Crista, Jill v. Wisconsin Physicians Service Insurance Corporation et al

Filing 50

Transmission of Notice of Appeal, Order, Judgment and Docket Sheet to Seventh Circuit Court of Appeals re: 48 Notice of Appeal, (Attachments: # 1 Order, # 2 Judgment, # 3 Docket Sheet) (lak)

IN THE UNITED STATES DISTRICT COURT
FOR THE WESTERN DISTRICT OF WISCONSIN
JILL CRISTA, TORIN HIGNELL,
and KAELAN HIGNELL,
Plaintiffs,

OPINION AND ORDER

v.
18-cv-365-wmc
WISCONSIN PHYSICIANS SERVICE
INSURANCE CORPORATION,
Defendant.
Defendant Wisconsin Physicians Service Insurance Corporation (“WPS”) is being
sued under the Employee Retirement Income Security Act, 29 U.S.C. § 1132(a) (“ERISA”)
after it denied prior authorization requests for administration of intravenous
immunoglobulin (“IVIG”) to plaintiffs Kaelan and Torin Hignell, the twin sons of plaintiff
Jill Crista. Before the court are the parties’ cross-motions for summary judgment. Plaintiffs
contend that WPS’s denial was arbitrary and capricious and constituted a breach of
fiduciary duties, while WPS counters that the denials were appropriate following a review
of the twins’ complete medical records. For the reasons that follow, the court concludes
that the undisputed facts and binding case law require entry of judgment for WPS.

UNDISPUTED FACTS1
A. Background
The plaintiffs all live in Rock County, Wisconsin. Crista is a participant in an
employee welfare benefit plan administered by defendant WPS, while Torin and Kaelan

1

The following facts are material and undisputed for purposes of summary judgment except where

are beneficiaries under that plan. WPS is a Wisconsin service insurance corporation. WPS
issued the original policy, an individual preferred provider organization policy, to Crista
on January 1, 2015, in which Torin and Kaelan were listed as covered dependents. The
policy renewed on January 1, 2016. On September 23, 2016, WPS informed Crista that
it would no longer offer individual Affordable Care Act coverage because of changes in the
health insurance market. As a result, WPS advised that her policy would end on December
31, 2016.
On January 16, 2017, Crista completed an application seeking small group
insurance coverage for her business, Center for Natural Medicine, LLC, to be effective
February 1, 2017. WPS issued a Group Master Policy, Group No. 10011017 to Center
for Natural Medicine, with a 2017 WPS PPO Certificate of Coverage effective February 1,
2017 (the “Plan”).2 This Plan qualifies as an employee welfare benefit plan under ERISA

noted below. The facts are drawn from the administrative record compiled by WPS in considering
plaintiffs’ claims. See Holmstrom v. Metro. Life Ins. Co., 615 F.3d 758, 761 (7th Cir. 2010).
Throughout this opinion, therefore, the court cites to portions of the administrative record (dkts.
#15, 15-1, 15-2, 15-3) as “WPS __.” Also before the court is plaintiffs’ motion to strike audio files
produced by WPS. (Dkt. #28.) The files were provided via USB port on November 13, 2018 -slightly more than two months after the September 7, 2018, deadline imposed by this court for
WPS to produce the entire administrative record and almost a month after plaintiffs had already
filed their summary judgment motion. (See dkts. #24, 11, 16.) Defendant has provided no
explanation for the belated disclosure, and so the delay is not justified, nor was the delay harmless
as it came after plaintiffs had already filed their own summary judgment motion. The court notes,
however, that the recordings were largely immaterial and would not have altered the opinion either
way. Regardless, for the purposes of this opinion and order, the court neither considered the audio
recordings nor the proposed findings of fact supported only by those recordings, and plaintiffs’
motion to strike is GRANTED.
On July 1, 2017, the employer’s name on the policy changed to “Crista Corporation” when the
company became an S-corporation.
2

2

with Crista a plan participant and her sons as beneficiaries. WPS serves as a fiduciary in
interpreting and applying the Plan terms.
The Plan vests “the sole and exclusive right to interpret and apply the Policy’s
provisions and to make factual determinations” in WPS, including determining “whether
benefits are payable for a particular health care service.” (WPS 1908.)3 The Plan “only
provides benefits for certain health care services,” and expressly notes that the policy does not
automatically cover services (1) “performed or prescribed” by a health care provider or (2)
that are “the only available health care service[s] for your illness or injury.” (Id.) The Plan
further lists a number of exclusions, including for: (1) “Health care services that we determine
are not medically necessary”; and (2) “Health care services that we determine are
experimental/investigational/unproven.” (WPS 1946.)
The Plan defines “medically necessary” as:
a health care service or facility that we determine to be:
1. Consistent with and appropriate for the diagnosis or
treatment of your illness or injury;
2. Commonly and customarily recognized and generally
accepted by the medical profession in the United States as
appropriate and standard of care for the condition being
evaluated or treated;
3. Substantiated by the clinical documentation;
4. The most appropriate and cost effective level of care that
can safely be provided to you. Appropriate and cost
effective does not necessarily mean least expensive;
5. Proven to be useful or likely to be successful, yield
additional information, or improve clinical outcome; and
6. Not primarily for the convenience or preference of the
covered person, his/her family, or any health care provider.

As quoted here, and throughout the Plan documents, a wide-range of terms are italicized and
defined elsewhere. Unless otherwise noted, any italics or other emphases appearing in the quotes
above are in the original.
3

3

(WPS 1976.) Similarly, the Plan expressly states that something “may not be considered
medically necessary even if the health care provider has performed, prescribed, recommended,
ordered, or approved the service, or if the service is the only available procedure or
treatment for your condition.” (Id.)
The Plan defines “Experimental/Investigational/Unproven” as “any health care service
or facility,” which is “determined by our Corporate Medical Director” to “meet[] at least
one of the following criteria:” (1) “It is not currently recognized as accepted medical
practice”; (2) “It is being used in a way that is not approved by the FDA or listed in the
FDA-approved labeling (i.e. off-label use), except for off-label uses that are accepted
medical practice”; (3) “Prevailing peer-reviewed medical literature in the United States has
failed to demonstrate that it is safe and effective for your condition”; and (4) insufficient
“evidence to . . . make a convincing argument that (a) it can measure or alter the sought
after changes . . .; or support conclusions concerning the effect of the drug, device,
procedure, service or treatment on health outcomes.”4 (WPS 1973.) Similarly, the Plan
states

that

“[a]

health

care

service

or

facility

may

be

considered

experimental/investigational/unproven even if . . . it is the only available procedure or treatment
for the condition.” (Id.)
Finally, under the Plan terms, WPS reserved “full discretionary authority to
determine whether a health care service is experimental/investigational/unproven” and states its
“determination will be upheld if it is based on any credible evidence.” (WPS 1974.) If

The definition of “Experimental/Investigational/Unproven” also listed other criteria not relevant
here. Moreover, the Plan explains that the list provided was “not all-inclusive.” (WPS 1973.)
4

4

WPS’s determination were reversed, the policy beneficiary “will not be entitled to receive
any compensatory damages, punitive damages, or attorney’s fees, or any other costs,” but
rather would be limited to the “provision of benefits in accordance with the Policy.” (Id.)

B. Prior Authorization Requests
Section 11 of the Plan outlines the process for submitting prior authorization
requests and benefits determinations. (WPS 1960-63.) The Plan explains that any “denial
notice will state the specific reason or reasons for the adverse benefit determination, the specific
Policy provision on which the determination is based, and a description of the internal and
external review procedures and associated timelines,” as well as “a description of any
additional material or information necessary for you to perfect the claim and an
explanation of why such material or information is necessary.” (WPS 1963.) If the denial
“is based on the definition of medically necessary or experimental/investigational/unproven, the
denial notice will include an explanation of the scientific or clinical judgment for the
determination” or “a statement that such explanation will be provided, free of charge, upon
your request.” (Id.)
Section 12 outlines the process for appealing an adverse benefits determination.
(WPS 1963-68.) A grievance can be filed by submitting to WPS’s Grievance/Appeal
Department “the concerns, issues, and comments” in writing, with “any supporting
documents” within three years following receipt of WPS’s “initial notice of denial or partial
denial.” (WPS 1964.) The policy provides the following example:
if we denied benefits for your claim because we determined that
a health care service provided to you was not medically necessary
and/or experimental/investigative/unproven, please send us all

5

additional medical information (including copies of your health
care provider’s medical records) that shows why the health care
service
was
medically
necessary
and/or
not
experimental/investigative/unproven under the Policy.
*
*
*
For decisions regarding medical judgment, the Committee will
consult with a health care professional who has the appropriate
training and experience in the field of medicine involved in the
medical judgment. Such health care professional will not be
the same individual who was consulted regarding the initial
adverse benefit determination or a subordinate of such
individual.
(Id.)

If after the completion of the grievance/appeal process, WPS determines that

treatment was experimental/investigational/unproven, a beneficiary could request an
external review by an independent review organization (“IRO”) under Section 13. (WPS
1968.) To invoke that process, the beneficiary must submit in writing a specific request
for independent external review.

(WPS 1968-69.)

Once the request is received, an

accredited IRO is then assigned to the case, and will then issue a decision after receiving
the request. (WPS 1969.) “Unless your case involves the rescission of the Policy, the
IRO’s decision is binding for both you and WPS.” (Id.)

C. Intravenous Immunoglobulin (IVIG) Treatment
There is no dispute that Torin and Kaelan had previously been diagnosed with
“hypogammaglobulinemia” by their treating physicians, Drs. Denis Bouboulis and Phillip
DeMio,

although

the

parties

dispute

whether

they

actually

suffer

from

it.

