Sunday 9 November 2014

Literature Review --- Infertility

2 Literature Review
2.2 Aetiology
The causes of infertility are variable with regard to the social and demographic profile of the individuals. The WHO provides a statistical analysis about the causes of infertility.
This study will concentrate mainly on the female pelvic causes of infertility rather than including all the general causes.
2-2-1.Uterine factors
Uterine factors represent 2-3% of the incidence of infertility and intrauterine pathology is the much more common in infertile women (40-50%) (Niknejadi & Haghighi 2012), therefore, female reproductive tract should be examined for any probable causes of infertility first part of the reproductive tract is the cervical canal. An irregular cervical mucus component, which interacts with the sperm, is not often regarded as one of the leading causes of infertility. However, the postcoital test (pct), the measurement and observance of the presence of the active sperm in the cervical mucus is still one of the infertility evaluation tests. Coussein and Vlahos (2012) identified that the uterine abnormality is relatively uncommon causes of female reproductive failure. Uterine malformation caused by mu¨llerian fusion defects are the most common types of congenital anomalies of the reproductive system (Homer et al 2000). This type of anomalies may occur during the Mu¨llerian developmental process (Saravelos, Cocksedge & Li 2008), (Wold, Pham, and Arici 2006). Furthermore, American Society of Reproductive Medicine developed specific calcification of the uterine malformation regarding the degree of failure of development of the Mu¨llerian duct. This calcification has become the most widely accepted and used globally, their calcification consist of seven regions 
(1) Mu¨llerian hypoplasia which may include the vagina, the cervix, the fundus, the tubes, or combined
 (2) Unicornuate uterus hypoplasia of one of the two Mu¨llerian ducts and this could be subdivided according to the present or absence of the rudimentary horn
 (3) Didelphys uterus (failure of lateral fusion of the vagina and uterus Mu¨llerian ducts)
(4) Bicornuate uterus (incomplete fusion of the uterine horns at the level of the fundus), which may be partial or Complete.
(5) Septate uterus (absent or incomplete resorption of the uterovaginal septum), ether Complete or Partial
(6) Arcuate uterus (a mild indentation at the level of the fundus)
(7) Diethylstilbestrol (DES) exposed uterus (T-shaped uterus resulting from DES exposure of the patient in utero)
Inthis calcification, there is no specific procedure or criteria for the diagnosis of each anomalies and the result will depend on the clinician impression (Woelfer et al 2001).It is important to know that this calcification exclude some of the other anomalies such as cervical atresia, vaginal anastomosis and vaginal septum (Pavone et al 2006).The diagnosis and indications for the treatment vary according to the different types of malformation. The septet uterus is the most common uterine anomalies among the other kind of anomalies (Homer et al 2000).
Figure F1    Calcification of the uterine malformation according to the American Society of   Reproductive Medicine ( Lee & Ku 2011).
Repair of these Müllerian anomalies or Caesarean section may result in synergy Uterine synechiae or uterine atresis and these can be defined as the presence of intrauterine adhesions (IUAs) or combined of fibrotic tissue can be either partial or complete (serious and severe adhesions resulting in menstrual dysfunction and infertility) (Ahmadi & Javam 2014).Imaging methods used in the diagnosis of these anomalies will be discussed in details in the next section.

2.2.2. Tubal-peritoneal factors.
In about 25–35 % of women, the risk factors for infertility are the result of the tubal peritoneal pathology. Pelvic inflammatory disease (PID) is the most common disease .In more than half of the these cases, tubal peritoneal factor infertility may occur as a result of ectopic pregnancy, pelvic PID, endometriosis, and pelvic or adnexal adhesions.  These factors may reveal some sort of pathology but cannot adequately specify the diagnosis (Coussein and Vlahos 2012). The outer end or ampullar section is responsible for Fertilization and the Fallopian tubes are responsible for oocyte uptake. For this reason, any change in anatomical or physiological aspect of the tubes is usually associated with the cause of the infertility. For example, contraceptives have a certain effect on fertility.  Brugo-Olmedo, Chillik and Kopelman (2002) also emphasised on this fact that there is an association between endometriosis and infertility.   Their study demonstrated approximately 48% infertile patients were found to have endometriosis compared with 5% of the normal fertile patient.Also, another study also found that 30-50 % of the patient with endometriosis were infertile (Bulletti et al 2010).  Endometriosis is actually the condition which is identified as the presence of endometrial tissue, stroma or glandes out of the uterine cavity, which leads to the onset ofchronic inflammatory reaction. It may affect about5-15% of women in their reproductive period.  Bulletti et al (2010) did an extensive research to explain the relation between infertility and endometriosis. They found that the prevalence of infertility in the females with endometriosis may relate to several situations such as anatomical disorders, anovulation and changing of the luteal phase. Abrao (2013) was also of the similar opinion. Some authors have identified that the changes in receptivity of endometriosis may affect on uterine implantation
    


