Abstract
Objective:
To investigate the association between the intraoperative diagnosis of placenta accreta at the time of cesarean hysterectomy and pathological diagnosis.
Study Design:
This is a retrospective cohort study of all patients undergoing cesarean hysterectomy for suspected placenta accreta from 2000–2016 at Barnes-Jewish Hospital. The primary outcome was presence of invasive placentation on the pathology report. We estimated predictive characteristics of clinical diagnosis of placenta accreta using pathologic diagnosis as the correct diagnosis.
Results:
There were 50 cesarean hysterectomies performed for suspected abnormal placentation from 2000–2016. Of these, 34 (68%) had diagnosis of accreta preoperatively, and 16 (32%) were diagnosed intraoperatively at the time of cesarean delivery. Two patients had no pathological evidence of invasion, corresponding to a false positive rate of 4.0% (95%CI 0.5%, 13.8%) and a positive predictive value of 96.0% (95%CI 86.3%, 99.5%). There were no differences in complications among patients diagnosed intraoperatively compared with those diagnosed preoperatively.
Conclusion:
Most patients undergoing cesarean hysterectomy for placenta accreta do have this diagnosis confirmed on pathology. However, since diagnosis of placenta accreta was made intraoperatively in nearly a third of cesarean hysterectomies, intraoperative vigilance is required as the need for cesarean hysterectomy may not be anticipated preoperatively.
Keywords: placenta accreta, cesarean hysterectomy, clinico-pathological correlation, clinical diagnosis
INTRODUCTION
As rates of cesarean delivery increase, there has been a proportional increase in the rates of placenta accreta.1 Clinically, placenta accreta is defined by placental invasion of the uterine wall, or an inability to separate the placenta from the uterine wall at the time of delivery.2 Pathologically, placenta accreta, increta, and percreta are diagnosed when the placenta extends through the decidua basalis and into the myometrium or uterine serosa respectively.3 Patients with placenta accreta are at high risk for maternal morbidity or mortality at the time of delivery and usually require cesarean hysterectomy.3
However, even despite advances in imaging and greater understanding of risk factors, rates of preoperative diagnosis of placenta accreta remain low: 30–80% depending on the practice setting and country, with a recent rate of 50% reported from a large United States database.4 This means that obstetrician-gynecologists are often making split-second decisions regarding the need for the morbid and sterilizing procedure of hysterectomy.5–7 Further research is needed to understand the accuracy and consequences of these decisions.5, 8–14
Therefore, the objectives of this study were to: 1) investigate the relative frequency of preoperative versus intraoperative diagnosis of placenta accreta; 2) investigate the association between the diagnosis of placenta accreta at the time of cesarean hysterectomy and pathological diagnosis; and 3) test the hypothesis that compared to intraoperative diagnosis, preoperative diagnosis of placenta accreta is associated with a lower risk of intraoperative complications.
MATERIALS AND METHODS
This is a retrospective cohort study of patients undergoing cesarean hysterectomy for suspected placenta accreta. All patients undergoing cesarean hysterectomy from 2000–2016 at Washington University School of Medicine in St. Louis for suspected placenta accreta were included. Placenta accreta was defined as placental invasion to (accreta), into (increta), or through (percreta) the myometrial wall.2 Patients were identified by searching the comprehensive billing database for relevant ICD-9 and CPT codes capturing hysterectomy at the time of cesarean and placenta accreta. Patients were excluded if they underwent cesarean hysterectomy for other indications (e.g. uterine rupture, atony) or if placenta pathology reports were unavailable. The electronic medical records of all eligible patients were reviewed. We abstracted patient and pregnancy characteristics including preoperative diagnoses, imaging studies when available, intraoperative findings, and placental pathology results. The operative report (specifically the listed preoperative diagnosis, postoperative diagnosis, and operative findings) was used to determine the preoperative diagnosis as well as the intraoperative findings. In cases of ambiguity, the report was reviewed by multiple authors to achieve consensus.
We defined “clinical diagnosis” as any nonpathological diagnosis (made either preoperatively or intraoperatively), “preoperative diagnosis” as having placenta accreta listed as a preoperative diagnosis on the operative report or included in the indications for procedure, and “intraoperative diagnosis” as a clinical diagnosis first made at the time of cesarean section.
