McCrann v. NC Department of Health & Human Services, Division of Mental Health

704 S.E.2d 899, 209 N.C. App. 241, 2011 N.C. App. LEXIS 81
CourtCourt of Appeals of North Carolina
DecidedJanuary 18, 2011
DocketCOA10-80
StatusPublished
Cited by2 cases

This text of 704 S.E.2d 899 (McCrann v. NC Department of Health & Human Services, Division of Mental Health) is published on Counsel Stack Legal Research, covering Court of Appeals of North Carolina primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
McCrann v. NC Department of Health & Human Services, Division of Mental Health, 704 S.E.2d 899, 209 N.C. App. 241, 2011 N.C. App. LEXIS 81 (N.C. Ct. App. 2011).

Opinion

HUNTER, JR., Robert N., Judge.

The North Carolina Department of Health and Human Services, Division of Mental Health, Developmental Disabilities, and Substance Abuse Services (hereinafter “DHHS” or “respondent”) appeals the superior court’s order finding respondent’s denial of benefits to petitioner Michael Jonathan McCrann, Jr., was arbitrary and capricious. Respondent argues that the denial of benefits was based upon a *243 federally authorized Medicaid waiver and was therefore proper. Petitioners urge this Court to affirm the superior court’s finding with respect to respondent’s denial of benefits, but seek our reversal of the superior court’s decision to deny reimbursement to petitioners for expenses incurred to maintain the denied services throughout this appeal. After careful review, we affirm the superior court’s decision finding the denial of benefits to be arbitrary and capricious, but reverse on the issue of reimbursement and remand for determination of the amount of reimbursement due to petitioners.

I. Factual and Procedural History

Michael Jonathan McCrann, Jr. (“Jonathan”) is the twenty-eight-year-old son of Michael and Kelly McCrann. Mr. and Mrs. McCrann are Jonathan’s legal guardians and join Jonathan as petitioners in this appeal. Since birth Jonathan has endured multiple disabilities including mental retardation, autism, cerebral palsy, and he is legally blind. To address the special needs of individuals such as Jonathan, North Carolina has developed a Medicaid-funded medical assistance program called the Community Alternatives Program for Persons with Mental Retardation and Other Developmental Disabilities (“CAP Program”).

The centerpiece of the CAP Program is an individualized Plan of Care, which is a schedule of services to be provided to the program participant. Plans of Care are reviewed each year and are tailored to ensure the medical and social needs of each patient are met. Jonathan’s Plan of Care reflects the significant amount of one-on-one services necessitated by his physical and mental disabilities and prescribes a personal caregiver to assist Jonathan with his daily functions. Without a personal caregiver, Jonathan would have significant difficulty with the most basic of daily activities such as using the bathroom, moving about safely, communicating with others, and learning. For most of his life, Jonathan has received these services under the CAP Program while living at home with his parents. In 2003, in an effort to help Jonathan become more independent, his parents moved him into a group home and continued to provide him care through a personal caregiver. Absent this intensive therapy Jonathan would require institutionalization.

For more than ten years, Edna McNeill has been the primary provider of these services for Jonathan. Ms. McNeill began caring for Jonathan in the McCranns’ home and has continued in her role as Jonathan’s primary caregiver since his admission to the Pinetree *244 Group Home (“Pinetree”). The two have developed a trusting bond that has facilitated Jonathan’s progress from a classification of “profoundly mentally retarded” to “moderately mentally retarded.” It is not surprising then that Jonathan’s Plan of Care, which was developed by a team of professionals, his family, and himself, designates Ms. McNeill as the person best suited to provide the “home support” component of the plan.

The Code of Federal Regulations authorizes federal grants to reimburse states for medical assistance programs for the disabled, such as the CAP Program. See 42 C.F.R. § 430.0 (2009). For a state to be eligible for reimbursement for program expenses, the state’s program must meet certain federal requirements. States are afforded flexibility, however, to implement changes in these assistance programs in order to try more cost-effective delivery of services or to tailor services to the specific needs of certain groups of benefit recipients. See 42 C.F.R. § 430.25(b) (2009). States must seek approval for such program changes from the federal government through a program “waiver.” See id. If a waiver is approved, the federal government thereby waives compliance with state program requirements while permitting states to remain eligible for reimbursement with federal grants. See id. Waivers do not permit states to implement permanent changes in their Medicaid assistance programs; waivers are initially approved for a period of two to three years and may be renewed thereafter. See 42 U.S.C. § 430.25(h).

Operating under the 2001 Waiver, the CAP Program paid for Ms. McNeill’s services from 2002 through 2005 as that waiver permitted rehabilitation services to be provided by a third-party provider in a group home setting. In 2005, however, DHHS revised the 2001 Waiver and received approval to implement the new waiver (hereinafter the “2005 Waiver”) by the Centers for Medicare and Medicaid Services, effective 1 July 2005. After the 2005 Waiver was approved, Jonathan’s case manager reviewed and updated Jonathan’s 2005 Plan of Care to bring it in compliance with the new waiver provisions. This updated Plan of Care requested that the services provided by Ms. McNeill be continued and that the services be provided in Jonathan’s group home. The Plan of Care was approved. In April of 2006, however, upon the next annual review of Jonathan’s Plan of Care, DHHS determined that these same services should be denied.

Revisions to the CAP Program that were approved in the 2005 Waiver provide, in pertinent part:

*245 Individuals who live in licensed residential settings or unlicensed alternative family living arrangements may only receive the community component of this service. The community component of Home and Community supports does not replace the Residential Support provider’s responsibility to provide support to individuals in their homes and the community, but is intended to support those who choose to engage in community activities that are not provided through a licensed day program.

DHHS interpreted this language to exclude third-party providers from providing services to benefit recipients in a group home setting. Thus, DHHS concluded that while the 2001 Waiver permitted Ms. McNeill to provide services to Jonathan in his group home, the 2005 Waiver precluded coverage for Ms. McNeill’s services under Jonathan’s Plan of Care — despite having approved the same services under the same waiver (the 2005 Waiver) the previous year. Jonathan could receive Ms. McNeill’s services if he lived at home or Pinetree employees could provide comparable services for which the State could be reimbursed through Medicaid.

On 25 April 2006, DHHS informed the McCranns that Ms. McNeill’s services would no longer be covered. The McCranns filed a petition for a contested case hearing in the Office of Administrative Hearings.

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Bluebook (online)
704 S.E.2d 899, 209 N.C. App. 241, 2011 N.C. App. LEXIS 81, Counsel Stack Legal Research, https://law.counselstack.com/opinion/mccrann-v-nc-department-of-health-human-services-division-of-mental-ncctapp-2011.