Wallace v. Dinello

CourtDistrict Court, N.D. New York
DecidedFebruary 7, 2025
Docket9:24-cv-00446
StatusUnknown

This text of Wallace v. Dinello (Wallace v. Dinello) is published on Counsel Stack Legal Research, covering District Court, N.D. New York primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Wallace v. Dinello, (N.D.N.Y. 2025).

Opinion

UNITED STATES DISTRICT COURT NORTHERN DISTRICT OF NEW YORK

DWAYNE WALLACE,

Plaintiff, 9:24-cv-446 (ECC/TWD) v.

DAVID DINELLO, et al.,

Defendants.

Amy J. Agnew, Esq., for Plaintiff Aimee Cowan, Asst. Attorney General, for Defendant Dinello Ryan T. Donovan, Esq., for Defendants Mannava, Chaudhry, and Mohammed Hon. Elizabeth C. Coombe, United States District Judge: MEMORANDUM-DECISION AND ORDER On March 29, 2024, Plaintiff Dwayne Wallace initiated this action pursuant to 42 U.S.C. § 1983 alleging claims of deliberate indifference under the Eighth Amendment against Defendants David Dinello, Venkata Mannava, Shazia Chaudhry, Asma Mohammed, and Carol Moores. Complaint (Compl.), Dkt. No. 1.1 Presently before the Court is Defendant Dinello’s motion to dismiss pursuant to Rule 12(b)(6) of the Federal Rules of Civil Procedure. Dkt. No. 30. The motion is fully briefed. Dkt. Nos. 30-1, 35, 36. For the following reasons, the motion to dismiss is granted, to the extent the complaint is dismissed without prejudice as against Defendant Dinello.

1 On June 24, 2024, Plaintiff filed a notice of voluntary dismissal as to Defendant Moores. Dkt. No. 28. Defendants Mannava, Chaudhry, and Mohammed filed an answer on June 25, 2024, Dkt. No. 29; the claims against them are not addressed here. I. FACTS2 A. Medications With Abuse Potential Policy Plaintiff was held in the custody of the New York State Department of Corrections and Community Supervision (DOCCS) from 2018 to 2021. He alleges that the discontinuation and denial of effective medication, pursuant to DOCCS policy, without an individualized assessment of his needs constitutes deliberate indifference. Compl. at ¶¶ 315-18, 321, 324-25, 342-43.

DOCCS’ “policy on Medications With Abuse Potential” (MWAP) was drafted by Defendant Dinello and promulgated on June 2, 2017. Compl. at ¶¶ 145-46.3 On its MWAP list, “DOCCS included a group of . . . ubiquitous medications, including” the medication at issue here: Neurontin (also known as Gabapentin), “an anticonvulsant generally taken to control seizures” and “often prescribed to relieve nerve pain.” Id. at ¶¶ 78, 88.4 The medications on the MWAP list “are not risk free,” and “[l]ike any medication they can be abused, but many of them—including Neurontin . . . —are considered to have low addiction potential.” Id. at ¶ 98. “DOCCS, its physicians and mid-level clinicians have been aware of the risks of these medications for decades.” Id. at ¶ 100.

2 These facts are drawn from the complaint. The Court assumes the truth of, and draws reasonable inferences from, the well-pleaded factual allegations, see Lynch v. City of New York, 952 F.3d 67, 74–75 (2d Cir. 2020), but does not accept as true any legal conclusions, see Ashcroft v. Iqbal, 556 U.S. 662, 678 (2009). 3 The MWAP policy was codified as DOCCS Health Services Policy 1.24, “Medications with Abuse Potential.” Plaintiff alleges that DOCCS allowed Defendant Dinello to draft this policy despite his lack of specialized training in addiction issues, and his guilty plea following charges in 2010 by the New York State Department of Health State Board of Professional Medical Conduct of “failing to adequately evaluate patients prior to discharge from an emergency room.” Compl. at ¶¶ 136–46. 4 Although Plaintiff appears to allege that Neurontin was in a 2019 Formulary Book and was therefore available to doctors to prescribe without approval from an administrator, Compl. at ¶¶ 39–40, 42, Plaintiff’s allegations as to the Medications With Abuse Potential policy and related customs suggest that the MWAP policy altered these practices. Under the MWAP policy, a provider “submitted the MWAP Request Form” to the Regional Medical Director (RMD) in charge of their hub. Compl. at ¶ 159. The MWAP Request Form “asked for relevant health information regarding the patient, the justification for use of the medication and a list of any alternatives tried to treat the medical issue.” Id. at ¶ 160. The MWAP

