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Case-crossover study to examine the change in postpartum risk of pulmonary embolism over time
© The Author(s). 2017
Received: 6 May 2016
Accepted: 21 March 2017
Published: 14 April 2017
Although the current guidelines recommend anticoagulation up until 6 weeks after delivery in women at high risk of venous thromboembolism (VTE), the risk of VTE may extend beyond 6 weeks. Our objective was to estimate the risk of a pulmonary embolism in successive 2-week intervals during the postpartum period.
In a population-based, case-crossover study, we analyzed the French national inpatient database from 2007 to 2013 (n = 5,517,680 singleton deliveries). Using ICD-10 codes, we identified women who were diagnosed with a postpartum pulmonary embolism between July 1st, 2008, and December 31st, 2013. Deliveries were identified during a case “period” immediately before the pulmonary embolism, and five different control periods one year before the pulmonary embolism. Using conditional logistic regression, Odds ratios (ORs) and 95% confidential intervals (CIs) were estimated for ten successive 2-week intervals that preceded the diagnosis of pulmonary embolism.
We identified 167,103 cases with a pulmonary embolism during the inclusion period. After delivery, the risk of pulmonary embolism declined progressively over time, with an OR [95%CI] of 17.2 [14.0–21.3] in postpartum weeks 1 to 2 and 1.9 [1.4–2.7] in postpartum weeks 11 to 12. The OR [95%CI] in postpartum weeks 13 to 14 was 1.4 [0.9–2.0], and the OR did not fall significantly after postpartum week 14.
Our findings indicate that women are at risk of a pulmonary embolism up to 12 weeks after delivery. The shape of the risk curve suggests that the risk decreases exponentially over time. Future research is needed to establish whether the duration of postpartum anticoagulation should be extended beyond 6 weeks.
The postpartum period is associated with an elevated risk of a venous thromboembolic event (VTE). The American College of Chest Physicians recommends that patients at high risk of thromboembolism should receive prophylactic anticoagulation therapy for 6 weeks following delivery . In France, recommendations for prophylactic anticoagulation are similar . However, based on the results of four studies [3–6], it is not clear whether the risk of VTE extends beyond 6 weeks postpartum. Studies by Ros et al.  and Heit et al.  (estimated by Jackson et al.  from reported data) did not find an elevated risk of VTE after 6 weeks, whereas studies by Pomp et al.  and Kamel et al.  evidenced an elevated risk for at least 12 weeks after delivery. Indeed, the most detailed of these studies (with 3-week time intervals) concluded that an elevated risk could extend up to 15 weeks postpartum .
In light of these findings, we decided to explore the relative risk of a postpartum VTE with a greater degree of precision. It is noteworthy that studies reporting incidence rates (without any assessment of the relative risk) give estimations for week-long intervals [4, 5, 8, 9]. Hence, a large population-based study of how the risk of a postpartum VTE decreases over time after delivery was warranted.
The objective of the present study was to assess the risk of a postpartum VTE in 2-week time epochs extending from the date of delivery.
Collection of the study data was approved by the French National Data Protection Commission (CNIL; authorization number: 1754053). The “acute care” section of the French national inpatient database contains information on 171,556,421 inpatient stays and 5,517,680 singleton deliveries linked to 4,252,507 mothers between January 1st, 2007 to December 31st, 2013. Summary data for each inpatient stay in an “acute care” department of a public -or private- sector hospital are collected by the French National Health Insurance Agency (Assurance Maladie ). The corresponding database contains the ICD-10 diagnostic codes , the medical procedures performed (coded according to the French national “CCAM Classification Commune des Actes Médicaux” classification), and the patient’s age, gender, and unique identifier. The time interval between two different hospital admissions are expressed as the number of days.