Hypogammaglobulinemia is a serious immune disorder that causes chronic respiratory and
gastrointestinal issues and recurring infections, which can lead to the development of
autoimmune conditions and premature death.

6

Hypogammaglobulinemia is an FDA-

approved indication for IVIG treatment. There is also no dispute that Torin and Kaelan
have received IVIG treatment since 2013, although again the parties dispute its medical
necessity.
1. Approval of First Prior Authorization Requests in 2015
The first prior authorization requests for IVIG treatment for Torin and Kaelan were
submitted to WPS in late January 2015, listing hypogammaglobulinemia as the
necessitating diagnosis. WPS’s specialty pharmacy benefits manager, Diplomat, approved
these requests, and WPS approved IVIG treatment for each child from January 22, 2015,
until January 28, 2016. (WPS 147, 353.)
2. Denial, Appeal, and Ultimate Approval of the 2016 Prior Authorization
Requests
Additional prior authorization requests for IVIG treatment were submitted to WPS
for Torin and Kaelan in late January 2016, again listing hypogammaglobulinemia as the
necessitating diagnosis. These prior authorization requests included some medical records
for the Hignells, but the parties dispute whether more documents were requested and
subsequently provided. (Def.’s PFOF (dkt. #38) ¶¶ 27, 31.) Specifically, WPS maintains
that it requested all office notes and laboratory reports from January 1, 2013, to December
31, 2014, but that plaintiffs did not turn over all of these records. (Id.) Plaintiffs dispute
that the records were even requested at that time. (Id. ¶ 27.) This dispute is addressed
further in the opinion that follows.
WPS then referred Kaelan’s prior authorization request to Dr. Betty Liu, an outside
board-certified pediatric allergist/immunologist at AllMed Healthcare Management

7

(“AllMed”).

Dr. Liu determined that the hypogammaglobulinemia diagnosis “is not

likely,” and she found that IVIG was “experimental / investigational and unproven” and
not medically necessary.

(WPS 158-59.)

Dr. Liu added that “additional testing is

necessary to confirm the member’s diagnosis as it is not clear if he has a qualified immune
deficiency.” (Id.)
In February 2016, Dr. Michael Ostrov, a WPS physician, next recommended
denying both Torin’s and Kaelan’s prior authorization requests, noting in part that:
Based upon my review of the submitted documentation, there
was
not
evidence
that
the
diagnosis
of
hypogammaglobulinemia was supported. The case was sent for
external review . . . . A pediatric immunologist performed the
review [and] . . . determined that the treatment with IVIG was
not medically necessary because the diagnosis was not
established. The recommendation was to stop the IVIG and
have reevaluation of immunoglobulin levels and antibody
response.
(WPS 146, 352.)
On February 9, 2016, WPS formally denied the twins’ prior authorization requests
via letter. (WPS 116-17, 271-72.) The letters stated that:
The request for the medication Gammagard (IVIG) is being
denied. After review of the documentation submitted it was
found that the diagnosis of hypogammaglobulinemia was not
supported and for this reason the Gammagard (IVIG) is
considered not medically necessary. The recommendation is
to stop the medication and have a reevaluation of
Immunoglobulin levels and antibody response.
(WPS 116, 271.)
In response, on February 17, 2016, the children’s physician, Dr. Bouboulis,
submitted letters explaining his reasons for prescribing IVIG. (WPS 115, 345.) Dr. Ostrov

8

reviewed those letters, but was unpersuaded and his “assessment remain[ed] unchanged.”
(WPS 146, 352.) On February 22, 2016, WPS contacted Bouboulis’s office to inform him
of the denial. (Id.) On February 25, Bouboulis’s office requested a review call with Dr.
Liu concerning both Hignells. That same day, Drs. Bouboulis and Liu had a peer-to-peer
call, after which Liu revised her original determination and concluded that the IVIG
treatment was medically necessary for Kaelan. (WPS 162-65.) “Based on the updated
medical information gained via the peer-to-peer call,” Dr. Liu explained that “the treating
provider has laboratory data that is supportive of an immune deficiency with
hypogammaglobulinemia and decreased antibody function (CVID)”; “[a]dditional testing
is not medically necessary to further confirm or remove support for this diagnosis”; and
“IVIG is medically necessary according to the member’s certificate of coverage.” (WPS
163.) That same day, plaintiff Jill Crista faxed the lab results apparently discussed on the
peer-to-peer call, which WPS apparently forwarded to Dr. Liu. (WPS 145 (“Clinical
advisor[] has been reviewing documentation, additional clinical faxed to outside reviewer
as requested by Dr. Ostrov.”), 351 (same).)
After reviewing those test results, Dr. Liu revised her determinations once again,
explaining “the provider [presumably Dr. Bouboulis] gave conflicting information on the
peer-to-peer call that was not supported by the written documentation.” (WPS 168.) In
particular, Liu ultimately concluded that Kaelan “does not have laboratory data that is
supportive of immune deficiency”; “[h]e should have repeat immune evaluation done 6
months after being off of IVIG”; “IVIG is not medically necessary”; and “[t]he request is

9

experimental / investigational per the certificate of coverage.”5 (WPS 168-69.) On March
2, WPS sent Dr. Bouboulis renewed denials of the prior authorization requests, again based
on a lack of medical necessity. (WPS 57-58, 279-80.)
After receiving the denials, Crista filed an appeal for both her sons on April 6, 2016.
(WPS 27.) In her appeal letter, she stated “[t]he only rationale I can imagine for your
company’s refusal is that we became too expensive for your company to meet the bottom
line.” (WPS 28.) She attached 2016 lab results and office visit notes. WPS acknowledged
her appeal on April 12, 2016. Around this time, Crista also faxed a letter dated April 4,
2016, seeking “the written clinical rationale used to make the decision to deny the
authorization.” (WPS 64.) In response, WPS sent a letter to Dr. Bouboulis, copying in
Crista, explaining the denial.
In April of 2016, another WPS physician, Dr. Kevin Rak, reviewed the medical
records for both Kaelan and Torin, ultimately agreeing that “if this truly were
hypogammaglobulinemia, one would expect the immunoglobulin levels to be much lower,
and in fact, many of the levels are actually normal,” so that “[t]he new lab values and data
do not conflict with the prior determination made by the AllMed specialty review.” (WPS
172, 362.) Rak added that “although the twins’ values of the immunoglobulins tested are
not exact, in both cases there are mild depressions in the levels of a few immunoglobulins,

The parties seem to disagree about which of the February 25, 2016, letters from Dr. Liu came
first. (See Def.’s PFOF (dkt. #38) ¶ 48.) However, the administrative record shows the letters were
faxed at different times, with the letter again concluding that the treatment was not medically
necessary sent later. (Cf. WPS 161 (fax cover sheet dated February 26, 2016); WPS 166 (fax cover
sheet dated March 2, 2016).)
5

10

but no severe deficiencies, and several of the values are within the range of normal.” (WPS
362.)
In late April and early May of 2016, WPS next mailed Crista several letters,
including a notification that the “appeal meeting” was scheduled for June 2, 2016. This
letter explained that “[y]our provider, at your option, may participate” in the meeting.
(WPS 78.) On May 19, 2016, WPS referred the children’s prior authorization requests to
Dr. Joshua Davidson, a board-certified allergist and immunologist with expertise in
pediatric allergy and immunology, also affiliated with AllMed. Dr. Davidson concluded
that “the existence of hypogammaglobulinemia diagnosis at this time cannot be
supported.” (WPS 371, 198.) Davidson also explained that a hypogammaglobulinemia
diagnosis
is dependent upon findings of quantitative and qualitative
deficit. The former is supported by low total IgG levels, as
IVIG largely consists of pooled IgG intended to replace what is
low and/or absent in a given patient. A low level is typically
defined as two standard deviations below the lower normal
limit. In this case, there are numerous total IgG values,
including data obtained prior to IVIG initiation in 2015.
These data show either normal or very mildly depressed values
that never f[e]ll two standard deviations below the lower
normal limit. The latter concern, a qualitative deficit, would
be supported by demonstrated failure to respond to a
vaccination, such as a specific immune stimulus; this is not
present in the documentation provided for review. Thus, with
this failure to demonstrate quantitative and qualitative deficit,
IVIG therapy is not supported at this time.
(WPS 371-72, 198-99.) WPS provided Dr. Davidson’s analyses to Crista before the appeal
meeting.

