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    O B S T E T R I C S

    Screening for placenta accreta at 11-14 weeks of gestationJulien J. Stirnemann, MD; Eve Mousty, MD; Gihad Chalouhi, MD; Laurent J. Salomon, MD, PhD;

    Jean-Pierre Bernard, MD; Yves Ville, MD

    OBJECTIVE: We sought to describe the potential value of 11-14 weeks

    screening for placenta accreta (PA).

    STUDY DESIGN: Patients with a history of lower segment cesarean

    section were prospectively included between 11-136 weeks over a

    1.5-year period. The first 258 were offered standard screening

    whereas the following 105 underwent screening for PA. Women were

    considered high-risk when the trophoblast overlapped the scar visual-

    ized by transvaginal ultrasound and low-risk otherwise.

    RESULTS: The group screened for PA did not differ from the non-

    screened group for demographic characteristics. In all, 6 of 105 (5.8%)

    women were considered high-risk. In the nonscreened group, 1 case of

    PA was discovered during an elective repeat cesarean. In the screened

    population, 1 case of PA occurred in a high-risk patient allowing a con-

    servative planned management at 35 weeks.

    CONCLUSION: At 11-14 weeks, ultrasound may help risk stratification

    for PA with a specific follow-up. Early recognition of patients at risk

    might improve the perinatal outcome of PA.

    Key words: cesarean, first trimester, placenta accreta, screening,

    ultrasound

    Cite this article as: Stirnemann JJ, Mousty E, Chalouhi G, et al. Screening for placenta accreta at 11-14 weeks of gestation. Am J Obstet Gynecol

    2011;205:547.e1-6.

    P lacenta accreta (PA) is a life-threat-ening obstetrical condition that oc-curs when a defect of the decidua basalis

    enables the direct apposition of chori-

    onic villi to the myometrium. As a result,

    at least part of the placenta cannot sepa-

    rate after delivery and this may lead to

    severe obstetric hemorrhage.1-5 It has

    become the principal indication forpostpartum hysterectomy as well as for

    related surgical injuries.6-10 The inci-

    dence of PA has increased 4-fold from

    199411 through 2002,12 following the in-

    crease in cesarean delivery rates over the

    same period of time. Most PA present as

    placenta previa in the third trimester

    with an incidence of 9.3% in this group

    compared with 0.005% when the pla-

    centa is normally inserted.11 Among

    women with placenta previa, maternal

    age35 years and previous cesarean de-

    livery are independent risk factors, with

    an incidence of 2% for women aged35

    years and no cesarean section up to 38%

    in women aged35 years and2 previ-ous cesarean sections.11

    It is important to diagnose PA prior to

    delivery, to allow for optimal concerted

    management planning and prevention

    of severe maternal morbidity and mor-

    tality.13-17 The diagnosis of PA by ultra-

    sound and magnetic resonance imaging

    (MRI) in the second and third trimester

    of pregnancy remains largely speculative,

    even in high prevalence cohorts,18-21 and

    most cases are only diagnosed at the time

    of delivery in cases with prepartum or

    postpartum hemorrhage.13-16 The timing

    of the defective trophoblast implantation

    leading to PA suggests that this condition

    couldbeidentifiedduringthe11-14weeks

    ultrasound.

    Signs of PA have been recognized as

    early as the first trimester in several case

    reports.22-26 However, these findings

    have never been implemented in a pro-

    spective early screening strategy. The

    main aim of our study was to describethe potential use of routine 11-14 weeks

    scan27 for screening for PA in women

    with a history of delivery by lower seg-

    ment cesarean section (LSCS).

    MATERIALS AND METHODS

    The screening procedure for PA was de-

    fined inpatients with a history of LSCS as

    follows: a transvaginal midsagittal planewas defined, including the cervical canal,the bladder, and the lower part of the

    gestational sac.28 Both the uterine scar

    and the location of the trophoblast were

    recognized and located. The relationship

    between the uterine scar and the tropho-

    blast thus defined the high-risk group. A

    patient was considered high-risk when

    the scar was exposed within the uterine

    cavity above the lowest part of the gesta-

    tional sac, which encompasses the cervix

    and part of the inferior segment togetherwith a covering low-lying placenta (Fig-

    ure 1).28 A patient was considered low-

    risk eitherwhen the uterine scar was pro-

    tected within the cervicoisthmic canal

    (Figure 2, A) or when the trophoblast

    was not covering the internal os (Figure

    2, B).28

    The population considered for this

    study comprises all consecutive cases of

    patients with a history of lower segment

    uterine scar over a 1.5-year period (Sep-

    tember 2008 through March 2010) at-tending our unit for first-trimester

    From the Department of Obstetrics and

    Maternal-Fetal Medicine, GHU Necker

    Enfants Malades, Universit Paris Descartes,Paris, France.

