2021
DOI: 10.1111/1471-0528.16938
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Effect of antithrombin III among patients with disseminated intravascular coagulation in obstetrics: a nationwide observational study in Japan

Abstract: Objective Pregnant women may develop disseminated intravascular coagulation (DIC), possibly resulting in massive maternal haemorrhage and perinatal death. The Japan guideline recommends use of antithrombin III (ATIII) for DIC in obstetrics; however, its effect remains uncertain. The present study aimed to investigate the effect of ATIII for DIC in obstetrics, using a national inpatient database in Japan. Design Nationwide observational study. Setting Japan. Population We used the Diagnosis Procedure Combinatio… Show more

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Cited by 7 publications
(8 citation statements)
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References 31 publications
(42 reference statements)
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“…Postpartum hemorrhage patients were defined as those with the following diagnoses: intrapartum hemorrhage ( ICD-10 codes, O679), disseminated intravascular coagulation after labor (O723), shock during labor (O751) or hemorrhage shock (R571), or patients who received blood transfusions. Postpartum hemorrhage patients who underwent cesarean delivery, and other delivery-related procedures were defined as patients who delivered during hospitalization 14 . We excluded patients with primary diagnoses of placenta previa (O441) or placenta accrete spectrum disorders (O720, O722, O730, and O731) because it was unclear whether REBOA was used for prophylactic or therapeutic intervention.…”
Section: Methodsmentioning
confidence: 99%
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“…Postpartum hemorrhage patients were defined as those with the following diagnoses: intrapartum hemorrhage ( ICD-10 codes, O679), disseminated intravascular coagulation after labor (O723), shock during labor (O751) or hemorrhage shock (R571), or patients who received blood transfusions. Postpartum hemorrhage patients who underwent cesarean delivery, and other delivery-related procedures were defined as patients who delivered during hospitalization 14 . We excluded patients with primary diagnoses of placenta previa (O441) or placenta accrete spectrum disorders (O720, O722, O730, and O731) because it was unclear whether REBOA was used for prophylactic or therapeutic intervention.…”
Section: Methodsmentioning
confidence: 99%
“…The database includes the following variables for each patient: sex; age; diagnoses, comorbidities at admission, and complications after admission recorded according to the International Classification of Diseases, Tenth Revision (ICD-10), codes and written in Japanese text; procedures recorded according to the Japanese medical procedure status and code (Supplemental Digital Content, Supplementary Table 2, http://links.lww.com/TA/ C518); drugs used; device code (Supplemental Digital Content, Supplementary Table 2, http://links.lww.com/TA/C518); referral from other facilities; teaching hospital; intensive care unit admission; pregnancy status (pregnant or not); gestational age at admission and delivery during hospitalization; readmitted within 1 week after delivery; date of admission, procedure, and discharge; and discharge status (in-hospital mortality, transportation to other hospital, or discharge to home). 14 Validation of various diagnostic records in this database was conducted to a high standard. 15,16 The sensitivity and specificity of the primary diagnoses were 78.9% and 93.2%, respectively.…”
Section: Study Design and Data Sourcementioning
confidence: 99%
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“…3 4 Moreover, most existing studies did not have population-based case ascertainment covering multiple DIC aetiologies. 6 Prior studies that relied on diagnosis codes from administrative registries to identify patients with DIC 5 did not capture mild, subclinical and transient DIC episodes, and thus were unable to account for disease severity in their analyses. Currently, only a few DIC registries and other data sources exist.…”
Section: Strengths and Limitations Of This Studymentioning
confidence: 99%
“…Despite the devastating prognosis of DIC, specific knowledge about its epidemiology remains limited. The few studies that have investigated the clinical epidemiology of DIC have been limited to selected patients, for example, patients in the intensive care unit (ICU) at university hospitals3 4; were mainly conducted in Japan3 5; were more than 10 years old3 4; were unable to track patients across transitions in sites of care, for example, transfer between hospitals4 6; and did not include rich clinical data on symptoms/signs, laboratory records, microbiology and in-hospital treatment, for example, transfusions or use of haemostatic drugs 3 4. Moreover, most existing studies did not have population-based case ascertainment covering multiple DIC aetiologies 6.…”
Section: Introductionmentioning
confidence: 99%