11

Crista submitted additional letters from Dr. DeMio, one of the twins’ other treating
physicians, who “st[oo]d by the diagnosis of hypogammaglobulinemia” for both boys.
(WPS 6, 238.) DeMio opined that the boys had “low gammaglobulins,” as well as “poor
immune function with repeatedly failed full-course antimicrobial treatment for multiple
infections, and . . . autoimmunity including neuroautoimmunity with resultant brain
dysfunction such as tics and OCD.” (WPS 6, 238.) He likewise opined that IVIG was
medically necessary.
The appeal meeting took place on June 2, 2016, as scheduled, with Dr. Bouboulis
in attendance. On June 7, 2016, WPS sent Crista letters approving the prior authorization
requests for IVIG treatment for both boys from June 7, 2016, until June 7, 2017. Those
letters emphasized that future treatment requests would also require prior authorization.
3. Denial of the 2017 Prior Authorization Requests
On April 26, 2017, obviously still unsatisfied with the state of the medical record
and any definitive diagnosis, WPS sent letters to Dr. Bouboulis asking for updated medical
documentation for the Hignell boys in advance of the expiration of the IVIG prior
authorizations on June 7, 2017. The letters asked for medical records from the past four
years and additional testing, stating that these records were necessary so that “an
appropriate clinical determination can be rendered.” (WPS 785, 1201.) On June 5, 2017,
Dr. DeMio submitted the boys’ February 2017 lab results as well as prior authorization
requests for IVIG therapy along with prescriptions for the therapy. Two days later, PA
Navigator Pharmacy Services explained in a letter on behalf of WPS that “[c]overage of
GAMMAGARD INJ 5GM/50ML requires review of progress notes detailing diagnosis,

12

previous therapeutic history, concurrent medications, and treatment and monitoring plan,”
and further asserting that “[w]e did not receive the above mentioned information.” (WPS
788-89, 1402-03.)
On June 13, 2017, WPS initially denied the prior authorization requests as “not
medically necessary because [Torin and Kaelan] do not meet the criteria as outlined in the
resources used to make coverage determinations.” (WPS 789, 1403.) The denial letter
added that “[c]ontinued coverage of IVIG requires review of progress notes detailing
diagnosis, previous therapeutic history, concurrent medications, and treatment and
monitoring plan,” which were “requested from [their] provider, but not received.” (WPS
789, 1403.) In response, on June 15 and 19, 2017, Dr. DeMio faxed to WPS various 2016
and 2017 lab results for both boys, as well as a letter summarizing the results. In this
letter, DeMio explained that “during the period with no IVIG treatment (12/15/1602/16/17), both children suffered for not having IVIG. Both reported viral infections,
headache, and increased school absences during the four to five-week period past the
treatment due date.” (WPS 840, 1450.) Notably, although WPS had asked on April 26,
2017, for the medical records from the past four years, Dr. DeMio did not include any pre2016 records in his June 2017 faxes.
On June 15, 2017, the prior authorization requests were again referred to outside
health care professionals at Advanced Medical Reviews (“AMR”) completed between June
20 and June 23, 2017. (WPS 1006, 1668.) Specifically, Dr. Wayne Imber, a board
certified allergist/immunologist, concluded that IVIG treatment was medically necessary

13

for Kaelan, while an unidentified neurologist concluded likewise for Torin.6 As to Kaelan,
Dr. Imber concluded that “[t]he diagnosis of primary immune deficiency is clear in this
patient, as is the need for IVIG treatment.” (WPS 1006.) His June 2017 report further
noted: (1) “infusions should not be interrupted to learn about a patient’s tolerance for
frequency of infusion as this will place the patient in harm’s way unnecessarily and also
would be consistent with medical malpractice”; (2) “[f]uture lapses in therapy should be
scrupulously avoided, as they could be a cause of probable morbidity and possible mortality
in this patient”; and (3) “it is not reasonable to anticipate that the IVIG/SCIG dose and/or
frequency may be tapered and ultimately discontinued according to relevant evidencebased medical literature.” (WPS 1007-08.)
As to Torin, the unidentified neurologist concluded that “IVIG would be considered
medically necessary and the treatment of choice for this patient with primary
immunodeficiency.”

(WPS 1668.)

The reviewer explained that “[c]ontinuation of

IVIG/SCIG is considered medically necessary for the diagnosis of hypogammaglobulinemia
as his laboratory values have improved,” Torin “is noted to be clinically unstable without
treatment,” and “IVIG/SCIG should be continued indefinitely for the treatment of
hypogammaglobulinemia without interruption.” (WPS 1669-70.) Further, the reviewer
noted that continued IVIG/SCIG was “essential to prevent permanent bodily harm from
infectious disease, and/or premature death.” (WPS 1669.)
Obviously still unsatisfied, WPS extended its approval of IVIG therapy for both
Torin and Kaelan based on these reports, but only for a one-month period from June 28

6

Plaintiffs refer to both known and unknown reviewers jointly as the “First Reviewer.”

14

through July 28, 2017, adding that their treating physician would need to seek
reauthorization to continue the treatment beyond that period, and “future authorizations
are not necessarily guaranteed and will be based on your physician submitting appropriate
clinical information along with the request.” (WPS 794, 1408.) On July 14, 2017, WPS
also expressly asked for “all medical records from 2012 through the current date” in order
“to make an informed, fair, and accurate determination as to the medical necessity of
IVIG.” (WPS 840.) Plaintiffs contend that this was the first time that WPS claimed pre2015 records were necessary to review authorization requests. Defendant disputes this,
maintaining that it had previously requested pre-2015 medical history records. (See Def.’s
Resp. to Pls.’ PFOF (dkt. #27) ¶ 66.) Again, this dispute is addressed further in the opinion
that follows.
Regardless, on July 19, 2017, Dr. DeMio responded with several additional faxes
containing the Hignells’ medical records, although the parties also dispute whether these
documents had been previously produced to WPS. (Def.’s Reply to Pls.’ Resp. to Def.’s
PFOF (dkt. #38) ¶ 85.) Those records indicate that a diagnosis of pediatric autoimmune
neuropsychiatric disorders associated with streptococcal infections (“PANDAS”) had been
originally discussed as a possible cause of Torin’s symptoms as early as 2012; and in 2013,
PANDAS specialist, Dr. Kovacevic, diagnosed Torin with PANDAS and recommended
IVIG therapy. (WPS 1578.) As a result, Torin apparently received IVIG therapy on July
5-6, 2013, and January 23-24, 2014. Then, on June 25, 2014, Torin began treatment with
Dr. Bouboulis, who recommended continuing IVIG treatment.

Torin received IVIG

treatment again in February 2015, with his PANDAS symptoms “improve[d] but not

15

gone,” and “[a]fter 5 weeks, all PANDAS [symptoms] return.” (WPS 1578-79.) Again,
following IVIG treatment on April 23-24, 2015, all Torin’s “PANDAS s[ymptoms]
disappear[ed] but return[ed] slowly at wk 6.” (WPS 1579.) In another record from UW
Health from 2011, Dr. James Conway of the Pediatrics Infectious Disease Department
noted, “Please let mother know that all infectious serologies negative . . . . Also GI serology
for infectious cause of [abdominal] pain negative.” (WPS 1627.)
As to Kaelan, the records included treatment notes from Dr. DeMio, who wrote that
he was “getting worse of[f] IVIG . . . ‘extremely fatigued,’ apathetic/mood & lose interest
w school . . . tics . . .” (WPS 966.) Another note from Dr. DeMio stated, “tics ~gone . . .
IVIG had been (now) resumed. . . . he remains w/more fatigue, malaise.” (WPS 974.)
On July 27, 2017, WPS responded by approving another month of IVIG for both
Hignells to avoid disruption while it continued its review of the prior authorization
requests. (WPS 797, 1411.) On August 4, Dr. DeMio faxed a letter similar to the letters
he sent in June summarizing Kaelan and Torin’s lab results from February 2017 and March
2016.
After receiving these July 19, 2017, records from Dr. DeMio, WPS also sought yet
another review from an outside health care professional. This time, WPS referred the prior
authorizations requests to Dr. Maureen Peterson, Board Certified in Allergy and
Immunology and in Pediatrics at the Medical Review Institute of America, Inc.
(“MRIOA”).7 While plaintiffs contend that the Plan did not authorize WPS to seek a
second opinion, defendant responds that it had the discretion to do so. (See Def.’s Resp.

7

Plaintiffs refer to Dr. Peterson as the “Second Reviewer.”

16

to Pls.’ PFOF (dkt. #27) ¶ 72.) Dr. Peterson attempted to reach Dr. DeMio before
rendering her opinion, as her report indicates that she called his office six times to schedule
a conversation, but she was apparently unsuccessful. Nevertheless, upon reviewing the
medical records of Torin Hignell, Dr. Petersen issued her report on August 17, 2017,
opining that: (1) the medical record “does not support the stated diagnosis, of either
hypogammaglobulinemia or of common variable immune deficiency, or of immunoglobulin
G (IgG) subclass deficiency” as to Torin; (2) no further testing would clarify his diagnosis
given his previous “extensive laboratory evaluation”; (3) Torin “more likely” had
“preservation of IgG antibody production,” making him “less likely to benefit from Ig
therapy”; (4) the “patient has no clinical symptoms of an immunodeficiency”; (5) IVIG
was “experimental/investigative/unproven” for Torin, who was “being treated for
[PANDAS], not hypogammaglobulinemia” as “[a]utomimmune features is not an
indication for supplemental IVIG”; (6) “[t]he evidence supporting the use of IVIG in the
treatment of PANDAS is as strong as the evidence refuting [it]”; (7) “no objective criteria
. . . demonstrated a clinically significant beneficial response during prior IVIG/SCIG
therapy”; (8) continuation of IVIG was not medically necessary; (9) Torin had received
“three times the usual replacement dose of immunoglobulins for treatment of
immunodeficiency,” so that “the total IgG count would take months before [the patient
would be] at significant risk for infections”; and (10) “[t]he patient should immediately
stop IVIG.” (WPS 1673-76.) Dr. Petersen came to the same basic conclusions regarding
Kaelan for the same reasons. (WPS 1012-17.)

