M.A. Mushow v. Doyle & Roth Mfg. (WCAB)

CourtCommonwealth Court of Pennsylvania
DecidedApril 12, 2022
Docket121 C.D. 2021
StatusUnpublished

This text of M.A. Mushow v. Doyle & Roth Mfg. (WCAB) (M.A. Mushow v. Doyle & Roth Mfg. (WCAB)) is published on Counsel Stack Legal Research, covering Commonwealth Court of Pennsylvania primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
M.A. Mushow v. Doyle & Roth Mfg. (WCAB), (Pa. Ct. App. 2022).

Opinion

IN THE COMMONWEALTH COURT OF PENNSYLVANIA

Michael A. Mushow, : Petitioner : : No. 121 C.D. 2021 v. : : Submitted: September 17, 2021 Doyle and Roth Manufacturing : (Workers’ Compensation Appeal : Board), : Respondent :

BEFORE: HONORABLE PATRICIA A. McCULLOUGH, Judge HONORABLE ELLEN CEISLER, Judge HONORABLE BONNIE BRIGANCE LEADBETTER, Senior Judge

OPINION NOT REPORTED

MEMORANDUM OPINION BY JUDGE McCULLOUGH FILED: April 12, 2022

Michael A. Mushow (Claimant) petitions for review of the January 14, 2021 order of the Workers’ Compensation Appeal Board (Board) that affirmed the decision of a workers’ compensation judge (WCJ) denying the Petition for Review of Utilization Review (UR) Determination (UR Petition) filed by Claimant. For the reasons that follow, we affirm. Background In December of 2012, Claimant sustained a work-related injury in the form of a right knee medial meniscus tear. Doyle and Roth Manufacturing (Employer) accepted liability for the injury and, pursuant to the provisions of the Workers’ Compensation Act (Act),1 issued a Notice of Compensation Payable. (Certified Record (C.R.), Item No. 18.) 2 In June of 2019, Employer and its insurer filed a request for a UR determination3 regarding the treatment rendered to Claimant by Avner R. Griver, M.D., Claimant’s pain management provider, beginning June 7, 2019, and ongoing. (C.R., Item No. 17.) Specifically, the request for a UR determination sought a review of the reasonableness and necessity of Claimant’s medical prescriptions for OxyContin 60 mg twice a day, and oxycodone 10 mg four times a day, prescribed by Dr. Griver. On August 15, 2019, Richard S. Kaplan, M.D., the Utilization Review Organization (URO) reviewer, rendered a UR determination on the reasonableness and necessity of Claimant’s treatment with Dr. Griver. Id. In doing so, Dr. Kaplan reviewed Claimant’s medical records and history, discussed Claimant’s case with Dr. Griver, and reviewed a written statement from Claimant. Id., Report at 1. Dr. Kaplan stated that the last office note in Dr. Griver’s records, dated February 28, 2019,4 indicated that Claimant had right knee and hip pain, and that Dr. Griver continued to prescribe him with OxyContin 60 mg twice per day and oxycodone 10 mg four times daily. Id. at 2. That office note also detailed that Dr. Griver discussed with Claimant

1 Act of June 2, 1915, P.L. 736, as amended, 77 P.S. §§1-1041.4, 2501-2710.

2 The Reproduced Record does not comply with Pa.R.A.P. 2173, in that it lacks pagination. Accordingly, we cite to the Certified Record throughout this opinion.

3 Section 306(f.1) of the Act, 77 P.S. §531, requires that disputes regarding the reasonableness and necessity of medical treatment be submitted for utilization review by a utilization review organization (URO) authorized by the Department of Labor and Industry to perform such reviews. According to Section 306(f.1)(6)(ii) and (iv) of the Act, 77 P.S. § 531(6)(ii) and (iv), the URO is to issue a report and the report is to be made part of the record before the WCJ, who shall consider it as evidence but is not bound by it.

