| Course | HA550 Health Care Law and Ethics |
|---|---|
| Unit | Unit 3 |
| Paper type | Informed consent scenario |
| Length | About 870 words, 6 pages double-spaced |
| Format | APA 7 student paper |
| School | Purdue University Global |
| Program | Master of Health Administration (MHA) |
| Updated | October 2026 |
Free sample paper for HA550 Unit 3
Six Cases Before Hers: An Informed Consent Scenario Asking Whether a Composite Surgeon's Limited Experience With Robotic-Assisted Hysterectomy Was Information the Law Required the Patient to Receive, Tested Under Both Disclosure Standards
[Student Name]
Purdue University Global
HA550: Health Care Law and Ethics
Unit 3 Informed Consent Scenario
[Instructor Name]
[Date]
The patient, surgeon and hospital are composite and bracketed for the writer's own data; the cases cited are real, and the analysis is coursework, not legal advice.
The Question
Was the surgeon's limited experience with this procedure material information that had to be disclosed? This scenario sets aside whether the operation was performed negligently, which is a separate claim.
Facts
The consent form listed general risks, including injury to nearby organs such as the bowel and bladder, conversion to open surgery and bleeding. The pre-operative note records a discussion of the procedure's benefits and risks, and of alternatives, including abdominal hysterectomy. It says nothing about the surgeon's experience. The patient later said she had chosen the hospital because its website described its robotic program as "among the region's most experienced."
The Rule
The principle that every adult of sound mind may decide what is done to their own body traces to a 1914 New York decision (Schloendorff v. Society of New York Hospital, 1914). Informed consent turns that principle into a duty to disclose. States use one of two standards. The professional standard measures disclosure against the customs of the physician's own specialty, shown through expert testimony. The reasonable patient standard, set out in Canterbury v. Spence (1972), asks instead what information someone standing where the patient stood would find significant when deciding. States divide roughly evenly between the two. A claim also requires causation: that a reasonable patient, properly informed, would have chosen differently, and that the undisclosed risk caused the injury.
Application Under the Reasonable Patient Standard
Would a reasonable patient consider her surgeon's experience material? There is a strong argument that she would. Studies of surgical outcomes find that surgeon volume is linked to lower complication and death rates for many procedures (Birkmeyer et al., 2003). In Johnson v. Kokemoor (1996), the Wisconsin Supreme Court held that evidence of a surgeon's limited experience with a difficult procedure, and of the higher risk when less experienced surgeons perform it, was admissible because a reasonable person would want to know it. Here, the patient chose the hospital partly for its claimed experience, which makes the information even more plainly material to her decision. The patient picked the hospital for its experience and was never told that her surgeon had little. Causation: she must show that, informed, she would have chosen a more experienced surgeon or a different procedure, and that a reasonable patient would have done the same. Given her stated reason for choosing the hospital, that is plausible.
Application Under the Professional Standard
Here the answer depends on expert testimony about what surgeons customarily disclose. Many surgeons do not routinely volunteer their case numbers, so an expert might testify that the disclosure met the standard. The claim is weaker under this standard, unless the patient asked directly and was misled.
Who Owns the Consent Process
Consent is usually treated as the physician's duty, and most courts hold the physician, not the hospital, responsible for the content of the disclosure. But hospitals own the forms, the policies on who obtains consent and the training of staff who witness signatures. When a hospital promotes a service, it also shapes what patients expect to hear. A hospital that requires consent conversations to cover certain topics, and audits whether they happen, reduces both patient harm and its own exposure. Here, the hospital's form listed risks but had no line for the surgeon's experience with a new technology, and nobody checked whether the conversation covered it.
Defenses the Surgeon May Raise
The surgeon may argue that experience is not a risk of the procedure but a fact about the surgeon, that disclosure of numbers can mislead patients because volume is only one factor, and that the bowel injury is a known complication that occurs even in experienced hands. Courts in reasonable patient states have not always accepted the first argument, as Johnson v. Kokemoor (1996) shows.
The Website Problem
Separately from the consent claim, the hospital's description of its program as highly experienced could support a claim of misrepresentation if it was misleading. That is a risk for the hospital, not just the surgeon.
Consequences for the Hospital
Under the reasonable patient standard, the hospital faces a serious consent claim, and the website increases its exposure. Under the professional standard, the claim is uncertain.
What the Hospital Should Change
1. Add a line to the consent conversation for new technology or new procedures: how many the surgeon has performed and who will assist.