17

After summarizing their files and the contradictory opinions therein, WPS’s internal
reviewer, Dr. Kevin Rak, also concluded that the prior authorization requests for both
Hignells should be denied on August 18, 2017. (WPS 998-1001, 1660-63.) Rak noted
that “if a serious underlying immune deficiency was truly present, than a greater need for
medical services or antiinfectious agents (other than those routinely taken) would have
arisen during the [gaps in IVIG treatment], but this is not borne out from the medical
records.” (WPS 1000-01, 1662-63.) As to Kaelan Hignell, Dr. Rak noted that the records
indicated

“IVIG

may

be

prescribed

for

alternative

diagnoses

other

than

hypogammaglobulinemia,” as notes about how Kaelan felt off the IVIG -- instead of
infectious diseases -- and how his tics responded to the IVIG “raise concerns that immune
deficiency is not the primary focus of IVIG therapy” in light of alternate diagnoses of OCD
and tics. (WPS 998.) Rak reached a similar conclusion about Torin Hignell’s condition.8
(WPS 1660-62.)
Armed once more with supportive opinions supporting a denial of benefits by both
an outside and internal physician, WPS again denied the prior authorization requests for
IVIG on August 18, 2017, explaining that “the provided documentation does not support
the stated diagnosis” and IVIG “[wa]s considered experimental/investigative/unproven for
the treatment of the member’s signs and symptoms.” (WPS 801, 1415.) Plaintiffs and

One difference between the twins was that Dr. Rak noted Torin did not see a doctor during the
gap in IVIG treatment, as opposed to Kaelan’s one medical visit. However, as plaintiffs point out,
that distinction is mistaken as Torin did in fact see a doctor during an IVIG hiatus. (See WPS 25152.)
8

18

the boys’ treating physicians disagree with this conclusion, and Crista appealed the denial
on September 7, 2017.
Five days later, WPS acknowledged receipt of her request for an appeal and
scheduled a review for late September. On September 15, WPS provided the clinical
rationale for its denial, explaining its concern that immune deficiency was not the primary
focus of the IVIG therapy. In particular, WPS noted that additional medical records had
been submitted on July 19, 2017 -- after the June 2017 external reviews by Dr. Imber and
the unidentified neurologist had been completed -- and that this prompted a subsequent
review “with the inclusion of these additional medical records.” (WPS 511-12, 1105-06.)
Moreover, WPS wrote that “it would be anticipated that if a serious underlying immune
deficiency was truly present, then there would have been a greater need for medical services
or anti-infectious agents (other than those routinely taken) during these gaps of IVIG
treatment, but this is not borne out from the medical records.” (WPS 512, 1106).
On September 18, 2017, WPS sent letters and provided appeals packet information
to be reviewed by the grievance and appeals committee. Dr. Michael Halwig of MRIOA,
specializing in allergy pediatrics, also was retained to review and issue opinions on the prior
authorization requests based on the medical records and a peer-to-peer call with the boys’
treating physician, Dr. DeMio. Although Dr. Halwig never treated either boy and only
spoke to Dr. DeMio for four minutes, he issued opinions as to both boys on September
22,

2017,

concluding

that:

(1)

while

the

documentation

supported

the

hypogammaglobulinemia diagnosis, there was no clinical evidence of a primary
immunodeficiency requiring IVIG; (2) IVIG was experimental/investigative/unproven for

19

treatment of this IgG subclass deficiency because it was not the current immunology
practice; (3) no alternative treatments should have been employed because there was no
evidence of recurrent bacterial infections; (4) the prescribed dose of IVIG would not be the
standard of care for a 17 year old with this diagnosis as the initial recommended dose
would be 400 mg/kg, adjusted by IgG levels; (5) a vaccine challenge would not assist in
diagnosing; and (6) IVIG was not medically necessary. In addition, for Torin, Dr. Halwig
added that “[t]he laboratory findings are consistent with an IgG subclass deficiency with a
possible IgA deficiency,” and “IVIG replacement would be considered if there was an
impaired response to antigenic stimulus and recurrent bacterial infections unresponsive to
aggressive medical management and the failure of prophylactic antibiotics to prevent
recurrent infections.” (WPS 1221.)
The grievance and appeal committee upheld WPS’s denials in letters dated
September 29, 2017, for each boy.

The letters explained that the committee had

considered “all of the available information,” including the full medical records, and cited
to treatment records from Dr. Bouboulis and Dr. DeMio. (WPS 422, 1065.) Ultimately,
WPS’s committee offered two related reasons for the denial of plaintiffs’ appeal. First, it
determined that IVIG “is considered experimental/investigative/unproven for treatment”
because “its use does not meet current immunology practice standards.” (WPS 423, 1066.)
The committee noted that “the provided documentation does support the laboratory
finding of IgG subclass hypogammaglobulinemia, but there is no evidence of a clinically
significant primary immunodeficiency.” (WPS 423, 1066.) According to WPS, “current
immunology practice standards require that the clinical history, physical exam, and

20

laboratory findings be consistent with a diagnosis of primary immunodeficiency,” while the
“[r]ecords that were provided did not demonstrate a clinical picture consistent with a
diagnosis of primary immunodeficiency.” (WPS 423-24, 1067.) As to Torin, the WPS
committee further wrote “it appears that IVIG is being prescribed for the alternative
diagnosis of PANDAS” and that “Dr. DeMio’s clinical records from the past year seem to
focus more on IVIG’s impact on symptoms of tics, obsessive compulsive disorder (OCD),
mood swings, irritability, anxiety, and fatigue,” rather than broader immunodeficiency
concerns. (WPS 1067.) Similarly, as to Kaelan, the committee noted that it appeared
from treatment notes that IVIG “is being prescribed primarily for other symptoms . . .
versus for the purpose of a primary immunodeficiency,” such as tics. (WPS 424.) Finally,
the committee explained that the use of IVIG to treat tics or PANDAS symptoms is not
currently recognized as accepted medical practice and, therefore, is considered
experimental/investigative/unproven. (WPS 424, 1067.) Plaintiffs do not dispute that
IVIG

treatment

for

PANDAS

symptoms

or

tics

would

be

experimental/investigative/unproven.
The second reason offered by the WPS appeal committee for its denial was that
“IVIG is not considered medically necessary because the diagnosis of primary
immunodeficiency is not established.” (WPS 424, 1067.) The committee again noted
that “the diagnosis requires . . . the patient’s documented history within his medical records
be consistent with a clinically significant immunodeficiency.” (WPS 425, 1068.) The
committee observed that “the medical records provided did not substantiate any recurrent
bacterial infections” or “indicate any assessment of or treatment for bacterial infections.”

21

(WPS 425, 1068.)

Instead, “the provided medical documentation only referenced

symptoms of headache, sore throat, muscle aches, fatigue, tics, obsessive compulsive
disorder (OCD), and anxiety,” but “[t]he presence of these symptoms do not warrant IVIG
treatment because they are not bacterial in nature.” (WPS 425, 1068.)
Disagreeing with the conclusions that IVIG was no covered by the Plan, plaintiffs
filed this lawsuit to challenge WPS’s final denial of their claims.

OPINION
Specifically, plaintiffs claim that WPS wrongfully denied them benefits owed under
the Plan and breached its fiduciary duties, all in violation of ERISA. To remedy these
claimed violations, plaintiffs seek: (1) reinstatement of benefits; (2) an injunction
providing that both boys’ treatment be continued without interruption; (3) removal of
WPS as a fiduciary making decisions on whether IVIG treatment is medically necessary;
and (4) a surcharge to prevent WPS’s unjust enrichment. Defendant does not dispute the
applicability of ERISA, contending instead that its actions were in line with the Act’s
requirements. Both parties have moved for summary judgment.
Summary judgment is appropriate if the moving party “shows that there is no
genuine dispute as to any material fact and the movant is entitled to judgment as a matter
of law.” Fed. R. Civ. P. 56(a). Generally, the court must view all facts and draw all
inferences in the light most favorable to the non-moving party. Anderson v. Liberty Lobby,
Inc., 477 U.S. 242, 255 (1986). Where, as here, a court is faced with cross-motions for
summary judgment, it must take care to apply the proper standard to each motion. See
Hotel 71 Mezz Lender LLC v. Nat'l Ret. Fund, 778 F.3d 593, 603 (7th Cir. 2015). Here, the

22

court will begin with defendant’s motion, construing the evidence in the light most
favorable to plaintiffs. Even under this unfavorable standard, however, defendant prevails.
Necessarily, this means the court must also deny plaintiffs’ motion. Id. (“Only if the court
can say, on that sympathetic reading of the record, that no finder of fact could reasonably
rule in the unsuccessful movant's favor may the court properly enter summary judgment
against that movant.”).

