Annals of Clinical Epidemiology
Online ISSN : 2434-4338
Development and Validation of Algorithms using the Diagnosis Procedure Combination for Identifying Fetal Outcomes in Japan
Sachiko Yamamoto-Kataoka, Noriko Furuita, Yumie Ikeda, Yuki Kataoka, Takuya Aoki, Yoshimitsu Takahashi, Hidenori Kawasaki, Shinya Yoshikoka, Takeo Nakayama
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ジャーナル オープンアクセス 早期公開

論文ID: 27011

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Background

Accurate identification of fetal outcomes among hospitalized pregnant women is essential for perinatal research. Japan’s Diagnosis Procedure Combination (DPC) database may enable outcome ascertainment, but the validity of DPC-derived algorithms remains unclear. This study aimed to develop and validate DPC-based algorithms to identify abortions and stillbirths.

Methods

This retrospective cohort study included hospitalized pregnant women at Kyoto Min-iren Chuo Hospital (January1, 2017–November 30, 2021) and Kobe City Medical Center General Hospital (October 1, 2018–March 31, 2024). We created expert-defined algorithms to predict fetal outcomes, including abortions/stillbirths. Predictions were compared using pregnancy and neonatal summary tables and electronic medical records. Sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were calculated with 95% confidence intervals.

Results

At Kyoto Min-iren Chuo Hospital, 865 pregnancies included 131 reference abortions/stillbirths (92 induced abortions). Sensitivity was 0.98 (95% CI, 0.94–1.00), specificity 1.00 (95% CI, 1.00–1.00), PPV 1.00 (95% CI, 0.97–1.00), and NPV 1.00 (95% CI, 0.99-1.00). At Kobe City Medical Center General Hospital, 2,694 pregnancies included 43 reference abortions/stillbirths (12 induced abortions). Sensitivity was 0.63 (95% CI, 0.47–0.77), specificity 1.00 (95% CI, 1.00–1.00), PPV 1.00 (95% CI, 0.87–1.00), and NPV 0.99 (95% CI, 0.99–1.00).

Conclusions

The DPC-derived algorithms demonstrated excellent specificity, PPV, and NPV, although the sensitivity varied considerably across hospitals. These findings support the use of inpatient DPC data for pharmacoepidemiological research, provided that institution-specific coding practices are considered. Accurate estimation of outcome prevalence may require site-specific algorithm recalibration.

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© 2026 Society for Clinical Epidemiology

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