   
 


References
Abrao, M.S., Muzii, L. & Marana, R.( 2013). Anatomical causes of female infertility and their management. International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 123 Suppl 2, pp.S18–24. Available at: http://www.ncbi.nlm.nih.gov/pubmed/24119894 [Accessed September 26, 2014].
Brugo-Olmedo, S., Chillik, C. & Kopelman, S. ( 2002). Review Definition and causes of infertility. Reproductive BioMedicine Online, 2(1), pp.173–185. Available at: http://dx.doi.org/10.1016/S1472-6483(10)62193-1.
Bulletti, C. et al., 2010. Endometriosis and infertility. Journal of assisted reproduction and genetics, 27(8), pp.441–7. Available at: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=2941592&tool=pmcentrez&rendertype=abstract [Accessed September 23, 2014].
Choussein, S. & Vlahos, N.F.( 2012). Female Fertility Assessment. Current Obstetrics and Gynecology Reports, 1(4), pp.174–181. Available at: http://link.springer.com/10.1007/s13669-012-0022-7 [Accessed September 23, 2014].
Derchi, L.E. et al.(2001). Ultrasound in gynecology. European radiology, 11(11), pp.2137–55. Available at: http://www.ncbi.nlm.nih.gov/pubmed/11702153 [Accessed September 23, 2014].
Fughesu, A. M., Ciampelli, M., Belosi, C., Apa, R., Pavone, V., & Lanzone, A. (2001). A new   ultrasound criterion for the diagnosis of polycystic ovary syndrome: the ovarian stroma/total area ratio. Fertility and sterility, 76(2), 326-331.Available at: http://www.sciencedirect.com/science/article/pii/S0015028201019197 [Accessed September 22, 2014].

Healy, D. L., Trounson, A. O. And Andersen, A. N. (1994). Female infertility: causes and treatment. [online] Lancet, 343(8912), pp.1539–44. Available at: http://www.ncbi.nlm.nih.gov/pubmed/7914278.
Homer, H. A., Li, T. C., & Cooke, I. D. (2000). The septate uterus: a review of  management and reproductive outcome. Fertility and sterility, 73(1), 1-14.
Karimpour A, Esmaeelenezhad A, Moslemizadeh, N, Mousanezhad. N, Peyvandi, S, Gahandar, M.(2005). Incidence and main causes of infertility in patients attending the infertility center of Imam khomeini hospital in 2002-2004. J Mazandaran Univ Med Sci.; 15 (49) :44-49

Krishnan, Sandhya, et al. (2011). Ovarian torsion in infertility management - missing the diagnosis means losing the ovary: A high price to pay. [online]. Journal of human reproductive sciences, 4 (1), 39-42. at: http://shu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwXV2xCgIxDC3uLoLi6A-cNEl7bWfx8AP0A5K0HW-6_8e2CIpblkCGkATee3nGEF7t9DcTGFV8je18rs7bLEChoESYsSjBcGj5vjH4pQQuB7Mr69G8lvvz9pg-BgGTUoftY3JjAXd9qXZT70jAQVRQBqBXs2sN6gtVmyS00yK3gFmLRhYQByez504kX7chOMtnc-nVWSvqOZCbUZLmJFkyYEu07N4_BjhF .
Lankford, J.C., Mancuso, P. & Appel, R., 2013. Congenital Reproductive Abnormalities. Journal of midwifery & women’s health, pp.546–551. Available at: http://www.ncbi.nlm.nih.gov/pubmed/24033893 [Accessed September 23, 2014].
Legro, R.S., Strauss, J.F.( 2002). Molecular progress in infertility : polycystic Overy Syndrome . , 78(3).

Saravelos, S., Cocksedge, K. & LI, T. (2008). Prevalence and diagnosis of congenital uterine anomalies in women with reproductive failure: a critical appraisal. Human Reproduction Update, 14(5), pp.415–429. Available at: http://humupd.oxfordjournals.org/content/14/5/415.short [Accessed September 22, 2014].
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Lee HJ, Ku SY.( 2011).  Diagnosis and current treatment of Müllerian duct anomaly.   Korean J Obstet Gynecol.Mar; 54(3):132-139.  Available at
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