A total of 153 data completeness and coherence checks  are performed routinely when the information on inpatient admissions is sent to the French National Health Insurance Agency. These include checks on the chronology of the inpatient admissions, data integrity/accuracy (i.e. missing, incorrect or imprecise values) of patient’s and admissions’ data (gender, age, date and mode of entry, and date and mode of discharge), the format of the procedure codes and the diagnostic codes, and the concordance between procedure codes, diagnostic codes, the length of stay, and patients’ age and gender. More specifically, consistency controls between the following duplets are conducted: “procedure or diagnosis” AND “the antepartum/postpartum period”; “procedure or diagnosis” AND “gestational age”; “diagnosis on delivery” AND “procedure on delivery”.
From March 1st, 2009, the code for the “primary diagnosis” corresponds to the primary medical indication for hospital admission, and is recorded at the time of the patient’s discharge. Emergency room visits that did not result in an inpatient hospital admission are not included in the database.
Inclusion criteria (definition of a case)
We identified inpatient admissions for a VTE between July 1st, 2008, to December 31st, 2013. If a patient suffered more than one VTE during that period, only the first-occurring event was analyzed.
Several algorithms for tracking VTEs in claims data have been developed and evaluated . Many of these algorithms refer to ICD-9 codes. In a study by Casez et al., ICD-10  discharge diagnosis codes were found to be sensitive tools for identifying pulmonary embolism (Sensitivity = 88.9% [85.6%–92.2%]) but not deep vein thrombosis (Sensitivity = 58% [51.9%–64.1%]). Furthermore, deep vein thrombosis does not necessarily require inpatient hospital admission. Accordingly, we chose pulmonary embolism as a marker of the risk of a VTE in the present crossover study.
The ICD-10 codes used to identify pulmonary embolism are detailed in the Additional file 1, as are the exclusion criteria.
Definition of exposure
Deliveries (i.e. the exposure of interest) for patients aged between 15 and 45 years (at the time of delivery) were identified during the case period and the control periods.
Inpatient delivery hospitalizations were classified by the presence of the diagnosis code Z37.0 (“Single live birth”) and the absence of the diagnosis codes O35.x (“Maternal care for known or suspected fetal abnormality and damage”) and O28.x (“Abnormal findings on antenatal screening of mother”). According to French guidelines , the diagnosis code Z37.0 must be entered for all single, live births. A prior comparison with national birth records has confirmed that the French national inpatient database’s use of this diagnosis code is reliable .
Retrospective calculation of the time interval between pulmonary embolism and delivery
The CCAM classification enabled us to identify all delivery procedures and the exact date of each delivery. We separated these events into two classes, according to whether the pulmonary embolism occurred during a later postpartum hospitalization or during the delivery hospitalization. In the former instance, we used the later admission date to calculate the time interval between delivery and the pulmonary embolism. In the latter instance (which was less frequent), calculating the time interval was more complicated. We had to (i) confirm that the VTE had occurred after the delivery and (ii) estimate the time interval between the delivery and the event. Firstly, the “primary diagnosis” (i.e. the reason for inpatient hospital admission) had to be compatible with a delivery, in order to confirm that the pulmonary embolism had occurred after delivery. Secondly, the dates of procedures (CCAM codes presented in the Additional file 1) required to diagnose pulmonary embolism enabled us to calculate the time interval.
Firstly, we performed a descriptive analysis of all singleton, live births between 2007 and 2013. Categorical and binary variables were expressed as frequencies. Continuous data were expressed as the mean ± standard deviation (SD). Based on previously published data, we studied the following risk factors for postpartum VTE : pre-term delivery (delivery ≤37 weeks’ gestation), maternal age > 35 years, preeclampsia or eclampsia, morbid obesity (BMI ≥40 kg/m2), cesarean section, postpartum hemorrhage, postpartum infection, and birth weight <2.5 kg.
Secondly, we calculated the number of pulmonary embolisms for each 14-day interval for the case period and for the control periods. The pulmonary embolism rate for 100,000 deliveries was also computed by using the number of deliveries between July 1st, 2008, and December 31st, 2013, as the denominator. Next, we compared the likelihood of a delivery occurring from 0 to 13 days before a pulmonary embolism with the likelihood of a delivery occurring during five, 2-week-long control periods: from day 330 to day 343 before the thromboembolic event, from day 344 to day 357, from day 358 to 371, from day 372 to 385, and from day 386 to day 399. We performed the same analysis ten times (using the case-crossover approach) for each 2-week interval before the pulmonary embolism. We used conditional logistic regression to calculate the odds ratio (OR) and the 95% confidence interval (CI) for each 2-week interval. An additional analysis was performed by stratifying by the mode of delivery; this enabled us to determine whether the risk was higher after cesarean section than after vaginal delivery. These results are presented in the Additional file 1.
