Edward Elder v. Kentucky Retirement Systems

CourtKentucky Supreme Court
DecidedSeptember 21, 2020
Docket2017 SC 000258
StatusUnknown

This text of Edward Elder v. Kentucky Retirement Systems (Edward Elder v. Kentucky Retirement Systems) is published on Counsel Stack Legal Research, covering Kentucky Supreme Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Edward Elder v. Kentucky Retirement Systems, (Ky. 2020).

Opinion

RENDERED: SEPTEMBER 24, 2020 TO BE PUBLISHED

Supreme Court of Kentucky 2017-SC-0258-DG

EDWARD ELDER APPELLANT

ON REVIEW FROM COURT OF APPEALS V. CASE NO. 2015-CA-0916-MR FRANKLIN CIRCUIT COURT NO. 14-CI-00468

KENTUCKY RETIREMENT SYSTEMS APPELLEE

OPINION OF THE COURT BY JUSTICE NICKELL

REVERSING AND REMANDING

Edward Elder appeals the decision of the Kentucky Court of Appeals

affirming denial of disability retirement benefits by the Board of Trustees of the

Kentucky Retirement Systems (Systems). In a matter of first impression, this

appeal addresses the proof required of a public employee with less than sixteen

years’ service credit1 to establish his genetic condition—present at conception

but dormant until after a dozen years on the job—was not a “pre-existing”

1 Kentucky Revised Statutes (KRS) 61.600(4)(b) exempts a public employee with

sixteen years’ service credit from proving a disabling condition did not pre-exist employment. condition, disqualifying him from receiving benefits under KRS 61.600(3)(d).2

We reverse the Court of Appeals, reaffirm as controlling law the legal principles

announced in Kentucky Retirement Systems v. Brown, 336 S.W.3d 8 (Ky. 2011),

and remand to Systems for proceedings consistent with this Opinion.

FACTUAL BACKGROUND

Elder was hired as a school custodian by the Graves County Board of

Education in August 1995. Upon employment, he became a member of the

County Employees Retirement System which is administered by Systems.3

Elder worked regularly until 2007, performing heavy activities and receiving

glowing evaluations. In 2007, he began accruing health-related absences,

particularly due to the onset of chronic nosebleeds and gastrointestinal

bleeding. He had previously enjoyed good health.4

Dr. Charles Winkler began treating Elder for colon cancer on October 24,

2007. In reviewing notes from Dr. Jeff Carrico, a family practitioner in

Mayfield, Kentucky, Dr. Winkler wrote in a letter he had learned Dr. Carrico

had diagnosed Elder with Hereditary Hemorrhagic Telangiectasia (HHT) on

2 In pertinent part, KRS 61.600(3)(d) establishes a public employee with less than sixteen years’ service credit may qualify for disability retirement benefits if objective medical evidence examined by licensed physicians establishes “[t]he incapacity does not result directly or indirectly from bodily injury, mental illness, disease, or condition which pre-existed membership in the system or reemployment, whichever is most recent.” 3 KRS 61.645(1). 4 Elder underwent successful back surgery in 1980, began medication for

anemia and iron deficiency in 1997, and also received treatment for high blood pressure, an allergic reaction to a bee sting, and sleep apnea.

2 August 29, 2007. No basis for the diagnosis was provided. We located no

notes from Dr. Carrico dated August 29, 2007, but a “patient abstract” of an

office visit dated August 31, 2007, lists the diagnosis as “HEREDIT HEMORR

TELANGIEC.”

On September 23, 2008, Elder received a definitive medical diagnosis of

HHT from Dr. Chandra Prakash Gyawali, a gastroenterology specialist at the

Washington University School of Medicine in St. Louis, Missouri, based on the

Curaçao diagnostic criteria.5 Even with treatment, Elder’s condition continued

to deteriorate, ultimately leading him to retire on September 1, 2011, with only

180 months (15 years) total service credit.6 His last day of paid employment

was May 3, 2011.

Though he experienced a single memorable nosebleed as a young adult,7

Elder first sought treatment for chronic and severe nosebleeds in 2007. Pre-

2007 medical records submitted by Elder contain no mention of long-term or

severe nosebleeds, but erroneously noted he had been diagnosed with HHT in

the 1980’s. Elder sought to correct the erroneous historical notations by filing

5 The Curaçao diagnostic criteria were developed in 1999 and involve four diagnostic factors for the diagnosis of HHT. A definitive diagnosis of HHT is medically- indicated if three of the four criteria are present. Dr. Gyawali diagnosed Elder’s HHT after establishing the co-existence of recurring and spontaneous epistaxis (nosebleeds), family history of HHT (mother and sister), and gastrointestinal telangiectasia. The fourth criteria is arteriorvenous malformations (AVMs). https://curehht.org/understanding-hht/diagnosis-treatment/diagnostic-criteria-hht/ 6 According to Systems, Elder had not purchased seven summer months and did not earn service credit for October-December 2002 while on medical leave. 7 Elder recalled his bride became upset when, as a newlywed, he suffered a nosebleed resulting in a bloodstained pillow.

3 an affidavit to clarify it was his mother who had been diagnosed with HHT in

the 1980s, and he testified consistently. In contrast, Elder’s post-2007 medical

records are replete with references to daily nosebleeds—sometimes five or six a

day—along with other associated HHT symptoms. As his nosebleeds and other

difficulties worsened, Elder became dependent on regular iron infusions and

blood transfusions.

PROCEDURAL SUMMARY

Without counsel, Elder applied for disability retirement benefits in

August 2011. Using Form 6000, Systems’ standard application, Elder

attributed his disability to the 2007 onset and worsening of the debilitating

symptoms of HHT, though he readily admitted the condition’s hereditary

nature. Under “Members Statement of Disability,” Elder copied the following

definition of HHT, obtained from the National Center for Biotechnology

Information (NCBI) website8:

Hereditary hemorrhagic telangiectasia (Osler-Weber- Rendu disease) is an autosomal dominant, systemic fibrovascular dysplasia in which telangiectases, arteriovenous malformations, and aneurysms may be widely distributed throughout the body vasculature. Major clinical manifestations include: recurrent bleeding from mucosal telangiectases and arteriovenous malformations; hypoxemia, cerebral embolism, and brain abscess due to pulmonary arteriovenous fistulas; high-output congestive heart failure and portosystemic encephalopathy from hepatic arteriovenous malformations; and a variety of neurologic symptoms due to central nervous system angiodysplasia. Therapy is primarily supportive, consisting of iron supplementation and blood

8 https://www.sciencedirect.com/science/article/abs/pii/0002934387901628

4 transfusion. Septal dermoplasty and oral estrogens may allow prolonged remission of epistaxis, but permanent surgical cure of gastrointestinal bleeding is rarely feasible because of diffuse angiodysplasia of the alimentary tract. Ligation, resection, or embolization may be indicated for pulmonary arteriovenous fistulas. The prognosis and survival of patients with hereditary hemorrhagic telangiectasia are favorable, providing treatable complications are accurately diagnosed.

Elder also described how HHT negatively impacted his health and physical

abilities. In support of his application, Elder filed more than 2,000 pages of

medical records, the earliest dating back to 2005. He had attempted to obtain

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