Out-of-Distribution Detection in Dermatology using Input Perturbation and Subset Scanning

TL;DR

This paper introduces an input perturbation and subset scanning method for detecting out-of-distribution skin disease samples in dermatology, improving robustness and fairness across different data sources and skin tones.

Contribution

It proposes a novel OOD detection approach using latent space scanning and input perturbation, validated across multiple dermatology datasets and fairness evaluations.

Findings

Competitive OOD detection performance across datasets

Effective identification of samples from different protocols

Detection of unknown disease classes

Abstract

Recent advances in deep learning have led to breakthroughs in the development of automated skin disease classification. As we observe an increasing interest in these models in the dermatology space, it is crucial to address aspects such as the robustness towards input data distribution shifts. Current skin disease models could make incorrect inferences for test samples from different hardware devices and clinical settings or unknown disease samples, which are out-of-distribution (OOD) from the training samples. To this end, we propose a simple yet effective approach that detect these OOD samples prior to making any decision. The detection is performed via scanning in the latent space representation (e.g., activations of the inner layers of any pre-trained skin disease classifier). The input samples could also perturbed to maximise divergence of OOD samples. We validate our ODD detection approach in two use cases: 1) identify samples collected from different protocols, and 2) detect samples from unknown disease classes. Additionally, we evaluate the performance of the proposed approach and compare it with other state-of-the-art methods. Furthermore, data-driven dermatology applications may deepen the disparity in clinical care across racial and ethnic groups since most datasets are reported to suffer from bias in skin tone distribution. Therefore, we also evaluate the fairness of these OOD detection methods across different skin tones. Our experiments resulted in competitive performance across multiple datasets in detecting OOD samples, which could be used (in the future) to design more effective transfer learning techniques prior to inferring on these samples.