Volume 14, Issue 9 (9-2016)                   IJRM 2016, 14(9): 583-588 | Back to browse issues page


XML Persian Abstract Print


Download citation:
BibTeX | RIS | EndNote | Medlars | ProCite | Reference Manager | RefWorks
Send citation to:

Salehpour S, Zamaniyan M, Saharkhiz N, Zadeh modares S, Hosieni S, Seif S, et al . Does intrauterine saline infusion by intrauterine insemination (IUI) catheter as endometrial injury during IVF cycles improve pregnancy outcomes among patients with recurrent implantation failure?: An RCT. IJRM 2016; 14 (9) :583-588
URL: http://ijrm.ir/article-1-782-en.html
1- Preventive Gynecology Research Center (PGRC), Shahid Beheshti University of Medical Sciences, Tehran, Iran
2- Preventive Gynecology Research Center (PGRC), Shahid Beheshti University of Medical Sciences, Tehran, Iran , marziehzamaniyan@gmail.com
3- Department of Veterinary Theriogenology and Obstetric, Tehran University of Medical Sciences, Tehran, Iran
4- Department of Health and Community Medicine, Faculty of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran
Full-Text [PDF 355 kb]   (933 Downloads)     |   Abstract (HTML)  (3911 Views)
Full-Text:   (435 Views)
Introduction
 
In assisted reproductive technology (ART), embryo culture conditions and transfer methods have improved over recent decades, but the pregnancy and delivery rate has not increased. It is predicted that about 10% of women who undergo in vitro fertilization (IVF) treatment will face specific problems (1). Recurrent implantation failure (RIF) is a main cause of repeated IVF failure (2). There are some differences in definition of RIF. One favorable definition of RIF is having at least three unsuccessful IVF with transfer of good-quality embryos without a successful implantation or alternatively another definition is when women fail to conceive from IVF after cumulative transfers exceeding 10 high-quality embryos (3). RIF is the most important dilemma that physicians and patients frequently encountered with it. Among the different causes of RIF, uterine factors, including thin endometrium, poor endometrial receptivity and immunological factors have received more attention (4). Numerous signaling molecules, including cytokines, growth factors and interleukins are secreted from the endometrium, which could modify endometrial receptivity and dysregulation of these factors, can result in RIF (5-7).
Several studies have indicated that local endometrial injury (EI) caused by hysteroscopy, scratching or biopsies during IVF cycles are associated with local inflammatory response which subsequently leads to improved implantation and pregnancy among women with RIF (8-20).
There is also some evidence showing that EI in IVF cycles immediately after oocyte retrieval does not have any deleterious effects on embryo implantation, but adverse effects could be observed when the biopsy is performed immediately before embryo transfer (21, 22). Some other studies have suggested that EI during the ongoing stimulation cycle could cause better pregnancy outcomes (9, 18, 23). Nevertheless, one study reported that EI on the day of oocyte retrieval had negative effects on clinical outcomes (24). There is also some evidence indicating that hysteroscopy per se in early follicular phase of proceeding cycles of IVF causes a higher pregnancy rate in experimental patients compared to the control group (14-16, 20).
The present study is the first study to investigate the intrauterine saline infusion as endometrial injury among RIF patients, which seems to act like hysteroscopy alone. In the present study, we assumed that, if a local EI can be a helpful factor for increased pregnancy outcomes, a local mechanical injury by intrauterine saline infusion and subsequently suctioning it at day 3-5 of ovarian stimulation during ongoing IVF cycle should produce similar effects with lower costs and complications compared to hysteroscopy or biopsy.
 
Materials and methods
 
The present study was approved by the institutional ethics committee review board of Shahid Beheshti University of Medical Science, Tehran, Iran. All women gave written informed consent before the start of the study.
 
