2f:I[703058,["/_next/static/immutable/chunks/3bhq_5eh1d760.js","/_next/static/immutable/chunks/1855-ogyi8eh4.js","/_next/static/immutable/chunks/2pfsjpn6k6zlg.js","/_next/static/immutable/chunks/26c7v3_3uwnwu.js","/_next/static/immutable/chunks/25a3ozcrvi1ff.js","/_next/static/immutable/chunks/2r4wx50nvjh_4.js","/_next/static/immutable/chunks/23fsw06hsi5b1.js","/_next/static/immutable/chunks/06_yt270h41rg.js","/_next/static/immutable/chunks/3ezsiz-7shkna.js","/_next/static/immutable/chunks/20x2y96ldu5wx.js","/_next/static/immutable/chunks/2lxntcm3pd1_h.js","/_next/static/immutable/chunks/00dgco8irq3jw.js","/_next/static/immutable/chunks/00nwe-kq0rboc.js","/_next/static/immutable/chunks/2051ffx3xzio9.js"],"PaperListPageClient"] 30:T68e,Placental abruption engenders powerful risks of maternal cardiovascular disease (CVD), but offspring risks are lacking. We examine the associations between abruption and the risks of all-cause mortality and fatal and nonfatal CVD events in the offspring. We designed a retrospective cohort study using the PACER (Placental Abruption and Cardiovascular Event Risk) cohort (births in New Jersey, 1993-2020). We fit Cox proportional hazards models to estimate the abruption-associated risks of mortality in singleton offspring and of fatal and nonfatal CVD events. These associations were replicated in a sibling-pair analysis to minimize familial confounding. Of 2 949 992 singleton pregnancies, the abruption prevalence was 1% (n=28 641). The median offspring follow-up was 14.5 years (range 0-28; 41.9 million person-years). The offspring CVD mortality rates among births with abruption and without abruption were 4 (n=17) and 1 (n=307) per 100 000 person-years, respectively (adjusted hazard ratio [HR], 4.64 [95% CI, 2.75-7.86]). The corresponding nonfatal CVD rates were 627 (n=2425) and 190 (n=79 360) per 100 000 person-years, respectively (HR, 2.86 [95% CI, 2.74-2.98]). The risks were higher in analyses restricted to offspring aged <1 year with CVD events. These associations were similar in the sibling pair analyses. Offspring born of pregnancies complicated by abruption suffer an increased burden of mortality and CVD. CVD risks associated with abruption are evident during the infancy period and persist throughout the life course. These data underscore how microvascular placental dysfunction due to abruption can affect the offspring's CVD risk.31:T960, Background Placental abruption engenders powerful risks of maternal cardiovascular disease (CVD), but offspring risks are lacking. We examine the associations between abruption and the risks of all‐cause mortality and fatal and nonfatal CVD events in the offspring. Methods We designed a retrospective cohort study using the PACER (Placental Abruption and Cardiovascular Event Risk) cohort (births in New Jersey, 1993–2020). We fit Cox proportional hazards models to estimate the abruption‐associated risks of mortality in singleton offspring and of fatal and nonfatal CVD events. These associations were replicated in a sibling‐pair analysis to minimize familial confounding. Results Of 2 949 992 singleton pregnancies, the abruption prevalence was 1% (n=28 641). The median offspring follow‐up was 14.5 years (range 0–28; 41.9 million person‐years). The offspring CVD mortality rates among births with abruption and without abruption were 4 (n=17) and 1 (n=307) per 100 000 person‐years, respectively (adjusted hazard ratio [HR], 4.64 [95% CI, 2.75–7.86]). The corresponding nonfatal CVD rates were 627 (n=2425) and 190 (n=79 360) per 100 000 person‐years, respectively (HR, 2.86 [95% CI, 2.74–2.98]). The risks were higher in analyses restricted to offspring aged <1 year with CVD events. These associations were similar in the sibling pair analyses. Conclusions Offspring born of pregnancies complicated by abruption suffer an increased burden of mortality and CVD. CVD risks associated with abruption are evident during the infancy period and persist throughout the life course. These data underscore how microvascular placental dysfunction due to abruption can affect the offspring's CVD risk. 25:[[["$","script","0",{"type":"application/ld+json","dangerouslySetInnerHTML":{"__html":"{\"@context\":\"https://schema.org\",\"@type\":\"CollectionPage\",\"name\":\"Placental Abruption: condition Research & Clinical Takeaways\",\"description\":\"Explore peer-reviewed papers on Placental Abruption (condition). Clinician-written summaries and actionable practice insights. Updated daily.