<?xml version="1.0" encoding="UTF-8"?><!DOCTYPE article  PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "http://dtd.nlm.nih.gov/publishing/3.0/journalpublishing3.dtd"><article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="3.0" xml:lang="en" article-type="research article"><front><journal-meta><journal-id journal-id-type="publisher-id">OJOG</journal-id><journal-title-group><journal-title>Open Journal of Obstetrics and Gynecology</journal-title></journal-title-group><issn pub-type="epub">2160-8792</issn><publisher><publisher-name>Scientific Research Publishing</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.4236/ojog.2018.85048</article-id><article-id pub-id-type="publisher-id">OJOG-84327</article-id><article-categories><subj-group subj-group-type="heading"><subject>Articles</subject></subj-group><subj-group subj-group-type="Discipline-v2"><subject>Medicine&amp;Healthcare</subject></subj-group></article-categories><title-group><article-title>
 
 
  Recurrent Miscarriage: Hysteroscopy-Assisted Management
 
</article-title></title-group><contrib-group><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Fady</surname><given-names>M. Shawky Moiety</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref><xref ref-type="corresp" rid="cor1"><sup>*</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Abdel</surname><given-names>Fattah Agameya</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib><contrib contrib-type="author" xlink:type="simple"><name name-style="western"><surname>Hisham</surname><given-names>Aly Saleh</given-names></name><xref ref-type="aff" rid="aff1"><sup>1</sup></xref></contrib></contrib-group><aff id="aff1"><addr-line>Department of Obstetrics and Gynecology, Faculty of Medicine, Alexandria University, Alexandria, Egypt</addr-line></aff><author-notes><corresp id="cor1">* E-mail:<email>fmoeity@yahoo.com(FMSM)</email>;</corresp></author-notes><pub-date pub-type="epub"><day>03</day><month>05</month><year>2018</year></pub-date><volume>08</volume><issue>05</issue><fpage>425</fpage><lpage>430</lpage><history><date date-type="received"><day>21,</day>	<month>December</month>	<year>2017</year></date><date date-type="rev-recd"><day>1,</day>	<month>May</month>	<year>2018</year>	</date><date date-type="accepted"><day>4,</day>	<month>May</month>	<year>2018</year></date></history><permissions><copyright-statement>&#169; Copyright  2014 by authors and Scientific Research Publishing Inc. </copyright-statement><copyright-year>2014</copyright-year><license><license-p>This work is licensed under the Creative Commons Attribution International License (CC BY). http://creativecommons.org/licenses/by/4.0/</license-p></license></permissions><abstract><p>
 
 
  Objective:
  <b> </b>
  To apply office hysteroscopy in assessment/management of patients with recurrent miscarriage, thus to/or not to recommend office hysteroscopy as a routine procedure in such cases.
   
  <b>Study design</b>
  : Retrospective analysis. Setting: University hospital’s 
  outpatient abortion clinic
  . Subjects &amp; Methodology: Patients’ 
  records during the period between March 2015 and January 2017 for subjects
   
  with at least 2 previous miscarriages, who had undergone office hysteroscopy were reviewed. <b>Results:</b>
  <b> </b>
  Cases with 2 previous miscarriages (n = 95) were assessed and compared with those with 3 or more miscarriages (n = 105). Abnormal uterine findings were diagnosed in 24.1% of the former, and 43.8% of the latter group. The prevalence of uterine lesions among cases with 2 recurrent miscarriages was 42.1%; meanwhile, for subjects with 3 or more consecutive miscarriages, it was 43.8%.
   
  <b>Conclusion:</b>
  <b> </b>
  In addition to safety profile, simplicity and outpatient basis of use, outpatient hysteroscopy in recurrent miscarriages would be an added-value
   
  to practitioners as a diagnostic and therapeutic tool.
 
