Leave No Patient Behind: Enhancing Medication Recommendation for Rare Disease Patients
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Abstract (arXiv)
Medication recommendation systems have gained significant attention in healthcare as a means of providing tailored and effective drug combinations based on patients' clinical information. However, existing approaches often suffer from fairness issues, as recommendations tend to be more accurate for patients with common diseases compared to those with rare conditions. In this paper, we propose a novel model called Robust and Accurate REcommendations for Medication (RAREMed), which leverages the pretrain-finetune learning paradigm to enhance accuracy for rare diseases. RAREMed employs a transformer encoder with a unified input sequence approach to capture complex relationships among disease and procedure codes. Additionally, it introduces two self-supervised pre-training tasks, namely Sequence Matching Prediction (SMP) and Self Reconstruction (SR), to learn specialized medication needs and interrelations among clinical codes. Experimental results on two real-world datasets demonstrate that RAREMed provides accurate drug sets for both rare and common disease patients, thereby mitigating unfairness in medication recommendation systems.
Key facts. Cited by 11 papers in the map (data through 7 Oct 2026). Builds on 15 of its 48 references that are in the map. First posted on arXiv 26 Mar 2024.
Builds on
15 of 48 references.
References · 15
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Citing papers per year: 2024: 1; 2025: 7; 2026: 3.
11 papers.
- 2024RareAgents: Autonomous Multi-disciplinary Team for Rare Disease Diagnosis and Treatmentcited by 6
- 2025Unveiling Discrete Clues: Superior Healthcare Predictions for Rare Diseasescited by 5
- 2025Fine-grained List-wise Alignment for Generative Medication Recommendationcited by 5
- 2025Bridging Data Gaps of Rare Conditions in ICU: A Multi-Disease Adaptation Approach for Clinical Predictioncited by 4
- 2026The Taxonomies, Training, and Applications of Event Stream Modelling for Electronic Health Recordscited by 3
- 2025Learning to Evolve: Bayesian-Guided Continual Knowledge Graph Embeddingcited by 2
- 2025Traceable Drug Recommendation over Medical Knowledge Graphscited by 1
- 2025Overview of CHIP 2025 Shared Task 2: Discharge Medication Recommendation for Metabolic Diseases Based on Chinese Electronic Health Recordscited by 1
- 2026SafeRx-Agent: A Knowledge-Grounded Multi-Agent Framework for Safe and Explainable Medication Recommendationcited by 1
- 2025Combating the Bucket Effect:Multi-Knowledge Alignment for Medication Recommendationcited by 0
- 2026Improving Rare Medication Recommendation with Counterfactual Data Augmentation and Large Language Modelscited by 0
- 2026Improving Rare Medication Recommendation with Counterfactual Data Augmentation and Large Language Models23 Jul 2026
- 2026SafeRx-Agent: A Knowledge-Grounded Multi-Agent Framework for Safe and Explainable Medication Recommendation27 May 2026
- 2026The Taxonomies, Training, and Applications of Event Stream Modelling for Electronic Health Records14 Mar 2026
- 2025Overview of CHIP 2025 Shared Task 2: Discharge Medication Recommendation for Metabolic Diseases Based on Chinese Electronic Health Records9 Nov 2025
- 2025Traceable Drug Recommendation over Medical Knowledge Graphs31 Oct 2025
- 2025Learning to Evolve: Bayesian-Guided Continual Knowledge Graph Embedding4 Aug 2025
- 2025Bridging Data Gaps of Rare Conditions in ICU: A Multi-Disease Adaptation Approach for Clinical Prediction8 Jul 2025
- 2025Fine-grained List-wise Alignment for Generative Medication Recommendation26 May 2025
- 2025Combating the Bucket Effect:Multi-Knowledge Alignment for Medication Recommendation25 Apr 2025
- 2025Unveiling Discrete Clues: Superior Healthcare Predictions for Rare Diseases23 Jan 2025
- 2024RareAgents: Autonomous Multi-disciplinary Team for Rare Disease Diagnosis and Treatment17 Dec 2024