Dhruv Naik

Elliot Schumacher, Daniel Rosenthal, Dhruv Naik et al.

Large language models (LLMs) have shown promise in safety-critical applications such as healthcare, yet the ability to quantify performance has lagged. An example of this challenge is in evaluating a summary of the patient's medical record. A resulting summary can enable the provider to get a high-level overview of the patient's health status quickly. Yet, a summary that omits important facts about the patient's record can produce a misleading picture. This can lead to negative consequences on medical decision-making. We propose MED-OMIT as a metric to explore this challenge. We focus on using provider-patient history conversations to generate a subjective (a summary of the patient's history) as a case study. We begin by discretizing facts from the dialogue and identifying which are omitted from the subjective. To determine which facts are clinically relevant, we measure the importance of each fact to a simulated differential diagnosis. We compare MED-OMIT's performance to that of clinical experts and find broad agreement We use MED-OMIT to evaluate LLM performance on subjective generation and find some LLMs (gpt-4 and llama-3.1-405b) work well with little effort, while others (e.g. Llama 2) perform worse.

Elliot Schumacher, Dhruv Naik, Anitha Kannan

Large language models (LLMs) have demonstrated impressive capabilities in disease diagnosis. However, their effectiveness in identifying rarer diseases, which are inherently more challenging to diagnose, remains an open question. Rare disease performance is critical with the increasing use of LLMs in healthcare settings. This is especially true if a primary care physician needs to make a rarer prognosis from only a patient conversation so that they can take the appropriate next step. To that end, several clinical decision support systems are designed to support providers in rare disease identification. Yet their utility is limited due to their lack of knowledge of common disorders and difficulty of use. In this paper, we propose RareScale to combine the knowledge LLMs with expert systems. We use jointly use an expert system and LLM to simulate rare disease chats. This data is used to train a rare disease candidate predictor model. Candidates from this smaller model are then used as additional inputs to black-box LLM to make the final differential diagnosis. Thus, RareScale allows for a balance between rare and common diagnoses. We present results on over 575 rare diseases, beginning with Abdominal Actinomycosis and ending with Wilson's Disease. Our approach significantly improves the baseline performance of black-box LLMs by over 17% in Top-5 accuracy. We also find that our candidate generation performance is high (e.g. 88.8% on gpt-4o generated chats).

Priyam Tejaswin, Dhruv Naik, Pengfei Liu

State-of-the-art summarization systems are trained and evaluated on massive datasets scraped from the web. Despite their prevalence, we know very little about the underlying characteristics (data noise, summarization complexity, etc.) of these datasets, and how these affect system performance and the reliability of automatic metrics like ROUGE. In this study, we manually analyze 600 samples from three popular summarization datasets. Our study is driven by a six-class typology which captures different noise types (missing facts, entities) and degrees of summarization difficulty (extractive, abstractive). We follow with a thorough analysis of 27 state-of-the-art summarization models and 5 popular metrics, and report our key insights: (1) Datasets have distinct data quality and complexity distributions, which can be traced back to their collection process. (2) The performance of models and reliability of metrics is dependent on sample complexity. (3) Faithful summaries often receive low scores because of the poor diversity of references. We release the code, annotated data and model outputs.