Orientador: Rogério Dias / Coorientador: Daniel Spadoto Dias / Banca: Nilton José Leite / Banca: Reginaldo Guedes Coelho Lopes / Resumo: Objetivo do estudo. Comparar os resultados entre duas técnicas de ablação endometrial de primeira geração. Tipo de estudo. Estudo prospectivo, longitudinal e analítico (Canadian Task Force II-2). Local do estudo. Hospital público terciário, centro universitário de ensino. Pacientes e métodos. Durante o período de outubro de 2011 a setembro de 2013, 73 pacientes com história de sangramento uterino anormal (SUA) e resposta insatisfatória ao tratamento clínico por um período mínimo de 12 meses, foram randomizadas e submetidas à ablação endometrial por ressecção com eletrodo monopolar em alça "U" seguida de eletrocoagulação com rollerball no grupo A (36 pacientes) e eletrocoagulação apenas com rollerball no grupo B (37 pacientes). As mulheres foram acompanhadas por período médio de 359 dias (280;751) e 370 dias (305;766), respectivamente. Intervenções. As pacientes foram submetidas à ablação endometrial conforme a técnica de cada grupo. Avaliações nos tempos 30, 90, 180 e 360 dias foram realizadas através de protocolo de pesquisa, que procurou avaliar o padrão de sangramento, sintomas associados, índice de falha e taxa de satisfação. Resultados. Os grupos foram clínico-epidemiologicamente homogêneos (P ≥ 0,05). O tempo cirúrgico e o volume utilizado do meio distensor foram menores nas pacientes do grupo B [média de 48,5 (±12,0) vs. 31,9 (±5,6) minutos; P < 0,001 e 5.700 mL vs. 3.500 mL; P < 0,01]. Observou-se uma considerável melhora no quadro clínico após ablação endometrial, em ambos os grupos, com redução do número de dias de sangramento (P < 0,01), assim como do número de absorventes utilizados no dia de maior fluxo (P < 0,01) e durante todo o período menstrual (P < 0,01). Houve também menor incidência de infecção do sítio cirúrgico no grupo B (30,5% vs. 8,1%; P < 0,05). A taxa de histerectomia observada no estudo foi de 9,6%, decorrente de ... / Abstract: Purpose of the study. Compare the results of two techniques of endometrial ablation first generation. Type of study. Prospective, longitudinal and analytical study (Canadian Task Force II-2). The study site. Tertiary public hospital, university teaching center. Patients and methods. During the period October 2011 to September 2013, 73 patients with a history of abnormal uterine bleeding (AUB) and poor response to medical treatment for a minimum period of 12 months, were randomized and underwent endometrial ablation with monopolar resection electrode handle "U" followed by rollerball electrocoagulation with the group a (36 patients) with rollerball electrocoagulation only in group B (37 patients). The women were followed for an average period of 359 days (280;751) and 370 days (305;766), respectively. Interventions. The patients were submitted to endometrial ablation technique according to each group. Ratings at 30, 90, 180 and 360 days were accomplished through research protocol, which sought to assess the pattern of bleeding, associated symptoms, failure rate and satisfaction rate. Results. The groups were homogeneous clinical and epidemiologically (P ≥ 0.05). Surgical time and the volume of distension medium used were lower in group B patients [mean of 48.5 (±12.0) vs. 31.9 (±5.6) minutes; P < 0.001 and 5.700 mL vs. 3.500 mL; P < 0.01]. There was a significant improvement in clinical symptoms after endometrial ablation in both groups, reducing the number of bleeding days (P < 0.01), as well as the number of pads used on the day of the flow rate (P < 0.01) and throughout the menstrual cycle (P < 0.01). There was also a lower incidence of surgical site infection in group B (30.5% vs. 8.1%; P < 0.05). The hysterectomy rate observed in the study was 9.6%, due to technical difficulties and intraoperative hemorrhage, persistence of SUA, development of incapacitating dysmenorrhea and / or pelvic pain ... / Mestre

