Post-Pellet Hormone Panel for Female Patients
For female patients receiving hormone pellet therapy, measure morning estradiol, testosterone, complete blood count (CBC), comprehensive metabolic panel (CMP), and lipid panel at 4 weeks post-insertion, then when symptoms return or at 3-4 month intervals. 1
Core Hormone Measurements
Timing of Laboratory Assessment
- Draw labs at 4 weeks post-pellet insertion to assess peak hormone levels and ensure therapeutic range has been achieved 1, 2
- Repeat testing when androgen deficiency symptoms return (typically 3-6 months), as this indicates declining hormone levels requiring re-implantation 1
- Morning samples are preferred for consistency, though estradiol pellets show less circadian variation than testosterone 1, 3
Essential Hormone Levels
- Serum estradiol: Target follicular phase range (50-70 pg/mL) for the first 3 months, declining to approximately 37 pg/mL by 6 months with 25 mg pellets 3
- Serum testosterone: Therapeutic levels average 299 ng/dL at week 4, declining to 171 ng/dL when symptoms return (significantly higher than endogenous female levels) 1
- Estrone (E1): Monitor to ensure estradiol:estrone ratio remains >1, which is characteristic of pellet therapy 3, 2
Metabolic and Safety Monitoring
Baseline and Follow-up Labs
Lipid panel: Monitor high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), total cholesterol, and triglycerides at baseline, 12 weeks, and 24 weeks 3, 2
Comprehensive metabolic panel (CMP): Assess renal function and electrolytes 4
Complete blood count (CBC): Baseline and periodic monitoring 4
- Hemoglobin may be affected by hormone therapy 4
Pituitary Hormone Assessment
- Luteinizing hormone (LH) and follicle-stimulating hormone (FSH): Measure at baseline and follow-up to assess pituitary suppression 3, 2
Additional Considerations
Bone Health Monitoring
- Urinary calcium/creatinine ratio: Consider measuring to assess bone resorption, as pellets reduce this ratio more consistently than other estrogen delivery methods 2
- Bone mineral density testing: Should be considered for patients with hypogonadism risk 4
Thyroid and Binding Proteins
- Sex hormone-binding globulin (SHBG): Remains relatively unchanged with estradiol pellets, unlike oral estrogen 3
- Corticosteroid-binding globulin (CBG): Also remains stable with pellet therapy 3
Critical Pitfalls to Avoid
Interpretation Challenges
- Expect massive inter-individual variance (coefficient of variation 36-43%) even with identical dosing, making single testosterone measurements unreliable for dose adjustments 1
- Intra-individual circadian variation can reach 25%, so timing consistency matters 1
- Clinical response and symptom relief should guide therapy more than absolute hormone levels, as pharmacologic testosterone dosing is required to produce physiologic effects in women 1
Contraindication Screening
- Screen for breast cancer history or active disease before initiating testosterone pellets 5
- Assess for history of deep vein thrombosis (DVT) as a contraindication to androgen therapy 5
Special Populations
- For patients with adrenal insufficiency, never initiate DHEA or androgen therapy before ensuring adequate cortisol replacement 5
- Baseline morning cortisol and ACTH should be checked if adrenal insufficiency is suspected 5
Monitoring Schedule Summary
Initial insertion: Baseline labs (estradiol, testosterone, CBC, CMP, lipids, LH, FSH)
Week 4: Estradiol, testosterone, estrone
3 months: Full panel repeat (hormones, CBC, CMP, lipids)
When symptoms return (typically 4-6 months): Estradiol, testosterone to guide re-implantation timing 1, 3