Patients
A total of 63 women with RIF were recruited in this clinical trial study which was done in Taleghani Hospital, Tehran, Iran, during April to December 2014. Finally, 59 women, who had failed three or more in vitro fertilization-embryo transfer (IVT-ET) cycles or took replacement of more than 10 embryos in previous failed IVF-ET cycles, met our criteria and recruited for the study. Women aged 20-40 years old with body mass index (BMI) ≤30 kg/m2 or ≥ 18 kg/m2, who underwent fresh intra cytoplasmic sperm injection-embryo transfer (ICSI-ET) cycles, and had normal endometrial thickening (7-12 mm) on the day of oocyte retrieval and did not have any visible endometrial pathology were included within the study. Women with poor ovarian reserve (defined as serum level or anti-Müllerian hormone (AMH) ≤1.1 ng/mL or antral follicular count (AFC) <5 or ≤3 oocytes were retrieved in previous IVF cycles), advanced endometriosis, pelvic or uterine adhesion, hypothyroidism and hyperprolactinemia, genital tuberculosis or two or less previous IVF failures were excluded (32).
Work up of RIF, such as ruling out uterine pathology (synechia, sub mucosal myoma, polyp) using diagnostic hysteroscopy, an autoimmune serology test and karyotype of couples, was performed for all participants. Couples, in whom there was no evidence of pathology, received an offer to undergo intra uterine saline infusion during ongoing assisted reproduction cycles. Out of 59 participants 20 women agreed and underwent this procedure and the remaining 39 patients underwent regular IVF.
 
Hyper stimulation protocol and saline infusion procedure
All women underwent GnRH antagonist protocol as follow: controlled ovarian stimulation (COS) started using recombinant FSH (rFSH, Gonal-F; Merck Serono SA, Geneva, Switzerland) 225-400 IU/day for the first five days. Subsequently, the rFSH dose was adjusted along with ovarian response, every other day. During the COS in the intervention group, intrauterine saline infusion procedure was performed on day 3-5 of stimulation using a gynecologic examination table.
No drug or anesthesia was used. Cusco’s speculum was inserted through the vagina in order to visualize the cervical orifice. After sterilization with Povidone iodine (10%) and full irrigation with normal saline, intrauterine insemination (IUI) catheter (Biorade, Berkeley, California) was introduced gently into the uterine cavity with a syringe and then 20ml of normal saline was introduced into the uterine cavity and aspirated immediately. Then follicular tracking and endometrial measurement were completed using a 7.5 MHZ transvaginal ultrasound transducer.
GnRH antagonist (Cetrotide 0.25 mg; Merck Serono SA) was started once the leading follicle reached 14-15 mm, and was continued until the day of hCG injection. A recombinant hCG (Ovitrelle; Merck Serono SA, Geneva, Switzerland, 250 μg) was injected to trigger final follicular maturation when three or more follicles reached a mean diameter of ≥17 mm (25). Oocyte retrieval was performed 36 hrs later under conscious sedation. Then each oocyte was denudated with hyaluronidase.
Conventional Intra-Cytoplasmic Sperm Injection (ICSI) was performed for all patients. The embryo grading was based on Veeck’s classification (26). One to two good or top quality embryos were transferred 72-96 hr after oocyte retrieval. Luteal phase was supported by the administration of micronized progesterone (600mg/day, Cyclogest; Actavis; Barnstaple; UK), which was stopped if the pregnancy test (serum β-HCG level test performed on day 15 after embryo transfer), was negative or after 12 wks of pregnancy.
 
Statistical analysis
Based on an Altman’s nomogram by power of 65% and a Standardized Difference of 0.6 to detect significant differences between two study groups, with respect to the pregnancy rate according to the previous pilot report on endometrial biopsy for increasing the success rate in IVF cycles, 20 cycles of IVF were required for each group (9).
We included 39 patients (about two times the number of case group) as the control group for achieving more reliable results. The statistical software package SPSS for windows, version 21.0 (SPSS, Armonk, NY: IBM Corp) was used for data analysis. T-test was used to compare the results between the groups. The proportions were compared using the c2test. p˂0.05 were considered as significant.
 
Results
 
During the eight-month period (April to December 2014), a total of 63 patients with RIF were recruited. Of these, 59 women met our inclusion criteria.Finally, 20 women were assigned to the intervention group after agreeing to undergo the new method and 39 remaining patients were included in the control group (Figure 1). The mean±SD age among the women in the intrauterine saline infusion group was 37.7±5.63 years and in the control group it was 34.0±6.04 years (p=0.49). Baseline and clinical characteristics among RIF patients with or without the intrauterine saline infusion procedures are presented (Table I).
Chemical (2 vs. 9, p=0.03), and clinical pregnancy numbers (1 vs. 9, p=0.01), as well as implantation rates (4.7% vs. 41.6%, p=0.0035), were significantly higher in control group compared to those in the saline infusion group. There was no significant difference in miscarriage rates (9.4% vs. 8.7%, p=0.403) and multiple pregnancy numbers (1 vs. 3, p=0.39) between two groups (Table II).


