Minimally Invasive Gynecological Surgery

7. Diagnostic Methods, Risk Factors of Niches, Related Symptoms and Therapies

J. A. F. Huirne M. BijdeVaate1L. Van der Voet2M. Witmer1 and H. A. M. Brölmann1


Department Obstetrics and Gynaecology, VUMC, Amsterdam, The Netherlands


Department Obstetrics and Gynaecology, Deventer Ziekenhuis, Deventer, The Netherlands

J. A. F. Huirne



7.1 Introduction and Nomenclature

7.2 Prevalence of Niches and Diagnostic Methods

7.3 Niche Shapes

7.4 Predisposing Factors for Niches

7.5 Related Symptoms

7.6 Etiology of Niche-Related Bleeding Disorders

7.7 Treatment Modalities

7.8 Hysteroscopic Niche Resection

7.8.1 Technique

7.8.2 Effectiveness of Hysteroscopic Niche Resection

7.9 Laparoscopic or Vaginal Niche Repair

7.9.1 Effectiveness of Laparoscopic or Vaginal Niche Repair

7.10 Conclusion


7.1 Introduction and Nomenclature

Incomplete healing of caesarean section (CS) scars may be associated with complications in later pregnancies, such as uterine rupture, abnormal adherent placenta. The first publications on CS scar defects in relation to bleeding symptoms date from 1975 (Stewart and Evans 1975). However, the relation of such defects with gynecological symptoms in non-pregnant state such as postmenstrual bleeding has only recently been proven in prospective cohort studies in a unselected population of women with a history of CS (BijdeVaate et al. 2011). Since then the number of publications describing CS scar defects is increasing. Different terminology in the assessment of CS scars has been used (Naji et al. 2012a). A hypoechoic triangular area at the site of previous CS scars observed using ultrasonography has been given the term “niche” (Fig. 7.1).


Fig. 7.1

Schematic diagram of a caesarean scar defect, also known as a niche

However, more shapes have been described (Figs. 7.2 and 7.3). A generally accepted definition for a niche is still under debate. Alternative terms for a niche are caesarean scar defect (Armstrong et al. 2003; Vikhareva Osser et al. 2009; Wang et al. 2009), deficient caesarean scar (Ofili-Yebovi et al. 2008), diverticulum (Surapaneni and Silberzweig 2008), pouch (Fabres et al. 2003), and isthmocele (Borges et al. 2010). Some of these terms are unfortunate as they imply a relationship between the appearance of the niche and function, particularly in any future pregnancy. Until now there is no evidence yet to underline a relation with the appearance of the CS and its function. In this chapter, we will use the term “niche.”


Fig. 7.2

Different niches on sonohysterography (Published in Bij de Vaate et al. 2011)


Fig. 7.3

Niche shape. Schematic diagram demonstrating classification used to assess niche shape: triangle, semicircle, rectangle, circle, droplet and inclusion cysts (Published in Bij de Vaate et al. 2011)