OBJETIVO: avaliar a histomorfometria do endométrio na fase lútea de mulheres férteis e inférteis. MÉTODOS: foram triadas 40 pacientes, 30 inférteis e 10 férteis, em seguimento na Clínica Ginecológica do HC-FMUSP, que concordaram em participar deste estudo. Foi realizada avaliação ultrassonográfica seriada a partir da menstruação, para determinação da ovulação. Na fase lútea as pacientes eram submetidas à histeroscopia. Foram excluídas 14 pacientes sendo 12 por falta durante a avaliação ultrassonográfica e 2 pela presença de pólipos. A casuística foi composta por 6 controles férteis, que foram comparadas a 20 casos inférteis (endometriose-8, causa tubo-peritoneal-5, causa masculina-5, sem causa aparente-2). Na histeroscopia foram coletadas duas biópsias dirigidas (sistema de Bettocchi) da parede posterior (terço distal), e da parede anterior (terço médio), e uma biópsia aspirativa com Pipelle. Foram avaliados parâmetros histomorfométricos endometriais. RESULTADOS: as duas formas de biópsia foram apropriadas para análise endometrial; a dirigida coletou menor área tecidual, porém sem sangue. Nenhum paciente fértil apresentou heterogeneidade endometrial (atraso de fase em algum sítio); isto ocorreu em 7 (35%) das inférteis (p=0,11). Foi diagnosticada endometrite em 2 (10%) casos. CONCLUSÃO: não foram observadas diferenças histomorfométricas entre o endométrio de mulheres férteis e inférteis na fase lútea. Parte das pacientes inférteis mostrou heterogeneidade endometrial e endometrite. A biópsia dirigida, assim como a aspirativa, foi adequada ao estudo endometrial na fase lútea / Objective: to evaluate the endometrial histomorphometry of fertile and infertile women during their luteal period. Methods: 40 female patients- 30 infertile and 10 fertile- who were being followed-up at the Gynecological Clinic at the Hospital das Clinicas (HC),-Faculdade de Medicina da Universidade de Sao Paulo (FMUSP), agreed to participate in the study. Serial ultra sonograms, starting from their menstrual period, were performed to identify their ovulation. In the luteal phase the patients underwent hysteroscopy. From the initial sample, 14 patients were excluded from the study, 12 of whom for being absent during scheduled ultra sonograms and 2 for presenting polyps. The final sample thus consisted of 6 fertile females (control subjects) who were compared to 20 patients with infertility, categorized as follows: 8 due to endometriosis, 5 due to peritoneal tube conditions, 5 due to male infertility, and 2 with no apparent cause. During the hysteroscopy 2 directed biopsies (Bettocchis System) of the posterior wall (distal third section) and of the anterior wall (medial third) were performed, as well as Pipelle sampling. Endometrial histomorpholometric parameters were evaluated. Results: the two forms of endometrial sampling performed were appropriate for the endometrial analysis. The directed biopsy collected tissue from a smaller area, but it had no blood. None of the fertile patients presented endometrial heterogeneity, i.e., phase delay in any site. In contrast, this occurred in 7(35%) of the infertile females (p=0.11). Endometritis was diagnosed in 2 (10%) of the cases. Conclusions: no histomorphometric differences were observed in the endometrium of the fertile and infertile female patients during their luteal phase. About a third of infertile cases (35%) displayed endometrial heterogeneity and a small percentage of which (10%) had endometritis. Both the directed biopsy and Pipelle sampling were found satisfactory for studies of endometrium during the luteal phase

OBJETIVO: avaliar a histomorfometria do endométrio na fase lútea de mulheres férteis e inférteis. MÉTODOS: foram triadas 40 pacientes, 30 inférteis e 10 férteis, em seguimento na Clínica Ginecológica do HC-FMUSP, que concordaram em participar deste estudo. Foi realizada avaliação ultrassonográfica seriada a partir da menstruação, para determinação da ovulação. Na fase lútea as pacientes eram submetidas à histeroscopia. Foram excluídas 14 pacientes sendo 12 por falta durante a avaliação ultrassonográfica e 2 pela presença de pólipos. A casuística foi composta por 6 controles férteis, que foram comparadas a 20 casos inférteis (endometriose-8, causa tubo-peritoneal-5, causa masculina-5, sem causa aparente-2). Na histeroscopia foram coletadas duas biópsias dirigidas (sistema de Bettocchi) da parede posterior (terço distal), e da parede anterior (terço médio), e uma biópsia aspirativa com Pipelle. Foram avaliados parâmetros histomorfométricos endometriais. RESULTADOS: as duas formas de biópsia foram apropriadas para análise endometrial; a dirigida coletou menor área tecidual, porém sem sangue. Nenhum paciente fértil apresentou heterogeneidade endometrial (atraso de fase em algum sítio); isto ocorreu em 7 (35%) das inférteis (p=0,11). Foi diagnosticada endometrite em 2 (10%) casos. CONCLUSÃO: não foram observadas diferenças histomorfométricas entre o