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Bailey v. Blue Cross Blue Shield of Virginia - United States Court of Appeals for the Fourth Circuit - October 11, 1995 - Robert E. Hoskins

Bailey v. Blue Cross Blue Shield of Virginia, 67 F.3d 53 (4th Cir. 1995) – decided October 11, 1995 – United States Court of Appeals for the Fourth Circuit – Robert E. Hoskins

 

I represented Bailey. Bailey is one of a series of many high dose chemotherapy cases in which I represented the plaintiff in the 1990s; many others are discussed in this site. To view them all, use the search function and put in the phrase “high dose chemotherapy”. Bailey involved a situation where the insurer, Blue Cross Blue Shield of Virginia, had a specific exclusion for bone marrow transplants and stem cell rescues (then commonly used support procedures for high dose chemotherapy treatment) in its policy language. The question presented was whether the exclusion language was so broad as to encompass the actual high dose chemotherapy treatment, itself. With the procedure known as high dose chemotherapy supported by a peripheral stem cell rescue (HDC/PSCR), the high dose chemotherapy actually treats the cancer and the stem cell rescue or bone marrow transplant, as the case may be, is a support and recovery procedure. I argued that the specific exclusion should not be read so broadly as to include the high dose chemotherapy. Obviously, Blue Cross argued to the contrary. The United States District Court for the Eastern District of Virginia ruled with Bailey. (Click here to view the district court opinion on the merits.) The defendant appealed to the United States Court of Appeals for the Fourth Circuit. The Fourth Circuit used Bailey to clarify the applicable standard of review for ERISA governed insured benefit plans. In fact, to this day, Bailey is my most often cited decision out of the Fourth Circuit. As of March 2008, Bailey had been cited over 220 times including by the United States Courts of Appeals for the Seventh and Tenth Circuit. Bailey is usually cited in connection with a discussion of the standard of review for insured ERISA plans or the applicability of the doctrine of contra proferentum which mandates that ambiguities in insured plans are construed against the drafter of the plan. On the former issue, the court stated in Bailey:

“Blue Cross Blue Shield concedes that it operated under a conflict of interest when it denied the benefits sought by Bailey. It argues, though, that the district court erred by not articulating the degree of (lessened) deference it accorded Blue Cross’s decision. Although the district court did not elaborate specifically on the degree of deference it considered appropriate, the lower court correctly articulated the legal standard we established in Doe. Joint Appendix at 364. Furthermore, after citing the relevant case law, it expressly found that Bailey was entitled to summary judgment “in light of the deference to be accorded to the administrator of the Policy under the facts of this case.” Id. at 373. Although a more extensive analysis might have been helpful, we cannot say that the district court erred in its application of the law. A more thorough explanation might have been necessary had the conflict of interest not been as total as that in this case, where Blue Cross stood as the single beneficiary of a substantial sum based on its denial of benefits. Cf. Brown v. Blue Cross Blue Shield, 898 F.2d 1556, 1564 (11th Cir. 1990) (“When the members of a tribunal - - for example, the trustees of a pension fund - - have a serious conflict of interest, the proper deference to give may be slight, even zero; the decision if wrong may be unreasonable.”).”

With regard to the contra proferentum issue, the court found that the policy was ambiguous and stated:

“Blue Cross next argues that even under the less deferential standard described above, its decision to deny Bailey benefits was proper, because the policy’s language unambiguously indicates that high dose chemotherapy is not covered. Construing the exclusion for “stem cell rescue (in which the patient is the donor) with high dose chemotherapy or radiation,” Blue Cross essentially interprets “with” as unambiguously meaning “and”. Joint Appendix at 180. In contrast, Bailey contends that the language is ambiguous as a matter of law. In assessing this argument, we must interpret the policy using ordinary principles of contract law, enforcing the plan’s plain language in its ordinary sense. Hardester v. Lincoln Nat. Life Ins. Co., 33 F.3d 330, 338 (4th Cir. 1994) (Hall, J., dissenting), vacated on reh’g, 52 F.3d 70 (4th Cir. 1995) (en banc) (adopting panel dissenting opinion). “Where a term is ambiguous, we must construe it against the drafter, and in accordance with the reasonable expectations of the insured.” Wheeler, F.3d at (citations omitted).

 

Both parties rely on our holdings in Doe, 3 F.3d at 80, and Hendricks v. Central Reserve Life Ins. Co., 39 F.3d 507 (4th Cir. 1994), as supporting their respective positions regarding whether the language at issue is ambiguous. In Doe, the “rescue” procedure preceding chemotherapy and radiation involved an autologous transplant of bone marrow, rather than peripheral stem cells. 3 F.3d at 82. The medical principles, however, were equivalent to those underlying the procedure for which Bailey seeks coverage. The insurance policy at issue in Doe excluded “services or supplies for or related to” the bone marrow transplant. Id. at 88. Elsewhere in the policy, coverage for chemotherapy and radiation specifically was provided. Id. at 87-88. Applying the less deferential abuse of discretion standard discussed above, we held that the policy covered the high dose chemotherapy portion of a cancer patient’s treatment, id. at 89.

 

In contrast, we held in Hendricks that the plaintiff’s insurance policy did not cover high dose chemotherapy. The policy at issue in that case excluded “treatment or services experimental or investigational in nature.” 39 F.3d at 511. After ruling that the desired HDC/PSCR treatment fell within the exclusion, the court rejected the plaintiff’s argument that phases of the treatment other than the high dose chemotherapy itself were covered. “To fragment the phrases of treatment and consider each in light of the policy language produces an unrealistic and distorted analysis.” Id. at 514.