2. Require proctoring for a surgeon's first [20] robotic cases and disclose proctoring to patients.
3. Review marketing claims with the medical staff office before publication.
4. Document the experience conversation in the pre-operative note.
Conclusion
In a reasonable patient state, surgeon experience was very likely material, especially for a patient who chose the hospital for experience. The safer course everywhere is to disclose it.
References
Birkmeyer, J. D., Stukel, T. A., Siewers, A. E., Goodney, P. P., Wennberg, D. E., & Lucas, F. L. (2003). Surgeon volume and operative mortality in the United States. New England Journal of Medicine, 349(22), 2117-2127. https://doi.org/10.1056/NEJMsa035205
Canterbury v. Spence, 464 F.2d 772 (D.C. Cir. 1972).
Johnson v. Kokemoor, 199 Wis. 2d 615, 545 N.W.2d 495 (1996).
Schloendorff v. Society of New York Hospital, 211 N.Y. 125, 105 N.E. 92 (1914).
The Purdue Global HA550 Unit 3 instructions
Unit 3 in HA 550 commonly asks students to analyze an informed consent scenario. Instructions usually require stating the question, the facts, the legal standard for disclosure, the application to the facts and the elements of a claim, including causation, with recommendations for the organization. State the question narrowly, and set aside separate issues such as surgical negligence. Explain both disclosure standards and apply the facts under each, since states differ. Cite the leading cases in APA style. Address causation: whether a reasonable patient, properly informed, would have decided differently. Consider the organization's role as well as the physician's, including forms, policies and marketing, and end with practical changes to the consent process.
How this HA550 Unit 3 example is built
The sample states its narrow question, with a margin note on why. Facts cover the form, the note and the patient's reason for choosing the hospital. The rule section traces consent to a 1914 New York decision and explains both disclosure standards. Under the reasonable patient standard, research on surgeon volume and the Wisconsin decision support materiality, and a highlighted line notes that she chose the hospital for its experience. Under the professional standard, the answer depends on expert testimony; a margin note explains why the application runs twice. Sections cover who owns the consent process, the surgeon's defenses and the website problem. Consequences, four changes and a conclusion, with a third margin note, follow.
HA550 Unit 3 rubric: what earns full points
HA 550 consent rubrics generally award points for a precise question, accurate facts, correct statement of both disclosure standards, careful application, attention to causation, consideration of the organization's role, practical recommendations, sources and presentation. Question points go to separating consent from negligence. Rule points reward accurate standards with leading cases. Application points depend on testing the facts under each standard. Causation points require addressing what the patient would have done. Organization points go to forms, policies and marketing. Recommendation points reward changes staff can follow. Analyses that recommend practice beyond the legal minimum tend to be marked highest, since they turn case law into policy.
HA550 Unit 3 help from the desk
Consent papers often lose points by treating any bad outcome as a consent failure, or by mixing consent with whether the surgery was done well. Others describe only one disclosure standard or skip causation. Many ignore the hospital's role. Ask one narrow question. Explain both standards and apply the facts under each. Use leading cases and, where relevant, research showing why the information matters to patients. Address causation directly. Then look at what the organization controls: the consent form, who conducts the conversation, training and the claims it makes in marketing. Recommend specific changes, such as adding a line about experience with new procedures and documenting the conversation.
Get an HA550 Unit 3 example written to your instructions
Share the Unit 3 scenario exactly as posted, the rubric, and any state it names. Both disclosure standards are applied unless your state is identified, causation gets its own section, and the hospital's role in the consent process is not left out. First custom sample free, 24-48h, written as coursework. The paper above is an original model document written by our desk, not a submitted student paper and not an official Purdue University Global document.
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HA550 Unit 3 questions, answered
Where can I find a free HA550 Unit 3 sample paper?
The complete HA550 Unit 3 informed consent scenario is here, testing whether a composite surgeon's limited robotic experience had to be disclosed.
What is the reasonable patient standard?
The approach from Canterbury v. Spence that measures disclosure by what an ordinary patient in the same situation would want to know before deciding.
Does surgeon experience have to be disclosed?
Under the reasonable patient standard it may be material, as a Wisconsin court held in Johnson v. Kokemoor.
What is causation in a consent claim?
Proof that a reasonable patient, properly informed, would have decided differently and that the undisclosed risk caused the injury.
How long is the HA550 Unit 3 scenario?
About five pages applying both disclosure standards.