Pro forma for ultrasound reporting in suspected abnormally invasive placenta ( AIP ): an international consensus

Accurate antenatal diagnosis of an abnormally invasive placenta (AIP), allowing multidisciplinary management at the time of delivery, has been shown to improve maternal and fetal outcomes1–3. AIP can be predicted as early as in the first trimester, by identifying cases of suspected Cesarean scar pregnancy (CSP), as there is evidence that CSP in the first trimester and AIP in the second and third trimesters may represent different stages of a similar pathology4. Grayscale ultrasonography, with or without color Doppler and performed both transabdominally and transvaginally, has been used widely for antenatal screening and diagnosis of AIP. Many signs have been suggested, with reports varying as to their sensitivity and specificity5. Most of these ‘signs’ are poorly defined and, consequently, it is difficult to assess which are the most robust. To address this, the European Working Group on AIP (EW-AIP) have produced a consensus proposal to standardize the ultrasound descriptions used to define each sign, published in this issue of the Journal6. We assembled an international group of experts in the field with the specific aim of reaching an agreement regarding a standardized means of reporting ultrasound assessment of suspected AIP. If adopted by sonographers, clinicians and researchers worldwide, such a pro forma may facilitate better communication, and better evaluation of our diagnostic performance, in cases of suspected AIP. The group of international experts comprised an e-mail discussion group (n = 50) led by Jose Palacios Jaraquemada, members of the EW-AIP (n = 19) and members of the ISUOG (International Society of Ultrasound in Obstetrics and Gynecology) Clinical Standards Committee (n = 7). Each expert was asked to participate in a survey which involved completion of an online questionnaire to indicate what they believed should be included in the pro forma for reporting ultrasound assessment of suspected AIP. The online questionnaire, created using Survey Monkey, included risk factors known to be associated with AIP and all commonly reported ultrasound signs and definitions related to the diagnosis of AIP5–11. Ultrasound signs were divided into three subgroups according to modality: grayscale ultrasound, color Doppler and three-dimensional (3D) power Doppler. Each ultrasound sign in each subgroup had between one and six associated definitions reported in the published literature. To each selected demographic characteristic and ultrasound sign we assigned three options: (i) definitely include in report; (ii) include optionally in report and (iii) do not include in report. The definitions for each ultrasound sign were also assigned three options: (i) include; (ii) do not include and (iii) unsure. Participants were also asked whether clinical interpretation and relevance of the ultrasound findings should be included in the report. Options for preferred method of reporting clinical interpretation included: (i) give probability of clinically significant AIP, (ii) state whether manual removal of placenta should be attempted, and (iii) give free text description to provide guidance to the local team. There was the opportunity to provide free text comments for each section. A reminder to complete the questionnaire was sent out after 2 weeks, and we allowed 4 weeks for a response. All demographic characteristics and ultrasound signs for which >50% respondents selected ‘definitely include in report’ were incorporated into the standardized report, while those for which >50% respondents selected ‘do not include in report’ were excluded. For each ultrasound sign, the definitions for which >50% of respondents selected either ‘include’ or ‘unsure’ were kept for further evaluation. A second questionnaire was created for such items requiring further evaluation, in which respondents could specify first and second choice for definition of the ultrasound sign, and included additional suggestions from the free text comments, such as assessment for suspected parametrial involvement. For confirmation, we distributed a third and final round of the survey, with three domains, addressing: demographic and risk factors, ultrasound signs and clinical interpretation. At this round, consensus was sought from all participants that the ultrasound signs previously agreed on should be defined using the standardized descriptors proposed by the EW-AIP6. There were 42 respondents in the first round of the survey (response rate, 55%). For all of the demographic characteristics, placental location and grayscale ultrasound parameters, and for all but one color Doppler parameter, >50% of respondents chose ‘definitely include in report’. Only seven respondents thought that 3D power Doppler volumes should definitely be included and thus this criterion was excluded. All