Table I. Baseline characteristics in RIF patients with and without the intrauterine saline infusion

Data are presented as Mean ± SD.                                            Independent t test was used. 


Table II. Comparison of clinical outcomes in RIF patients with and without the intrauterine saline infusion

* Data are presented as %.                                                       ** Data are presented as Mean±SD
a c2 test                                                                                     b Independent t test



Figure 1. Flow chart of the eligible patients.


Discussion
 
In this present study, we investigated the effects of intrauterine saline infusion as endometrial injury on day 3-5 during ongoing ovarian stimulation in IVF cycles on pregnancy and implantation rates. Our objective was to introduce intrauterine saline infusion as a novel procedure to induce endometrial injury for improving implantation in IVF cycles for patients with RIF.
Some animal studies have reported that oil injections into the uterine cavity result in uterine decidualization (27, 28). We assumed that if hysteroscopy without biopsy has been found in some studies to lead to increased pregnancy rate, a less invasive procedure like intrauterine saline infusion, which has no adverse effects or does not require anesthesia, may improve implantation in IVF cycles as well (14-16). Contrary to previous results, our study showed that chemical and clinical pregnancy and implantation rates were significantly lower in intervention compared with control group (9-11, 18, 20, 29).
There are inconsistent clinical results concerning EI. Some studies have reported that endometrial injury causes better clinical outcomes, but other studies have reported similar results (9, 10, 12, 18, 20, 29, 30). In one meta-analysis, mechanical endometrial injury (by hysteroscopy or biopsy or scratching) carried out as ovarian stimulation during IVF cycle was found to increase clinical pregnancy rates in women with RIF. The authors concluded that this procedure may yield iatrogenic effects and it should not be done routinely in clinical practice due to insufficient evidence (10).
In a recent Cochrane's review by Nastri et al it was reported that EI in women undergoing ART between seven days of preceding cycle and the day of ET cycle versus no intervention was associated with increased live birth rate (LBR) in women with more than two previous embryo transfers. These researchers found no evidence regarding the effect of EI on miscarriage, multiple pregnancies or bleeding except mild pain (11). In another study, endometrial scratching by Pipple twice on day 21 or 22 immediately prior to IVF cycle, had similar LBR compared to the control group, but in a subgroup of patients with two or more previous IVF failures, it improved LBR. These researchers noted that this procedure should be used in luteal phase of preceding IVF cycle to stimulate gene expression for implantation, since when this procedure was used in the pre ovulatory phase of the ongoing IVF cycle; it could disrupt the endometrial proliferation and embryo implantation (30).
In contrast Baum et al reported that local injury to the endometrium by Pipple twice in follicular and luteal phase of preceding IVF cycle did not have any benefits in high-order RIF patients and that clinical outcomes in the intervention group were significantly lower than those in the control group. They suggested that these lower clinical results might be due to intrinsic embryonic factors in high-order RIF patients and did not correlate with endometrial receptivity (31). To our knowledge the present study is the only study aiming to incorporate an intra-uterine saline infusion procedure as local endometrial injury to improve pregnancy outcomes.
This experimental study included only 20 patients undergoing this procedure, but the sample size was insufficient to demonstrate definitive unfavorable results. Our results suggested that patients with RIF get no advantage from injury to the endometrium as intra uterine saline infusion in ongoing cycle.
 
Conclusion
 
When intrauterine saline infusion as a form of endometrial injury is performed during the ongoing IVF cycles it has negative effect on reproductive outcomes among patients with recurrent implantation failure.
 
Acknowledgments
 
With thanks to the health providers and patients at Shahid Beheshti University and Taleghani Hospital for their assistance.
 
Conflict of interest
 
The authors have no conflict of interest with the subject matter of the present manuscript.
 
