Boland v. King County Medical Blue Shield

798 F. Supp. 638, 15 Employee Benefits Cas. (BNA) 2905, 1992 U.S. Dist. LEXIS 10007, 1992 WL 160390
CourtDistrict Court, W.D. Washington
DecidedJuly 9, 1992
DocketC92-504D
StatusPublished
Cited by4 cases

This text of 798 F. Supp. 638 (Boland v. King County Medical Blue Shield) is published on Counsel Stack Legal Research, covering District Court, W.D. Washington primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Boland v. King County Medical Blue Shield, 798 F. Supp. 638, 15 Employee Benefits Cas. (BNA) 2905, 1992 U.S. Dist. LEXIS 10007, 1992 WL 160390 (W.D. Wash. 1992).

Opinion

ORDER

DIMMICK, District Judge.

Plaintiff Lyn Boland has brought this action under the Employment Retirement Income Security Act of 1974, as amended, 29 U.S.C. § 1001 et seq. (ERISA), contesting defendants’ denial of coverage under an employer’s medical plan. Defendants have filed separate motions for summary judgment, but refer to and incorporate each other’s briefs and affidavits and will be referred to collectively as “defendants.” The Boeing Company (“Boeing”) emphasizes contract principles to argue for dismissal. Boeing contends that the plan lan *640 guage and the underlying bargaining agreement classify as an excluded experimental procedure any procedure so defined by the national Blue Cross and Blue Shield Association (“national Blue Cross”). Defendant King County Medical Blue Shield (“King County Medical”) on the other hand emphasizes the plan’s exclusion of any experimental procedure that is not generally recognized by the medical profession. Plaintiff insists that defendants’ decisions as to what constitutes experimental treatment should not be entitled to deference because of a conflict of interest or because the decisions were not made by a fiduciary.

The Court has considered the briefs and affidavits filed by the parties and concludes that summary judgment in favor of defendants is justified insofar as the employer medical plan relies on the classification of a third party — national Blue Cross. This conclusion involves no disputed issue of material fact and can be decided by the Court as a question of law premised on the plain language of the plan. Fed.R.Civ.P. 56.

FACTS

Plaintiff Lyn Boland was diagnosed with breast cancer in August of 1991. She subsequently underwent surgery and has received extensive chemotherapy. There is no question that this earlier treatment is covered by the terms of the plan. In January of 1992, Mrs. Boland’s treating physicians recommended that she be treated at the Fred Hutchinson Cancer Research Center with high dose chemotherapy with auto-logous bone marrow transplant (“HDC with ABMT”). Mrs. Boland sought pre-authorization for this treatment under the Boeing Medical Plan. Mrs. Boland was covered under the medical plan because of her husband’s employment as a Boeing engineer.

The details of the medical plan at issue here were negotiated between Boeing and Seattle Professional Engineering Employees Association (“SPEEA”). See Collective Bargaining Agreement, CP 34, Exhibit B. The Boeing Company is the plan sponsor and pays for all benefits under the plan with no limitation as to amount of payments; the Welfare Benefit Plans Committee (“Committee”) is the plan administrator and hears appeals. See Health Care Plans, 1990 Edition, CP 34, Exhibit A, page 54. The four members of the Committee are Boeing executives. Cannon Deposition, CP 50, Exhibit 13, page 12.

The Boeing Company signed an agreement January 1, 1987, with defendant King County Medical to act as the service representative for the medical plan and as an agent for Boeing to process claims and disburse payments. See Administrative Services Agreement, CP 34, Exhibit C. King County Medical is a nonprofit organization, which is paid an annual fee by Boeing unaffected by any benefits paid. 1 CP 60.

The collective bargaining agreement and the Health Care Plans document exclude coverage for experimental or investigational medical services or supplies. The SPEEA agreement states the exclusion as follows:

Experimental or investigational medical services or supplies (and related complications) meaning any services so classified by the National Blue Cross and Blue Shield Association and any service whose use is still under clinical investigation by health professionals or is not generally recognized by the medical profession as tested and accepted medical practice. This exclusion also applies to items requiring Federal Drug Administration or other governmental agency approval if such approval was not granted at the time the service or supply was ordered.

Id. at ¶ 19, A-28. The Health Care Plans document refers to exclusions of “[e]x-penses for experimental or investigational services and supplies (as defined on page 57), and related complications.” CP 34, *641 Exhibit A, page 28. This definition follows:

An experimental or investigational service or supply is one that meets at least one of the following:
1. Is under clinical investigation by health professionals and is not generally recognized by the medical profession as tested and accepted medical practice.
2. Requires approval by the Federal Drug Administration or other governmental agency, and such approval has not been granted at the time the service or supply is ordered.
3. Has been classified by the national Blue Cross and Blue Shield Association as experimental or investigational.

CP 34, Exhibit A, page 56-57.

Following Mrs. Boland’s request for authorization of HDC with ABMT treatment, King County Medical’s director Dr. Stanley Pomerantz advised Mrs. Boland that the treatment was not covered under the terms of the plan. Letter dated February 19, 1992. 2 This denial was appealed to the Committee which also denied coverage. Defendants denied coverage on grounds of “experimental or investigational service” as defined in numbers 1 and 3 above.

Mrs. Boland filed suit March 27, 1992. On April 1, 1992, Mrs. Boland filed a motion for preliminary injunction. The motion for preliminary injunction was ultimately resolved by the parties permitting Mrs. Bo-land to proceed with treatment, but the issues raised therein were retained for trial. The Court set an expedited trial schedule, with trial date set for August 23, 1992.

ISSUES

1. Although it is conceded that the plan gives the administrator discretion to interpret the plan, the entity named as plan administrator (Committee) is a fiduciary with a conflict of interest; therefore, is a less deferential standard of review appropriate? 3

2. Can defendants properly base a determination of the experimental nature of a particular medical treatment on a third party’s decision — national Blue Cross — when it is specified in the collective bargaining agreement with SPEEA and the language in its medical plan?

3. Applying the appropriate standard of review, can the Court conclude as a matter of law (applying summary judgment standards) that the plan administrator properly denied treatment.

DISCUSSION

Discussion below will focus first on the standard of review for defendants’ decisions. Then the above two bases for denial ((1) not generally recognized by the medical profession, and (3) classified as experimental by national Blue Cross) will be covered under the appropriate standard.

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Bluebook (online)
798 F. Supp. 638, 15 Employee Benefits Cas. (BNA) 2905, 1992 U.S. Dist. LEXIS 10007, 1992 WL 160390, Counsel Stack Legal Research, https://law.counselstack.com/opinion/boland-v-king-county-medical-blue-shield-wawd-1992.