|First use||China 1958 and
|Figures are combined usage of MVA and EVA.|
|UK: Eng. & Wales||64% (2006)|
|United States||88.3% (2003)|
Vacuum or suction aspiration uses aspiration to remove uterine contents through the cervix. It may be used as a method of induced abortion, a therapeutic procedure used after miscarriage, or a procedure to obtain a sample for endometrial biopsy. The rate of infection is lower than any other surgical abortion procedure at 0.5%. Some sources may use the terms dilation and evacuation or "suction" dilation and curettage to refer to vacuum aspiration, although those terms are normally used to refer to distinct procedures.
Vacuuming as a means of removing the uterine contents, rather than the previous use of a hard metal curette, was pioneered in 1958 by Drs Wu Yuantai and Wu Xianzhen in China, but their paper was only translated into English on the fiftieth anniversary of the study that "ultimately led to the technique becoming the world’s commonest and safest obstetric procedure".
In Canada, the method was pioneered and improved on by Henry Morgentaler, achieving a complication rate of 0.48% and no deaths in over 5,000 cases. He was the first doctor in North America to use the technique, which he trained other doctors to use.
Harvey Karman in the United States refined the technique in the early 1970s with the development of the Karman cannula, a soft, flexible cannula that avoided the need for initial cervical dilatation and so reduced the risks of puncturing the uterus.
Vacuum aspiration may be used as a method of induced abortion, as a therapeutic procedure after miscarriage, to aid in menstrual regulation, and to obtain a sample for endometrial biopsy. It is also used to terminate molar pregnancy.
When used as a miscarriage treatment or an abortion method, vacuum aspiration may be used alone or with cervical dilation anytime in the first trimester (up to 12 weeks gestational age). For more advanced pregnancies, vacuum aspiration may be used as one step in a dilation and evacuation procedure. Vacuum aspiration is the procedure used for almost all first-trimester abortions in many countries.
Vacuum aspiration is an outpatient procedure that generally involves a clinic visit of several hours. The procedure itself typically takes less than 15 minutes. Suction is created with either an electric pump (electric vacuum aspiration or EVA) or a manual pump (manual vacuum aspiration or MVA). A hand-held 25cc or 50cc syringe can function as a manual pump. Both methods use the same level of suction, and so can be considered equivalent in terms of effectiveness and safety.
The clinician may first use a local anesthetic to numb the cervix. Then, the clinician may use instruments called "dilators" to open the cervix, or sometimes medically induce dilation with drugs. Finally, a sterile cannula is inserted into the uterus and attached via tubing to the pump. The pump creates a vacuum which empties uterine contents.
After a procedure for abortion or miscarriage treatment, the tissue removed from the uterus is examined for completeness. Expected contents include the embryo or fetus, as well as the decidua, chorionic villi, amniotic fluid, amniotic membrane and other tissue.
Post-treatment care includes brief observation in a recovery area and a follow-up appointment approximately two weeks later. These would tend to include tests for infection in case any biological material was not properly removed.
Advantages over dilation and curettage
Dilation and curettage (D&C), also known as sharp curettage, was once the standard of care in situations requiring uterine evacuation. However, vacuum aspiration has a number of advantages over D&C and has largely replaced D&C in many settings.
Vacuum aspiration may be used earlier in pregnancy than dilation and curettage (D&C). Manual vacuum aspiration is the only surgical abortion procedure available earlier than the 6th week of pregnancy. Vacuum aspiration has lower rates of complications when compared to D&C.
Vacuum aspiration - especially manual vacuum aspiration - is significantly cheaper than D&C. The equipment needed for vacuum aspiration costs less than a curette set. Unlike D&C, vacuum aspiration does not require general anesthesia and so can be performed as an outpatient procedure at a clinic rather than in a hospital surgical setting. While D&C is generally provided only by physicians, vacuum aspiration may be performed by advanced practice clinicians such as physician's assistants and midwives.
Manual vacuum aspiration does not require electricity and so can be provided in locations that have unreliable electrical service or none at all. Manual vacuum aspiration also has the advantage of being quiet, without the noise of an electric vacuum pump.
When used for uterine evacuation, vacuum aspiration is 98% effective in removing all uterine contents. Retained products of conception require a second aspiration procedure. This is more common when the procedure is performed very early in pregnancy, before 6 weeks gestational age.
Other complications occur at a rate of less than 1 per 100 procedures and include excessive blood loss, infection, injury to the cervix or uterus, including perforation, and uterine adhesions.
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- Baird, Traci L. and Susan K. Flinn (2001). Manual Vacuum Aspiration: Expanding women's access to safe abortions services (PDF). Ipas. p. 3. Retrieved 2008-01-28., which cites:
- Greenslade, Forrest; Janie Benson, Judith Winkler, Victoria Henderson and Ann Leonard (1993). "Summary of clinical and programmatic experience with manual vacuum aspiration". Advances in Abortion Care 3 (2).
- "Managing complications in pregnancy and childbirth: A guide for doctors and midwives". World Health Organization. 2003. Retrieved 2006-09-14.
- Baird (2001), pp. 4-5,14 (sidebars and information box).
- Baird (2001), p. 10 (table).
- Baird (2001), pp. 4-6.
- Baird (2001), p. 2.
- Baird (2001), pp. 5,8-13.
- Dalton, VK; Saunders NA; Harris LH; Williams JA; Lebovic DI (June 2006). "Intrauterine adhesions after manual vacuum aspiration for early pregnancy failure". Fertility and Sterility 85 (6): 1823.e1–3. doi:10.1016/j.fertnstert.2005.11.065. PMID 16674955.