Moore v. Regents of the University of California

793 P.2d 479 (1990)

Quick Summary

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John Moore (plaintiff) underwent medical treatment where Dr. Golde of Regents of the University of California (defendant), used Moore’s cells for profitable research without his consent.

The dispute involved whether Moore’s rights were violated due to non-disclosure of financial interests and lack of informed consent. The Supreme Court concluded that while there was a breach of fiduciary duty, the cells were not subject to conversion claims.

Facts of the Case

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John Moore (plaintiff) was treated for leukemia at UCLA Medical Center, where Dr. David Golde (defendant) recommended and performed a splenectomy. Without Moore’s consent, Golde used Moore’s cells to establish a patented cell line, which he licensed for commercial development, resulting in significant financial gain. Moore was unaware of Golde’s intents and filed a lawsuit for conversion, lack of informed consent, and breach of fiduciary duty among other claims.

The patent was held by the Regents of the University of California (defendant), with Golde and researcher Shirley Quan (defendant) listed as inventors. Moore alleged that the defendants did not disclose their financial interests in his cells before obtaining his consent for medical procedures, thus violating his rights.

Procedural Posture and History

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  1. Moore underwent treatment and had his spleen removed at UCLA Medical Center.
  2. Dr. Golde used Moore’s cells for research without permission, leading to a patented cell line.
  3. Moore filed a lawsuit including a claim for conversion against the defendants.
  4. The trial court granted summary judgment on the conversion claim and dismissed the case.
  5. Moore appealed, and the California Court of Appeal reversed, reinstating the conversion claim.
  6. The defendants then appealed to the Supreme Court of California.

I.R.A.C. Format

Issue

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Whether a patient has stated a cause of action against his physician and other defendants for using his cells in medical research without his permission, potentially violating informed consent and property rights.

Rule of Law

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The court must determine if the physician’s undisclosed research and economic interests in the patient’s cells before obtaining consent constitute a breach of fiduciary duty and if the patient’s cells can be considered personal property subject to conversion.

Reasoning and Analysis

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The court concluded that the physician had an obligation to disclose any personal interests that could affect his judgment when seeking patient consent for medical procedures. The ruling emphasized that such disclosure is crucial for patient autonomy in making informed decisions regarding treatment.

However, the court also decided that Moore’s excised cells did not constitute personal property that could be converted, as no precedent supported this claim within existing law.

The opinion further clarified that even if Moore’s cells were considered property, the establishment of a cell line is distinct from the original cells and thus not owned by Moore. The court weighed potential implications for medical research and determined that extending conversion liability could hinder access to necessary materials for scientific advancement.

Conclusion

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The complaint states a cause of action for breach of fiduciary duty but not for conversion. The case was remanded to determine secondary liability issues and other claims.

Dissenting Opinions

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The dissenting opinion argued that Moore should be recognized as having a property interest in his cells, which would support a cause of action for conversion. It emphasized the ethical imperative to respect bodily autonomy and fairness in benefiting from one’s own biological materials.

Key Takeaways

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  1. Patients must be informed of physicians’ research and economic interests that may affect their judgment when obtaining consent for medical procedures.
  2. Excised human cells are not considered personal property for purposes of a conversion claim under current California law.
  3. The case establishes limits on property rights over one’s own body parts once removed, particularly concerning commercial development.

Relevant FAQs of this case

What are the ethical considerations for a doctor when their medical research interests might affect patient treatment?

The ethical considerations include the necessity for transparency and managing any potential conflicts of interest to prioritize the patient’s welfare. Doctors need to disclose any personal gain that might influence their clinical judgment. A key component of this is the doctrine of informed consent, which mandates that patients should understand any risks, benefits, and alternatives to treatment, including the doctor’s related interests.

  • For example: A dentist discovers a new method of treating cavities that could become commercially lucrative and must inform their patient if this method will be used instead of traditional treatment.

How do courts define property rights in relation to parts of the human body?

Courts typically draw a distinction between an individual’s rights over their body while alive and intact versus separated biological materials. Generally, once bodily materials are separated from the person, such as blood or tissue samples, they are not considered the individual’s personal property under the law. The material’s transformation through a process like establishing a cell line can further sever property claims.

  • For example: A person donates blood at a clinic. While they retain no property rights over the donated blood, they also cannot claim any ownership over potential products developed from it, like synthesized plasma.

Is informed consent required if a medical procedure can result in commercial benefits for the physician?

Informed consent is imperative when a medical procedure entails potential commercial gains for a physician. The physician must disclose any resulting conflicts of interest to ensure that the patient’s consent is both fully informed and voluntary.

  • For example: If an orthopedic surgeon patents a new type of knee implant that they plan to use in a patient’s surgery, they must inform the patient about their financial stake in the product before proceeding.

References

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