Asherman's syndrome

Asherman's syndrome
Classification and external resources
Specialty urology
ICD-10 N85.6
ICD-9-CM 621.5
DiseasesDB 946
MedlinePlus 001483
MeSH D006175
Ultrasound view.

Asherman's syndrome (AS) or Fritsch syndrome, is a condition characterized by adhesions and/or fibrosis of the endometrium particularly but can also affect the myometrium. It is often associated with dilation and curettage of the intrauterine cavity.[1] A number of other terms have been used to describe the condition and related conditions including: intrauterine adhesions (IUA), uterine/cervical atresia, traumatic uterine atrophy, sclerotic endometrium, endometrial sclerosis, and intrauterine synechiae.[2]

History

The condition was first described in 1894 by Heinrich Fritsch (Fritsch, 1894)[3] and further characterized by Israeli gynecologist Joseph Asherman[4] in 1948.[5]

It is also known as Fritsch syndrome, or Fritsch-Asherman syndrome.

Causes and features

HSG view. Note: not the same uterus as in ultrasound or hysteroscopic view; this uterus appears to be T-shaped.
Hysteroscopic view.

The cavity of the uterus is lined by the endometrium. This lining is composed of two layers, the functional layer (adjacent to the uterine cavity) which is shed during menstruation and an underlying basal layer (adjacent to the myometrium), which is necessary for regenerating the functional layer. Trauma to the basal layer, typically after a dilation and curettage (D&C) performed after a miscarriage, or delivery, or for surgical termination of pregnancy, can lead to the development of intrauterine scars resulting in adhesions that can obliterate the cavity to varying degrees. In the extreme, the whole cavity can be scarred and occluded. Even with relatively few scars, the endometrium may fail to respond to estrogen. Often, patients experience secondary menstrual irregularities characterized by a decrease in flow and duration of bleeding (amenorrhea, hypomenorrhea, or oligomenorrhea)[6] and become infertile. Menstrual anomalies are often but not always correlated with severity: adhesions restricted to only the cervix or lower uterus may block menstruation. Pain during menstruation and ovulation is sometimes experienced and can be attributed to blockages. It has been reported that 88% of AS cases occur after a D&C is performed on a recently pregnant uterus, following a missed or incomplete miscarriage, birth, or during an elective termination (abortion) to remove retained products of conception.[1]

It affects women of all races and ages equally, suggesting no underlying genetic predisposition for its development.[7] Depending on the degree of severity, AS may result in infertility, repeated miscarriages, pain from trapped blood, and future obstetric complications[8](see Prognoses below). If left untreated, the obstruction of menstrual flow resulting from adhesions can lead to endometriosis in some cases.[2][9]

AS can also result from other pelvic surgeries including cesarean sections,[7][10] removal of fibroid tumours (myomectomy) and from other causes such as IUDs, pelvic irradiation, schistosomiasis[11] and genital tuberculosis.[12] Chronic endometritis from genital tuberculosis is a significant cause of severe intrauterine adhesions (IUA) in the developing world, often resulting in total obliteration of the uterine cavity which is difficult to treat.[13]

One study found a significant correlation between Paramesonephric duct anomalies and intrauterine adhesions.[14] This apparent correlation is attributed to women with congenital uterine anomalies being predisposed to miscarriages,[9][15] and therefore having higher rates of D&Cs performed than the general population, which could account for the higher rate of IUA observed.[16] It is also feasible that women with septate uteri and other Müllerian defects are at a higher risk of sustaining endometrial damage after blind D&C due to their atypical anatomy, particularly if the doctor performing the surgery was unaware of it.

An artificial form of AS can be surgically induced by endometrial ablation in women with excessive uterine bleeding, in lieu of hysterectomy.

Incidence

AS has a reported incidence of 25% of D&Cs performed 1–4 weeks post-partum,[9][10][17] up to 30.9% of D&Cs performed for missed miscarriages and 6.4% of D&Cs performed for incomplete miscarriages.[18] In another study, 40% of patients who underwent repeated D&C for retained products of conception after missed miscarriage or retained placenta developed AS.[19]

In the case of missed miscarriages, the time period between fetal demise and curettage may increase the likelihood of adhesion formation due to fibroblastic activity of the remaining tissue.[7][20]

The risk of AS also increases with the number of procedures: one study estimated the risk to be 16% after one D&C and 32% after 3 or more D&Cs.[21] However, a single curettage often underlies the condition.