Request Form “also asked if there is any recent evidence of drug diversion or abuse by the patient.” Id. ¶ 161. “Based on the MWAP Request Form contents—the RMD and not the patient’s medical provider—determined whether a patient will receive an MWAP.” Id. at ¶ 164. The treating physicians and mid-level clinicians “had to discontinue an MWAP prescription if it was not approved by the RMD[,]” “pharmacies would not fill a prescription for an MWAP without RMD approval[,]” and providers “had no ability to provide the medication once an RMD refused to approve the prescription.” Id. at ¶ 168. The MWAP policy “had the immediate impact of abruptly discontinuing the effective treatment of hundreds of inmates on MWAPs[.]” Compl. at ¶ 174. “As implemented, the MWAP Policy was an almost wholesale restriction on the prescription of MWAPs, except in cases of acute

need or palliative care.” Id. at ¶ 107. This stands in contravention of the positions of several other agencies, such as the National Commission on Correctional Health Care, of which DOCCS is an accredited member, that published a position statement directing that “[c]linicians should not approach the treatment of chronic pain as a decision regarding the use or nonuse of opioids (as in acute pain)[;] [r]ather clinicians should consider all aspects of the problem and all available proven modalities[,]” and “[p]olicies banning opioids should be eschewed.” Id. at ¶¶ 107–11. Similarly, the Federal Bureau of Prisons’ (BOP) Clinical Guideline does not prohibit use of opioids or neuromodulating medications like Neurontin but instead “lists Neurontin . . . as [a] second line treatment[] for neuropathic pain.” Id. at ¶¶ 112–13. The American Correctional Association, by which DOCCS is accredited, “lists the BOP’s Clinical Guideline . . . as its clinical guideline standard.” Id. at ¶ 114. The New York State Department of Health “has only two main concerns regarding Neurontin/Gabapentin: it recommended avoiding prescriptions in doses higher than 3600 mg per day because there is no evidence of increase in therapeutic dose, and it recommended

avoidance of use of Neurontin by a patient benefiting from concurrent opioid treatment.” Id. at ¶ 115. The American Medical Association “also does not restrict the prescription of many of the medications on the MWAP list.” Id. at ¶ 116. In fact, “[t]he standard in the medical community is to use medications like Neurontin . . . and other non-opioid MWAPS to treat chronic conditions to reduce the number of opioid prescriptions;” “[t]he standard in the medical community is not to restrict all effective treatment.” Id. at ¶ 118. In February 2021, “as a direct result of class action litigation, DOCCS . . . rescinded the MWAP Policy and promulgated a new policy[,] 1.24A,” entitled “Prescribing for Chronic Pain.” Compl. at ¶ 286.5 “The new policy demanded ‘Pain management medication should only be discontinued after a provider has met with the patient, discussed the issues regarding the use of the

medication, analyzed the patient’s situation, and subsequently determined that it is in the best interest of the patient for the medication to be discontinued.[’]” Id. at ¶ 287. B. Plaintiff’s Medical Issues Plaintiff entered DOCCS’s custody in 2018 with an active prescription for Gabapentin to treat his diabetic neuropathy. Compl. at ¶ 314. Immediately after Plaintiff’s intake, a DOCCS medical provider “discontinued his Gabapentin prescription without an examination or even seeing” Plaintiff. Id. at ¶ 315. “The provider did not even submit an MWAP Request to [Plaintiff’s

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