endométrio de mulheres férteis e inférteis na fase lútea. Parte das pacientes inférteis mostrou heterogeneidade endometrial e endometrite. A biópsia dirigida, assim como a aspirativa, foi adequada ao estudo endometrial na fase lútea / Objective: to evaluate the endometrial histomorphometry of fertile and infertile women during their luteal period. Methods: 40 female patients- 30 infertile and 10 fertile- who were being followed-up at the Gynecological Clinic at the Hospital das Clinicas (HC),-Faculdade de Medicina da Universidade de Sao Paulo (FMUSP), agreed to participate in the study. Serial ultra sonograms, starting from their menstrual period, were performed to identify their ovulation. In the luteal phase the patients underwent hysteroscopy. From the initial sample, 14 patients were excluded from the study, 12 of whom for being absent during scheduled ultra sonograms and 2 for presenting polyps. The final sample thus consisted of 6 fertile females (control subjects) who were compared to 20 patients with infertility, categorized as follows: 8 due to endometriosis, 5 due to peritoneal tube conditions, 5 due to male infertility, and 2 with no apparent cause. During the hysteroscopy 2 directed biopsies (Bettocchis System) of the posterior wall (distal third section) and of the anterior wall (medial third) were performed, as well as Pipelle sampling. Endometrial histomorpholometric parameters were evaluated. Results: the two forms of endometrial sampling performed were appropriate for the endometrial analysis. The directed biopsy collected tissue from a smaller area, but it had no blood. None of the fertile patients presented endometrial heterogeneity, i.e., phase delay in any site. In contrast, this occurred in 7(35%) of the infertile females (p=0.11). Endometritis was diagnosed in 2 (10%) of the cases. Conclusions: no histomorphometric differences were observed in the endometrium of the fertile and infertile female patients during their luteal phase. About a third of infertile cases (35%) displayed endometrial heterogeneity and a small percentage of which (10%) had endometritis. Both the directed biopsy and Pipelle sampling were found satisfactory for studies of endometrium during the luteal phase

Made available in DSpace on 2015-05-14T16:53:12Z (GMT). No. of bitstreams: 0 Previous issue date: 2014-10-10Bitstream added on 2015-05-14T16:59:16Z : No. of bitstreams: 1 000825160.pdf: 709651 bytes, checksum: 51e908d6fe4712ab7da7bea551017d14 (MD5) / Objetivo do estudo. Comparar os resultados entre duas técnicas de ablação endometrial de primeira geração. Tipo de estudo. Estudo prospectivo, longitudinal e analítico (Canadian Task Force II-2). Local do estudo. Hospital público terciário, centro universitário de ensino. Pacientes e métodos. Durante o período de outubro de 2011 a setembro de 2013, 73 pacientes com história de sangramento uterino anormal (SUA) e resposta insatisfatória ao tratamento clínico por um período mínimo de 12 meses, foram randomizadas e submetidas à ablação endometrial por ressecção com eletrodo monopolar em alça U seguida de eletrocoagulação com rollerball no grupo A (36 pacientes) e eletrocoagulação apenas com rollerball no grupo B (37 pacientes). As mulheres foram acompanhadas por período médio de 359 dias (280;751) e 370 dias (305;766), respectivamente. Intervenções. As pacientes foram submetidas à ablação endometrial conforme a técnica de cada grupo. Avaliações nos tempos 30, 90, 180 e 360 dias foram realizadas através de protocolo de pesquisa, que procurou avaliar o padrão de sangramento, sintomas associados, índice de falha e taxa de satisfação. Resultados. Os grupos foram clínico-epidemiologicamente homogêneos (P ≥ 0,05). O tempo cirúrgico e o volume utilizado do meio distensor foram menores nas pacientes do grupo B [média de 48,5 (±12,0) vs. 31,9 (±5,6) minutos; P < 0,001 e 5.700 mL vs. 3.500 mL; P < 0,01]. Observou-se uma considerável melhora no quadro clínico após ablação endometrial, em ambos os grupos, com redução do número de dias de sangramento (P < 0,01), assim como do número de absorventes utilizados no dia de maior fluxo (P < 0,01) e durante todo o período menstrual (P < 0,01). Houve também menor incidência de infecção do sítio cirúrgico no grupo B (30,5% vs. 8,1%; P < 0,05). A taxa de histerectomia observada no estudo foi de 9,6%, decorrente de ... / Purpose of the study. Compare the results of two techniques of endometrial ablation first generation. Type