7.2 Prevalence of Niches and Diagnostic Methods

Various methods to detect and measure a niche have been described. In earlier publications, it was observed during hystesterosalpingraphy (Surapaneni and Silberzweig 2008). However, this method may be considered as less imprecise for this objective and small niches may be missed. The most applied techniques are transvaginal sonography (TVS) (BijdeVaate et al. 2011; Vikhareva Osser et al. 2009; Armstrong et al. 2003) and sonohysterography (SHG) (BijdeVaate et al. 2011; Vikhareva Osser et al. 2009; Regnard et al. 2004; Valenzano et al. 2006). The latter technique is proposed to be more accurate due to improved delineation of the borders of a niche in comparison with TVS (Vikhareva Osser 2010a). This is underlined by a larger proportion of patients with a niche after SHG in comparison to TVS. BijdeVaate et al. (2011) observed in 56 % of women a niche using SHG compared to 24 % using TVS 6–12 months after a CS in a prospective cohort study. This is in line with an other prospective cohort study, studying niches in women after a CS, reporting a niche in 84 % of women using SHG compared to 70 % using TVS (Vikhareva Osser 2010a). Using SHG, the prevalence of niches in relatively unselected women after CS varies between 56 and 84 % (BijdeVaate et al. 2011; Regnard et al. 2004; Valenzano 2006; Vikhareva Osser 2010a). Reported prevalence of niches in women after CS using hysteroscopy varies between 31 and 88 % (Borges et al. 2010; El-Mazny et al. 2011). Besides the applied diagnostic methods, the prevalence of niches is highly dependent on the population, the awareness of the observers and of course the applied definitions. Until now there is no agreement about the gold standard for the detection and measurement of a niche. Higher prevalence is expected in women undergoing examination because of symptoms such as bleeding disorders or fertility problems. CS scar assessment during pregnancy is a different topic and requires other techniques and definitions since a SHG is not possible to apply. Naji et al. studied CS scars during pregnancy using TVS and was able to detect CS scars with low inter- and intra-observer variability (Naji et al. 2012b).

7.3 Niche Shapes

Various niche shapes have been described using sonography (see Figs. 7.2 and 7.3). Most studies report on a triangular shape (Vikhareva Osser et al. 2009; Chen et al. 1990). Using sonohysterography, the semicircular and triangular shapes were reported to be most prominent (BijdeVaate et al. 2011). Another reported classification based on the direction of the external surface is inward protrusion (internal surface bulging toward the bladder), outward protrusion (external surface bulging toward the bladder) or inward retraction (external surface of the scar dimpling toward the myometrial layer). (Chen et al. 1990).

7.4 Predisposing Factors for Niches

As not all women with a history of CS develop a niche, it is a subject of interest to identify the risk factors for the development of a niche. Several publications tried to elucidate the main risk factors, however, most individual publications are of insufficient power to study all relevant risk factors. Different diagnostic methods were used to identify niches in a selected population of women with gynaecological symtoms and used definitions were not uniform and often not clearly defined. So far only two studies have studied risk factors in an unselected population after a CS (Armstrong et al. 2003; Vikhareva Osser 2010a). Three other studies were performed in a population of women who were assessed for a variety of gynecological symptoms (Monteagudo 2001; Wang et al. 2009; Ofili-Yebovi et al. 2008).

Cervical dilatation and station of the presenting fetal part below pelvic inlet at the time of CS were the only predictive factors in one prospective study including patients with only one previous CS using TVS or SHG (Vikhareva Osser 2010, 2). Prolonged labor and multiple caesarean sections were identified as risk factors for niches in an unselected population using TVS (Armstrong et al. 2003). Using TVS, multiple caesarean sections were also identified as predisposing factor for niches (Ofili-Yebovi et al. 2008) and for larger niches (Wang et al. 2009). Uterine retroflexion was also associated with niches Moeten er geen referenties bij aangezien er staat ‘several’? (Vikhareva Osser et al. 2009) However, it is not clear if the retroflected position is a predisposing factor for the development of a niche or that retroflexion is caused by insufficient CS scar healing. Suturing technique should be considered as a predisposing factor as well. There are two small randomized trials and one prospective trial studying the effect of the suturing technique on the prevalence of a niche using ultrasound 4–6 weeks after the CS (Hayakawa et al. 2006; Hamar et al. 2007; Yazicioglu et al. 2006). There was no difference in myometrial thickness between one-layer or two-layer closure (Hamar et al. 2007), but there were less niches identified after double-layer closure compared to single layer (Hayakawa et al. 2006) or to split-level closure without inclusion of the endometrial layer (Yazicioglu et al. 2006).