\",\"url\":\"https://www.reachrx.ai/hub/tag/condition/Placental%20Abruption\",\"breadcrumb\":{\"@type\":\"BreadcrumbList\",\"itemListElement\":[{\"@type\":\"ListItem\",\"position\":1,\"name\":\"Home\",\"item\":\"https://www.reachrx.ai\"},{\"@type\":\"ListItem\",\"position\":2,\"name\":\"Research Hub\",\"item\":\"https://www.reachrx.ai/hub\"},{\"@type\":\"ListItem\",\"position\":3,\"name\":\"Conditions\",\"item\":\"https://www.reachrx.ai/hub/tag/condition\"},{\"@type\":\"ListItem\",\"position\":4,\"name\":\"Placental Abruption\",\"item\":\"https://www.reachrx.ai/hub/tag/condition/Placental%20Abruption\"}]}}"}}]],["$","$L2f",null,{"title":"Placental Abruption: Research & Clinical Takeaways","description":"Discover peer-reviewed research on Placental Abruption with concise clinician summaries and next-step guidance.","papers":[{"doi":"10.1093/eurheartj/ehag564","pmid":"42554048","title":"Adverse pregnancy outcomes in successive pregnancies and maternal cardiovascular mortality: a Norwegian nationwide study","journal_title":"European Heart Journal","journal_issn":"0195-668X","published_at":"2026-08-05T00:00:00.000Z","url":"https://doi.org/10.1093/eurheartj/ehag564","source_score":8,"is_retracted":false,"is_open_access":true,"raw_metadata":{"pubmed":true,"crossref":true,"unpaywall":true},"created_at":"2026-08-11T13:26:21.274Z","updated_at":"2026-08-11T13:26:21.274Z","tags":[{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"age_group","value":"adult","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"category","value":"Cardiac & Cardiovascular Systems","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Cardiovascular Disease Mortality","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Gestational Hypertension","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Perinatal Loss","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Placental Abruption","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Preeclampsia","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Preterm Delivery","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"condition","value":"Small For Gestational Age","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"impact_flag","value":"practice_changing","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"level_of_evidence","value":"2","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"sample_size","value":"n=1001409","value_numeric":1001409},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"sex","value":"female","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"study_design","value":"Nationwide Cohort Study","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"warning","value":"Individual APO subtypes (e.g., placental abruption, perinatal loss) are analyzed separately but specific HRs for each subtype by sequence are not reported in the abstract — only composite APO results are detailed here.","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"warning","value":"The cohort spans over 50 years (1967–2020); secular trends in obstetric and cardiovascular care may limit direct applicability to contemporary patients.","value_numeric":null},{"paper_doi":"10.1093/eurheartj/ehag564","tag_type":"warning","value":"The 'practice_changing' impact flag is applied because the study reframes how APO history should be taken (sequence-based rather than binary), but the observational design means clinical guidelines would need formal endorsement before changing protocols.","value_numeric":null}],"summaries":{"what_studied":"This Norwegian nationwide cohort study evaluated how the **sequence** of adverse pregnancy outcomes (APOs) across complete pregnancy histories — rather than simple presence/absence — relates to premature CVD mortality (≤70 years) in 1,001,409 women followed from 1967 to 2020.","key_result":"Women with APOs in their **first pregnancy and no further pregnancies** had the highest CVD mortality risk (aHR 3.30, 95% CI 2.97–3.66). APOs in both first and later pregnancies carried aHR 2.41 (95% CI 2.16–2.69). Women with APOs in first pregnancy followed by uncomplicated pregnancies had the lowest risk (aHR 1.39, 95% CI 1.27–1.53). Binary classification (APO yes/no) yielded only an overall 1.73-fold higher CVD mortality — masking substantial variation.","limitations":"- Observational design limits causal inference.\n- Registry-based data may lack granularity on comorbidities, lifestyle factors, or treatment received after APO diagnosis.\n- Study spans 1967–2020; management of APOs changed substantially over this period, which may affect generalizability to current practice.","practice_takeaway":"Ask about the **full obstetric history** — not just whether a patient ever had an APO, but when and how often. Women who had APOs only in a first pregnancy and never became pregnant again carry the steepest CVD mortality risk and may warrant the most proactive cardiovascular surveillance."