    Received Feb. 9, 2011; revised May 29, 2011;accepted July 13, 2011.

    This study was supported by the SocitFranaise pour lAmlioration des PratiquesEchographiques in setting teaching sessions.

    The authors report no conflict of interest.

    Reprints: Yves Ville, MD, Maternit, HpitalNeckerEnfants Malades, 149 rue de Svres,75015 Paris, France. [email protected].

    0002-9378/$36.00 2011 Mosby, Inc. All rights reserved.

    doi: 10.1016/j.ajog.2011.07.021

    Research www.AJOG.org

    DECEMBER 2011 American Journal of Obstetrics &Gynecology 547.e1

    mailto:[email protected]:[email protected]:[email protected]
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    screening at 11-136 weeks as defined

    by a crown-rump length between 45-84

    mm. During a first period of time, pa-

    tients were not specifically screened for

    placenta and scar location. In a second

    period, patients were screened for PA by

    transvaginal ultrasound.All ultrasounds were performed usinga General Electrics Voluson E8 or 730

    Expert (GEMedical SystemEurope, Buc,

    France) with a 3.5- to 5-MHz or 6- to

    8-MHz transvaginal transducer.

    Demographic data as well as obstetri-

    cal and perinatal management and out-

    come were prospectively recorded in our

    electronic database (Astraia, Munich,

    Germany). Patients considered high-risk

    were followed up prospectively with se-

    rial ultrasound focusing on ultrasoundsigns of placental invasion in our unit up

    until delivery.

    The statistical analysis was conducted

    using R (www.r-project.org). Quantita-

    tive variables are summarized by the me-

    dian and interquartile range (25th-75th

    centile) and qualitative variables are de-

    scribed by N (%). Comparisons of de-

    mographic characteristics between the

    screened and nonscreened populations

    were performed using Mann-WhitneyU

    tests for quantitative variables and Fisherexact tests for qualitative variables.Since transvaginal ultrasound is of-

    fered routinely for first-trimester screen-

    ing in our practice, this study did not re-

    quire an institutional review board;

    however, written informed consent was

    obtained from all women.

    RESULTS

    Over the study period, 363womenwith a

    history of LSCS attended our unit forfirst-trimester screening at 11-136

    weeks gestation. Among these, the first

    258women were screened only for aneu-

    ploidy and fetal defects whereas the fol-

    lowing 105 were also prospectively

    screened for PA. No significant differ-

    ences in demographic characteristics

    were found between thescreenedand the

    nonscreened populations (Table 1). In

    particular, considering risk factors for

    PA, maternal age (P .12), parity (P

    .46), number of scars (P

    .28), andratesof emergency cesarean operations (P

    FIGURE 1

    Exposed scar with overlapping trophoblast (T) defining high-risk group

    Arrows uterine scar.

    B, bladder; C, cervix; GS, gestational sac.

    Stirnemann. Screeningfor placenta accreta at 11-14weeks. Am J Obstet Gynecol 2011.

    FIGURE 2

    Protected and exposed scars

    A, Protected scar with trophoblast (T) overlapping internal os. B, Exposed scar with nonoverlapping T.Arrows uterine scar.

    B, bladder; C, cervix; GS, gestational sac.

    Stirnemann. Screeningfor placenta accreta at 11-14weeks. Am J Obstet Gynecol 2011.

    Research Obstetrics www.AJOG.org

    547.e2 American Journal of Obstetrics &Gynecology DECEMBER 2011

    http://www.r-project.org/http://www.r-project.org/
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    .06) were similar. The overall rate of loss

    to follow-up was 38/363 (10.5%) and

    was similar in both groups(9/105 [8.6%]

    and 29/258 [11.2%], P .57). The deliv-

    ery mode was unknown in 5 cases.

