A Study on Multimodal Data- and Explainable AI-Based Risk Prediction and Intervention for Postpartum Depression in Nursing Care Settings
DOI:
https://doi.org/10.62177/apjcmr.v2i5.1788Keywords:
Postpartum Depression, Multimodal Data, Explainable Artificial Intelligence, Nursing Decision Support, Risk StratificationAbstract
Objective: To evaluate a nursing-centered dynamic prediction and risk-stratified intervention system for postpartum depression (PPD) using multimodal longitudinal data and explainable artificial intelligence (AI). Methods: A quasi-experimental controlled study included 300 postpartum women enrolled within 6 hours after delivery and allocated by admission sequence to AI-assisted stratified nursing (n=150) or routine nursing care (n=150). Physiological, behavioral, psychological, and social-support indicators were collected, with EPDS assessments on postpartum days 7, 14, 28, and 42. A hybrid model combined temporal convolution, long short-term memory, text and voice representations, and multilayer fusion; SHAP and attention mechanisms supported case-level explanations. Outcomes included time to risk identification, EPDS trajectory, remission among high-risk women, nursing workload, and internally validated model performance. Results: Risk was identified earlier in the intervention group than in the control group (1.21 +/- 0.68 vs. 4.73 +/- 1.92 days, P<0.05). Mean EPDS reduction by day 42 was greater (-5.62 +/- 3.14 vs. -2.13 +/- 2.87, P<0.05), and remission was more frequent (78.3% vs. 42.6%; chi-square=36.41, P<0.05). High-risk identification reached 92.0% versus 64.0%. Time per follow-up decreased by 34.7%, and nurses reported fewer women requiring daily follow-up and lower work-related stress. The model achieved an AUC of 0.864, accuracy of 0.82, recall of 0.77, and F1-score of 0.79. Conclusion: A multimodal explainable AI system integrated with risk-stratified nursing care was associated with earlier risk recognition, improved depressive symptom trajectories, and lower nursing workload. External validation and a fully randomized multicenter evaluation are required before broad implementation.
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