</p></abstract><kwd-group><kwd>Hysteroscopy</kwd><kwd> Office</kwd><kwd> Recurrent</kwd><kwd> Miscarriage</kwd></kwd-group></article-meta></front><body><sec id="s1"><title>1. Introduction</title><p>By definition, 3 pregnancy terminations in a row before 20 weeks, is termed recurrent pregnancy loss [<xref ref-type="bibr" rid="scirp.84327-ref1">1</xref>] . Some couples, however would start seeking a professional advice, and investigating recurrent miscarriages after the second pregnancy loss, as thought to be helping detect the cause early enough to treat. However, this has not been shown beneficial [<xref ref-type="bibr" rid="scirp.84327-ref2">2</xref>] . Uterine abnormalities, are implicated as one of the causes of recurrent miscarriages, and have been estimated to be diagnosed in as many as 10% to 15% of patients with repeated miscarriages. Exclusion of any intrauterine pathology is an important step before subjecting the patient to another pregnancy at risk [<xref ref-type="bibr" rid="scirp.84327-ref3">3</xref>] . Hysterosalpingogram (HSG) has classically been used to assess the uterine cavity for defects, Sonohysterography could be also used with more information on endometrial lesions, however, hysteroscopy, the gold standard for evaluating the uterine cavity, can be performed reliably and safely as an office, minimally invasive procedure [<xref ref-type="bibr" rid="scirp.84327-ref4">4</xref>] . The role of hysteroscopy is to detect possible intrauterine changes that could interfere with implantation or growth, or both, of the conceptus [<xref ref-type="bibr" rid="scirp.84327-ref5">5</xref>] . However the hysteroscopy is still an invasive procedure and its role in routine management of recurrent miscarriages is to be evaluated. Other tests for recurrent pregnancy loss may include investigating parental genetic disorders, thrombophilias, and maternal hormonal dysfunction [<xref ref-type="bibr" rid="scirp.84327-ref2">2</xref>] . The aim of this study was to test the application of office hysteroscopy in assessment/management of patients with recurrent miscarriage, thus to/or not to recommend it as a routine procedure in such cases.</p></sec><sec id="s2"><title>2. Subjects and Methodology</title><p>This retrospective study included patients’ medical record during the period between March 2015 and January 2017, at Shat by-Alexandria University hospital’s, recurrent miscarriage clinic. To be included, each record must confirm having two or more consecutive pregnancy losses before completing 20 weeks of gestation. In addition, having undergone an office hysteroscopy on outpatient basis under the care of the first author. Subjects with history of chromosomal defects, endocrinopathies, or thrombophilias were excluded. Office hysteroscopy (OH) was performed, using A2.9 mm semi-rigid hysteron scope (Gynecare, Ethicon, USA&#210;). Distention of the uterine cavity was accomplished with normal saline solution. The procedure was considered complete only when the entireuterine cavity and both Tubal Ostia were visualized. Reports of 3D Ultrasonographic scans, done after the procedure, and confirming the diagnosis of uterine lesion if any, were also reviewed. Statistical Analysis was perform educing the Student’s t-test. A result of P ≤ 0.05 was considered significant.</p></sec><sec id="s3"><title>3. Results</title><p>The total number of patients fulfilling the inclusion criteria was 200. Cases with 2 previous miscarriages (n = 95) were assessed and compared with those with 3 or more miscarriages (n = 105), where no significant differences were found between both groups in terms of age, parity, or body mass index (BMI). The number of cases with more than 3 miscarriages was 18 cases. Abnormal uterine findings were diagnosed in 24.1% of the former, and 43.8% of the latter group. No statistically significant difference was seen between the 2 groups regarding the type and incidence of uterine lesions, except submucus fibroids, being significantly more frequent in the 2<sup>nd</sup> group. The prevalence of uterine lesions among cases with 2 recurrent miscarriages was 42.1% (22.1% Acquired, and 20% congenital), meanwhile, for subjects with 3 or more consecutive miscarriages, it was 43.8% (31.4% Acquired, and 12.4% congenital) (<xref ref-type="table" rid="table1">Table 1</xref>, <xref ref-type="fig" rid="fig1">Figure 1</xref>).The duration of OH procedure ranged from 10 - 15 minutes. The procedure was acceptable in almost all patients. The majority of the patients did not feel any significant pain during the procedure; and all were discharged within 30 minutes after the procedure, without any reported complications.