}},{"doi":"10.1186/s12884-026-09762-2","pmid":null,"title":"Algorithm for classifying the underlying pathologies in postpartum hemorrhage using bleeding rate, fibrinogen, and fibrin/fibrinogen degradation products: a case series study","journal_title":"BMC Pregnancy and Childbirth","journal_issn":"1471-2393","published_at":"2026-08-03T00:00:00.000Z","url":"https://doi.org/10.1186/s12884-026-09762-2","source_score":1,"is_retracted":false,"is_open_access":true,"raw_metadata":{"pubmed":false,"crossref":true,"unpaywall":true},"created_at":"2026-08-11T13:26:23.868Z","updated_at":"2026-08-11T13:26:23.868Z","tags":[{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"age_group","value":"adult","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"category","value":"Obstetrics & Gynecology","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"condition","value":"Disseminated Intravascular Coagulation","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"condition","value":"Placental Abruption","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"condition","value":"Postpartum Hemorrhage","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"impact_flag","value":"limited_evidence","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"level_of_evidence","value":"4","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"modality","value":"Clinical Decision Algorithm","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"sample_size","value":"n=171","value_numeric":171},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"sex","value":"female","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"study_design","value":"Case Series","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"warning","value":"Only 3 DIC cases were identified; the predictive formula distinguishing DIC from LIPC is statistically underpowered and should not yet guide clinical decisions independently.","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"warning","value":"Placental abruption cases were included regardless of blood loss, which may skew the coagulopathy subgroup distribution compared to a general severe PPH population.","value_numeric":null},{"paper_doi":"10.1186/s12884-026-09762-2","tag_type":"warning","value":"The algorithm was derived and internally tested on the same 171-patient dataset with no external validation cohort—classification thresholds (e.g., bleeding rate ≥61 mL/min, fibrinogen ≥237 mg/dL, FDP <2 mg/dL) should be interpreted cautiously until prospectively validated.","value_numeric":null}],"summaries":{"what_studied":"A multicenter case series (9 perinatal centers, Japan; Aug 2020–Jun 2024) developed and tested a classification algorithm for underlying pathologies in postpartum hemorrhage (PPH) using three clinical parameters—bleeding rate, fibrinogen, and FDP—in 171 patients with severe PPH (blood loss >2000 mL) or placental abruption.","key_result":"The algorithm sorted 171 cases into four categories: non-coagulopathy (NCP, n=88), coagulation factor consumption (CFC, n=62), whole blood loss with low bleeding rate (WBLL, n=12), and whole blood loss with high bleeding rate (WBLH, n=9); within CFC, 59 had locally initiated consumptive coagulopathy (LIPC) vs. 3 with DIC. WBLL showed the lowest hemoglobin (median 6.3 g/dL) and CFC the lowest fibrinogen (median 168.5 mg/dL), both significantly lower than the other categories (P<0.05).","limitations":"Small overall sample (n=171) with very few DIC cases (n=3), limiting validation of the DIC/LIPC distinction; single-country, multicenter design may reduce generalizability; the algorithm was developed and tested on the same dataset without external validation.","practice_takeaway":"Clinicians managing severe PPH may use a sequential assessment of bleeding rate, fibrinogen, and FDP to distinguish coagulopathic from non-coagulopathic causes, guiding targeted treatment. This is a pilot tool—external validation is needed before broad clinical adoption."}},{"doi":"10.1016/j.ajog.2026.07.008","pmid":"42431247","title":"Ischemic Placental Disease and Hospitalization for Neurological and Psychiatric Disorders","journal_title":"American Journal of Obstetrics and Gynecology","journal_issn":"0002-9378","published_at":"2026-07-10T00:00:00.000Z","url":"https://doi.org/10.1016/j.ajog.2026.07.008","source_score":10,"is_retracted":false,"is_open_access":true,"raw_metadata":{"pubmed":true,"crossref":true,"unpaywall":true},"created_at":"2026-07-25T13:57:45.287Z","updated_at":"2026-07-25T13:57:45.287Z","tags":[{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"age_group","value":"adult","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"category","value":"Obstetrics & Gynecology","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Fetal