I. Standard of Review
Before turning to plaintiffs’ substantive claims under ERISA, the court must first
address the deferential standard of review it must apply in reviewing the decision-making
by an administrator of an ERISA plan. Where an ERISA plan grants the plan administrator
discretionary authority to determine eligibility for benefits, the court must review the
decision under an “arbitrary and capricious” standard. Holmstrom v. Metro. Life Ins. Co.,
615 F.3d 758, 766 (7th Cir. 2010) (citing Firestone Tire & Rubber Co. v. Bruch, 489 U.S.
101, 115 (1989); Metropolitan Life Ins. Co. v. Glenn, 554 U.S. 105, 111 (2008); Jenkins v.
Price Waterhouse Long Term Disability Plan, 564 F.3d 856, 860-61 (7th Cir. 2009)). 9 Under
this standard, the court “is not to decide whether it would reach the same decision as the
administrator”; rather, the administrator’s decision will be upheld as long as specific
reasons for the denial are communicated to the claimant and supported by record
evidence.” Raybourne v. Cigna Life Ins. Co. of New York, 576 F.3d 444, 449 (7th Cir. 2009)

This standard is also used interchangeably by the parties and the court as an “abuse of discretion”
standard. See Raybourne, 576 F.3d at 449 (the “arbitrary-and-capricious standard . . . is synonymous
with abuse of discretion” in ERISA cases).
9

23

(citing Davis v. Unum Life Ins. Co. of Am., 444 F.3d 569, 576 (7th Cir. 2006); Leger v. Tribune
Co. Long Term Disability Ben. Plan, 557 F.3d 823, 831 (7th Cir. 2009)). Even so, “[r]eview
under this deferential standard is not a rubber stamp,” and a court will not uphold a plan
administrator’s decision “when there is an absence of reasoning in the record to support
it.” Holmstrom, 615 F.3d at 766 (quoting Hackett v. Xerox Corp. Long-Term Disability Income
Plan, 315 F.3d 771, 774-75 (7th Cir. 2003)).
Moreover, “[a]n administrator's conflict of interest is a key consideration under this
deferential standard.” Id. Such a conflict exists where an administrator “both determines
whether an employee is eligible for benefits and pays benefits out of its own pocket.” Glenn,
554 U.S. at 108 (emphasis added). In such a case, “a reviewing court should consider that
conflict as a factor in determining whether the plan administrator has abused its discretion
in denying benefits.” Id.; see also Jenkins, 564 F.3d at 861-62 (“When the case is borderline
. . . the inherent conflict of interest . . . can push it over the edge -- towards a finding of
capriciousness.”).
Here, the parties agree that the Plan granted WPS discretionary authority to
determine benefits allocations, meaning an arbitrary and capricious standard applies. (See
Pls.’ Br. (dkt. #17) 14; Def.’s Br. (dkt. #22) 14; WPS 1974.) What’s more, both parties
acknowledge that WPS had a conflict of interest insofar as it bore the responsibility to
determine the Hignells’ eligibility for the requested benefits fairly and the obligation to pay
for any approved benefits. (See Def.’s Resp. to Pls.’ PFOF (dkt. #27) ¶ 96.) Accordingly,
the court will review WPS’s decision to deny plaintiffs’ prior authorization requests under

24

the arbitrary and capricious standard, while considering its obvious conflict of interest as a
factor.

II. Wrongful Denial of Benefits
ERISA § 502(a)(1)(B) authorizes a participant or beneficiary to bring a civil action
“to recover benefits due to him under the terms of his plan, to enforce his rights under the
terms of the plan, or to clarify his rights to future benefits under the terms of the plan.”
ERISA § 502(a)(1)(B) (codified at 29 U.S.C. § 1102(a)(1)(B)). According to plaintiffs,
WPS’s determination that IVIG treatment for the Hignell twins fell outside a covered
benefit under the Plan was arbitrary and capricious. Generally, WPS contends that it
“completed a thorough, carefully documented, and fully articulated decision that was in
no way influenced by the cost of IVIG treatment.” (Def.’s Opp’n (dkt. #26) 5-11.)
According to WPS, its decision rested on its findings that the IVIG treatment was
“experimental/investigative/unproven” and not medically necessary because it was
prescribed

primarily

to

treat

PANDAS

or

other

symptoms,

not

to

treat

hypogammaglobulinemia as was its intended use.
As noted above, while hypogammaglobulinemia is an FDA-approved indication for
IVIG treatment, there is no dispute that IVIG treatment for PANDAS symptoms or tics
would be experimental/investigative/unproven, and as such, not covered under the Plan.
Plaintiffs, however, contend that: (1) a diagnosis of hypogammaglobulinemia had been
established; (2) IVIG was medically necessary and not experimental/investigative/unproven
for this diagnosis; and (3) PANDAS is nothing more than “a red herring.” (Pls.’ Br. (dkt.
#17) 20.)

25

At the outset, the court acknowledges that the medical record in this case is a mixed
bag. Certainly, there is evidence that supports plaintiffs’ position, including the opinions
of the boys’ two treating physicians, as well as those of Dr. Imber, an internist with
specialties in allergy and immunology, and the unidentified neurologist, both of whom
were outside experts with AMR retained by WPS.

However, there is also evidence

supporting WPS’s decision, including the opinions from Drs. Liu, Ostrov, Rak, and
Davidson in 2016, and Drs. Peterson, Rak, and Halwig in 2017, with Drs. Liu and Davison
outside specialists in outside specialists in immunology pediatrics at AllMed and Drs.
Peterson and Halwig outside specialists in immunology pediatrics at MRIOA. Moreover,
Drs. Peterson, Rak, and Halwig were the only medical reviewers who had the benefit of the
boys’ full, pre-2015 medical records, something Dr. Imber and the neurologist did not have
available in forming their opinions. In the discussion that follows, this court considers
plaintiffs’ various arguments regarding the alleged capriciousness of WPS’s denial. As
discussed below, the court is troubled by some of WPS’s actions during its multi-year
review process, but concludes that even factoring in WPS’s profit motive under the
deferential standard of review, WPS’s decision must be upheld because of the ultimate
review of all available medical records by MRIOA’s two, outside specialists, and particularly
the detailed findings in Dr. Peterson’s reports.

A. Pre-2015 Medical Records
To begin, the parties’ dispute regarding the boys’ earliest medical records must be
addressed as it affects the court’s consideration of the rest of the evidence. As indicated in
the summary of facts above, the parties dispute when WPS requested what records, as well

26

as the timing of the actual production of those records. Specifically, WPS asserts that as
early as January 14, 2016, it requested all office notes and laboratory reports from January
1, 2013, to December 31, 2014.

To support this assertion, WPS points to records

summarizing two phone calls from its consultant. The first note refers to a call with “Jill
(mbr. mom),” during which the consultant “let her know that MD office was contacted for
request for documentation.” (WPS 147, 352.) The second note concerns a call to Superior
Associates, which appears to be the boys’ doctors’ office, during which the WPS consultant
left a voicemail requesting “all documentation for 2 years be sent including all office notes
and laboratory reports for the past 2 years ending Jan 2015&to include pretreatment
assessment.”

(WPS 147, 352.)

In turn, plaintiffs object that these records do “not

establish or substantiate any requests actually communicated to either Plaintiff Crista or
Dr. Bouboulis,” and they further aver that the “lack of any physical or paper
communication to either Plaintiffs or their treatment physicians is noteworthy and calls
the veracity of these notes into question.” (Pls.’ Resp. to Def.’s PFOF (dkt. #38) ¶ 27.)
While plaintiffs’ purported dispute regarding this request for older records is rather
weak, viewing the evidence in the light most favorable to them, the court will assume for
purposes of summary judgment that WPS did not request the boys’ pre-2015 medical
records in 2016. However, there is no dispute that WPS requested these records in 2017,
including: (1) on April 26, 2017, when WPS sent letters to Dr. Bouboulis asking in part
for medical records from the past four years, and explaining that the records were necessary
to render an appropriate clinical determination; (2) on June 7, 2017, when PA Navigator
Pharmacy Services requested (among other things) on behalf of WPS, the boys’ previous

27

therapeutic history; and (3) on July 14, 2017, when WPS asked for all medical records
beginning in 2012, explaining that the records were required to make a determination as
to the medical necessity of IVIG.
There is also no reasonable dispute that on July 19, 2017, Dr. DeMio sent several
faxes to WPS containing a number of previously unproduced medical records for the
Hignell twins. While plaintiffs purport to dispute this fact -- pointing out that some of the
records produced by Dr. DeMio had been previously provided -- WPS maintains that
many, other records were newly produced. In particular, WPS notes that the records
produced in July of 2017 included: (1) records indicating a possible diagnosis of PANDAS
for both boys and related symptoms, including OCD and tics; (2) a note from PANDAS
specialist Dr. Kovacevic diagnosing Torin with PANDAS and recommending IVIG therapy;
and (3) notes indicating that after Torin received IVIG treatment his PANDAS symptoms
improved but were not gone, and those symptoms returned after 5-6 weeks. Since plaintiffs
fail to identify any portion of the administrative record suggesting that these records in
particular were provided earlier, the court will accept WPS’s evidence as establishing that
records related to the boys’ PANDAS symptoms were produced for the first time in July of
2017.
In fairness, plaintiffs also dispute the relevance of these older records, suggesting
that WPS’s request for and consideration of these records was unreasonable. Specifically,
plaintiffs argue that “[n]othing in [Dr. Imber’s or the neurologist’s] independent review
indicated that more documentation was necessary or that [their] report suggested it was
anything other than ‘final.’” (Pls.’ Br. (dkt. #17) 21.) Instead, plaintiffs characterize

28

WPS’s request for the historical medical records as a search for “any justification to deny
the claim.” (Pls.’ Br. (dkt. #17) 17-18.) On the other hand, defendants contend that these
records were “quite material,” since “they showed that the IVIG therapy was being used to
treat PANDAS, not hypogammaglobulinemia, as was stated in the prior authorization
requests for IVIG.” (Def.’s Opp’n (dkt. #26) 5.) Additionally, it must be noted that
WPS’s request for historical records was made prior to Dr. Imber and the neurologist’s
review -- there is no dispute that in April of 2017, WPS requested the past four years of
the boys’ medical records.
Certainly, a claimant’s medical history has been found to be relevant in considering
denials of ERISA benefits. See Holmstrom, 615 F.3d at 773 (“Holmstrom's overall objective
medical history is also highly relevant.”); Diaz v. Prudential Ins. Co. of Am., 499 F.3d 640,
646 (7th Cir. 2007) (finding claimant’s history of treatment relevant to his claim for
benefits). Moreover, the undisputed evidence suggests that contemporaneous immunology
practice standards required a patient’s clinical history, as well as his laboratory findings, to
be consistent with a diagnosis of primary immunodeficiency to support IVIG treatment.
Thus, given the specific facts of this case, the boys’ historical medical records were plainly
relevant to WPS’s determination, whatever its underlying motives may have been.
That said, the court, like plaintiffs, is somewhat suspicious of the fact that WPS
apparently felt it had sufficient information in 2015 and 2016 to render a decision, but in
2017 determined that additional historical information was required. Moreover, neither
Dr. Imber nor the neurologist suggested in their opinions that any additional records would
be required to arrive at an appropriate diagnosis. Still, the Seventh Circuit has cautioned

29

that a plan administrator is “entitled to seek and consider new information and, in
appropriate cases, to change its mind.” Geiger v. Aetna Life Ins. Co., 845 F.3d 357, 363-64
(7th Cir. 2017) (quoting Holmstrom, 615 F.3d at 767). And WPS, perhaps fairly, insists
that its leniency towards plaintiffs in 2015 and 2016 should not be held against it. Thus,
while the court looks at WPS’s middle-of-the-game request with a skeptical eye, that WPS
asked for older medical records (or considered them once they were produced) does not,
standing alone, render WPS’s decision unreasonable, particularly given the conflicting
views of medical experts from the very beginning of plaintiffs’ prior authorization requests
in 2016.

