# Mounting Challenges: A Tragic Case of Rheumatoid Arthritis-Associated Interstitial Lung Disease in an Incarcerated Patient, Highlighting Healthcare Access Barriers in Correctional Settings

**Authors:** Shaivya Pathak

PMC · DOI: 10.7759/cureus.102545 · Cureus · 2026-01-29

## TL;DR

A case study shows how limited healthcare access in prisons worsened a man's rheumatoid arthritis and lung disease, leading to severe complications.

## Contribution

Highlights healthcare access barriers in correctional settings through a tragic case of RA-ILD.

## Key findings

- Discontinuation of tofacitinib due to formulary restrictions led to severe respiratory failure.
- Incarcerated patients face significant challenges in accessing rheumatologic care and specialist services.
- Lack of treatment continuity in correctional facilities can result in life-threatening complications.

## Abstract

Rheumatoid Arthritis-associated Interstitial Lung Disease (RA-ILD) is a serious extra-articular manifestation associated with significant morbidity and mortality. We present the case of a 48-year-old incarcerated male with seropositive rheumatoid arthritis who was clinically stable on tofacitinib and methotrexate for over one year. Following the discontinuation of tofacitinib, which the patient attributed to correctional facility formulary changes and restrictions, he developed progressive respiratory symptoms. He presented to the hospital two months later with acute hypoxic respiratory failure necessitating intubation. Computed tomography of his lungs revealed extensive ground-glass opacities with honeycombing consistent with usual interstitial pneumonia pattern ILD, a condition previously undiagnosed in this patient. Despite aggressive management including pulse-dose corticosteroids, bronchoscopy, empiric antimicrobial treatment and comprehensive infectious workup, he continued to deteriorate over an eight-day intensive care unit course. He was deemed not a candidate for extracorporeal membrane oxygenation or lung transplantation due to acute illness severity, and the family eventually elected to transition to comfort care. This case highlights the profound challenges of managing rheumatoid arthritis in incarcerated populations, including barriers to accessing expensive targeted therapies, limited specialist availability, and the importance of treatment continuity for patients with complex autoimmune diseases. We discuss the practical implications of these healthcare disparities and advocate for policy reforms to ensure adequate rheumatologic care in correctional settings.

## Linked entities

- **Chemicals:** tofacitinib (PubChem CID 9926791), methotrexate (PubChem CID 4112)
- **Diseases:** Rheumatoid Arthritis (MONDO:0008383), Interstitial Lung Disease (MONDO:0015925), Rheumatoid Arthritis-associated Interstitial Lung Disease (MONDO:0004586)

## Full-text entities

- **Genes:** CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}
- **Diseases:** connective tissue disease (MESH:D003240), traction bronchiectasis (MESH:D001987), poor (MESH:D009123), arthritis (MESH:D001168), RA (MESH:D001172), cough (MESH:D003371), subcutaneous emphysema (MESH:D013352), leukocytosis (MESH:D007964), Rheumatologic (MESH:D012216), infection (MESH:D007239), UIP (MESH:D054990), incarcerated (MESH:D060725), COVID-19 (MESH:D000086382), Interstitial Lung Disease (MESH:D017563), hepatitis (MESH:D056486), hand tenderness (MESH:D063806), coccidioides (MESH:D003047), Depression (MESH:D003866), infectious (MESH:D003141), pulmonary hypertension (MESH:D006976), neuromuscular blockade (MESH:D020879), joint destruction (MESH:D008105), aspergillus (MESH:D001228), HIV (MESH:D015658), sleep problems (MESH:D012893), influenza (MESH:D007251), rheumatologic complication (MESH:D008107), inflammatory (MESH:D007249), PJP (MESH:D011020), Epstein-Barr virus (MESH:D020031), morning stiffness (MESH:D048968), neck deformities (MESH:D006258), ulnar deviation of the fingers (MESH:D010262), eosinophilia (MESH:D004802), emphysema (MESH:D004646), shortness of breath (MESH:D004417), pulmonary disease (MESH:D008171), fatigue (MESH:D005221), hyperemia (MESH:D006940), acute kidney injury (MESH:D058186), pneumomediastinum (MESH:D008478), weight gain (MESH:D015430), interstitial opacities (MESH:D003318), hypoxemic (MESH:D012131), hypoxic (MESH:D002534), cytomegalovirus (MESH:D003586), multi-organ dysfunction (MESH:D009102), autoimmune disease (MESH:D001327), hypoxia (MESH:D000860), hypotension (MESH:D007022), pulmonary embolism (MESH:D011655), fever (MESH:D005334)
- **Chemicals:** Beta-D-glucan (-), guaifenesin (MESH:D006140), piperacillin-tazobactam (MESH:D000077725), ceftriaxone (MESH:D002443), meloxicam (MESH:D000077239), prednisone (MESH:D011241), creatinine (MESH:D003404), oxygen (MESH:D010100), azithromycin (MESH:D017963), tofacitinib (MESH:C479163), galactomannan (MESH:C012990), vancomycin (MESH:D014640), Atovaquone (MESH:D053626), adalimumab (MESH:D000068879), methylprednisolone (MESH:D008775), methotrexate (MESH:D008727), epoprostenol (MESH:D011464), cyclic citrullinated peptide (MESH:C487763)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12949528/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12949528/full.md

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Source: https://tomesphere.com/paper/PMC12949528