</p></sec><sec id="s4"><title>4. Discussion</title><p>One of the basic steps of workup for recurrent pregnancy loss is to evaluate the shape and regularity of the uterine cavity [<xref ref-type="bibr" rid="scirp.84327-ref6">6</xref>] . After 2 consecutive miscarriages,</p><table-wrap id="table1" ><label><xref ref-type="table" rid="table1">Table 1</xref></label><caption><title> Hysteroscopic findings in 200 subjects with recurrent pregnancy loss</title></caption><table><tbody><thead><tr><th align="center" valign="middle" >Findings</th><th align="center" valign="middle" >Two pregnancy losses (n = 95) (%)</th><th align="center" valign="middle" >Three or more pregnancy losses (n = 105) (%)</th><th align="center" valign="middle" >P Value</th></tr></thead><tr><td align="center" valign="middle" >Normaluterinecavity</td><td align="center" valign="middle" >55 (57.9)</td><td align="center" valign="middle" >59 (56.2)</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Abnormal intrauterine finding</td><td align="center" valign="middle" >40 (42.1)</td><td align="center" valign="middle" >46 (43.8)</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Acquired Finding</td><td align="center" valign="middle" >21 (22.1)</td><td align="center" valign="middle" >33 (31.4)</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Submucous fibroid _</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >&lt;0.04*</td></tr><tr><td align="center" valign="middle" >Endometrial polyp</td><td align="center" valign="middle" >8</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Multiple focal findings</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Intrauterine adhesions</td><td align="center" valign="middle" >4</td><td align="center" valign="middle" >5</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Cervical polyp</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Endometritis</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Blocked Ostia</td><td align="center" valign="middle" >3</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Congenital Malformation</td><td align="center" valign="middle" >19 (20)</td><td align="center" valign="middle" >13 (12.4)</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Uterine septum</td><td align="center" valign="middle" >17</td><td align="center" valign="middle" >13</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Ashermansyndrome</td><td align="center" valign="middle" >2</td><td align="center" valign="middle" >0</td><td align="center" valign="middle" >NS</td></tr><tr><td align="center" valign="middle" >Total</td><td align="center" valign="middle" >95</td><td align="center" valign="middle" >105</td><td align="center" valign="middle" ></td></tr></tbody></table></table-wrap><p>*: Statistically significant at p ≤ 0.05. NS: Not significant.</p><p>the patient would usually start to seek medical assistance, not waiting for a third “round” that would be highly probable, thus a suggestion has been made to modify the original definition, and accept 2 consecutive spontaneous pregnancy losses instead of 3 to fulfill the definition [<xref ref-type="bibr" rid="scirp.84327-ref7">7</xref>] . In this work, we studied a representative sample of patients with recurrent miscarriage (200 patients), which is, to our knowledge, the largest number studied for such an uncommon condition. A similar study by Ventolini G. et al., for instance, was conducted on only 23 patients [<xref ref-type="bibr" rid="scirp.84327-ref8">8</xref>] . Another published work by Dendrinos S. et al. reported 48 patients with 3 consecutive miscarriages without dividing them into groups [<xref ref-type="bibr" rid="scirp.84327-ref9">9</xref>] .</p><p>Our results demonstrated that the prevalence of uterine lesions among cases with 2 recurrent miscarriages was 42.1% (22.1% Acquired, and 20% congenital), meanwhile, for subjects with 3 or more consecutive miscarriages, it was 43.8 (31.4% Acquired, and 12.4% congenital). A prevalence of uterine anomalies causing recurrent abortion was reported to vary between 15% - 27% [<xref ref-type="bibr" rid="scirp.84327-ref10">10</xref>] [<xref ref-type="bibr" rid="scirp.84327-ref11">11</xref>] [<xref ref-type="bibr" rid="scirp.84327-ref12">12</xref>] , and up to 50% by Keltz et al. [<xref ref-type="bibr" rid="scirp.84327-ref13">13</xref>] The variable number of recruits and the different design of each research could be the cause of such vast variation.