B. Competing Opinions and Cherry-Picking Evidence
The Seventh Circuit has said that one “hallmark of an arbitrary and capricious
decision” is the rejection of evidence “based on selective readings that are not reasonably
consistent with the entire picture.” Holmstrom, 615 F.3d at 777. In other words, a plan
administrator cannot cherry-pick evidence that supports its decision while ignoring
contrary evidence. See Leger, 557 F.3d at 832-33. Still, where there is a “contest of
competing medical opinions,” a court cannot second-guess the plan administrator’s choice
between opinions so long as that choice is rationally supported by record evidence. See
Black v. Long Term Disability Ins., 582 F.3d 738, 745-46 (7th Cir. 2009) (in “a contest of
competing medical opinions, . . . under our deferential standard of review, we must defer
to [the plan administrator’s] choice between competing medical opinions so long as it is
rationally supported by record evidence”); Davis, 444 F.3d at 578 (“[R]eaching a decision
amid . . . conflicting medical evidence is a question of judgment that should be left to [the

30

plan administrator] under the arbitrary-and-capricious standard.”); Semien v. Life Ins. Co. of
N. Am., 436 F.3d 805, 812 (7th Cir. 2006) (while plaintiff’s treating physicians reached
different conclusions as to her abilities than the physicians hired by plan administrator,
“under an arbitrary and capricious review, neither this Court, nor the district court, will
attempt to make a determination between competing expert opinions”).
Plaintiffs argue that WPS “impermissibly ignored the conclusions of the [twins’]
treating physicians and of the two independent reviewers from AMR that treatment was
medically necessary” -- “cherry-picking” which reviewers’ conclusions to adopt, while
ignoring the rest. (Pls.’ Br. (dkt. #17) 18, 23.) As plaintiffs point out, the Hignells’
treating physicians -- Drs. Bouboulis and DeMio -- both consistently stood by their
conclusions that the boys suffered from hypogammaglobulinemia and that IVIG treatment
was medically necessary. In 2017, WPS’s designated reviewer, Dr. Imber, himself an
internist with relevant specialization in allergy and immunology with AMR, also found
that Kaelan’s diagnosis of a primary immune deficiency was “clear” (WPS 1006), and its
other MRIOA reviewer, an unidentified neurologist, arrived at a similar finding for Torin
(WPS 1668). As a result, both Dr. Imber and the neurologist concluded that continuation
of IVIG treatment was medically necessary as well.
At the same time, other physicians had come to contrary conclusions both before
and after the MRIOA reviewers. Specifically, in 2016, Dr. Liu -- also an outside reviewer
hired by WPS -- determined as to Kaelan that a hypogammaglobulinemia diagnosis was
“not likely” and found that IVIG was “experimental / investigational and unproven.”
While Dr. Liu revised her opinion after a phone call with Dr. Bouboulis, she changed her

31

opinion back after receiving the actual historic lab results for both boys, explaining in her
final opinion that: (1) information provided by Dr. Bouboulis was not supported by the
written documentation; (2) Kaelan’s laboratory data did not support a diagnosis of
immune deficiency; and (3) IVIG was experimental/investigational and not medically
necessary. Also in 2016, WPS physicians, Drs. Ostrov and Rak, concluded that a diagnosis
of hypogammaglobulinemia was not supported -- in part because the lab values were not
entirely consistent with such a diagnosis -- and both recommended denying the IVIG
requests. Another outside reviewer, Dr. Davidson, likewise concluded in 2016 that: (1)
hypogammaglobulinemia diagnoses were not supported, finding neither quantitative nor
qualitative deficits in the boys’ lab values; and (2) IVIG therapy was “not supported at this
time.” (WPS 371-72.)
Additionally, in 2017, Dr. Peterson, a specialist in immunology pediatrics at
MRIOA, opined that the medical record did not support hypogammaglobulinemia
diagnoses or other common, variable immune deficiencies, making IVIG treatment both
experimental/investigative/unproven and not medically necessary. After WPS physician
Dr. Rak affirmed Dr. Peterson’s conclusions, a final opinion was rendered by another
MRIOA allergy pediatric specialist, external reviewer Dr. Halwig, acknowledged that the
documentation supported a laboratory finding of hypogammaglobulinemia, but that there
was no clinical evidence of a primary immunodeficiency, and thus that IVIG was
experimental/investigative/unproven and not medically necessary. (WPS 422-25, 106568.)

32

Thus, the record contains mixed opinions from a variety of qualified physicians from
the beginning of WPS’s review of plaintiffs’ authorization requests. Ideally, WPS should
have at least sought further input from Dr. Imber and the neurologist as to whether the
newly-produced information from Dr. DeMio in July of 2017 would have changed their
opinions, instead of immediately seeking another outside expert’s opinion. Moreover,
WPS’s own monetary incentive to deny treatment makes its actions smell of “opinion
shopping.” Nevertheless, the court cannot ignore the fact that WPS sought out two
eminently qualified experts in the relevant field of allergy pediatrics to take a fresh look at
all the medical records, nor that both doctors, after having the opportunity to examine the
full medical record concluded that IVIG was not medically necessary. Further, arguably the
most appropriate remedy to resolve such a muddied record as the one before WPS would
be to submit the evidence to a qualified, neutral decisionmaker. Were there a basis to
question the integrity of Dr. Peterson or her report, the court’s deference would be
substantially less, but there is not on this record. Far from it, Dr. Peterson appears
eminently qualified to undertake this review, and her reports are the most thorough and
persuasive of those presented to the court.

Plus, even after its initial denial, WPS

submitted the question to Dr. Halwig for a final review and determination. Although,
again, WPS’s flip-flopping and motives raise significant questions, and another course of
action could have been taken, WPS’s ultimate decision to give greater weight to the outside
medical experts from MRIOA who concluded that IVIG was not medically necessary does
not support a finding of capriciousness.

33

C. Treating Physicians
Relatedly, plaintiffs fault WPS for not giving greater credit to the opinions from
Drs. Bouboulis and DeMio, the boys two treating physicians. While plan administrators
generally “may not arbitrarily refuse to credit a claimant's reliable evidence, including the
opinions of a treating physician,” the Supreme Court has held that ERISA does not require
plan administrators to give special consideration to the opinions of treating physicians.
Black & Decker Disability Plan, 538 U.S. at 834; see also Love v. Nat'l City Corp. Welfare
Benefits Plan, 574 F.3d 392, 397-98 (7th Cir. 2009) (“While plan administrators do not
owe any special deference to the opinions of treating physicians, they may not simply
ignore their medical conclusions or dismiss those conclusions without explanation.”)
(internal citation omitted).10
Here, WPS generally explained that it considered “all of the available information,”
including references to a number of treatment notes from the two treating physicians in
the final denial letter. Additionally, both WPS and its external doctors made efforts to
include both treating physicians in the determination. For example, WPS explained that
the boys’ medical provider could participate at the appeals meetings in 2016 and 2017,
although Dr. Bouboulis only attended the 2016 meeting and Dr. DeMio did not attend

Plaintiffs also emphasize that Drs. Bouboulis and DeMio were the only ones who personally
examined the boys, pointing to cases where courts have criticized plan administrators for rejecting
conclusions reached by every doctor that personally examined the claimant and accepting only
opinions based on paper records. See Love, 574 F.3d at 397; Holmstrom, 615 F.3d at 775; Clark v.
Cuna Mut. Long Term Disability Plan, 2016 WL 1060344, *28 (W.D. Wis. Mar. 15, 2016). In the
cases cited by plaintiffs with respect to the need for a personal exam, however, the issue was the
claimant’s functional ability to engage in full-time work -- a determination that could be better
understood or ascertained via physical examination. See Love, 574 F.3d at 397; Holmstrom, 615 F.3d
at 775; Clark, 2016 WL 1060344, *28. Here, by contrast, plaintiffs do not explain how such an
examination would provide unique insight into the boys’ condition.
10

34

either meeting. Additionally, among other things, Dr. Halwig called Dr. DeMio’s office
and spoke with him (albeit only for four minutes) before rendering his ultimate review,
and Dr. Peterson called Dr. DeMio’s office six times, although was not able to successfully
connect with him. (WPS 1011.)
Still, plaintiffs’ general argument has some force as WPS does not appear -- at least
expressly -- to have given significant consideration to the opinions of Drs. Bouboulis and
DeMio in its final denials. Arguably, WPS did not need to address specifically these
opinions as it presented a full explanation as to why it concluded they were not adequately
supported by the medical record, but the court considers WPS’s lack of express
consideration of the boys’ treating physicians’ opinions in its denials as a factor cutting
against granting its motion for summary judgment. That said, the court also observes that
there are internal inconsistencies within Drs. Bouboulis’s and DeMio’s own records.
Although in 2016

and 2017,

both physicians

stood by

their

diagnoses of

hypogammaglobulinemia, their own records from 2015 suggest that IVIG treatment was
being used to treat PANDAS or OCD symptoms, including tics. This inconsistency came
up again in 2016, when Dr. Liu noted that Dr. Bouboulis had given her “conflicting
information on the peer-to-peer call that was not supported by the written
documentation.” (WPS 168.)

