Kaplan Hospital Investigates Suspected Unconsented Blood Draws for Research
Translated & summarized from Haaretz by baba
Kaplan Hospital in Rehovot has filed a police complaint over suspicions that blood was taken from patients without their consent for a research study. The hospital administration has also notified the Ministry of Health, which has pledged to coordinate with police on the investigation. Medical procedures, including blood draws for research, require informed patient consent according to Israeli law. Failure to obtain consent can be considered assault or negligence.
The story in 5 lines · by baba
- Kaplan Hospital in Rehovot is investigating allegations of blood being drawn from patients without consent for research.
- The hospital filed a police complaint and informed the Ministry of Health about the suspected misconduct.
- The Ministry of Health will coordinate with police to investigate the serious complaint.
- Patient consent is legally required for medical procedures and research in Israel.
- Performing procedures without informed consent can be classified as assault or negligence.
Kaplan Hospital in Rehovot announced Sunday that it filed a police complaint last week concerning alleged misconduct within its cardiology department. The hospital suspects that blood was drawn from patients without their consent as part of a research study conducted in a hospital laboratory. In addition to the police complaint, the hospital administration has informed the Ministry of Health about the suspicions and the actions taken. The Ministry of Health stated it received a report from the hospital director regarding the complaint's details and the investigation process, including the decision to file a police report. The ministry affirmed it would pursue the serious complaint in coordination with the police, utilizing its legal authority. Taking blood, like any medical procedure, requires patient consent, who must be aware of all risks, consequences, and alternatives. Except in rare circumstances, informed consent is mandatory for all medical procedures and research to ensure patients understand the implications and can freely agree. Under the Patient Rights Law and Public Health Regulations, performing a medical procedure or research without informed consent can be considered assault or negligence.
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