A post-hoc conservative analysis was also performed by computing the risk after the exclusion of (i) cases with a length of stay (for delivery) greater or equal to 10 days (n = 126) and (ii) cases with an intercurrent admission between the time of the inpatient stay for delivery and the time of the inpatient stay for pulmonary embolism (n = 112).
Lastly, we implemented a negative control by assessing exposure that was not expected to lead to an elevated risk of a VTE. To this end, we analyzed the CCAM code AHPA009 (“Release of the median nerve in the carpal tunnel, using a direct approach”) and the ICD-10 diagnosis code G56.0 (“carpal tunnel syndrome”) over seven successive 30-day intervals.
Description of the study population
Risk factors for VTEs during inpatient stays with delivery from 2007 to 2013
n = 5,517,680a
12.8%b (n = 475,935)
Maternal age >35 years
14.4% (n = 798,074)
Preeclampsia or eclampsia
4.1% (n = 229,853)
Morbid obesity (BMI ≥40 kg/m2)
0.3% (n = 18,871)
19.6% (n = 1,084,005)
3.6% (n = 201,338)
1.4% (n = 77,968)
Birth weight <2.5 kg
5.8%c (n = 266,174)
Risk estimation for each 2-week interval
The risk of a VTE during the postpartum period, as a function of the time after delivery
Time period (days after delivery)
Number of events b
Number of events a, b
The post-hoc conservative analysis yielded slightly lower ORs; for weeks 7 to 8, weeks 9 to 10, and weeks 11 to 12, the ORs [95%CI] were respectively 3.0 [2.1–4.2], 1.9 [1.3–2.7] and 1.4 [0.9–2.0]. The results for the negative control are presented in the Additional file 1, the corresponding odds-ratios were systematically close to 1.
Our present results showed that an elevated risk of a VTE was present for nearly 12 weeks after delivery. The shape of the risk curve suggests that this risk decreases exponentially over time. Beyond 12 weeks, the risk was no longer elevated.
The incidence of pulmonary embolism in our study is similar to that reported by Jacobsen et al.  (22.0 per 100,000 deliveries) and by Lindqvist et al.  (21 per 100,000 [estimated from reported data]), but is greater than the incidence reported by Gherman et al. : 8 per 100,000 (estimated from reported data).
Odds ratios reported by other studies, by 6-week intervals
Our use of a crossover design can be justified in two respects. Firstly, this design gave us more statistical power. Secondly, rigorous empirical evaluation by the OMOP has demonstrated that crossover design are superior in pharmaco-epidemiological studies  - particularly when compared with “new user”-type cohorts  and case-control studies . The OMOP also showed that crossover cohort and case-crossover designs had similar methodological quality; these two cross-over designs were applied to data initially collected in a retrospective cohort. The use of these designs requires short exposure periods and events that have short durations and brief effects; these conditions were met in the present study. Finally, the results obtained in the complementary analysis, showing a greater risk of thrombosis after caesarean delivery, are in line with the results of Morris et al. , and in line with the most recent recommendations for thromboprophylaxis in United States (National Partnership for Maternal Safety)  and United Kingdom (Royal College of Obstetrician and Gynaecologists) ; However, the results of this additional analysis are not adjusted (in this case, the analysis compares groups of patients with each other -with or without cesarean section-, and no more the patient to herself) and no evaluation of the benefit-risk balance of thromboprophylaxis was conducted: For these reasons, these additional results do not assess the value of such thromboprophylaxis after cesarean.
