Wheeler v. United States of America
Filing
74
ORDER denying in part 35 Motion to Compel. Signed by Magistrate Judge James P. O'Hara on 6/5/2018. (srj)
IN THE UNITED STATES DISTRICT COURT
FOR THE DISTRICT OF KANSAS
RICKY WHEELER, personally and as
Special Administrator of the
Estate of Gretchen A. Konrad, Deceased,
and as the father and natural guardian
of L.W., a minor,
Plaintiff,
v.
Case No. 17-2249-JTM
UNITED STATES OF AMERICA,
Defendant.
ORDER
Ricky Wheeler, the surviving spouse of Gretchen A. Konrad, brings this wrongfuldeath and survival action against the United States of America under the Federal Tort
Claims Act. Plaintiff alleges physicians and other healthcare providers at Irwin Army
Community Hospital (“IACH”) negligently failed to properly manage Ms. Konrad’s
delivery of her son and failed to properly assess and treat Ms. Konrad thereafter. This
case is before the court on plaintiff’s motion to compel defendant to provide complete
responses to his first interrogatories and request for production of documents (ECF No.
35).
On April 30, 2018, the undersigned U.S. Magistrate Judge, James P. O’Hara,
issued an order (ECF No. 59) taking under advisement the portion of plaintiff’s motion
seeking two documents defendant claims are protected by the medical quality assurance
1
privilege contained in 10 U.S.C. § 1102—specifically, a note written by Sean Pozarek,
CRNA, and a memorandum written by Mary Ellen Raymond, CNM.1 The court’s order
directed defendant to submit the two documents to the court for in camera review, and to
submit an affidavit clarifying how the documents have been held by IACH, and how the
documents have been moved (if at all). The order further provided both parties the
opportunity to file supplemental briefs. The undersigned has reviewed the documents,
the affidavits, and the supplemental briefing, and is now prepared to rule on the
remainder of plaintiff’s motion to compel.
10 U.S.C. § 1102(a) provides that “[m]edical quality assurance records created by
or for the Department of Defense as part of a medical quality assurance program are
confidential and privileged.” The statute goes on to specifically provide that “[n]o part
of any medical quality assurance record … may be subject to discovery or admitted into
evidence in any judicial … proceeding”2 except under certain enumerated exceptions,3
none of which apply in this case. Congress had one overriding concern in mind when it
enacted this medical quality assurance privilege:
to produce an effective mechanism allowing the military departments to
monitor and ensure that quality medical care [is] provided to Department of
Defense beneficiaries through a collegial review process operating in “an
environment of confidentiality in order to elicit candid appraisals and
1
The remainder of plaintiff’s motion to compel was granted in part and denied in
2
10 U.S.C. § 1102(b)(1) (emphasis added).
3
Id. § 1102(c).
part.
2
evaluations of fellow professionals” without the fear that such records
would be subject to discovery during litigation, thereby causing such
beneficiaries to “receive less than the high quality of care they deserve.”4
The statute defines “medical quality assurance program” as:
any peer review activity carried out … to assess the quality of medical care,
including activities conducted by individuals, military medical or dental
treatment facility committees, or other review bodies responsible for quality
assurance, credentials, infection control, patient care assessment ….,
medical records, health resources management review and identification
and prevention of medical or dental incidents and risks.5
The term “medical quality assurance record” is defined as “the proceedings, records,
minutes, and reports that emanate from quality assurance program activities described
[above] and are produced or compiled by the Department of Defense as part of a medical
quality assurance program.”6
Upon review of the documents submitted in camera, the affidavits, and
supplemental briefing, the court concludes the documents sought constitute records
emanating from quality assurance program activities (i.e., risk management) that are
produced or compiled as part of the medical quality assurance program. Defendant has
demonstrated that the Raymond memorandum and “a version of” the Pozarek note have
been held and continue to be held as part of the risk management record. Although
4
Smith ex rel. Smith v. United States, 193 F.R.D. 201, 208 (D. Del. 2000) (quoting
1986 U.S.C.C.A.N. 6413, 6440).
5
10 U.S.C. § 1102(j)(1).
6
Id. § 1102(j)(2).
3
plaintiff argues he’s entitled to the original draft version of the Pozarek note insofar as it
exists on a drive outside of the risk management file, the court finds plaintiff’s argument
unpersuasive.
Accordingly, plaintiff’s motion, to the extent not already granted in part and
denied in part, is denied.
IT IS SO ORDERED.
Dated June 5, 2018, at Kansas City, Kansas.
s/ James P. O’Hara
James P. O’Hara
U.S. Magistrate Judge
4
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