7.5 Related Symptoms

Several complications of a scar defect have been reported, including niche pregnancies (BijdeVaate et al. 2010), malplacentation (Naji et al. 2013a), and perforated intrauterine devices (Voet et al. 2009). Recently, it has been shown that the thickness of the residual myometrium is an independent prognostic factor for success rate after trial of labor (Naji et al. 2013). However, the exact risk of niches on uterine ruptures has to be elucidated.

The relation between a niche and gynecological symptoms in non-pregnant patients has been acknowledged only recently. An association between a niche and prolonged menstrual bleeding and postmenstrual spotting has been reported in several studies (BijdeVaate et al. 2011; Fabres et al. 2003; Regnard et al. 2004; Thurmond et al. 1999; Wang et al. 2009; Borges et al. 2010). A niche is observed in almost 60 % of all women after a CS. The incidence of postmenstrual spotting is higher in these patients compared to those without a niche (OR 3.1 [95 % CI, 1.5–6.3]) (BijdeVaate et al. 2011). An association between the size of the niche and postmenstrual spotting is reported in three studies (Wang et al. 2009; Bij de Vaate et al. 2011; Uppal et al. 2011). Whilst a larger niche volume was demonstrated in women with postmenstrual spotting, there was no relation with the shape of the niche (BijdeVaate et al. 2011). In another study (Wang et al. 2009), scar defects were significantly wider in women with postmenstrual spotting, dysmenorrhea or chronic pelvic pain. In the third study, the incidence of postmenstrual spotting or prolonged menstrual bleeding was higher with an increase of the diameter of the niche (Uppal et al. 2011). Niche-related menstrual bleeding disorders do often not respond to hormonal therapies and are associated with cyclic pain (Gubbini et al. 2008) and may be responsible for a substantial part of gynecological consultations and interventions. Other reported symptoms in women with a niche were dysmenorrhea (53.1 %), chronic pelvic pain (36.9 %), and dyspareunia (18.3 %) (Wang et al. 2009).

7.6 Etiology of Niche-Related Bleeding Disorders

It has been assumed that abnormal uterine bleeding may be due to the retention of menstrual blood in the niche, which is intermittently expelled after the majority of the menstruation has ceased, causing postmenstrual spotting and pain (Thurmond et al. 1999; Fabres et al. 2005). The presence of fibrotic tissue below the niche may impair the drainage of menstrual flow (Fabres et al. 2003). Additional new formed fragile vessels in the niche may also attribute to the accumulation of in situ produced blood (Morris 1995).

7.7 Treatment Modalities

Since the recent acknowledged association between CS-related niches and bleeding disorders, several innovative surgical therapies have been developed. The effectiveness of surgical interventions for the treatment of niche-related uterine bleeding disorders has been reported in a limited number of studies. Most studies include case reports or small prospective or retrospective case series. Surgical treatment includes hysteroscopic resection (Chang et al. 2009; Fabres et al. 2005; Gubbini et al. 20082011; Wang et al. 2011), laparoscopic (Donnez et al. 2008; Klemm et al. 2005) or vaginal repair (Klemm et al. 2005).

7.8 Hysteroscopic Niche Resection

The least invasive surgical therapy, which can be performed in day care, is the hysteroscopic resection of the niche. The proposed theory behind this treatment is to improve outflow of menstrual blood and to prevent in situ produced hemorrhage by the fragile vessels in the niche itself.

7.8.1 Technique

The hysteroscopic resection was all done by a monopolar resectoscoop varying between 9 and 12 mm. In most studies, the distal part of the niche was resected with (Fabres et al. 2005; Chang et al. 2009) or without coagulation of the bottom of the niche (Fernandez et al. 1996) (see Fig. 7.4). In some studies both the distal and the proximal part of the niche were resected (see Fig. 7.4b) in combination with coagulation of the bottom with a rollerball (see Figs. 7.4band 7.5) (Wang et al. 2009; Gubbini et al. 20082011). Given the potential risk on perforation or bladder injury a certain distance between the niche and bladder is required, also known as residual myometrium, presented as 2 in Fig. 7.6. Minimal required residual myometrium thickness varies among the different studies between 2 and 2.5 mm (Wang et al. 2009; Gubbini et al. 20082011).