The present study had several limitations. Firstly, it is also well known that survival bias can influence the findings from observational, pharmaco-epidemiological studies [28–30], since the inclusion criteria can sometimes lead to the selection of low-risk patients. We cannot rule out the presence of survival bias because all patients with a VTE between January 1st, 2007 and June 30th, 2008 were excluded. Secondly, the use of a statistical test for each 2-week interval inevitably increases the type I error. This may have biased our estimates of the time point beyond which the risk of postpartum pulmonary embolism is no longer elevated, but not the temporal decrease in pulmonary embolism incidence. Thirdly, the use of hospital administrative databases always raises the question of data accuracy [31, 32]. However, the codes we used for pulmonary embolism and delivery are both known to be associated with a good level of recall. In addition, it seems reasonable to consider that misclassification of VTE may occur in both case and control periods, which would not necessarily change the odds ratios and could thus be a non-differential bias. Fourthly, some dates of delivery could be inaccurate, since this date has only been mandatory since 2010. Before 2010, the database’s default delivery date is set to zero and so it is (sometimes wrongly) considered that delivery occurs on the first day of hospitalization. To some extent, this choice may have artificially lengthened the time period between delivery and the occurrence of a VTE. Furthermore, the analysis of events that only account for a proportion of the total events of interest constitutes another study limitation, and raises the question of whether our findings can be generalized to the entire set of events concerned. In the case of VTEs, it is unclear whether PE events are a good proxy for deep venous thromboses . In addition, it is possible that some massive pulmonary embolisms, leading to death without prior hospitalization, have not been detected. Finally, although our database is comprehensive for hospitalizations in France, some patients who gave birth in France could then have been lost to follow-up (e.g. emigration).
Lastly, we did not perform additional subgroup analyses as a function of the presence of anticoagulation therapy, since this information was not available in the database. It would be of value to evaluate the risk of bleeding associated with anticoagulation therapy. This could be performed by analyzing a drug prescription database. Measures of association, computed in our study, do not account for the use of mechanical or pharmacological VTE prophylaxis: It is likely that the measures of association computed for the first 6 weeks are modified by the use of prophylaxis in our population; Contrariwise, it seems reasonable to think that our estimation beyond 6 weeks is less modified. In addition, the presence of a prophylaxis beyond 6 weeks (for some patients in our analyzed sample) would be conservative regarding the results obtained for the intervals beyond 6 weeks, as it would decrease the risk of a pulmonary embolism.
An elevated risk of a postpartum pulmonary embolism is present for nearly 12 weeks after delivery, and appears to decay exponentially. In groups at high risk of a VTE, it may be of value to assess the relevance of extending the duration of preventive anticoagulation therapy beyond 6 weeks. To adequately assess the risks vs benefits of extended anticoagulation therapy after delivery, comparative effectiveness studies in large populations are needed.
All the authors of the present study are employed by the University of Lille or Lille University Hospital. These funding organizations did not suggest the subject of this study, and did not have access to the results before publication. This study did not receive any third-party funding.
Availability of data and materials
To ensure the validity and the reproducibility of our analysis, the R code is available on demand. The French national inpatient database is available from the Agence technique de l’information sur l’hospitalisation (http://www.atih.sante.fr/bases-de-donnees/commande-de-bases/) after approval by the French National Data Protection Commission (http://www.cnil.fr/).
All authors declare: no support from any organization for the submitted work; no financial relationships with any organizations that might have an interest in the submitted work; no other relationships or activities that could appear to have influenced the submitted work.
GF, JBB and EC contributed to the study’s conception and design, and planned the statistical analysis; YJJ collected and abstracted the data; GF and AC performed the statistical analysis; GF and LF drafted the manuscript; GF, RB and CG performed the literature search. All authors contributed to the interpretation of findings and revision the manuscript for important intellectual content. All authors approved the final version for publication. Lastly, all authors had full access to all the data, including statistical reports and tables.
Consent for publication
Ethics approval and consent to participate
Collection of the study data was approved by the French National Data Protection Commission (CNIL; authorization number: 1754053). According to French legislation on retrospective registry-based studies, approval by an investigational review board and formal consent by patients was not required. The data were structured so that individual patients could not be identified.
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