Prevalence

In an attempts to estimate the prevalence of AS in the general population, it was found in 1.5% of women undergoing hysterosalpingography HSG,[22] and between 5 and 39% of women with recurrent miscarriage.[23][24][25]

After miscarriage, a review estimated the prevalence of AS to be approximately 20% (95% confidence interval: 13% to 28%).[26]

Diagnosis

The history of a pregnancy event followed by a D&C leading to secondary amenorrhea or hypomenorrhea is typical. Hysteroscopy is the gold standard for diagnosis.[8] Imaging by sonohysterography or hysterosalpingography will reveal the extent of the scar formation. Ultrasound is not a reliable method of diagnosing Asherman's Syndrome. Hormone studies show normal levels consistent with reproductive function.

Classification

Various classification systems were developed to describe Asherman’s syndrome (citations to be added), some taking into account the amount of functioning residual endometrium, menstrual pattern, obstetric history and other factors which are thought to play a role in determining the prognoses. With the advent of techniques which allow visualization of the uterus, classification systems were developed to take into account the location and severity of adhesions inside the uterus. This is useful as mild cases with adhesions restricted to the cervix may present with amenorrhea and infertility, showing that symptoms alone do not necessarily reflect severity. Other patients may have no adhesions but amenorrhea and infertility due to a sclerotic atrophic endometrium. The latter form has the worst prognosis.

Treatment

Fertility may sometimes be restored by removal of adhesions, depending on the severity of the initial trauma and other individual patient factors. Operative hysteroscopy is used for visual inspection of the uterine cavity during adhesion dissection (adhesiolysis). However, hysteroscopy is yet to become a routine gynaecological procedure and only 15% of US gynecologists perform office hysteroscopy {Isaacson, 2002}. Adhesion dissection can be technically difficult and must be performed with care in order to not create new scars and further exacerbate the condition. In more severe cases, adjunctive measures such as laparoscopy are used in conjunction with hysteroscopy as a protective measure against uterine perforation. Microscissors are usually used to cut adhesions. Electrocauterization is not recommended.[27]

As IUA frequently reform after surgery, techniques have been developed to prevent recurrence of adhesions. Methods to prevent adhesion reformation include the use of mechanical barriers (Foley catheter, saline-filled Cook Medical Balloon Uterine Stent, IUCD) and gel barriers (Seprafilm, Spraygel, autocrosslinked hyaluronic acid gel Hyalobarrier) to maintain opposing walls apart during healing {Tsapanos, 2002}; {Guida, 2004};{Abbott, 2004}, thereby preventing the reformation of adhesions. Antibiotic prophylaxis is necessary in the presence of mechanical barriers to reduce the risk of possible infections. A common pharmacological method for preventing reformation of adhesions is sequential hormonal therapy with estrogen followed by a progestin to stimulate endometrial growth and prevent opposing walls from fusing together {Roge, 1996}. However, there have been no randomized controlled trials (RCTs) comparing post-surgical adhesion reformation with and without hormonal treatment and the ideal dosing regimen or length of estrogen therapy is not known. The absence of prospective RCTs comparing treatment methods makes it difficult to recommend optimal treatment protocols. Furthermore, diagnostic severity and outcomes are assessed according to different criteria (e.g. menstrual pattern, adhesion reformation rate, conception rate, live birth rate). Clearly, more comparable studies are needed in which reproductive outcome can be analysed systematically.

Follow-up tests (HSG, hysteroscopy or SHG) are necessary to ensure that adhesions have not reformed. Further surgery may be necessary to restore a normal uterine cavity. According to a recent study among 61 patients, the overall rate of adhesion recurrence was 27.9% and in severe cases this was 41.9%.[28] Another study found that postoperative adhesions reoccur in close to 50% of severe AS and in 21.6% of moederate cases.[8] Mild IUA, unlike moderate to severe synechiae, do not appear to reform.

Prognosis

The extent of adhesion formation is critical. Mild to moderate adhesions can usually be treated with success. Extensive obliteration of the uterine cavity or fallopian tube openings (ostia) and deep endometrial or myometrial trauma may require several surgical interventions and/or hormone therapy or even be uncorrectable. If the uterine cavity is adhesion free but the ostia remain obliterated, IVF remains an option. If the uterus has been irreparably damaged, surrogacy or adoption may be the only options.