Fig. 7.4

Technique of hysteroscopic resection: (a) resection of distal part of the niche, (b) resection of both distal and proximal part (b was published in Gubbini et al. 2008)


Fig. 7.5

(a) Resectoscope for resection of the distal part of the niche. (b) Coagulation of the niche bottom with a rollerball (Published in Gubbini et al. 2008)


Fig. 7.6

Schematic diagram on the measurement of niches. Niche characteristics: niche depth (1), thickness of the residual myometrium (2), total thickness of adjacent myometrium (3), (Published in Bij de Vaate et al. 2011)

7.8.2 Effectiveness of Hysteroscopic Niche Resection

So far only three prospective cohort, one case–control study and four retrospective cohort studies are published on hysteroscopic resections. Apart from one case–control study (Florio et al. 2011), which compared hysteroscopic resection with medical therapy, all studies were single-arm studies. The populations varied, all had an observed niche, however the niche was not always clearly defined and the minimal required thickness of the residual myometrium was only reported in one study, in which it had to be at least 2.5 mm (Chang et al. 2009). Symptoms of the patients varied, these included postmenstrual spotting in four studies (Wang et al. 2009; Gubbini et al. 2008; Chang et al. 2009; Fernandez et al. 1996). Reported success rates were as high as 60–84 % (Wang et al. 2009; Gubbini et al. 20082011; Chang et al. 2009). The three prospective studies included a total of 61 patients receiving a hysteroscopic intervention. Mean reported reduction of postmenstrual spotting varied between 3 and 3.4 days (Gubbini et al. 20082011; Chang et al. 2009). One retrospective case–control study reported better outcomes of the hysteroscopic niche resection in comparison to applied hormonal therapies (Florio et al. 2011).

Complications were not reported. However exact methodology, follow-up or used (validated) tools to measure outcomes are mostly not reported. In theory, several complications could be expected. In case of a very thin residual myometrium, one should be aware of perforation and bladder injuries. Therefore, some studies propose preoperative installation of methylene blue dye in the bladder to enable the identification of any bladder injury in case of an unintended perforation.

7.9 Laparoscopic or Vaginal Niche Repair

Large niches with thin residual myometrium are less suitable for hysteroscopic resection. In these cases, surgical resection of the entire CS scar and suturing is proposed in case of severe symptoms. Such a niche repair or uterine reconstruction can be performed either by a laparoscopic (Donnez et al. 2008; Kostov et al. 2009; Klemm et al. 2005), robot-assisted (Yalcinkaya et al. 2011), or a vaginal (Khoshnow et al. 2010; Klemm et al. 2005) approach (Fig. 7.7).


Fig. 7.7

Part that is removed during a laparoscopic or vaginal niche resection

7.9.1 Effectiveness of Laparoscopic or Vaginal Niche Repair

There is only limited evidence for good results. So far only small case series reported on niche reconstruction in non-pregnant patients. In total only 14 patients underwent a laparoscopic repair (Donnez et al. 2008; Kostov et al. 2009; Klemm et al. 2005), 2 patients a robot-assisted (Yalcinkaya et al. 2011), and 4 patients a vaginal repair (Kostov et al. 2009; Hoorenbeeck 2002; Klemm et al. 2005). Indications for niche repair were diverse, these included women with secondary infertility, pelvic pain or metrorrhage, abnormal uterine bleeding, postmenstrual spotting, and previous cesarean scar pregnancy. Although an association between a niche and symptoms was presumed in these studies, one may still question if a niche is responsible for these symptoms. Outcome parameters in the reported publications were symptom reduction or MRI or hysteroscopic appearance of the niche. However, structural evaluation of clearly defined outcome parameters or follow-up was mostly not described. Although these techniques seem to be promising, more prospective studies are required with sufficient sample sizes and structural follow-up for the evaluation of the efficacy. In addition, long-term follow-up is required to draw conclusion on implications of these techniques on later pregnancies.