of study. Prospective, longitudinal and analytical study (Canadian Task Force II-2). The study site. Tertiary public hospital, university teaching center. Patients and methods. During the period October 2011 to September 2013, 73 patients with a history of abnormal uterine bleeding (AUB) and poor response to medical treatment for a minimum period of 12 months, were randomized and underwent endometrial ablation with monopolar resection electrode handle U followed by rollerball electrocoagulation with the group a (36 patients) with rollerball electrocoagulation only in group B (37 patients). The women were followed for an average period of 359 days (280;751) and 370 days (305;766), respectively. Interventions. The patients were submitted to endometrial ablation technique according to each group. Ratings at 30, 90, 180 and 360 days were accomplished through research protocol, which sought to assess the pattern of bleeding, associated symptoms, failure rate and satisfaction rate. Results. The groups were homogeneous clinical and epidemiologically (P ≥ 0.05). Surgical time and the volume of distension medium used were lower in group B patients [mean of 48.5 (±12.0) vs. 31.9 (±5.6) minutes; P < 0.001 and 5.700 mL vs. 3.500 mL; P < 0.01]. There was a significant improvement in clinical symptoms after endometrial ablation in both groups, reducing the number of bleeding days (P < 0.01), as well as the number of pads used on the day of the flow rate (P < 0.01) and throughout the menstrual cycle (P < 0.01). There was also a lower incidence of surgical site infection in group B (30.5% vs. 8.1%; P < 0.05). The hysterectomy rate observed in the study was 9.6%, due to technical difficulties and intraoperative hemorrhage, persistence of SUA, development of incapacitating dysmenorrhea and / or pelvic pain ...

Introduction: Actually 0.7-1 percent of all deliveries can be followed by secondary uterine bleeding. There is a residual trophoblastic tissue diagnosed in most of these cases and it is often managed by repeat intrauterine interventions. These operations are connected with high risk of formation of intrauterine adhesions and their early diagnosis and management can be important for next fertility. Material and methods: There were generally 188 patients included into the study. All patients underwent ultrasound examination in 6 weeks after delivery and ambulant hysteroscopy after next 2 months without anesthesia. Described intrauterine pathologies (residual tissue and adhesions) were managed in one step. Results: In cases with suspect ultrasound finding, the retained trophoblastic tissue was diagnosed by hysteroscopy in 66 percent vs. in 96 percent with sensitivity 85 percent and specificity 85 percent. Patients with intrauterine adhesions had normal ultrasound finding in 74 percent and it did not recognized patients with severe adhesions in 94 percent. Clinical signs had generally 72 percent of patients with diagnosed left residual tissue. Number of severe residual tissue is increasing with delay of instrumental evacuation from delivery (10 vs. 30 percent). When is necessary to repeat the operation...

Introduction: Actually 0.7-1 percent of all deliveries can be followed by secondary uterine bleeding. There is a residual trophoblastic tissue diagnosed in most of these cases and it is often managed by repeat intrauterine interventions. These operations are connected with high risk of formation of intrauterine adhesions and their early diagnosis and management can be important for next fertility. Material and methods: There were generally 188 patients included into the study. All patients underwent ultrasound examination in 6 weeks after delivery and ambulant hysteroscopy after next 2 months without anesthesia. Described intrauterine pathologies (residual tissue and adhesions) were managed in one step. Results: In cases with suspect ultrasound finding, the retained trophoblastic tissue was diagnosed by hysteroscopy in 66 percent vs. in 96 percent with sensitivity 85 percent and specificity 85 percent. Patients with intrauterine adhesions had normal ultrasound finding in 74 percent and it did not recognized patients with severe adhesions in 94 percent. Clinical signs had generally 72 percent of patients with diagnosed left residual tissue. Number of severe residual tissue is increasing with delay of instrumental evacuation from delivery (10 vs. 30 percent). When is necessary to repeat the operation...