D. Physician Specializations
Plaintiffs also argue that WPS’s consideration of the opinions of Dr. Rak was an
abuse of discretion as the Wisconsin licensing website shows that he specialized in
radiology, and was not an immunologist, allergist, or other specialist in a field familiar with

35

autoimmune diagnoses. (See Pls.’ Reply (dkt. #30) 4. n.4.) Certainly, a reviewer’s medical
specialty may be relevant to a plan administrator’s determination of benefits, but there are
a number of problems with plaintiffs’ position. First, to establish Dr. Rak’s specialty,
plaintiffs are inappropriately introducing evidence outside of the administrative record. See
Krolnik v. Prudential Ins. Co. of Am., 570 F.3d 841, 843 (7th Cir. 2009) (“When review is
deferential -- when the plan's decision must be sustained unless arbitrary and capricious -then review is limited to the administrative record.”) (emphasis omitted). Second, as
defendant points out, if external evidence may be submitted to prove specialties, and if
only physicians with a specialty in autoimmune disorders are qualified to offer an opinion,
then one of plaintiffs’ treating physicians, Dr. DeMio, would not be qualified, as he has an
emergency medicine specialty. (See Def.’s Reply to Pls.’ Resp. to Def.’s PFOF (dkt. #38)
¶ 99.) Finally, Drs. Liu, Davidson, Peterson, and Halwig were all board certified in allergy
and immunology, with further special expertise in pediatrics, and all rendered opinions
consistent with that of Dr. Rak. Overall, it would seem that plaintiffs’ argument regarding
specializations hurts rather than helps them, certainly does not support a finding that
WPS’s decision was arbitrary and capricious.

E. Previous Grant of Benefits
Plaintiffs also criticize WPS for its “course-reversal,” having granted plaintiffs’ prior
authorization requests in 2015 and 2016 and for a month in 2017, but ultimately denying
them in August of 2017. Under Seventh Circuit case law, the previous payment of benefits
has been held to be a circumstance or factor to be considered in the court’s review process,
but it does not create a presumptive burden for the plan to overcome. Leger, 557 F.3d at

36

832. Rather, a “plan administrator is entitled to seek and consider new information and,
in appropriate cases, to change its mind.” Holmstrom, 615 at 767.
In this case, WPS had conflicting medical evidence and questions from at least
2016. Plus, additional historical medical records from plaintiffs’ doctor in July of 2017
provided a legitimate basis for WPS to request further outside reviews by Drs. Peterson
and Halwig, both board certified in allergy pediatrics, and both of whom concluded that
IVIG treatment was experimental/investigative/unproven and not medically necessary
given the boys most likely diagnosis. It should also be noted that the 2017 reversal was
not out of the blue, since Drs. Liu, Ostrov, Rak, and Davidson had previously come to
similar conclusions in 2016, and WPS had initially denied prior authorization requests,
only approving them on appeal. Accordingly, WPS’s previous grant of benefits cuts neither
for nor against either party.

F. Moving Target
The Seventh Circuit has held that “[a]n ERISA benefit cannot be a moving target
where the plan administrator continues to add conditions precedent to the award of
benefits.” Dabertin v. HCR Manor Care, Inc., 373 F.3d 822, 831 (7th Cir. 2004). In
Dabertin, a plan administrator’s denial of benefits was found to be unlawful because, inter
alia, the administrator imposed three additional qualifications that did not exist in the
plain language of the plan.

Id. at 831.

Similarly, in Holmstrom, MetLife (a plan

administrator) was held to have acted arbitrarily and capriciously in part because it:
invited additional evidence to establish disability, but when
Holmstrom provided it, MetLife repeatedly found that the new

37

evidence was not sufficient under new standards or
expectations that had not been communicated to Holmstrom.
Holmstrom, 615 F.3d at 775-76.
According to plaintiffs, “WPS concedes that the [hypogammaglobulinemia]
diagnosis is supported, but decided to deny the benefits anyway, because -- referencing a
standard for the first time -- that diagnosis may not be a ‘clinically significant primary
immunodeficiency.’” (Pls.’ Br. (dkt. #17) 23 (emphasis in original).) It is not clear to this
court, nor do plaintiffs explain, how a hypogammaglobulinemia diagnosis differs from a
diagnosis of a clinically significant primary immunodeficiency. Regardless, WPS did not
concede that a hypogammaglobulinemia diagnosis had been established; rather, WPS’s
final denials noted that, consistent with Drs. Peterson’s and Halwig’s findings, while “the
provided documentation does support the laboratory finding of IgG subclass
hypogammaglobulinemia,” immunology practice standards require a patient’s laboratory
findings and clinical history to be consistent with a diagnosis of a primary
immunodeficiency. (WPS 423, 1066.)
Moreover, WPS’s requests for medical records not previously required in 2015 and
2016 were consistent and clearly communicated in advance of the denial. In particular,
beginning in early 2017, WPS consistently sought additional documentation:
•

On April 26, 2017, letters to Dr. Bouboulis, WPS requested medical records from
the past four years.

•

In a letter on June 7, 2017, PA Navigator Pharmacy Services (on behalf of WPS)
wrote to plaintiffs, explaining that “[c]overage of GAMMAGARD INJ 5GM/50ML
requires review of progress notes detailing diagnosis, previous therapeutic history,

38

concurrent medications, and treatment and monitoring plan. We did not receive
the above mentioned information.” (WPS 788-89, 1402-03.)
•

On June 13, 2017, WPS denied the prior authorizations and stated that
“[c]ontinued coverage of IVIG requires review of progress notes detailing diagnosis,
previous therapeutic history, concurrent medications, and treatment and
monitoring plan” which were “requested from [their] provider, but not received.”
(WPS 789, 1403.)

•

On June 28, 2017, WPS approved IVIG therapy for both boys for one month, but
added that “future authorizations are not necessarily guaranteed and will be based
on your physician submitting appropriate clinical information along with the
request.” (WPS 794, 1408.)

Finally, when the records were provided, WPS ultimately determined that they were not
supportive of a hypogammaglobulinemia diagnosis, explaining in part that “it would be
anticipated that if a serious underlying immune deficiency was truly present, then there
would have been a greater need for medical services or anti-infectious agents (other than
those routinely taken) during these gaps of IVIG treatment, but this is not borne out from
the medical records.” (WPS 512, 1106). Requesting historical medical documents, then
considering those documents in rendering an ultimate result, cannot reasonably be
considered “moving the target,” and so the court does not find capriciousness on this basis.

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G. Conclusion
Overall, although the court looks at WPS’s motives in this case with some
skepticism, and considering the evidence as a whole, a different decision could have been
justified under the circumstances, this court’s inquiry is more limited as a matter of law.
See Hess v. Reg-Ellen Mach. Tool Corp., 423 F.3d 653, 658 (7th Cir. 2005) (“[W]e will not
set aside a denial of benefits based on any reasonable interpretation of the plan . . . .
Indeed, whether or not we would have reached the same conclusion is irrelevant.”) (internal
citations omitted). The inquiry is whether WPS’s decision was arbitrary and capricious.
Here, the undisputed evidence suggests that it was not. Accordingly, summary judgment
will be granted in defendant’s favor as to this claim.

III. Breach of Fiduciary Duties
In addition to alleging wrongful denial of benefits, plaintiffs also contend that WPS
was a fiduciary to the Plan yet breached its fiduciary duties of loyalty and prudence when
it “looked for any reason to deny coverage” and by not following the Plan terms. (Pls.’ Br.
(dkt. #17) 13-17.) Defendant contends generally that a breach of fiduciary action is not
appropriate as a matter of law because it is duplicative of plaintiffs’ wrongful denial of
benefits claim. (Def.’s Br. (dkt. #22) 21.)
To understand the parties’ arguments, a review of the structure of ERISA is helpful.
Section 402 (codified at 29 U.S.C. § 1102) requires every ERISA plan to provide for one
or more named fiduciaries who have the authority to control and manage the operation
and administration of the plan. Here, there is no dispute that WPS is a fiduciary to the
Plan at issue. In turn, § 404 (codified at 29 U.S.C. § 1104) defines the duties of those

40

fiduciaries, and provides that the fiduciary “shall discharge his duties with respect to the
plan solely in the interests of the participants and beneficiaries.” ERISA § 404(a)(1)
(codified at 29 U.S.C. § 1104(a)(1)). It also requires the fiduciary to act “in accordance
with the documents and instruments governing the plan insofar as such documents and
instruments are consistent with the provisions of this subchapter and subchapter III.”
ERISA § 404(a)(1)(D) (codified at 29 U.S.C. § 1104(a)(1)(D)).
Finally, ERISA § 502 “identifies who is entitled to bring a civil action to enforce the
prescriptions of the statute and what relief may be obtained.”