4 Dr. Griver advised that Claimant was also seen on June 20, 2019, but the office note was not in the chart.

2 a possible total hip replacement and that Claimant’s opioid dosing was above the Centers for Disease Control and Prevention’s (CDC) recommended dosing guidelines. Id. Dr. Kaplan reported that, on July 26, 2019, he discussed with Dr. Griver complications associated with a possible hip replacement procedure, and Dr. Griver indicated that he planned to perform a genicular nerve block with possible radiofrequency ablation, and thereafter reduce Claimant’s morphine equivalent dose (MED) below 100 until the hip replacement surgery was performed. Id. Dr. Kaplan also stated that their discussion focused on possible alternative treatments, including Cymbalta, topical Pennsaid, and a trial test using a walker. Id. In Claimant’s written statement, he indicated that his current opioid dosing keeps his knee more limber and functional, and without the medication he is unable to walk. Id. Dr. Kaplan began his analysis by noting that Claimant’s current MED is 240, an amount that “is substantially higher than the 50 mg[ ]to[ ]90 mg MED range[, which is indicated] as a red flag level discussed in Pennsylvania and CDC [g]uidelines . . . .” (C.R., Item No. 17, Report at 3.) He stated that he and Dr. Griver “agreed that a target MED would be 60 mg[ ]to[ ]90 mg morphine equivalent, and that this may be helped with the addition of Cymbalta and Pennsaid as adjuvant medications along with a trial use of a walker.” Id. He acknowledged, however, that those other possible treatments were not part of his review. Id. Accordingly, Dr. Kaplan found the challenged treatment reasonable and necessary, in part. He found that Claimant’s total daily OxyContin and oxycodone dosage of 160 mg, or an MED of 240, exceeded recognized medication guidelines and CDC guidelines, and, as such, the prescriptions were not justified during the period under review. Id. Dr. Kaplan further found, however, that OxyContin and oxycodone are reasonable and medically necessary at a

3 continuing tapering dosage with a target total of 90 MED or less, “or, in other words, a total daily usage of OxyContin plus oxycodone of 60 mg or less.” Id. On September 17, 2019, Claimant filed his UR Petition of Dr. Kaplan’s August 15, 2019 UR determination, which was assigned to a WCJ. (C.R., Item Nos. 2 & 3.) Before the WCJ, Claimant submitted an affidavit in support of his UR Petition, stating that he sustained a work-related injury to his right knee in December of 2012, has had two surgeries and two total knee replacements since then, and has developed intractable pain syndrome as a result of the injury and subsequent surgeries. (C.R., Item No. 15.) He attested that Dr. Griver prescribed him 60 mg of OxyContin, which Claimant takes twice a day, and 10 mg of oxycodone, which Claimant takes four times a day, for pain. Claimant explained that the medication allows him to move more freely and with less pain, though he is never pain-free. He claimed that his mobility is severely limited without the medication. Claimant also submitted a December 17, 2019 report from Dr. Griver, in which Dr. Griver described his attempts to manage Claimant’s chronic right knee pain since 2017. (C.R., Item No. 13.) Dr. Griver noted that Claimant has had multiple right knee surgeries with secondary infection and has been on “relatively high dosages” of opioid pain medication for many years. Id. Dr. Griver explained that when Claimant came under his care in July of 2017, his MED was 330. However, when seen on September 23, 2019, Dr. Griver noted that he was continuing to follow Claimant’s complaints of right knee and right hip pain, and that Claimant was taking lower dosages (an approximate one-third decrease to an MED of 240) compared to the dosages prescribed to him in July 2017. Dr. Griver explained that he discussed Claimant’s case with Dr. Kaplan, who recommended that Dr. Griver further cut back Claimant’s opioid dosage in line with CDC guidelines. Dr. Griver noted that he discussed alternative

4 treatments with Claimant at his September 23, 2019 appointment, including the use of a walker, the drug Cymbalta, a genicular nerve block, opioid reduction, and a new medication called Tanezumab. Dr. Griver stated that he tried the genicular nerve block on Claimant in November of 2019, without success, and that Cymbalta and use of a walker were also not successful. As a result, according to Dr. Griver, the only remaining options are Claimant’s possible use of the new drug, Tanezumab, and/or weaning Claimant off of his opioid pain medications “without any attention being paid toward his function or pain complaints.” Id. Dr.

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Bluebook (online)
M.A. Mushow v. Doyle & Roth Mfg. (WCAB), Counsel Stack Legal Research, https://law.counselstack.com/opinion/ma-mushow-v-doyle-roth-mfg-wcab-pacommwct-2022.