The Senate of Puerto Rico held a joint public hearing May 29 to investigate how medical evaluations under Law 25 (1992) were carried out in the case of Hermes Ávila, whose release after receiving a "pase extendido" preceded a later homicide. Senators pressed contracted correctional health clinicians and community supervision staff for details on forms, panel composition and record access.
The chair opened the hearing with the resolution ordering the probe and identified witnesses from the contracted provider and the correctional medical complex. Dr. Débora Arús Rosado, who testified she evaluated Ávila on Aug. 9, 2021, told senators she completed the standard evaluation form and relied on available documentation and observation in the medical dormitory. "I used my best clinical judgment at that time," Arús said. She acknowledged she did not always have the full historical files before her and that, at times, she worked without direct written access to the applicable regulation text.
Senators repeatedly noted that Ávila had prior negative evaluations in 2013, 2015 and 2019 that recommended against release and asked why those earlier determinations were not visible or considered. "If a person has been denied three times before, that is relevant information for any subsequent decision," said Senator Rafael Bernabé during questioning. Witnesses said the panel typically received the evaluating clinician's form and a subset of recent records rather than the entire medical archive; one doctor described the record set presented to the panel as "a few pages" rather than the voluminous tomes maintained elsewhere.
Panel members — including Drs. Gladys Quiles Santiago, Cristóbal Antrón Ávila, Jeffrey E. González Morales and Pedro Pérez Arrindel — described how the medical panel is composed on the day of review from available physicians. Several acknowledged that panels often lacked a specialist in the precise disease under review, despite regulatory language that calls for a specialist when relevant. "The practice has been to convene the physicians who are available the day the panel meets," said Dr. Quiles. "We have not always had a specialist present."
The committee also discussed a May 1, 2024 audit carried out by UTICORP that the chair said identified discrepancies in records and diagnostic conclusions. The chair said the audit and the apparent administrative gaps had real consequences: "that blindness of that corporation cost the life of a woman," he said, linking systemic failings to the fatal outcome.
Community supervision staff testified about the field checks they perform. Technicians from the program that vets residence plans told senators their role is to confirm housing viability, family resources and neighbor acceptance; they do not make the final release recommendation. Erick Dávila, the technician who inspected the proposed home for Ávila, said the property had an independent ground-floor unit and basic utilities and that neighbours did not object to the placement. Dávila and his supervisors confirmed they were sometimes unaware of clinical details — including whether the person used a wheelchair — because the referral packet did not always include full medical specifics.
Senators identified several problem areas: routine reliance on an initial clinician's checklist rather than a full file review; panels formed from "available" physicians rather than a designated multidisciplinary body; inconsistent use of specialists on panels; and field investigators working without full clinical context. The committee also drew attention to differences between the 1992 statute, which focuses on terminal illness, and subsequent regulations that expanded eligibility to some "incapacitante" conditions; senators asked whether policy changes had been communicated and trained to clinical staff.
Witnesses said that, after the fatal incident, the department had suspended Law 25 recommendations while procedures are reviewed. Senators called for specific fixes, including better cross‑agency sharing of records, a standing multidisciplinary review committee, consistent requirements for documentation presented to panels, and written procedures for community investigators to follow when the candidate requires specialized medical equipment or assistance.
The hearing closed with senators saying the next steps should include written submissions, review of the UTICORP audit, and further testimony from agency leaders. The Senate recessed to arrange follow‑up sessions.