Patient and pregnancy information included maternal age, gestational age at delivery, race, height and weight at the time of delivery, obstetric history, number of prior cesarean deliveries, multiple pregnancy, tobacco use, and presence of placenta previa. Gestational age was based on the best obstetrical estimate as recorded in the medical record. All types of placenta previa (marginal, complete, etc.) were categorized as placenta previa. Imaging data included ultrasound and in some cases magnetic resonance imaging reports. Pathological diagnoses were determined from the pathology report. In cases of multiple levels of invasion the most severe was used (e.g. “placenta accreta with focal increta” was coded as “increta”). Surgical findings and complications were based on the operative report. The type of surgery was categorized as either cesarean total hysterectomy or cesarean supracervical hysterectomy. Intraoperative complications were categorized as cystotomy, ureteral injury, or other. Intentional cystotomies were recorded as “cystotomy.” Admission to the intensive care unit was noted. Estimated blood loss was obtained from the operative report. Intraoperative blood transfusion of packed red blood cells was recorded in units based on the operative report and anesthesia record.
The primary outcome was diagnosis of invasive placentation in the pathology report. Secondary outcomes were estimated blood loss and intraoperative complications. Test characteristics including positive predictive value and false positive rate with 95% confidence intervals (CI) of clinical diagnosis were estimated with pathology diagnosis of placenta accreta as the gold standard. Patients were categorized into two groups based on the timing of diagnosis of placenta accreta: preoperative or intraoperative, as discussed above. Baseline characteristics and outcome measures were compared with the Mann Whitney U or Fisher exact tests as appropriate.
Study data were collected and managed using REDCap electronic data capture tools hosted at Washington University School of Medicine in St. Louis. 15 The study was approved by the Washington University in St. Louis Human Research Protection Office. Given that we included all women who met inclusion criteria and the sample size was fixed, we did not perform an a priori sample size calculation. Analyses were performed in SAS software (version 9.2; SAS Institute, Inc, Cary, NC). A p-value <0.05 was considered statistically significant. We did not adjust for multiple comparisons.
RESULTS
From 2000–2016 There were 80 cesarean hysterectomies performed: 52 of which were for suspected placenta accreta (2 had a missing pathology report leaving a final sample size of 50) (Figure 1). The majority of these were in the years from 2013–2016 (n=28) with the remainder distributed relatively evenly over the preceding years. Of the 50 patients, 34 (68%) had a preoperative diagnosis of placenta accreta, while the diagnosis was first made intraoperatively in the remaining 16 (32%) at the time of cesarean delivery. The majority of patients (n=38, 76%) had a preoperative diagnosis of placenta previa and at least one prior cesarean delivery.
Figure 1:
Study Flow Diagram
Baseline characteristics were similar among patients diagnosed preoperatively and intraoperatively with the notable exception that placenta previa and prior cesarean were more common among patients diagnosed preoperatively: placenta previa (97% versus 44%, p<0.0001) and mean number of prior cesareans (3 versus 2, p=0.02). (Table 1).
Table 1:
Preoperative Characteristics (n=50)
| Characteristic | Entire Cohort (n=50) | Invasion diagnosed preoperatively (n=34) | Invasion first diagnosed intraoperatively (n=16) | P* |
|---|---|---|---|---|
| Maternal age, y | 31.4 (5.9) | 31.7 (5.3) | 30.8 (7.2) | 0.44 |
| Gestational age at delivery, wk | 33.0 (3.1) | 33.4 (3.2) | 32.3 (3.8) | 0.24 |
| Race | 0.72 | |||
| Black | 17 (34) | 10 (29) | 7 (44) | |
| Caucasian | 29 (58) | 21 (62) | 8 (50) | |
| Other | 4 (8) | 3 (9) | 1 (6) | |
| Body mass index (kg/m2) | 31.5 (7.3) | 31.3 (8.2) | 31.9 (5.1) | 0.44 |
| Gravidity | 5 (2) | 5 (2) | 4 (1) | 0.04 |
| Parity | 3 (2) | 3 (2) | 2 (1) | 0.16 |
| Prior cesarean delivery | 46 (94) | 32 (94) | 14 (88) | 0.58 |
| Number of prior cesareans | 2 (1) | 3 (2) | 2 (1) | 0.02 |
| Multiple pregnancy | 4 (8) | 1 (3) | 3 (18) | 0.09 |
| Tobacco use | 8 (16) | 6 (18) | 2 (13) | 1.00 |
| Placenta Previa | 40 (80) | 33 (97) | 7 (44) | <0.0001 |
Data presented as n (%) or mean (SD)
P from Mann Whitney U or Fisher exact test
In all, 48 (96%) patients had confirmed placenta accreta in the pathology report while two patients (4%) had no evidence of invasion. This corresponds to an overall positive predictive value of a clinical diagnosis of 96.0% (95%CI 86.3%, 99.5%), and a false positive rate of 4.0% (95%CI 0.5%, 13.8%) (Table 2).