<p>Uvod: Infertilitet pogađa 10-15% parova reproduktivnog doba. Vanetesna oplodnja (VTO) je najefikasniji vid tret-mana infertiliteta, ali uprkos značajnom napretku stopa uspeha VTO u proseku iznosi oko 30% po ciklusu. Glavnim razlogom neuspeha smatra se neadekvatan kvalitet embriona, dok se pretpostavlja da u 10-20% slučajeva razlog neuspeha leži u neadekvatnoj receptivnosti uterusa. Na osnovu inicijalnih istraživanja histeroskopija, koja predstvalja zlatni standard u dijagnostici i tretmanu patologije kavuma uterusa, se često izvodi u svakodnevnoj kliničkoj praksi kako bi se povećala uspe&scaron;nost VTO. Uprkos &scaron;irokoj primeni i dalje ne postoji dovoljno kvalitetnih dokaza o realnoj ulozi histeroskopije na ishod VTO kako kod patolo&scaron;kih stanja kavuma tako i rutinski, pre prvog ili rekurentnog poku&scaron;aja VTO. Cilj disertacije bio je da se utvrdi uticaj sprovođenja histeroskopije na ishod VTO, ustanovi učestalost prethodno neprepoznate patologije kavuma uterusa, kao i da se ispitaju stavovi pacijenata o primeni rutinske histeroskopije pred VTO. Materijal i metode: Istraživanje je sprovedeno u Kliničkom centru Vojvodine, u formi prospektivne studije u dve sukcesivne etape od 01.01.2015. do 01.04.2017. U prvoj etapi poređen je ishod VTO kod pacijentkinja kojima pred postupak VTO nije sprovedena histeroskopija (Grupa A), pacijentkinja kod kojih je dobijen uredan nalaz histeroskopije pred postupak VTO (Grupa B) i pacijentkinja gde je pred postupak VTO dobijen patolo&scaron;ki nalaz kavuma na histeroskopiji koji je u istom aktu tertian (Grupa C). Druga etapa istraživanja predstavljala je randomiziranu kontrolisanu studiju (RCT &ndash; randomised controlled trial). Nakon verifikacije urednog ultrazvučnog nalaza pred prvi postupak VTO, pacijentkinje su randomizirane u Grupu A2 kojima pred postupak VTO nije sprovedena histeroskopija i Grupu B2 kojima je pred postupak VTO sprovedena rutinska histeroskopija. Statistička analiza sprovedena je upotrebom odgovarajućeg softvera (JMP Ver. 9). Poređeni su podaci o osnovnim karakteristikama pacijenata, toka i ishoda ciklusa VTO. Primarni parametar ishoda bila je stopa kliničke trudnoće po embriotransferu. Pored analize ishoda primarno konstruisanih grupa, urađena je analiza i naknadno konstruisanih subgrupa, kao i predikcioni model uspeha VTO baziran na logističkoj regresiji. Rezultati: Studija je uključila 253 pacijentkinje (52 pacijentkinja iz Grupe A, 50 iz Grupe B, 50 iz Grupe C, 51 iz Grupe A2 i 50 iz Grupe B2). Nije postojala statistički značajna razlika u karakteristikama pacijentkinja, parametrima ovarijalne rezerve, broju dobijenih jajnih ćelija ni drugim parametrima toka postupka VTO među posmatranim grupama. U prvoj etapi istraživanja dobijena je statistički značajno (p=0,013) veća stopa kliničkih trudnoća kod pacijentkinja kojima je pred postupak VTO sprovedena histeroskopija - 50 % za Grupu B i 42% za grupu C u odnosu na 30,77% kod pacijentkinja bez histeroskopije (Grupa A), bez statistički značajne razlike među histeroskopskim grupama. U drugoj etapi istraživanja stopa kliničkih trudnoća prilikom upotrebe rutinske histeroskopije pred prvu VTO (Grupa B2) iznosila je 46% naspram 31,37% kod pacijentkinja bez histeroskopije pred prvu VTO (Grupa A2), iako uočena razlika nije dostigla statističku značajnost (p =0,089), uz relativan rizik (RR) za ostvarivanje kliničke trudnoće nakon primene histeoskopije uiznosio od 1,47 (95% CI 0,88-2,43) (p=0,13). Analizon subgrupa kod 100 pacijentkinja sa rutinski sprovedenom histeroskopijom pred VTO i 103 pacijentkinje bez histeroskopije pred VTO, dobijena je statistički značajnao veća stopa kliničkih trudnoća (48% naspram 31,07%, istim redom), uz RR od 1,54 (95% CI 1,08-2,20) (p=0,013), kao i stopa tekućih trudnoća od RR 1,49 (CI 1,01-2,19) (p= 0,039). Analiza ukupnog uticaja izvođenja histeroskopije pred VTO dobila je statistički značanjno veću stopu kliničkih trudnoća po ET za grupu histeroskopije uz RR 1,48 (CI 1,06-2,07) (p=0,017). Histeroskopijom je nakon urednog ultrazvučnog nalaza ustanovljeno postojanje patolo&scaron;kog nalaza kod 34,65% pacijenata i to 22,7% major patologije i 11,88% minor patologije kavuma. Nije postojala statistički značajna razlika u uspehu VTO u odnosu na sam nalaz histeroskopije. 