Here is a comprehensive overview of the MTP Kit:
MTP Kit (Medical Termination of Pregnancy Kit)
Composition
The MTP kit is a combipack containing:
- Mifepristone 200 mg - 1 tablet
- Misoprostol 200 mcg - 4 tablets (total 800 mcg)
Mechanism of Action
Mifepristone (RU-486)
- An analog of the progestin norethindrone
- Selective progesterone receptor modulator (SPRM)
- Binds to the progesterone receptor with higher affinity than progesterone itself, but blocks its action
- Causes decidual breakdown and sensitizes the uterus to prostaglandins
- Also has some antiglucocorticoid activity
Misoprostol
- Synthetic prostaglandin E1 analogue
- Stimulates uterine contractions and cervical ripening
- Acts synergistically with mifepristone for expulsion
The combination works by:
- Mifepristone blocks progesterone support of the pregnancy
- Misoprostol causes uterine contractions to expel the products of conception
Approved Regimens
Standard (FDA-approved / WHO-recommended) regimen:
- Mifepristone 200 mg orally on Day 1
- Misoprostol 800 mcg buccally (or vaginally / sublingually) 24-48 hours later
- Approved up to 70 days (10 weeks) from the last menstrual period
Older/alternate regimen:
- Mifepristone 600 mg on Day 1
- Misoprostol 400 mcg orally on Day 3
(This is less preferred; 200 mg mifepristone is equally effective)
Efficacy: ~97% in early first trimester; 96-99% complete abortion rate with combined regimen. - Berek & Novak's Gynecology, p. 781
Misoprostol Routes
| Route | Notes |
|---|
| Buccal | Placed between gum and cheek; standard preferred route |
| Vaginal | High efficacy; similar blood levels to buccal |
| Sublingual | Also effective; may have more GI side effects |
| Oral | Less effective (400 mcg oral < 800 mcg buccal/vaginal) |
Contraindications
- Known allergy/hypersensitivity to mifepristone, misoprostol, or other prostaglandins
- Confirmed or suspected ectopic pregnancy or undiagnosed adnexal mass
- IUD in place (must be removed first)
- Chronic adrenal failure
- Concurrent long-term corticosteroid therapy
- Hemorrhagic disorder or concurrent anticoagulant therapy
- Inherited porphyria
- No access to emergency medical facilities (for managing incomplete abortion or hemorrhage)
Side Effects
- Common (intended): Uterine cramping, vaginal bleeding
- Less common: Nausea, vomiting, diarrhea, chills, fever
- Serious (rare, ~0.3%):
- Excessive bleeding requiring blood transfusion
- Infection (rare cases of Clostridium sordellii reported historically - now mitigated by buccal route and prophylactic doxycycline where indicated)
Mortality risk: ~0.00063% - approximately 14 times lower than the risk associated with live birth. - Goldman-Cecil Medicine
Follow-up
- Patient must return for follow-up ~14 days after mifepristone
- Confirm complete termination by clinical exam or ultrasound
- If ongoing pregnancy detected: risk of fetal malformation - surgical termination is strongly recommended
Special Notes
- Home administration of misoprostol is permitted (and widely practiced)
- Telemedicine prescribing is now allowed in many jurisdictions (including the US, post-FDA 2023 ruling)
- Misoprostol at 24, 48, or 72 hours after mifepristone gives equal efficacy
- The kit can be used by non-specialist providers (family physicians, midwives, nurse practitioners, physician assistants)
Recent Evidence
A 2025
systematic review (PMID 39384382) confirmed that home use of mifepristone for medical abortion is safe and effective with high patient satisfaction. A
2025 meta-analysis (PMID 39444194) also confirmed the combination of mifepristone + misoprostol is superior to misoprostol alone for managing miscarriage and intrauterine fetal death.
Sources: Park's Textbook of Preventive & Social Medicine (p. 592), Berek & Novak's Gynecology (p. 781), Goldman-Cecil Medicine