7.10 Conclusion

Niches are frequently seen after caesarean sections and are related to postmenstrual spotting and potentially associated with menstrual pain (therapies). Related postmenstrual spotting can be treated by hysteroscopic resection or more invasive niche reconstructions by an abdominal, laparoscopic or vaginal approach. Type of treatment depends on symptomatology and on the measured residual myometrium, given the risk on perforation or bladder injury during hysteroscopic resection in case it is less than 2.5 mm. More studies are needed to study the effect of niches on fertility and pregnancy outcome, to elucidate etiology of niches and related symptoms and to study the effect of current applied therapies on symptoms and later pregnancies.


Armstrong V, Hansen WF, Van Voorhis BJ, Syrop CH (2003) Detection of cesarean scars by transvaginal ultrasound. Obstet Gynecol 101(1):61–65PubMedCrossRef

BijdeVaate AJ, Brolmann HA, van der Slikke JW, Wouters MG, Schats R, Huirne JA (2010) Therapeutic options of caesarean scar pregnancy: case series and literature review. J Clin Ultrasound 38(2):75–84

BijdeVaate AJ, Brolmann HA, van der Voet LF, van der Slikke JW, Veersema S, Huirne JA (2011) Ultrasound evaluation of the cesarean scar: relation between a niche and postmenstrual spotting. Ultrasound Obstet Gynecol 37(1):93–99

Borges LM, Scapinelli A, de Baptista Depes D, Lippi UG, Coelho Lopes RG (2010) Findings in patients with postmenstrual spotting with prior cesarean section. J Minim Invasive Gynecol 17(3):361–364PubMedCrossRef

Chang Y, Tsai EM, Long CY, Lee CL, Kay N (2009) Resectoscopic treatment combined with sonohysterographic evaluation of women with postmenstrual bleeding as a result of previous cesarean delivery scar defects. Am J Obstet Gynecol 200(4):370 e1–4CrossRef

Chen HY, Chen SJ, Hsieh FJ (1990) Observation of cesarean section scar by transvaginal ultrasonography. Ultrasound Med Biol 16(5):443–447PubMedCrossRef

Donnez O, Jadoul P, Squifflet J, Donnez J (2008) Laparoscopic repair of wide and deep uterine scar dehiscence after cesarean section. Fertil Steril 89(4):974–980PubMedCrossRef

El-Mazny A, Abou-Salem N, El-Khayat W, Farouk A (2011) Diagnostic correlation between sonohysterography and hysteroscopy in the assessment of uterine cavity after cesarean section. Middle East Fertil Soc J 16(1):72–76CrossRef

Fabres C, Aviles G, De La Jara C, Escalona J, Munoz JF, Mackenna A et al (2003) The cesarean delivery scar pouch: clinical implications and diagnostic correlation between transvaginal sonography and hysteroscopy. J Ultrasound Med 22(7):695–700; 01–2PubMed

Fabres C, Arriagada P, Fernandez C, Mackenna A, Zegers F, Fernandez E (2005) Surgical treatment and follow-up of women with intermenstrual bleeding due to cesarean section scar defect. J Minim Invasive Gynecol 12(1):25–28PubMedCrossRef

Fernandez E, Fernandez C, Fabres C, Alam V (1996) Hysteroscopic correction of cesarean section scars in women with abnormal uterine bleeding. J Am Assoc Gynecol Laparosc 3:S13

Florio P, Gubbini G, Marra E, Dores D, Nascetti D, Bruni L, Battista R, Moncini I, Filippeschi M, Petraglia F (2011) A retrospective case-control study comparing hysteroscopic resection versus hormonal modulation in treating menstrual disorders due to isthmocele. Gynaecol Endocrinol 27(6):434–438CrossRef