Growth Restriction","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Ischemic Placental Disease","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Neurological Disorders","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Placental Abruption","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Postpartum Depression","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Post-Traumatic Stress Disorder","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Preeclampsia","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Psychiatric Disorders","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"condition","value":"Stroke","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"impact_flag","value":"practice_changing","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"level_of_evidence","value":"3","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"sample_size","value":"n=17368071","value_numeric":17368071},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"sex","value":"female","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"study_design","value":"Retrospective Cohort Study","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"warning","value":"Brain disorder diagnoses are based on administrative ICD codes, which may undercount or misclassify conditions; the authors applied quantitative bias analysis but residual misclassification is possible.","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"warning","value":"The 'impact_flag' of practice_changing reflects the large sample size and dose-response finding, but causality cannot be established from this observational design.","value_numeric":null},{"paper_doi":"10.1016/j.ajog.2026.07.008","tag_type":"warning","value":"The study uses calendar-year follow-up rather than a fixed postpartum window (e.g., 12 months from delivery date), which may introduce variability in follow-up duration across patients.","value_numeric":null}],"summaries":{"what_studied":"This population-based retrospective cohort study used the US Nationwide Readmissions Database (2010–2020) to examine whether ischemic placental disease (preeclampsia, placental abruption, and/or fetal growth restriction) is associated with postpartum hospitalization for neurological and psychiatric disorders in women aged 15–54, within the calendar year of delivery.","key_result":"Among 17,368,071 deliveries, 10.7% had ischemic placental disease. Brain disorder hospitalization rates were 1,219 vs. 730 per 10,000 deliveries (with vs. without ischemic placental disease; adjusted HR 1.50, 95% CI 1.48–1.51). Risk rose in a dose-dependent fashion: HR 1.47 with 1 condition, 1.66 with 2, and 1.85 with all 3.","limitations":"- Administrative claims data rely on coded diagnoses, introducing potential outcome misclassification (though quantitative bias analysis was applied).\n- Unmeasured confounding cannot be fully excluded despite bias corrections.\n- Follow-up was limited to the calendar year of delivery, so longer-term outcomes are not captured.","practice_takeaway":"Women with ischemic placental disease face a ~50% higher risk of hospitalization for brain disorders—including stroke, depression, PTSD, and suicide attempt—within the postpartum year. Clinicians should treat ischemic placental disease as a neurological and psychiatric risk signal, prompting closer postpartum mental health and neurological surveillance."}},{"doi":"10.1161/jaha.125.045199","pmid":"41878836","title":"Cardiovascular Disease in Singleton Offspring Born of Pregnancies Complicated by Placental Abruption: A Population‐Based Retrospective Cohort Study","journal_title":"Journal of the American Heart Association","journal_issn":"2047-9980","published_at":"2026-03-25T00:00:00.000Z","url":"https://doi.org/10.1161/jaha.125.045199","source_score":108,"is_retracted":false,"is_open_access":true,"raw_metadata":{"ooir":{"day":"2026-04-30","doi":"10.1161/jaha.125.045199","days":"14","issn":"2047-9980","rank":"8","field":"Clinical Medicine","score":"108","category":"Cardiac & Cardiovascular Systems","categories":["Cardiac & Cardiovascular Systems"],"_categories":["Cardiac & Cardiovascular Systems"]},"pubmed":{"doi":"10.1161/JAHA.125.045199","title":"Cardiovascular Disease in Singleton Offspring Born of Pregnancies Complicated by Placental Abruption: A Population-Based Retrospective Cohort Study.","journal":"Journal of the American Heart Association","methods":"","results":"Of 2 949 992 singleton pregnancies, the abruption prevalence was 1% (n=28 641). The median offspring follow-up was 14.5 years (range 0-28; 41.9 million person-years). The offspring CVD mortality rates among births with abruption and without abruption were 4 (n=17) and 