Patients who carry a pregnancy even after treatment of IUA may have an increased risk of having abnormal placentation including placenta accreta[29] where the placenta invades the uterus more deeply, leading to complications in placental separation after delivery. Premature delivery,[30] second-trimester pregnancy loss,[31] and uterine rupture[32] are other reported complications. They may also develop incompetent cervix where the cervix can no longer support the growing weight of the fetus, the pressure causes the placenta to rupture and the mother goes into premature labour. Cerclage is a surgical stitch which helps support the cervix if needed.[31]

Pregnancy and live birth rate has been reported to be related to the initial severity of the adhesions with 93, 78, and 57% pregnancies achieved after treatment of mild, moderate and severe adhesions, respectively and resulting in 81, 66, and 32% live birth rates, respectively.[8] The overall pregnancy rate after adhesiolysis was 60% and the live birth rate was 38.9% according to one study.[33]

Age is another factor contributing to fertility outcomes after treatment of AS. For women under 35 years of age treated for severe adhesions, pregnancy rates were 66.6% compared to 23.5% in women older than 35.[29]

Prevention

A review in 2013 came to the conclusion that there were no studies reporting on the link between intrauterine adhesions and long-term reproductive outcome after miscarriage, while similar pregnancy outcomes were reported subsequent to surgical management (e.g. D&C), medical management or conservative management (that is, watchful waiting).[26] There is an association between surgical intervention in the uterus and the development of intrauterine adhesions, and between intrauterine adhesions and pregnancy outcomes, but there is still no clear evidence of any method of prevention of adverse pregnancy outcomes.[26]

In theory, the recently pregnant uterus is particularly soft under the influence of hormones and hence, easily injured. D&C (including dilation and curettage, dilation and evacuation/suction curettage and manual vacuum aspiration) is a blind, invasive procedure, making it difficult to avoid endometrial trauma. Medical alternatives to D&C for evacuation of retained placenta/products of conception exist including misoprostol and mifepristone. Studies show this less invasive and cheaper method to be an efficacious, safe and an acceptable alternative to surgical management for most women.[34][35] It was suggested as early as in 1993[21] that the incidence of IUA might be lower following medical evacuation (e.g. Misoprostol) of the uterus, thus avoiding any intrauterine instrumentation. So far, one study supports this proposal, showing that women who were treated for missed miscarriage with misoprostol did not develop IUA, while 7.7% of those undergoing D&C did.[36] The advantage of misoprostol is that it can be used for evacuation not only following miscarriage, but also following birth for retained placenta or hemorrhaging.

Alternatively, D&C could be performed under ultrasound guidance rather than as a blind procedure. This would enable the surgeon to end scraping the lining when all retained tissue has been removed, avoiding injury.

Early monitoring during pregnancy to identify miscarriage can prevent the development of, or as the case may be, the recurrence of AS, as the longer the period after fetal death following D&C, the more likely adhesions may be to occur.[21] Therefore, immediate evacuation following fetal death may prevent IUA.

The use of hysteroscopic surgery instead of D&C to remove retained products of conception or placenta is another alternative that could theoretically improve future pregnancy outcomes, although it could be less effective if tissue is abundant. Also, hysteroscopy is not a widely or routinely used technique and requires expertise.

There is no data to indicate that suction D&C is less likely than sharp curette to result in Asherman's. A recent article describes three cases of women who developed intrauterine adhesions following manual vacuum aspiration.[37]