Gubbini G, Casadio P, Marra E (2008) Resectoscopic correction of the “isthmocele” in women with postmenstrual abnormal uterine bleeding and secondary infertility. J Minim Invasive Gynecol 15(2):172–175PubMedCrossRef

Gubbini G, Centini G, Nascetti D, Marra E, Moncini I, Bruni L, Petraglia F, Florio P (2011) Surgical hysteroscopic treatment of cesarean-induced isthmocele in restoring fertility: prospective study. J Minim Invasive Gynecol 18(2):234–237PubMedCrossRef

Hamar BD, Saber SB, Cackovic M, Magloire LK, Pettker CM, Abdel-Razeq SS, Rosenberg VA, Buhimschi IA, Buhimschi CS (2007) Ultrasound evaluation of the uterine scar after cesarean delivery: a randomized controlled trial of one- and two-layer closure. Obstet Gynecol 110(4):808–813PubMedCrossRef

Hayakawa H, Itakura A, Mitsui T, Okada M, Suzuki M, Tamakoshi K, Kikkawa F (2006) Methods for myometrium closure and other factors impacting effects on cesarean section scars of the uterine segment detected by the ultrasonography. Acta Obstet Gynecol Scand 85(4):429–434PubMedCrossRef

Khoshnow Q, Pardey J, Uppal T (2010) Transvaginal repair of caesarean scar dehiscence. Aust N Z J Obstet Gynaecol 50(1):94–95PubMedCrossRef

Klemm P, Koehler C, Mangler M, Schneider U, Schneider A (2005) Laparoscopic and vaginal repair of uterine scar dehiscence following cesarean section as detected by ultrasound. J Perinat Med 33(4):324–331PubMedCrossRef

Kostov P, Huber AW, Raio L, Mueller MD (2009) Uterine scar dehiscence repair in rendezvous technique. Gynaecol Surg 6(Suppl 1) (S65)

Monteagudo A, Carreno C, Timor-Tritsch IE (2001) Saline infusion sonohysterography in nonpregnant women with previous caesarean delivery: the “niche” in the scar. J Ultrasound Med 20:1105–15

Morris H (1995) Surgical pathology of the lower uterine segment caesarean section scar: is the scar a source of clinical symptoms? Int J Gynecol Pathol 14(1):16–20PubMedCrossRef

Naji O, Abdallah Y, Bij De Vaate AJ, Smith A, Pexsters A, Stalder C, McIndoe A, Ghaem-Maghami S, Lees C, Brölmann HA, Huirne JA, Timmerman D, Bourne T (2012a) Standardized approach for imaging and measuring cesarean section scars using ultrasonography. Ultrasound Obstet Gynecol 39:252–259. doi:10.1002/uog.12334PubMedCrossRef

Naji O, Daemen A, Smith A, Abdallah Y, Bradburn E, Giggens R, Chan D, Stalder C, Ghaem-Maghami S, Timmerman D, Bourne T (2012b) Does the presence of a caesarean section scar influence the site of placental implantation and subsequent migration in future pregnancies: a prospective case-control study. Ultrasound Obstet Gynecol 40:557–561. doi:10.1002/uog.11133PubMedCrossRef

Naji O, Wynants L, Smith A, Abdallah Y, Stalder C, Sayasneh A, McIndoe A, Ghaem-Maghami S, Van Huffel S, Van Calster B, Timmerman D, Bourne T (2013) Predicting successful vaginal birth after Cesarean section using a model based on Cesarean scar features examined by transvaginal sonography. Ultrasound Obstet Gynecol 41(6):672-8. doi: 10.1002/uog.12423.