1 (n=307) per 100 000 person-years, respectively (adjusted hazard ratio [HR], 4.64 [95% CI, 2.75-7.86]). The corresponding nonfatal CVD rates were 627 (n=2425) and 190 (n=79 360) per 100 000 person-years, respectively (HR, 2.86 [95% CI, 2.74-2.98]). The risks were higher in analyses restricted to offspring aged <1 year with CVD events. These associations were similar in the sibling pair analyses.","abstract":"$30","keywords":["cardiovascular disease","multistate models","offspring","placental abruption","sibling design","unmeasured confounding bias"],"pubmed_id":"41878836","conclusions":"","publication_date":"2026-03-25T00:00:00"},"crossref":{"DOI":"10.1161/jaha.125.045199","URL":"https://doi.org/10.1161/jaha.125.045199","ISSN":["2047-9980"],"link":[{"URL":"https://www.ahajournals.org/doi/full/10.1161/JAHA.125.045199","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"page":null,"type":"journal-article","issue":"7","score":1,"title":["Cardiovascular Disease in Singleton Offspring Born of Pregnancies Complicated by Placental Abruption: A Population‐Based Retrospective Cohort Study"],"author":[{"given":"Cande V.","family":"Ananth","sequence":"first","affiliation":[{"name":"Rutgers Robert Wood Johnson Medical School"},{"name":"Rutgers Robert Wood Johnson Medical School"},{"name":"Rutgers Robert Wood Johnson Medical School"},{"name":"Rutgers School of Public Health"},{"name":"Environmental and Occupational Health Sciences Institute, Rutgers Robert Wood Johnson Medical School"}]},{"given":"Emily B.","family":"Rosenfeld","sequence":"additional","affiliation":[{"name":"Rutgers Robert Wood Johnson Medical School"},{"name":"Rutgers Robert Wood Johnson Medical School"}]},{"given":"Rachel","family":"Lee","sequence":"additional","affiliation":[{"name":"Rutgers Robert Wood Johnson Medical School"}]},{"given":"Linda","family":"Valeri","sequence":"additional","affiliation":[{"name":"Columbia University"},{"name":"Harvard T.H. Chan School of Public Health"}]},{"given":"William J.","family":"Kostis","sequence":"additional","affiliation":[{"name":"Rutgers Robert Wood Johnson Medical School"},{"name":"Rutgers Robert Wood Johnson Medical 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guidelines for this population do not yet exist.","value_numeric":null},{"paper_doi":"10.1161/jaha.125.045199","tag_type":"warning","value":"Median follow-up of 14.5 years means most offspring had not yet reached peak adult CVD risk age; long-term absolute risks may be underestimated.","value_numeric":null},{"paper_doi":"10.1161/jaha.125.045199","tag_type":"warning","value":"The sibling-pair analysis helps reduce familial confounding but cannot fully exclude shared genetic cardiovascular susceptibility.","value_numeric":null}],"summaries":{"what_studied":"This retrospective cohort study (PACER cohort, New Jersey births 1993–2020) examined whether singleton offspring born of pregnancies complicated by placental abruption face higher risks of all-cause mortality and fatal/nonfatal cardiovascular disease (CVD) events, with a sibling-pair analysis to control for familial confounding.","key_result":"Among ~2.95 million singleton pregnancies (1% abruption prevalence), offspring of abruption-affected pregnancies had a 4.64-fold higher CVD mortality rate (4 vs. 1 per 100,000 person-years; HR 4.64, 95% CI 2.75–7.86) and a 2.86-fold higher nonfatal CVD rate (627 vs. 190 per 100,000 person-years; HR 2.86, 95% CI 2.74–2.98) over a median follow-up of 14.5 years; risks were highest in infancy and persisted across the life course.","limitations":"Median follow-up of only 14.5 years limits detection of adult-onset CVD outcomes; study is limited to New Jersey births, which may reduce generalizability; residual confounding from unmeasured factors (e.g., shared genetic cardiovascular risk) cannot be fully excluded despite sibling-pair analysis.","practice_takeaway":"Clinicians should recognize offspring of abruption-complicated pregnancies as a high-risk group for CVD from infancy onward, supporting earlier and closer cardiovascular surveillance in this population. Documenting placental abruption in perinatal history may be a practical first step in identifying children who warrant long-term cardiac monitoring."}}],"initialOffset":4,"fetchConfig":{"kind":"tags","tags":[{"tag_type":"condition","value":"Placental Abruption"}]},"breadcrumbItems":[{"name":"Home","href":"/"},{"name":"Research Hub","href":"/hub"},{"name":"Conditions","href":"/hub/tag/condition"},{"name":"Placental Abruption"}],"hrefConfig":{"basePath":"/hub/papers","webViewQueryParams":{"hub_ctx":"tag","hub_tag_type":"condition","hub_tag_value":"Placental Abruption"}}}]]

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