98,67% pacijenata podržalo je rutinsku upotrebu histeroskopije pred prvi postupak VTO, dok je 83% pacijenata podržavlo rutinsku upotrebu histeroskopije pred svaki postupak VTO. U finalnom predikcionom modelu se uz AUC od 0,748 jedino postojanje visokokvalitetnog embriona uz odnos &scaron;ansi (OR) 7,91 (95% CI 1,80-56,06; p=0,0047), transfer blastociste uz OR 3,80 (95% CI 1,90-7,98; p=0,0001) i izvođenje histeroskopije pred VTO uz OR 2,13 (95% CI 1,14-4,08, p=0,0169) pokazalo statistički značajnim prediktorima trudnoće. Diskusija: Studija je dobila pozitivan uticaj histeroskopije na ishod postupka VTO, iskazan pre svega povećanjem stope kliničkih trudnoća nakon sprovođenja histeroskopije (bilo da je na histeroskopiji nađen uredan ili patolo&scaron;ki nalaz). Dodatna prednost histeroskopije predstavljala je i i detekcija prethodno nepropoznate patologije kavuma. Umeren efekat na ukupno pobolj&scaron;anje stope kliničkih trudnoća prilikom rutinskog sprovođenja histeroskopije pred prvu VTO, koji je statističku značajnost dostigao tek analizom subgrupa u skladu je sa nalazima novijih dobro dizajniranih studija koji donekle limitiraju nekritičku upotrebu histeroskopije. Biolo&scaron;ko obja&scaron;njenje potencijalnog pozitivnog uticaja histeroskopije najverovatnije leži u detekciji i tretmanu prethodno nepropoznate patologije kavuma, olak&scaron;avanju procedure embriotransfera, kao i humoralnim i molekularnim promenama koje nastaju u endometrijumu kao posledica odgovarajuće histeroskopske traume a koji su u dosa&scaron;anjim istraživanjima apostrofirani kao faktori koji mogu povećati receptivnost uterusa. Zaključak: Histeroskopija je efikasna, bezbedna i visoko prihvatljiva procedura koja dovodi do povećanja uspeha VTO u standardnim kliničkim indikacijama (prethodnog neuspelog postupka VTO i sumnje na patolo&scaron;ki nalaz kavuma uterusa) bilo da se na samoj histeroskopiji nađe uredan ili patolo&scaron;ki nalaz. Rutinska primena histeroskopije pred prvi postupak VTO se na osnovu rezultata studije ne može smatrati apsolutno opravdanom usled statistički nedovoljno značajnog povećanja stope kliničke trudnoće. Uzev&scaron;i u obzir visoku prihvatljivost od strane pacijenata i najverovatniji pozitivan efekat na stopu trudnoće primena rutinske histeroskopije pred prvu VTO bila bi opravdana ukoliko se implementira koncept ambulantne histeroskopije.</p> / <p>Introduction: Infertility affects 10-15% of all couples. In vitro fertilisation (IVF) is the most effective method of infertility treatment, but despite a significant improvement, success rate of IVF is still around 30% per cycle. The main reason for the IVF failure is inadequate embryo quality, but in 10-20% of cases the cause of IVF failure lies in impaired uterine receptivity. Based on earlier studies hysteroscopy, gold standard in the diagnosis and treatment of uterine cavity pathology, is often performed to increase IVF success. Despite its wide use, there is lack of high quality evidence regarding real contribution of hysteroscopy on IVF outcome in situations of uterine cavity pathology or routinely prior to first IVF or after recurrent implantation failure. The aim of this dissertation was to determine the influence of performing hysteroscopy on IVF outcome, as well as the incidence of previously unrecognized uterine pathology, and to examine patient&#39;s attitudes about performing routine hysteroscopy prior to IVF. Material and methods: The research was conducted in a prospective manner in two successive stages at Clinical Center of Vojvodina from 01.01.2015. until 01.04.2017. During first stage of the study IVF outcome was compared between patients who did not have a hysteroscopy prior to