Type of Study: Original Article |

References
1. Kupka MS, Ferraretti AP, de Mouzon J, Erb K, D'Hooghe T, Castilla JA, et al. Assisted reproductive technology in Europe, 2010: results generated from European registers by ESHRE. Hum Reprod 2014; 29: 2099-2113. [DOI:10.1093/humrep/deu175]
2. Coughlan C, Ledger W, Wang Q, Liu F, Demirol A, Gurgan T, et al. Recurrent implantation failure: definition and management. Reprod Biomed Online 2014; 28: 14-38. [DOI:10.1016/j.rbmo.2013.08.011]
3. Patil M. Recurrent Implantation Failure. In: Rao KA, et al (Eds.), Principles and Practice of Assisted Reproductive Technology. India, Jaypee Brothers Medical Publishers; 2014: 704-705.
4. Margalioth EJ, Ben-Chetrit A, Gal M, Eldar-Geva T. Investigation and treatment of repeated implantation failure following IVF-ET. Hum Reprod 2006; 21: 3036-3043. [DOI:10.1093/humrep/del305]
5. Aghajanova L. Leukemia inhibitory factor and human embryo implantation. Ann N Y Acad Sci 2004; 1034: 176-183. [DOI:10.1196/annals.1335.020]
6. Kao LC, Tulac S, Lobo S, Imani B, Yang JP, Germeyer A, et al. Global gene profiling in human endometrium during the window of implantation. Endocrinology 2002; 143: 2119-2138. [DOI:10.1210/endo.143.6.8885]
7. Horcajadas JA, Pellicer A, Simón C. Wide genomic analysis of human endometrial receptivity: new times, new opportunities. Hum Reprod Update 2007; 13: 77-86. [DOI:10.1093/humupd/dml046]
8. Kalma Y, Granot I, Gnainsky Y, Or Y, Czernobilsky B, Dekel N, et al. Endometrial biopsy-induced gene modulation: first evidence for the expression of bladder-transmembranal uroplakin Ib in human endometrium. Fertil Steril 2009; 91: 1042-1049. [DOI:10.1016/j.fertnstert.2008.01.043]
9. Huang SY, Wang CJ, Soong YK, Wang HS, Wang ML, Lin CY, et al. Site-specific endometrial injury improves implantation and pregnancy in patients with repeated implantation failures. Reprod Biol Endocrinol 2011; 9: 140. [DOI:10.1186/1477-7827-9-140]
10. Potdar N, Gelbaya T, Nardo LG. Endometrial injury to overcome recurrent embryo implantation failure: a systematic review and meta-analysis. Reprod Biomed Online 2012; 25: 561-571. [DOI:10.1016/j.rbmo.2012.08.005]
11. Nastri CO, Lensen SF, Gibreel A, Raine-Fenning N, Ferriani RA, Bhattacharya S, et al. Endometrial injury in women undergoing assisted reproductive techniques. Cochrane Database Syst Rev 2015; 3: CD009517. [DOI:10.1002/14651858.CD009517.pub3]
12. Bosteels J, Weyers S, Puttemans P, Panayotidis C, Van Herendael B, Gomel V, et al. The effectiveness of hysteroscopy in improving pregnancy rates in subfertile women without other gynaecological symptoms: a systematic review. Hum Reprod Update 2010; 16: 1-11. [DOI:10.1093/humupd/dmp033]
13. Gnainsky Y, Granot I, Aldo PB, Barash A, Or Y, Schechtman E, et al. Local injury of the endometrium induces an inflammatory response that promotes successful implantation. Fertil Steril 2010; 94: 2030-2036. [DOI:10.1016/j.fertnstert.2010.02.022]
14. Demirol A, Gurgan T. Effect of treatment of intrauterine pathologies with office hysteroscopy in patients with recurrent IVF failure. Reprod Biomed Online 2004; 8: 590-594. [DOI:10.1016/S1472-6483(10)61108-X]
15. Rama Raju GA, Shashi Kumari G, Krishna KM, Prakash GJ, Madan K. Assessment of uterine cavity by hysteroscopy in assisted reproduction programme and its influence on pregnancy outcome. Arch Gynecol Obstet 2006; 274: 160-164. [DOI:10.1007/s00404-006-0174-7]
16. Karimzadeh MA, Ayazi Rozbahani M, Tabibnejad N. Endometrial local injury improves the pregnancy rate among recurrent implantation failure patients undergoing in vitro fertilisation/intra cytoplasmic sperm injection: a randomised clinical trial. Aust N Z J Obstet Gynaecol 2009; 49: 677-680. [DOI:10.1111/j.1479-828X.2009.01076.x]
17. Makrakis E, Hassiakos D, Stathis D, Vaxevanoglou T, Orfanoudaki E, Pantos K. Hysteroscopy in women with implantation failures after in vitro fertilization: findings and effect on subsequent pregnancy rates. J Minim Invasive Gynecol 2009; 16: 181-187. [DOI:10.1016/j.jmig.2008.12.016]