References

  1. 1 2 Schorge, John O.; et al. (2008). Williams Gynecology. New York: McGraw-Hill Medical. ISBN 9780071472579.
  2. 1 2 Palter S (2005). "High Rates of Endometriosis in Patients With Intrauterine Synechiae (Asherman’s Syndrome)". Fertility and Sterility 86 (null): S471–S471. doi:10.1016/j.fertnstert.2005.07.1239.
  3. ↑ synd/1521 at Who Named It?Fritsch H, Ein Fall von volligem Schwaund der Gebormutterhohle nach Auskratzung. Zentralbl Gynaekol 1894; 18:1337-1342.
  4. ↑ Adhesions & Asherman's Syndrome
  5. ↑ Asherman JG. (December 1950). "Traumatic intra-uterine adhesions". J Obstet Gynaecol Br Em 57 (6): 892–6. doi:10.1111/j.1471-0528.1950.tb06053.x. PMID 14804168.
  6. ↑ Klein SM, Garcia C-R (1973). "Asherman's syndrome: a critique and current review". Fertility and Sterility 24 (9): 722–735. PMID 4725610.
  7. 1 2 3 Schenker JG, Margalioth EJ. (1982). "Intra-uterine adhesions: an updated appraisal". Fertility and Sterility 37 (5): 593–610. PMID 6281085.
  8. 1 2 3 4 Valle RF, and Sciarra JJ (1988). "Intrauterine adhesions: Hystreoscopic diagnosis, classification, treatment and reproductive outcome". Am J Obstet 158 (6Pt1): 1459–1470. doi:10.1016/0002-9378(88)90382-1. PMID 3381869.
  9. 1 2 3 Buttram VC, Turati, G (1977). "Uterine synechiae: variations in severity and some conditions which may be conducive to severe adhesions". Int J Fertil 22 (2): 98–103. PMID 20418.
  10. 1 2 Rochet Y, Dargent D, Bremond A, Priou G, Rudigoz RC (1979). "The obstetrical outcome of women with surgically treated uterine synechiae (in French)". J Gynecol Obstet Biol Reprod 8 (8): 723–726. PMID 553931.
  11. ↑ Krolikowski A, Janowski K, Larsen JV. (1995). "Asherman syndrome caused by schistosomiasis". Obstet Gynecol. 85 (5Pt2): 898–9. doi:10.1016/0029-7844(94)00371-J. PMID 7724154.
  12. ↑ Netter AP, Musset R, Lambert A Salomon Y (1956). "Traumatic uterine synechiae: a common cause of menstrual insufficiency, sterility, and abortion". Am J Obstet Gynecol. 71 (2): 368–75. PMID 13283012.
  13. ↑ Bukulmez O, Yarali H, Gurgan T. (1999). "Total corporal synechiae due to tuberculosis carry a very poor prognosis following hysteroscopic synechialysis". Hum Reprod 14 (8): 1960–1961. doi:10.1093/humrep/14.8.1960. PMID 10438408.
  14. ↑ Stillman RJ, Asarkof, N (1985). "Association between mullerian duct malformations and Asherman syndrome in infertile women". Obstet Gynecol 65 (5): 673–7. PMID 3982744.
  15. ↑ Worthen NJ, Gonzalez F. (1984). "Septate uterus: sonographic diagnosis and obstetric complications". Obstet Gynecol 64 (3 Suppl): 34S–38S. doi:10.1097/00006250-198409001-00009. PMID 6472746.
  16. ↑ March CM. (1995). "Intrauterine adhesions". Obstet Gynecol Clin N Am 22 (3): 98–103. PMID 8524533.
  17. ↑ Parent B, Barbot J, Dubuisson JB. Uterine synechiae (in French). Encyl Med Chir Gynecol 1988; 140A (Suppl): 10-12.
  18. ↑ Adoni A, Palti Z, Milwidsky A, Dolberg M. (1982). "The incidence of intrauterine adhesions following spontaneous abortion". Int J Fertil. 27 (2): 117–118. PMID 6126446.
  19. ↑ Westendorp ICD, Ankum WM, Mol BWJ, Vonk J. (1998). "Prevalence of Asherman's syndrome after secondary removal of placental remnants or a repeat curettage for incomplete abortion". Hum Reprod 13 (12): 3347–3350. doi:10.1093/humrep/13.12.3347. PMID 9886512.
  20. ↑ Fedele L, Bianchi S, Frontino G (December 2006). "Septums and synechiae: approaches to surgical correction". Clin Obstet Gynecol 49 (4): 767–88. doi:10.1097/01.grf.0000211948.36465.a6. PMID 17082672.
  21. 1 2 3 Friedler S, Margalioth EJ, Kafka I, Yaffe H. (1993). "Incidence of postabortion intra-uterine adhesions evaluated by hysteroscopy: a prospective study". Hum Reprod 8 (3): 442–444. PMID 8473464.