IVF (group A), patients with normal hysteroscopic finding prior to the IVF (Group B) and patients with abnormal hysteroscopic findings prior to IVF which was treated at the same time (Group C). The second stage of the study was a randomized controlled trial (RCT). After verification of normal ultrasound findings prior to the first IVF, patients were randomized to group A2 in who me hysteroscopy was not performed and group B2 who had routine hysteroscopy prior to first IVF. Statistical analysis was carried out using the appropriate statistical software (JMP Ver. 9). Patient characteristics, course and outcome of IVF cycle were compared between groups. The primary outcome was clinical pregnancy rate (CPR) per embryotransfer. In addition to analyzing the IVF outcomes in primarily defined groups, subgroup analysis was also performed, as well as IVF success pre-diction model based on logistic regression. Results: The study included 253 patients (52 patients in Group A, 50 in Group B, 50 in Group C, 51 in Group A2 and 50 in Group B2). There was no statistically significant difference in patient characteristics, ovarian reserve parameters, number of retrieved oocytes, or other relevant parameters of IVF course between the observed groups. In the first stage of the study there was statistically significant (p = 0.013) higher clinical pregnancy rate in patients who had a hysteroscopy before IVF - 50% for Group B and 42% for group C versus 30,77 % in patients without hysteroscopy before IVF (Group A), without statistically significant difference between hysteroscopic groups. In the second stage of the study, routine hysteroscopy prior to first IVF (Group B2) led to clinical pregnancy rate 46% versus 31.37% in patients without hysteroscopy prior to first IVF (Group A2), although without statistical significance (p = 0.089. Relative risk (RR) for achieving clinical pregnancy after performing hysteroscopy was 1.47 (95% CI 0.88-2.43) (p = 0.13). Subgroup analysis of 100 patients with routinely performed hysteroscopy before IVF and 103 patients without hysteroscopy prior to the IVF showed statistically significant higher rates of clinical pregnancies (48% versus 31.07%, in the same order), with RR of 1.54 (95% CI 1.08-2.20), (p = 0.013), and for ongoing pregnancies RR was 1.49 (95% CI 1.01-2.19) (p = 0.039). Overall effect of performing hysteroscopy prior to IVF resulted in a statistically significant increase in the clinical pregnancy with RR 1.48 (95% CI 1.06-2.07) (p = 0.017). After normal ultrasound finding hysteroscopy revealed 34.65% of pathological finding, 22.7% of major and 11.88% of minor pathology of the cavity). There was no statistically significant difference in IVF outcome based on hysteroscopy findings. 98.67% of patients supported the routine use of hysteroscopy before the first IVF procedure, while 83% of patients supported the routine use of the hysteroscopy before every IVF procedure. In the final prediction model, with the AUC of 0.748, only the presence of high quality embryos with odds ratio (OR) 7,91 (95% CI 1,80-56,06; p=0,0047), blastocyst transfer with OR 3,80 (95% CI 1,90-7,98; p=0,0001) and performing hysteroscopy prior to IVF with OR 2,13 (95% CI 1,14-4,08, p=0,0169) proved to be statistically significant predictors of pregnancy. Discussion: The study shoved a positive influence of hysteroscopy on the IVF outcome by increasing clinical pregnancy rate after performing hysteroscopy (whether hysteroscopy revealed normal or pathological finding). Additional benefit of hysteroscopy was detection of previously unrecognized uterine pathology. A moderate effect on the overall improvement in clinical pregnancy rate with use of routine hysteroscopy, which reached statistical significance only by subgroup analysis, is in line with findings of recent well designed studies that somewhat limit the noncritical use of hysteroscopy. A biological explanation of the potential positive effect of hysteroscopy is most likely due to