    Obstetrical and perinatal manage-

    ment of the study population is summa-rized in Figure 3. Two patients under-went termination of pregnancy and 3

    miscarried 24 weeks gestation. These

    patients together with 3 cases of intra-

    uterine fetal demise delivered vaginally.

    All live-born pregnancies with at least 2

    uterine scars delivered by elective cesar-

    ean whereas patients with only 1 scar

    attempted vaginal birth in 162/262

    (61.8%) with a 105/262 (64.8%) success

    rate.

    Perinatal complications related to priorcesarean included 2 cases (0.6%) of PA, 16

    cases (5%) of severe postpartum hemor-

    rhage requiring sulprostone or surgery, 2

    cases (0.6%)of placentaprevia, and2 cases

    (0.6%) of complete uterine rupture. The

    occurrenceofPAinthestudypopulationis

    summarized in Figure 4 with respect to

    screening results.

    Within the nonscreened population, 1

    case of placenta percreta was discovered

    during elective cesarean at 395 weeks

    in a 31-year-old, 4-parous patient with ahistory of 2 cesareans. This patient hadan uneventful follow-up until delivery.

    Upon opening of the peritoneum, pla-

    cental bulging through the anterior uter-

    ine wall required a fundal incision. A con-

    servative management was performed

    leavingtheplacentaand theuterus. Embo-

    lizationof uterineandinternaliliacarteries

    was subsequently performed. Follow-up

    was uneventful apart from episodic bleed-

    ing without signs of infection, with MRI

    examinations showingprogressive involu-tion of the placenta at 8 months after

    cesarean.

    Withinthe screened population, 1 scar

    was not visualized, 6 of 104 (5.8%) pa-

    tients were considered high-risk based

    upon a trophoblast overlapping an ex-

    posed scar, and 98 of 104 were consid-

    ered low-risk.One case of PA wasdiscov-

    ered in the sixth high-risk patient. This

    patient had been followed-up by serial

    ultrasound at 161,181,221,251,

    and 29

    1 weeks confirming signs of PAboth on ultrasound and MRI with a low-

    lying anterior placenta. Elective cesarean

    section was performed at 35 weeks under

    epidural anesthesia after a course of be-

    tamethasone given for fetal lung matu-

    rity enhancement. The inferior segment

    was richly vascularized. Hysterotomywas performed through a fundal vertical

    incision.No attempt was made to extract

    the placenta. Uterine and internal iliac

    arteries embolization was then per-

    formed systematically. Blood loss was

    300 mL and the postpartum period was

    uneventful. The placenta was still intra-uterine at 3 months when she developed

    TABLE 1

    Comparison of demographic characteristics betweenscreened and nonscreened populations

    Characteristic

    OverallWithout 11-14 wkscreening

    With 11-14 wkscreening

    Pvaluen 363 n 258 n 105

    Age, y .12..............................................................................................................................................................................................................................................

    Median (IQR) 35 (3138) 35 (3239) 34 (3038).....................................................................................................................................................................................................................................

    Missing 0..............................................................................................................................................................................................................................................

    Parity .46.....................................................................................................................................................................................................................................

    1 212 (58.4%) 157 (60.9%) 52 (55.9%).....................................................................................................................................................................................................................................

    1 139 (38.3%) 101 (39.1%) 41 (44.1%).....................................................................................................................................................................................................................................

    Missing 12 (3.3%)..............................................................................................................................................................................................................................................

    No. of scars .28.....................................................................................................................................................................................................................................

    1 305 (84.0%) 221 (85.7%) 84 (80%).....................................................................................................................................................................................................................................

    2 54 (14.9%) 34 (13.2%) 20 (19%).....................................................................................................................................................................................................................................3 4 (1.1%) 3 (1.1%) 1 (1%).....................................................................................................................................................................................................................................

    Missing 0..............................................................................................................................................................................................................................................

    Interval since last delivery, mo .14.....................................................................................................................................................................................................................................

    Median (IQR) 28 (1249) 26.5 (11.745.5) 32 (1454).....................................................................................................................................................................................................................................

    Missing 137 (37.7%)..............................................................................................................................................................................................................................................

    History of vaginal birth .36.....................................................................................................................................................................................................................................

    Yes 64 (17.6%) 42 (17.4%) 22 (21.8%).....................................................................................................................................................................................................................................

    No 279 (76.9%) 200 (82.6%) 79 (78.2%).....................................................................................................................................................................................................................................