  22. ↑ Dmowski WP, Greenblatt RB. (1969). "Asherman's syndrome and risk of placenta accreta". Obstet Gynecol 34 (2): 288–299. PMID 5816312.
  23. ↑ Rabau E, David A. (1963). "Intrauterine adhesions:etiology, prevention, and treatment". Obstet Gynecol 22: 626–629. PMID 14082285.
  24. ↑ Toaff R. (1966). "Some remarks on posttraumatic uterine adhesions.in French". Rev Fr Gynecol Obstet 61 (7): 550–552. PMID 5940506.
  25. ↑ Ventolini G, Zhang M, Gruber J. (2004). "Hysteroscopy in the evaluation of patients with recurrent pregnancy loss: a cohort study in a primary care population". Surg Endosc 18 (12): 1782–1784. doi:10.1007/s00464-003-8258-y. PMID 15809790.
  26. 1 2 3 Hooker, A. B.; Lemmers, M.; Thurkow, A. L.; Heymans, M. W.; Opmeer, B. C.; Brolmann, H. A. M.; Mol, B. W.; Huirne, J. A. F. (2013). "Systematic review and meta-analysis of intrauterine adhesions after miscarriage: Prevalence, risk factors and long-term reproductive outcome". Human Reproduction Update 20 (2): 262–78. doi:10.1093/humupd/dmt045. PMID 24082042.
  27. ↑ Kodaman PH, Arici AA. (2007). "Intra-uterine adhesions and fertility outcome: how to optimize success?". Current Opinion in Obstetrics and Gynecology 19 (3): 207–214. doi:10.1097/GCO.0b013e32814a6473. PMID 17495635.
  28. ↑ Yu D, Li T, Xia E, Huang X, Peng X. (2008). "Factors affecting reproductive outcome of hysteroscopic adhesiolysis for Asherman's syndrome". Fertility and Sterility 89 (3): 715–722. doi:10.1016/j.fertnstert.2007.03.070. PMID 17681324.
  29. 1 2 Fernandez H, Al Najjar F, Chauvenaud-Lambling; et al. (2006). "Fertility after treatment of Asherman's syndrome stage 3 and 4". J Minim Invasive Gynecol 13 (5): 398–402. doi:10.1016/j.jmig.2006.04.013. PMID 16962521.
  30. ↑ Roge, P; D'ercole, C; Cravello, L; Boubli, L; Blanc, B (1996). "Hysteroscopic management of uterine synechiae: a series of 102 observations". Eur J Obstet Gynecol Reprod Biol 65 (2): 189–193. doi:10.1016/0301-2115(95)02342-9. PMID 8730623.
  31. 1 2 Capella-Allouc S, Morsad F, Rongieres-Bertrand C; et al. (1999). "Hysteroscopic treatment of severe Asherman's syndrome and subsequent fertility". Hum Reprod 14 (5): 1230–1233. doi:10.1093/humrep/14.5.1230. PMID 10325268.
  32. ↑ Deaton JL, Maier D, Andreoli J. (1989). "Spontaneous uterine rupture during pregnancy after treatment of Asherman's syndrome". Am J Obstet Gynecol 160 ((5Pt1)): 1053–1054. doi:10.1016/0002-9378(89)90159-2. PMID 2729381.
  33. ↑ Siegler AM, Valle RF. (1988). "Therapeutic hysteroscopic procedures". Fertil Steril 50 (5): 685–701. PMID 3053254.
  34. ↑ Zhang J, Gilles JM, Barnhart K, Creinin MD, Westhoff C, Frederick MM (2005). "National Institute of Child Health Human Development (NICHD) Management of Early Pregnancy Failure Trial. A comparison of medical management with misoprostol and surgical management for early pregnancy failure". N Engl J Med. 353 (8): 761–9. doi:10.1056/NEJMoa044064. PMID 16120856.
  35. ↑ Weeks A, Alia G, Blum J, Winikoff B, Ekwaru P, Durocher J, Mirembe F. (2005). "A randomized trial of misoprostol compared with manual vacuum aspiration for incomplete abortion". Obstet Gynecol. 106 (3): 540–7. doi:10.1097/01.AOG.0000173799.82687.dc. PMID 16135584.
  36. ↑ Tam WH, Lau WC, Cheung LP, Yuen PM, Chung TK. (2002). "Intrauterine adhesions after conservative and surgical management of spontaneous abortion". J Am Assoc Gynecol Laparosc. 9 (2): 182–185. doi:10.1016/S1074-3804(05)60129-6. PMID 11960045.
  37. ↑ Dalton VK, Saunders NA, Harris LH, Williams JA, Lebovic DI (2006). "Intrauterine adhesions after manual vacuum aspiration for early pregnancy failure". Fertil. Steril. 85 (6): 1823.e1–3. doi:10.1016/j.fertnstert.2005.11.065. PMID 16674955.

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