Smith v. Med. Benefit

Administrators Grp., Inc., 639 F.3d 277, 282 (7th Cir. 2011) (citing ERISA § 502, codified
at 29 U.S.C. § 1132). This section provides in relevant part that:
A civil action may be brought -(1) by a participant or beneficiary -...
(B) to recover benefits due to him under the terms of
his plan, to enforce his rights under the terms of the
plan, or to clarify his rights to future benefits under the
terms of the plan;
...
(3) by a participant, beneficiary, or fiduciary (A) to enjoin any
act or practice which violates any provision of this subchapter
or the terms of the plan, or (B) to obtain other appropriate
equitable relief (i) to redress such violations or (ii) to enforce
any provisions of this subchapter or the terms of the plan.
...
ERISA § 502(a) (codified at 29 U.S.C. § 1132(a)). In addition to bringing a wrongful
denial of benefits claim under § 502(a)(1)(B), plaintiffs here also seek relief under §

41

502(a)(3) for alleged violations of WPS’s fiduciary duties. 11 As the Seventh Circuit has
explained, § 502(a)(3) “permits a participant to obtain relief for a breach of fiduciary duty
on behalf of himself as opposed to the plan.” Smith, 639 F.3d at 283.
As noted above, defendant argues that this court should dismiss plaintiffs’ breach
of fiduciary duty claims as duplicative, but case law does not appear to support the
proposition that a wrongful denial of benefits can never be brought under both §
502(a)(1)(B) and § 502(a)(3). While not directly on point, the U.S. Supreme Court in
Varity Corp. v. Howe, 516 U.S. 489 (1996), held that an individual could bring a breach of
fiduciary claim on behalf of himself through § 502(a)(3), and in doing so, addressed
concerns regarding a beneficiary’s potential ability to “repackage his or her ‘denial or
benefits’ claims as a ‘breach of fiduciary duty.’” Id. at 513. The Court explained that
“characterizing a denial of benefits as a breach of fiduciary duty does not necessarily change
the standard a court would apply when reviewing the administrator's decision to deny
benefits.” 516 U.S. at 514. The Court also went on to note that § 502(a)(3) authorizes
only “appropriate” equitable relief. Id. at 515 (“we should expect that where Congress
elsewhere provided adequate relief for a beneficiary's injury, there will likely be no need for
further equitable relief, in which case such relief normally would not be ‘appropriate’”).

The court does not understand plaintiffs to be asserting a claim under § 502(a)(2), as they cite
only to §§ 502(a)(1)(B) and 502(a)(3) in their amended complaint and briefing. Regardless, as
defendant points out, a § 502(a)(2) claim would not be available as the Supreme Court held in
Massachusetts Mutual Life Insurance Co. v. Russell, 473 U.S. 134 (1985), that that subsection was
available only to seek recovery on behalf of the entire plan, rather than recovery for an individual
injury. Id. at 144, 154.
11

42

Thus, the Court contemplated that a beneficiary could bring concurrent § 502(a)(1)(B)
and § 502(a)(3) claims, while still noting the limitations of such a strategy.
This question was more directly examined by the Sixth Circuit in Rochow v. Life
Insurance Co. of North America, 780 F.3d 364 (6th Cir. 2015), which held that:
A claimant can pursue a breach-of-fiduciary-duty claim under
§ 502(a)(3), irrespective of the degree of success obtained on a
claim for recovery of benefits under § 502(a)(1)(B), only where
the breach of fiduciary duty claim is based on an injury
separate and distinct from the denial of benefits or where the
remedy afforded by Congress under § 502(a)(1)(B) is
otherwise shown to be inadequate.
Id. at 372. While this issue does not appear to have been addressed in detail by the Seventh
Circuit, in Sumpter v. Metro. Life Ins. Co., 683 F. App'x 519, 521 (7th Cir. 2017)
(unpublished), the court stated that “a denial of benefits, without more, does not constitute
a breach of fiduciary duty that can be remedied under the equitable-relief provision; that’s
what section 1132(a)(1)(B) is for.” Id. at 521 (emphasis added). This appears largely
consistent with Rochow. Thus, case law suggests that a plaintiff can pursue both a §
502(a)(3) and a § 502(a)(1)(B) if she shows, for example, that the remedy under §
502(a)(1)(B) is inadequate.
Here, plaintiffs seek not only a reinstatement of benefits (a remedy available under
§ 502(a)(1)(B)) but also (1) an injunction ordering that both boys’ IVIG treatment be
continued without interruption; (2) removal of WPS as a fiduciary making decisions on
whether IVIG treatment is medically necessary; and (3) a surcharge to prevent WPS’s
unjust enrichment. As such, a legal remedy under § 502(a)(1)(B) would not be adequate
to make them whole, and additional relief under § 502(a)(3) may be appropriate. At least

43

as a matter of law, therefore, plaintiffs’ fiduciary duty claims do not appear to be
completely duplicative of their wrongful denial of benefits claim and will not be dismissed
outright on that ground. However, this is a pyrrhic victory for plaintiffs here, since their
fiduciary duty claims fail on the merits.
Plaintiffs allege that WPS violated its fiduciary duties in two ways, but as to both
claims plaintiffs fail to show that WPS acted contrary to its duties under ERISA for reasons
largely already addressed. First, plaintiffs argue that WPS failed to act in accordance with
its duties of loyalty and prudence when it denied plaintiffs’ 2017 preauthorization requests
for IVIG treatment. Specifically, they contend that WPS elevated “its own financial
interests above either boy’s health to deny coverage that it was obligated to provide under
the Plan” and that it actively looked “for any reason to deny coverage.” (Pls.’ Br. (dkt.
#17) 16.) But this argument fails to recognize that a plan administrator’s fiduciary duties
include “the need to preserve assets to satisfy future, as well as present, claims and requires
a trustee to take impartial account of the interests of all beneficiaries.” Varity Corp., 516
U.S. at 514. Here, WPS owed fiduciary obligations to all beneficiaries under the Plan, not
just to plaintiffs. Other than pointing out WPS’s obvious financial conflict, plaintiffs’
argument is simply that IVIG treatment was a covered benefit under the Plan, but as
discussed above, WPS reasonably determined that it was not. Indeed, once arriving at that
determination, WPS’s fiduciary duties arguably required it to deny plaintiffs’ coverage given
its obligation to preserve the Plan’s assets. Considered in this way, plaintiffs’ first breach
of fiduciary duty claim fails, and the undisputed evidence compels judgment in favor of
defendant.

44

Second, plaintiffs argue that WPS breached its fiduciary duty to follow the terms of
the Plan. As noted above, ERISA § 404(a)(1)(D) requires a fiduciary to act “in accordance
with the documents and instruments governing the plan insofar as such documents and
instruments are consistent with the provisions of this subchapter and subchapter III.”
ERISA § 404(a)(1)(D) (codified at 29 U.S.C. § 1104(a)(1)(D)). Plaintiffs claim that: (1)
under the Plan, an external reviewer’s decision on medical necessity is binding on WPS;
(2) Dr. Imber’s and the neurologist’s reviews concluding that IVIG was medically necessary
were binding; and (3) contrary to the Plan terms, WPS sought additional and contradictory
external reviews from Drs. Peterson and Halwig. To support the proposition that an
external reviewer’s decision is binding in particular, plaintiffs initially cite to Section 13 of
the Plan. However, as defendant points out, that section is only invoked if the beneficiary
submits in writing a specific request for independent external review, after which a specific
sequence of events is set in motion. Only then is the independent review organization’s
decision binding on the beneficiary and WPS. Here, plaintiffs have produced no evidence
that they invoked Section 13 or that Dr. Imber’s or the neurologist’s review were provided
under that section of the Plan.
Apparently recognizing this, plaintiffs argue in their reply brief that WPS’s actions
violated a different section of the Plan, Section 11.E, which provides that if a decision to
deny coverage is based on medical necessity or because treatment is experimental,
investigational, or unproven, then the denial “will include an explanation of the scientific
or clinical judgment for the determination applying the terms of the Policy to your medical
circumstances.” (WPS 1963.) Plaintiffs then go on to argue that “[s]uch explanations

45

would obviously include why WPS chose to drop the First Reviewers after receiving their
adverse clinical judgment that IVIG treatment was medically necessary and sought out a
different reviewer at a different company. WPS provides none, however, except to say that
the First Reviewers did not have the pre-2014 medical records.” (Pls.’ Reply (dkt. #30)
8.) But plaintiffs themselves supply the explanation: WPS sought an additional review
because new information had been provided after plaintiffs submitted the older medical
records. Because WPS continued to question coverage in light of conflicting medical
opinions from the outset of plaintiffs’ prior authorization requests and this additional
information supplied reasonable grounds to seek an additional outside review, the court is
persuaded that WPS followed the terms of the Plan. Thus, the undisputed facts establish
that plaintiffs’ second fiduciary duty claim fails and again compel judgment in favor of
defendant.

ORDER
IT IS ORDERED that:
1) Plaintiffs’ motion for summary judgment (dkt. #16) is DENIED.
2) Defendant’s motion for summary judgment (dkt. #21) is GRANTED.
3) Plaintiffs’ motion to strike (dkt. #28) is GRANTED.
Entered this 10th day of August, 2021.
BY THE COURT:
/s/
__________________________________
WILLIAM M. CONLEY
District Judge

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