    Missing 20 (5.5%)..............................................................................................................................................................................................................................................

    VBAC .16.....................................................................................................................................................................................................................................

    Yes 33 (9.1%) 27 (11.3%) 6 (5.8%).....................................................................................................................................................................................................................................

    No 309 (85.1%) 212 (88.7%) 97 (94.2%).....................................................................................................................................................................................................................................

    Missing 21 (5.8%)..............................................................................................................................................................................................................................................

    Emergency cesarean .06.....................................................................................................................................................................................................................................

    Yes 119 (32.8%) 77 (29.8%) 42 (40%).....................................................................................................................................................................................................................................

    No 244 (67.2%) 181 (70.2%) 63 (60%).....................................................................................................................................................................................................................................

    Missing 0..............................................................................................................................................................................................................................................

    Postpartum pyrexia .38.....................................................................................................................................................................................................................................

    Yes 15 (4.1%) 9 (3.5%) 6 (5.7%).....................................................................................................................................................................................................................................No 348 (95.9%) 249 (96.5%) 99 (94.3%).....................................................................................................................................................................................................................................

    Missing 0..............................................................................................................................................................................................................................................

    IQR, interquartile range; VBAC, vaginal birth after cesarean.

    Stirnemann. Screeningfor placenta accreta at 11-14weeks. Am J Obstet Gynecol 2011.

    www.AJOG.org Obstetrics Research

    DECEMBER 2011 American Journal of Obstetrics &Gynecology 547.e3

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    endometritis and hysterectomy was eas-

    ily performed without technical prob-

    lems. She was discharged home after 54

    days. Pathology examination confirmed

    placenta increta. The 5 other patients

    considered high-risk based upon 11-14

    weeksultrasound hadan uneventful fol-low-up (Table 2) and delivered vaginally(n 2) or by cesarean (n 3) without

    complications at between 38-40 weeks

    gestation.

    COMMENT

    PA is a life-threatening obstetrical emer-

    gency. Its incidence has risen in parallel

    with that of cesarean deliveries and it re-

    mains a major cause of maternal mortal-

    ity and morbidity as the principal indi-cation for postpartum hysterectomy

    with high blood loss, intensive care unit

    admission, and intraoperative injury to

    the bladder or bowel.13,15,16

    Efforts have been made to refine the

    ultrasound diagnosis of PA in the second

    and third trimester of pregnancy, con-

    sisting in the presence of placental lacu-

    nae (irregularly shaped vascular spaces

    with turbulent blood flow at the color

    Doppler), loss of retroplacental clear

    space, thinning of the myometriumoverlying the placenta and interruptionof the bladder line with protrusion of the

    placenta into the bladder, or evidence of

    hypervascularization by Doppler.21,29-31

    The performance of ultrasound has been

    studied in very high-risk populations,

    with a prevalence of PA ranging from

    9-44%. In these studies the sensitivity

    of ultrasound, with 1 contemporary

    signs, varies from 77-93% and the posi-

    tive predictive value from 65-93%.18-21

    Although MRI may help refine the diag-nosis following ultrasonography,32,33 its

    overall sensitivity remains unclear.19,29

    However, most cases of PA remain undi-

    agnosed until the time of delivery.13,15,16

    PA, however, is likely to develop at the

    time of the trophoblast invasion in the

    first trimester.34,35 The study of the tro-

    phoblasts location in the first trimester

    is feasible as part of the routine 11-136

    weeks scan. Mustaf et al36 in 2002 have

    well established the probability of pla-

    centa previa at termin relationto the dis-tance/overlap of the lower placental edge

    FIGURE 3

    Obstetric management of delivery in study population

    IUFD, intrauterine fetal demise; LSCS, lower segment cesarean section; LTFU, lost to follow-up; TOP, termination of pregnancy.

    Stirnemann. Screeningfor placenta accreta at 11-14weeks. Am J Obstet Gynecol 2011.

    FIGURE 4Flowchart of study population with respect toscreening and occurrence of placenta accreta

    LSCS, lower segment cesarean section; LTFU, lost to follow-up.

    Stirnemann. Screeningfor placenta accreta at 11-14weeks. Am J Obstet Gynecol 2011.

    Research Obstetrics www.AJOG.org

    547.e4 American Journal of Obstetrics &Gynecology DECEMBER 2011

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    with respect to the internal cervical os.

