.12 for premature ovarian failure) but require initiation before or concurrent with alkylating agents 4

Critical Exclusions and Contraindications

Absolute Contraindications:

  • Active SLE or APS disease flare; IVF is only safe with quiescent disease 4
  • Uncontrolled hypertension or diabetes 1
  • Active cervical dysplasia requiring treatment 3
  • Untreated intrauterine pathology 3

Relative Contraindications Requiring Optimization:

  • Inadequately treated hypothyroidism or hyperthyroidism 4
  • Severe obesity (BMI >40) without weight optimization 1
  • Active tobacco use without cessation attempts 1, 2

Common Pitfalls to Avoid

  • Do not proceed with IVF without documenting rubella immunity, as congenital rubella syndrome is preventable with pre-conception vaccination 3
  • Do not skip male partner evaluation, as 25% of infertility has a male factor component and female partners may undergo unnecessary invasive procedures 4
  • Do not assume prior normal Pap smears are sufficient; 5% of newly referred IVF patients have undiagnosed cervical dysplasia 3
  • Do not overlook uterine cavity assessment; 11% have pathology and some conceive after correction without requiring IVF 3
  • Do not initiate IVF in patients with active autoimmune disease, as pregnancy complications are significantly increased without disease quiescence 4

References

Research

Preconception Evaluation Before In Vitro Fertilization.

Obstetrical & gynecological survey, 2020

Research

Prerequisite work-up of the couple before in-vitro fertilization.

Human reproduction (Oxford, England), 1992

Guideline

Guideline Directed Topic Overview

Dr.Oracle Medical Advisory Board & Editors, 2025

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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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