 

Applying these cases, the ambiguity in Bailey’s policy becomes apparent. The desire in Hendricks to avoid excessive fragmentation supports Blue Cross’s view that HDC/PSCR is a unified treatment. On the other hand, if high dose chemotherapy was not a service “related to” the autologous bone marrow transplant in Doe, it is reasonable to conclude that the policy exclusion covers only the distinct PSCR. Moreover, as the district court found, “the record does not preclude the possibility that there may indeed be cases where HDC is not accompanied by PSCR.” Joint Appendix at 371. That possibility is consistent with Bailey’s interpretation of the policy as providing coverage for all types of chemotherapy - - including treatment with high doses. We have held repeatedly that ambiguous language must be construed against the drafter. Doe, 3 F.3d at 89; Glocker v. W.R. Grace & Co., 974 F.2d 540, 544 (4th Cir. 1992). Particularly because “Blue Cross’ discretionary interpretation to the contrary is not entitled to the deference we might otherwise accord,” Doe, 3 F.3d at 87, the district court’s ruling prohibiting Blue Cross from denying coverage for Bailey’s high dose chemotherapy was proper as a matter of law.” (Click here to see the Fourth Circuit opinion)

The Doe and Hendricks cases obviously weighed heavily into the Fourth Circuit’s decision in Bailey as discussed above. In the Hendricks case, I represented Mr. Hendricks (click here to see a discussion of the Hendricks in this website). I did not represent Doe. (However, to view the Doe decision click here.)

 

The defendant petitioned the United States Supreme Court for cert. The Supreme Court denied the Blue Cross’ petition. Interestingly, the very issues raised by Blue Cross Blue Shield of Virginia in its petition to the US Supreme Court are the same issues that the Supreme Court is scheduled to decide in 2008 in the case of Barron v. Metropolitan Life Insurance Company. (Click here, to see the entry for the Barron Supreme Court case at the Supreme Court level as compiled at SCOTUS Wiki.)

 

As an aside, the Bailey case also resulted in an interesting opinion from District Court Judge Calvet Clark on vacating judgments. (Click here to that opinion.)

 

As an interesting end note to this case and all of the cases where I represented individuals seeking health insurance coverage for individuals to undergo HDC/PSCR in the 1990s, I would highly recommend the article “We Were All Sold A Bill of Goods: “Litigating the Science of Breast Cancer Treatment””, Jacobson and Doebler, 52 Wayne L. Rev. 43, Spring 2006. In that article, the authors provide an excellent discussion about the litigation boom over HDC/PSCR for breast cancer in the late 1980s and particularly in the 1990s. They cite to six or seven of my cases which are discussed in this case log in analyzing the causation of the 1990s litigation boom. The article begins:

“In the late 1980s and 1990s, thousands of women elected to undergo high-dose chemotherapy with autologous bone marrow transplant (HDC-ABMT) as a last chance treatment for breast cancer, despite the fact that the procedure cost upwards of $100,000 and was also expensive in terms of risks and side effects. When their health insurers refused to cover the treatment, many women sought payment through the judicial system. The result was a series of nearly a hundred courtroom battles, not to mention thousands of settlement negotiations, in which judges and juries were forced to determine whether women would have access to a new procedure that offered their only hope for survivial. Without it they would almost certainly die. By the time studies were published conclusively showing that the procedure was ineffective, more than 30,000 women had already received the treatment, which often shortened their lives and added to their suffering, at a total cost of approximately $3 billion.

What went wrong? Howe could so much money have been spent and such suffering imposed for no apparent benefit? The natural reaction to these devastating accounts is to assign blame. Depending on one’s political and philosophical views, blame might be apportioned in the following ways. First, in their quest to slash costs and raise the bottom-line, health insurers and managed care organizations ignored the needs of their policyholders. Second, physicians pressured their patients into undergoing a procedure with essentially unknown risks and benefits, in a desperate attempt to give them at least a few more years of life. Third, plaintiffs’ attorneys saw the opportunity to make the insurers pay - - both literally and figuratively - - for their cold-heartedness and pursued these cases aggressively. Finally, courts, moved by the plight of the dying women who came before them, let sympathy trump the law.

These attempts to apportion blame are certainly plausible and accord with the conventional wisdom which views lawyers and the courts as especially culpable. In this Article, we question the conventional system. We examine the role that attorneys and the court system played in this unfortunate set of outcomes and explores alternatives to avoid replicating these results in the future.” (52 Wayne L. Rev. 43, 44, 45)

Personally, I am very pleased that the authors concluded:

“In the end, it is hard to blame the attorneys for what occurred. Each attorney represented his or her client in a manner that professional ethics demands and each acted with the best of intentions. Was their advocacy overly aggressive under the circumstances? Arguably so. But keep in mind the reality that the patient had what amounted to a death sentence and chose to undertake a risky procedure as a last chance.

As a society, we have yet to reach a balance between individual access to last chance therapies and the costs to society. The nation’s culture of technology is embedded too deeply to accept limits very easily. Like it or not, the legal system performed as it is designed to do-to protect individual litigants - - even if the judiciary is not the best forum for resolving controversial clinical scientific disputes. Are we prepared instead to delegate that responsibility to insurers? We doubt it. A much better alternative is for policymakers to focus on improving the technology assessment process and funding randomized control trials to determine a procedure’s effectiveness before its widespread diffusion into medical practice.” (52 Wayne L. Rev. 43, 111, 112)

 
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