    The cesarean scar has been studied and

    describedin nonpregnant women as part

    of the investigation of the relationship

    between scar defects and postmenstrual

    spotting, dysmenorrhea, and pelvic

    pain.

    37-40

    The sonographic diagnosis in the firsttrimester has been reported in a few

    cases22-25 mainly as a low gestational sac

    in early first trimester, suggesting a direct

    implantation of the trophoblast over the

    scar.26 However, these cases are difficult

    to differentiate from ectopic pregnancies

    developing in the LSCS scar. These cases

    of PA detected in early pregnancy all

    showed very specific sonographic fea-

    tures. These findings, however, are un-

    likely to be fit for 11-14 weeks screeningpolicy, since their prevalence in PA as

    well as in normal pregnancies has not

    been formally studied. We believe these

    ultrasound findings should be used in

    second-line diagnostic scans in screen-

    positive patients.

    Ultrasound examination is now rou-

    tinely offered to all pregnant women at

    11-14 weeks of gestation in many devel-

    oped countries.41 Todate,the aim ofthis

    examination is mainly to confirm viabil-

    ity and gestational age, diagnose and de-termine chorionicity of multiple preg-nancies, as well as screening for fetal

    aneuploidy and for some severe malfor-

    mations. Promising attempts at predict-

    ing severe obstetrical conditions devel-

    oping in the second or third trimester

    such as preeclampsia by ultrasound and

    Doppler examination at 12 weeks are

    promising.42,43 We believe that screen-

    ing for PA in a high-risk group with pre-

    vious cesarean section is justified by the

    severity of this condition at the time ofdelivery andby thefeasibility of both scar

    and placental examination at 11-14

    weeks.28 Early recognition of PA is likely

    to be associated with lesser maternal

    morbidity.15,16 Elective cesarean section

    with a conservative approach of the pla-

    centa left in place has shown to improve

    the prognosis for the mother.14 In our

    population, a case of placenta percreta

    went to delivery undiagnosed in thenon-

    screened group, whereas early recogni-

    tion of PA in the high-risk group allowedfor planning optimal management. This

    suggests that the rationale for 11-14

    weeks screening is to help plan further

    investigations and follow-up thus avoid-

    ing unanticipated peripartum discover-

    ies of PA as well as to reassure patients

    otherwise at risk based upon demo-

    graphic characteristics. Nonetheless, it islikely that a trophoblast overlapping thescar is notthe only factorthat determines

    the occurrence of PA. Indeed, as shown

    by Miller et al,11 PA may develop at a

    distance from the scar at a rate of 3.7%

    and 9.1% for patients 35 years and

    35 years with 1 previous cesarean sec-

    tion. Therefore, although 11-14 weeks

    screening is likely to identify most cases

    it is anticipated that it will fail in identi-

    fying all cases.

    We propose that systematic evaluationof the uterine scar and placental location

    be tested in a large prospective study at

    the time of the 11-14 weeks ultrasound

    examination in women with a uterine

    scar. Our data suggest that 5.8% of

    women with1 previous LSCS could be

    considered at high risk of PA with scars

    covered by the trophoblast insertion

    at 12 weeks. Conversely, scars located

    within the cervical canal or yet undevel-

    oped isthmus appear to be protected

    from this risk even with a low-lying tro-phoblast over the internal os. Account-

    ing for maternal age and history could

    lead to objective individual risk calcula-

    tion for PA as early as 12 weeks and help

    refine the care of women, including spe-

    cialized imaging investigations such as

    an early ultrasound at 16-18 weeks21 or

    MRI together with a planned delivery inan appropriate obstetrical unit. f

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    Ultrasound follow-up of 6 cases considered high-riskfor placenta accreta by 11-14 weeks screening

    CasesGestational age atfollow-up, wk Placental location

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    2 176 Anterior, high..............................................................................................................................................................................................................................................

    3 183 Posterolateral, low lying............................................................................................................................................................................

    222 Posterior, high..............................................................................................................................................................................................................................................

    4 160 Posterior, high..............................................................................................................................................................................................................................................

    5 284 Posterior, high..............................................................................................................................................................................................................................................

    6 161 Anterolateral low-lying............................................................................................................................................................................

    181 US signs of placenta accreta............................................................................................................................................................................

    221............................................................................................................................................................................

    251............................................................................................................................................................................

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