Table 2:
Pathological Outcomes (n=50)
| Outcome | n (%) |
|---|---|
| No invasion | 2 (4) |
| Accreta | 19 (38) |
| Increta | 18 (36) |
| Percreta | 11 (22) |
Of the 16 patients with initial intraoperative diagnosis, 9 (56%) had an initial attempt to remove the placenta. The remainder did not have such an attempt due to visibly abnormal placentation at the time of the delivery. All patients who were first diagnosed intraoperatively (n=16) had pathologic confirmation of placenta accreta.
Table 3 shows the relationship between intraoperative diagnosis of the degree of abnormality and the pathological diagnosis. Of the two false positive clinical diagnosis of placental invasion, one was thought to be a placenta accreta while the other was a suspected placenta increta. Both patients had a preoperative ultrasound diagnosis of placenta accreta.
Table 3:
Relationship between Intraoperative and Pathological Diagnoses (n=50)
| Pathological Diagnosis | |||||
|---|---|---|---|---|---|
| No invasion | Accreta | Increta | Percreta | ||
| Intraoperative Diagnosis | Accreta | 1 (2) | 14 (28) | 13 (26) | 4 (8) |
| Increta | 1 (2) | 1 (2) | 3 (6) | 2 (4) | |
| Percreta | 0 (0) | 4 (8) | 2 (4) | 5 (10) | |
Most patients (84%) had total cesarean hysterectomy, and the remainder (16%) had supracervical hysterectomy. There was no difference in total hysterectomy rates in patients with preoperative and postoperative diagnosis of placenta accreta (88% versus 75%, p=0.25). The median blood loss was 2,500 mL for the entire cohort with mean hospital length of stay of 4.5 days, with no differences between the groups diagnosed preoperatively versus intraoperatively. Nearly 1 in 5 women were admitted to the intensive care unit, with no differences in those diagnosed preoperatively and intraoperatively (21% versus 13%, p=0.70) (Table 4). There were no maternal deaths. Intraoperative surgical injury was common with nearly 1 in 3 patients sustaining a cystostomy, ureteral injury or other type of injury (n=16, 32%).
Table 4:
Surgical Outcomes (n=50)
| Outcome | Entire Cohort | Invasion diagnosed preoperatively (n=34) | Invasion diagnosed intraoperatively (n=16) | P |
|---|---|---|---|---|
| Surgical Procedure | 0.25 | |||
| Cesarean total hysterectomy | 42 (84) | 30 (88) | 12 (75) | |
| Cesarean supracervical hysterectomy | 8 (16) | 4 (12) | 4 (25) | |
| Intraoperative complication | 16 (32) | 14 (41) | 2 (12) | 0.26 |
| Cystotomy | 13 (26) | 11(32) | 2 (13) | |
| Ureteral injury | 1 (2) | 1 (3) | 0 (0) | |
| Other | 2 (4) | 2 (6) | 0 (0) | |
| Intensive care unit admission | 9 (18) | 7 (21) | 2 (13) | 0.70 |
| Estimated blood loss (mL) | 2400 (1500–3100) | 2600 (1500–3500) | 2000 (1250–2750) | 0.13 |
| Packed red blood cells transfused intraoperatively (units) | 2.5 (1–4) | 3 (1–5) | 2 (0.5–4) | 0.37 |
| Length of postoperative admission (days, mean (standard deviation)) | 4.5 (1.2) | 4.7 (1.4) | 4.1 (0.6) | 0.22 |
Data presented as n(%) or median (interquartile range). P from Mann Whitney U or Fisher exact test comparing preoperative to intraoperative diagnosis groups
DISCUSSION
We found that nearly one-third of diagnoses of placenta accreta were only made at the time of delivery. Additionally, although overall clinical diagnosis (preoperative and intraoperative) was largely accurate, there was a 4% false positive rate where the clinical diagnosis of placenta accreta was not confirmed on pathological examination. There were no significant differences in outcomes between patients diagnosed preoperatively compared to those diagnosed intraoperatively.