detection and treatment of the previously unrecognized uterine pathology, facilitating embryotransfer procedure, as well as the humoral and molecular changes that occur in the endometrium as a consequence of the hysteroscopic trauma. Those changes were hypothesized as factors that can increase uterine receptivity by numerous research. Conclusion: Hysteroscopy is an effective, safe and highly acceptable procedure that increases IVF success when performed for accepted clinical indications (previous IVF failures, pathological findings of uterine cavity), whether hysteroscopy reveals normal or pathological finding. The routine use of hysteroscopy prior to first IVF based on this study can not be considered justified since increase in clinical pregnancy rate did not reach statistical significance. Given the high acceptance of this concept by the patients and moderate but probable positive effect on IVF outcome, implementation of routine hysteroscopy prior to first VTO would be justified only in office hysteroscopy setting.</p>

Η αυτόματη επεξεργασία εικόνων του ενδομητρίου αποτελεί ένα δύσκολο και πολυδιάστατο πρόβλημα, το οποίο έχει απασχολήσει πλήθος ερευνητών και για το οποίο έχει αναπτυχθεί μεγάλος αριθμός τεχνικών. Στην παρούσα διατριβή, παρουσιάζεται μια μεθοδολογική προσέγγιση, η οποία βασίζεται στη χρήση αλγορίθμων ψηφιακής επεξεργασίας και ανάλυσης εικόνων, για την αυτόματη εκτίμηση χαρακτηριστικών που περιγράφουν την αγγείωση και την υφή εικόνων του ενδομητρίου. Αφορμή της μελέτης αποτελεί ο ρόλος που διαπιστώνεται ότι διαδραματίζει η μεταβολή των τιμών των εν λόγω χαρακτηριστικών στην έγκαιρη διάγνωση των παθήσεων του ενδομητρίου. Στα πλαίσια της διατριβής, υλοποιήθηκε κατάλληλη μεθοδολογία για τον υπολογισμό ενός συνόλου χαρακτηριστικών τόσο για υστεροσκοπικές εικόνες, όσο και για ιστολογικές εικόνες του ενδομητρίου. Ιδιαίτερη βαρύτητα δόθηκε στην προ – επεξεργασία των εικόνων προκειμένου να προκύψει βελτίωση της ποιότητας καθώς και ενίσχυση της αντίθεσης αυτών. Στη συνέχεια, ανιχνεύτηκαν τα σημεία που αποτελούν τους κεντρικούς άξονες των υπό εξέταση αγγείων με χρήση διαφορικού λογισμού για τις υστεροσκοπικές εικόνες και υπολογίστηκε ένα σύνολο χαρακτηριστικών μεγεθών που περιγράφουν την αγγείωση και την υφή των εικόνων τόσο για τις υστεροσκοπικές όσο και για τις ιστολογικές εικόνες. Τέλος, εφαρμόστηκαν κατάλληλοι αλγόριθμοι με σκοπό την κατηγοριοποίηση των υστεροσκοπικών και των ιστολογικών εικόνων και συγκεκριμένα τον διαχωρισμό των παθολογικών και των φυσιολογικών εικόνων του ενδομητρίου. Παράλληλα, χρησιμοποιήθηκε η ROC ανάλυση στην απεικόνιση και ανάλυση της συμπεριφοράς των εν λόγω κατηγοριοποιητών. / Automatic analysis of the endometrial images is a difficult and multidimensional problem. For this reason, the number of papers and techniques regarding this issue is numerous. In this Thesis, a methodology is presented, based on advance image processing techniques in order to automatically estimate texture and vessel’s features in endometrial images. Motivation for the Thesis is the fact that the variation of the measurements of the specific features plays significant role in the seasonable diagnosis of endometrial disorders. Throughout this Thesis, an appropriate methodology is developed in order to estimate the features for the hysteroscopical and histological images of the endometrium. An important step is the pre – processing of the images in order to enhance the image quality and the image contrast. Then, the pixels that constitute the centerlines of vessels are detected by using differential calculus for the hysteroscopical images, only. Furthermore, the texture and vessel’s features in hysteroscopical and histological images are estimated. Finally, appropriate algorithms are applied in order to classify the hysteroscopical and histological images and distinguish pathological and normal endometrial images. ROC analysis is used in order to evaluate the discrimination power of the features that were estimated.