Naji O, Daemen A, Smith A, Abdallah Y, Saso S, Stalder C, Sayasneh A, McIndoe A, Ghaem-Maghami S, Timmerman D, Bourne T (2013a) Changes in cesarean section scar dimensions during pregnancy: a prospective longitudinal study. Ultrasound Obstet Gynecol 41:556–562PubMedCrossRef

Ofili-Yebovi D, Ben-Nagi J, Sawyer E, Yazbek J, Lee C, Gonzalez J et al (2008) Deficient lower-segment cesarean section scars: prevalence and risk factors. Ultrasound Obstet Gynecol 31(1):72–77PubMedCrossRef

Regnard C, Nosbusch M, Fellemans C, Benali N, van Rysselberghe M, Barlow P et al (2004) Cesarean section scar evaluation by saline contrast sonohysterography. Ultrasound Obstet Gynecol 23(3):289–292PubMedCrossRef

Stewart KS, Evans TW (1975) Recurrent bleeding from the lower segment scar–a late complication of caesarean section. Br J Obstet Gynaecol 82(8):682–686PubMedCrossRef

Surapaneni K, Silberzweig JE (2008) Cesarean section scar diverticulum: appearance on hysterosalpingography. AJR Am J Roentgenol 190(4):870–874PubMedCrossRef

Thurmond AS, Harvey WJ, Smith SA (1999) Cesarean section scar as a cause of abnormal vaginal bleeding: diagnosis by sonohysterography. J Ultrasound Med 18(1):13–16; quiz 17–8PubMed

Uppal T, Lanzarone V, Mongelli M (2011) Sonographically detected caesarean section scar defects and menstrual irregularity. J Obstet Gynaecol 31(5):413–416PubMedCrossRef

Valenzano MM, Mistrangelo E, Lijoi D, Fortunato T, Lantieri PB, Risso D, Costantini S, Ragni N (2006) Transvaginal sonohysterographic evaluation of uterine malformations. Eur J Obstet Gynecol Reprod Biol 124:246–249PubMedCrossRef

Vikhareva Osser O, Valentin L (2010a) Risk factors for incomplete healing of the uterine incision after caesarean section. BJOG 117(9):1119–1126PubMedCrossRef

Vikhareva Osser O, Jokubkiene L, Valentin L (2009) High prevalence of defects in cesarean section scars at transvaginal ultrasound examination. Ultrasound Obstet Gynecol 34(1):90–97PubMedCrossRef

Vikhareva Osser O, Jokubkiene L, Valentin L (2010) Cesarean section scar defects: agreement between transvaginal sonographic findings with and without saline contrast enhancement. Ultrasound Obstet Gynecol 35(1):75–83PubMedCrossRef

Voet LF van der, Graziosi GCM, Veersema S, BijDeVaate M, Huirne J, Brolmann HAM (2009) Perforation of an intra uterine device in a cesarean section scar. Gynecol Surg 6(Suppl. 1) (S106)

Wang CB, Chiu WW, Lee CY, Sun YL, Lin YH, Tseng CJ (2009) Cesarean scar defect: correlation between cesarean section number, defect size, clinical symptoms and uterine position. Ultrasound Obstet Gynecol 34(1):85–89PubMedCrossRef

Wang CJ, Huang HJ, Chao A, Lin YP, Pan YJ, Horng SG (2011) Challenges in the transvaginal management of abnormal uterine bleeding secondary to cesarean section scar defect. Eur J Obstet Gynecol Reprod Biol 154(2):218–222PubMedCrossRef

Yalcinkaya TM, Akar ME, Kammire LD, Johnston-MacAnnay EB, Mertz HL (2011) Robotic-assisted laparoscopic repair of symptomatic caesarean section defect:a report of two cases. J Reprod Med 56(5–6):265–270PubMed

Yazicioglu F, Gökdogan A, Kelekci S, Aygün M, Savan K (2006) Incomplete healing of the uterine incision after caesarean section: is it preventable? Eur J Obstet Gynecol Reprod Biol 124(1):32–36PubMedCrossRef