</p><p>Portuondo et al., also compared cases with 2 or 3 recurrent miscarriages, in terms of uterine abnormalities using HSG, and found no difference [<xref ref-type="bibr" rid="scirp.84327-ref14">14</xref>] . We confirmed the diagnosis of uterine M&#252;llerian anomalies using a 3D ultrasonographic scan. This was also reported by Raga F. et al. and Wu MH et al. [<xref ref-type="bibr" rid="scirp.84327-ref15">15</xref>] [<xref ref-type="bibr" rid="scirp.84327-ref16">16</xref>] . The European Society of Human Reproduction and Embryology (ESHRE) guidelines indicate hysteroscopy may be only necessary, for the confirmation and treatment of doubtful intrauterine pathology [<xref ref-type="bibr" rid="scirp.84327-ref17">17</xref>] . In the current study, Assessment of the uterine cavity in patients with recurrent pregnancy loss was the main indication for performing diagnostichysteroscopy. It appears that many patients interpreted as normal following a HS Gare found to have a uterine abnormality after diagnostichysteroscopy, which might be a sign if I cant cause of reproductive failure [<xref ref-type="bibr" rid="scirp.84327-ref6">6</xref>] .</p><p>Donnez and Jadoul concluded that those uterine anomalies do influence pregnancy course [<xref ref-type="bibr" rid="scirp.84327-ref18">18</xref>] . Office hysteroscopy allows complete, accurate identification of intrauterine abnormalities that might negatively affect pregnancy continuation. We identified 11 cases with intrauterine adhesions using office hysteroscopy in this series. All of those cases were managed by hysteroscopicadhesiolysis, which would help improve their pregnancy outcome. Valli et al., also concluded that the role of hysteroscopy in lysing the intrauterine adhesions would improve pregnancy outcome in patients having recurrent miscarriages [<xref ref-type="bibr" rid="scirp.84327-ref19">19</xref>] . In concordance, Bouet PE et al. confirmed that office hysteroscopy is a useful tool in the management of women with recurrent pregnancy loss, preferably when complemented by a biopsy from the endometrium to diagnose chronic endometritis [<xref ref-type="bibr" rid="scirp.84327-ref20">20</xref>] . Dendrinos S. et al. also stated that hysteroscopy is superior to HSG for identification of intrauterine pathology, thus being a reliable assessment tool of the uterine cavity with a high specificity and sensitivity [<xref ref-type="bibr" rid="scirp.84327-ref9">9</xref>] .</p><p>In our work, office hysteroscopy was very acceptable by patients with extremely high safety profile and significant diagnostic potential on any intrauterine lesion. The large number of subjects studied, and the considerable amount of data obtained on each, are good points of strength adding to the value of this research. A weak point, however, is its retrospective type.</p></sec><sec id="s5"><title>5. Conclusion</title><p>We justify the introduction of office hysteroscopy in the routine work-up of cases with recurrent miscarriages. Intervention after 2 miscarriages would be more beneficial, based on the high incidence of uterine anomalies detected in this work, most of which were missed by other diagnostic modalities. We also confirm a good safety profile, acceptability and outstanding diagnostic potential of office hysteroscopy.</p></sec><sec id="s6"><title>Acknowledgements</title><p>The authors wish to thank the University of Alexandria for their support during most of the steps of this study.</p></sec><sec id="s7"><title>Conflict of Interest</title><p>There has been no conflict of interest of any kind with the authors of this work.</p></sec><sec id="s8"><title>Cite this paper</title><p>Moiety, F.M.S., Agameya, A.F. and Saleh, H.A. (2018) Recurrent Miscarriage: Hysteroscopy-Assisted Management. Open Journal of Obstetrics and Gynecology, 8, 425-430. https://doi.org/10.4236/ojog.2018.85048</p></sec></body><back><ref-list><title>References</title><ref id="scirp.84327-ref1"><label>1</label><mixed-citation publication-type="other" xlink:type="simple">Li, T.C., Makris, M., Tomsu, M., Tuckerman, E. and Laird, S. (2002) Recurrent Miscarriage: Aetiology, Management and Prognosis. 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