These findings indicate that when faced with a “surprise” potential placenta accreta, clinical diagnosis is highly accurate. The majority of the 16 patients with initial intraoperative diagnosis had an initial attempt to remove the placenta, suggesting that the diagnosis was indeed unexpected. Notably, all of these patients had pathological confirmation of placenta accreta, further suggesting that the abandonment of the placenta delivery attempt and decision to perform hysterectomy was justified.
The proportion of intraoperative versus preoperative diagnosis of placenta accreta in our study were similar to those in other studies, which have ranged from a preoperative diagnosis rate of 30–80%.5, 6, 10, 14, 16 In a retrospective case series of 99 pathologically-confirmed placenta accreta cases, 63% were diagnosed antepartum with the remaining 37% diagnosed at delivery.14 On the other hand, in a recent study of 205 cases from the Nordic countries, 70% were undiagnosed preoperatively.5 However, that study considered only clinical diagnosis, not pathological diagnosis. In our study, patients with risk factors were more likely to be diagnosed preoperatively, perhaps reflecting provider bias in more vigilantly searching for placenta accreta in patients with risk factors.
Further work is needed to improve rates of preoperative diagnosis.17 The diagnostic accuracy of ultrasound for abnormal placentation is variable with a recent report citing a false negative rate as high as 16%.10 However, a meta-analysis noted that in experienced units ultrasound is highly sensitive and specific for diagnosis of placenta accreta with prenatal detection rates >90%.11 This variability in accuracy of ultrasound diagnosis of abnormal placentation is likely due to the operator-dependent nature of ultrasound examinations.
It is recognized that patients with placenta accreta have better outcomes when treated in a specialty center with multidisciplinary care.7–9 However, it is unclear to what degree the patients managed by regular care in these studies had a suspected diagnosis prior to surgery.8 Notably a recent study from across the United States actually found worse outcomes in patients with a preoperative diagnosis compared to an initial intraoperative diagnosis, perhaps due to more severe disease.4 The lack of significant differences in outcomes between patients with preoperative versus intraoperative diagnoses in our study may be attributable to the fact that patients were treated in a regional perinatal health care center with continuous access to advanced pelvic surgeons as well as robust intensive care and blood bank services.18 Thus, outcomes may not be the same as in a community setting where an unplanned cesarean hysterectomy confers significantly more morbidity.9
There were a number of strengths to our study. The study was conducted in an institution with common approaches to diagnosis and management of placenta accreta. In addition, detailed data were abstracted allowing for comprehensive analysis. However, there are limitations to be considered when interpreting our results. This is a retrospective cohort study based on chart review of patients identified through billing codes. While we used exhaustive codes to in an attempt to identify all patients meeting inclusion criteria, there is the possibility some patients were missed. Moreover, accuracy of the distinction between preoperative and intraoperative diagnosis of placenta was based on the listed diagnoses and descriptions in the operative reports, which may reflect provider bias. Although our sample size is comparable to prior studies, it is relatively small and may have impacted our ability to find statistically significant differences.1, 14, 16 Finally, we did not have information about preoperative diagnoses of placenta accreta that were not clinically corroborated intraoperatively and therefore did not lead to cesarean hysterectomy. This made it impossible to estimate the test characteristics of preoperative imaging and diagnosis.
In conclusion, in our cohort, diagnosis of placenta accreta was first made intraoperatively in nearly a third of cesarean hysterectomies. While most patients undergoing cesarean hysterectomy for clinically diagnosed placenta accreta had the diagnosis confirmed on pathologic examination, there was a 4% false positive rate. When faced with a clinical situation concerning for placenta accreta, clinicians can be reassured that clinical diagnosis is highly accurate. These findings re-enforce the need for vigilance intraoperatively as the need for cesarean hysterectomy may not be anticipated preoperatively. As summarized in a recent editorial by Nageotte, clinicians must remain alert and ready for the potential for an undiagnosed placenta accreta at all times.19
Acknowledgments
Funding: This work was supported by the National Institutes of Health [grant numbers UL1 TR000448 and P30 CA091842]. Dr. Tuuli is supported by U01HD077384-03 and 1R01HD086007-01 grants. The contents of this publication are solely the responsibility of the authors and do not necessarily represent the official view of the NIH. The funder had no role in the study design, collection, analysis or interpretation of data, in the writing of the report, or in the decision to submit the article for publication.
Footnotes
Financial Disclosure: The authors report no conflict of interest.
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