18. Narvekar SA, Gupta N, Shetty N, Kottur A, Srinivas M, Rao KA. Does local endometrial injury in the nontransfer cycle improve the IVF-ET outcome in the subsequent cycle in patients with previous unsuccessful IVF? A randomized controlled pilot study. J Hum Reprod Sci 2010; 3: 15-19. [DOI:10.4103/0974-1208.63116]
19. Barash A, Dekel N, Fieldust S, Segal I, Schechtman E, Granot I. Local injury to the endometrium doubles the incidence of successful pregnancies in patients undergoing in vitro fertilization. Fertil Steril 2003; 79: 1317-1322. [DOI:10.1016/S0015-0282(03)00345-5]
20. Raziel A, Schachter M, Strassburger D, Bern O, Ron-El R, Friedler S. Favorable influence of local injury to the endometrium in intracytoplasmic sperm injection patients with high-order implantation failure. Fertil Steril 2007; 87: 198-201. [DOI:10.1016/j.fertnstert.2006.05.062]
21. Abate V, De Corato R, Cali A, Stinchi A. Endometrial biopsy at the time of embryo transfer: correlation of histological diagnosis with therapy and pregnancy rate. J In Vitro Fertil Embryo Trans 1987; 4:173-176. [DOI:10.1007/BF01555466]
22. Ubaldi F, Bourgain C, Tournaye H, Smitz J, Van Steirteghem A, Devroey P. Endometrial evaluation by aspiration biopsy on the day of oocyte retrieval in the embryo transfer cycles in patients with serum progesterone rise during the follicular phase. Fertil Steril 1997; 67: 521-526. [DOI:10.1016/S0015-0282(97)80080-5]
23. Zhou L, Li R, Wang R, Huang HX, Zhong K. Local injury to the endometrium in controlled ovarian hyperstimulation cycles improves implantation rates. Fertil Steril 2008; 89: 1166-1176. [DOI:10.1016/j.fertnstert.2007.05.064]
24. Karimzade MA, Oskouian H, Ahmadi S, Oskouian L. Local injury to the endometrium on the day of oocyte retrieval has a negative impact on implantation in assisted reproductive cycles: a randomized controlled trial. Arch Gynecol Obstet 2010; 281: 499-503. [DOI:10.1007/s00404-009-1166-1]
25. Kim CH, You RM, Kang HJ, Ahn JW, Jeon I, Lee JW, et al. GnRH antagonist multiple dose protocol with oral contraceptive pill pretreatment in poor responders undergoing IVF/ICSI. Clin Exp Reprod Med 2011; 38: 228-233. [DOI:10.5653/cerm.2011.38.4.228]
26. Veeck L. The morphological assessment of human oocytes and early conception. In: Keel BA. Webster, BW., editors. Handbook of the laboratory diagnosis and treatment of infertility. Boca Raton FL: CRC Press; 1990: 353-69.
27. Humphrey KW. Interactions between oestradiol 3, 17 beta and progesterone on the induction and growth of deciduomata in ovariectomized mice. Aust J Biol Sci 1969; 22: 689-699. [DOI:10.1071/BI9690689]
28. Finn CA, Martin L. Endocrine control of the timing of endometrial sensitivity to a decidual stimulus. Biol Reprod 1972; 7: 82-86. [DOI:10.1093/biolreprod/7.1.82]
29. Parsanezhad ME, Dadras N, Maharlouei N, Neghahban L, Keramati P, Amini M. Pregnancy rate after endometrial injury in couples with unexplained infertility: A randomized clinical trial. Iran J Reprod Med 2013; 11: 869-874.
30. Gibreel A, El-Adawi N, Elgindy E, Al-Inany H, Allakany N, Tournaye H. Endometrial scratching for women with previous IVF failure undergoing IVF treatment. Gynecol Endocrinol 2015; 31: 313-316. [DOI:10.3109/09513590.2014.994603]
31. Baum M, Yerushalmi GM, Maman E, Kedem A, Machtinger R, Hourvitz A, et al. Does local injury to the endometrium before IVF cycle really affect treatment outcome? Results of a randomized placebo controlled trial. Gynecol Endocrinol 2012; 28: 933-936. [DOI:10.3109/09513590.2011.650750]
32. Ferraretti A, La Marca A, Fauser BC, Tarlatzis B, Nargund G, Gianaroli L, ESHRE working group on Poor Ovarian Response Definition. ESHRE consensus on the definition of 'poor response'to ovarian stimulation for in vitro fertilization: the Bologna criteria. Hum Reprod 2011; 26: 1616- 1624 [DOI:10.1093/humrep/der092]

Send email to the article author


Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Designed & Developed by : Yektaweb