Charette v. Wexford Health Sources Inc.

CourtDistrict Court, D. Maryland
DecidedSeptember 11, 2023
Docket1:19-cv-00033
StatusUnknown

This text of Charette v. Wexford Health Sources Inc. (Charette v. Wexford Health Sources Inc.) is published on Counsel Stack Legal Research, covering District Court, D. Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Charette v. Wexford Health Sources Inc., (D. Md. 2023).

Opinion

IN THE UNITED STATES DISTRICT COURT FOR THE DISTRICT OF MARYLAND

ANGELA CHARETTE, Personal * Representative of the Estate of Michael Anthony Miller, *

Plaintiff, * Civil Action No. GLR-19-33

v. *

WEXFORD HEALTH SOURCES, INC. * et al., * Defendants. *** MEMORANDUM OPINION THIS MATTER is before the Court on Defendants Wexford Health Sources, Inc. (“Wexford”), Nurse Bernard Alenda, Dr. Gedion Atnafu, Dr. Melaku Ayalew, Dr. Zowie Barnes, Nurse Wondaye Deressa, Physician Assistant (“PA”) Robert Giangrandi, Dr. Kenneth Lee, PA Priscilla Momoh, Dr. Ayoku Oketunji, Dr. Bolaji Onabajo, Nurse Titilayo Otunuga, Nurse Jennifer Pope, and Dr. Kasahun Temesgen’s (collectively, “Defendants”) Motion for Summary Judgment (ECF No. 115) and Plaintiff Angela Charette’s Cross-Motion for Partial Summary Judgment (ECF No. 129). The Motions are ripe for disposition, and no hearing is necessary. See Local Rule 105.6 (D.Md. 2023). For the reasons outlined below, the Court will grant in part and deny in part Defendants’ Motion for Summary Judgment. Additionally, the Court will deny Charette’s Cross-Motion for Partial Summary Judgment. I. BACKGROUND A. Factual Background

Michael Miller spent the last two decades of his life caught in a revolving door of incarceration. (See Defs.’ Ex. 1, Inmate Traffic History [“Inmate Traffic Hist.”], ECF No. 115-3). Miller’s imprisonment was defined by cascading medical complications related to chronic cirrhosis, hepatitis B, and hepatitis C—conditions that ultimately caused his death. This dispute focuses mainly on Miller’s medical care while incarcerated at Jessup Correctional Institution (“JCI”) between September 2, 2015 and March 24, 2017. During

this time, Wexford, a private medical company, provided health care services to inmates in Maryland. The other thirteen Defendants are individual health care providers employed or contracted by Wexford. These individual Defendants each participated in Miller’s care in some fashion. The Court recounts Miller’s complicated medical history with attention to the care that was—or was not—provided by Defendants.

1. Miller’s Early Detection of Hepatitis B and C Miller first entered the Maryland state prison system in 1997. (Inmate Traffic Hist. at 8). He spent several years cycling between prison and mandatory supervision on release before starting a decade-long prison sentence in 2005. (Id.; see also Defs.’ Ex. 2, Sentence Status Change Report [“Sentence Rep.”], ECF No. 115-4).1

1 Miller’s convictions are recorded under two different names, Michael A. Miller and Robert A. Williams. (See Sentence Rep. at DPSCSBF000031). Mr. Miller, at times, would refer to himself as Robert Williams. The parties’ briefs refer to the decedent as Michael Miller, so the Court will do the same. Miller was likely infected with at least one form of hepatitis before his re- imprisonment in 2005. (Defs.’ Ex. 4, Kali Zhou, M.D., Dep. Tr. [“Dr. Zhou Dep.”] at

43:17–44:12, ECF No. 115-6). This was no secret to Miller, who believed he contracted hepatitis C in 1999. (Defs.’ Ex. 10, Integris Medical Records [“Integris Med. Rs.”] at IMBC-SUB-000033, ECF No. 115-12). On October 12, 2007, Miller told a nurse practitioner he was infected with both hepatitis B and hepatitis C. (Defs.’ Ex. 3, Wexford Medical Records [“Wexford Med. Rs.”] at DPSCS000038, ECF No. 115-5). Because nothing at that time corroborated Miller’s belief, the nurse practitioner ordered lab reports

and noted that she would follow-up with Miller once she received the results. (Id.). It is worth pausing to discuss the risks associated with hepatitis B, hepatitis C, cirrhosis, and esophageal varices—each of which contributed to Miller’s deteriorating health. Hepatitis B is a potentially-life threatening liver infection caused by the hepatitis B virus (“HBV”). HBV is generally transmitted through blood, sexual contact, or childbirth.

See generally World Health Organization, Fact Sheet: Hepatitis B (June 24, 2022), https://www.who.int/news-room/fact-sheets/detail/hepatitis-b. Some symptoms associated with hepatitis B include “yellowing of the skin and eyes (jaundice), dark urine, extreme fatigue, nausea, vomiting, and abdominal pain.” Id. Hepatitis B can take on both acute and chronic forms. Id. While acute hepatitis B involves a short-term infection, a person has

chronic hepatitis B when the virus remains active in a body for more than six months. (See Pl.’s Ex. O, Ryan D. Herrington, M.D., Expert Rep. [“Dr. Herrington Rep.”] at 18, ECF No. 127-15). Chronic hepatitis B infects cells within the liver, causing an “inflammatory response that injures or ‘scars’ the liver,” a process called “fibrosis.” (Id. at 17). While healthy livers

can regenerate, “long-term inflammation/injury from presence of HBV in the liver leads to progression of fibrosis until there is so much scar tissue the liver can no longer regenerate and begins to fail – the time point called cirrhosis.” (Id.). A person may eventually experience “decompensated cirrhosis,” which happens when complications related to liver failure start appearing. (Id.). These complications include “bleeding from varices (dilated esophageal veins from excess pressure in liver vessels), ascites (fluid in abdomen), and

encephalopathy (confusion due to toxic ammonia build-up).” (Id.). A hepatitis B infection may move between an inactive state (with an undetectable viral load) and an active state (with a detectable viral load) throughout a patient’s life. (Id. at 19). Like hepatitis B, hepatitis C is a viral disease that affects the liver. And just as hepatitis B has both acute and chronic forms, so too does hepatitis C. Chronic hepatitis C

similarly presents risks of fibrosis, cirrhosis, and liver failure. On May 2, 2010, Miller took serology tests for hepatitis A, hepatitis B, and hepatitis C. (Defs.’ Ex. 5, BioReference Laboratory Report [“BioReference Lab’y Rep.”] at BIO000011, ECF No. 115-7).2 Although Miller tested negative for hepatitis A, he tested positive for hepatitis B surface antigen. (Id.). A positive surface antigen test signifies a

person currently has a hepatitis B infection. Miller also tested positive for hepatitis C

2 Serologic testing involves measuring specific viral antigens and antibodies. In the context of hepatitis B, for instance, different serologic “markers” help identify different phases of HBV infections. antibodies. (Id.). Antibodies indicate a person has been infected with hepatitis B in the past. As a follow-up, on May 17, 2010, Miller underwent genotype and quantitative PCR testing

for hepatitis C viral RNA. (Id. at BIO000013). Those tests revealed Miller did not have detectable levels of hepatitis C viral RNA. (Id.). Taken together, these results established that Miller did not have an active, treatable hepatitis C infection in May 2010, despite having been exposed to hepatitis C at some point. (Dr. Zhou Dep. at 41:17–18, 42:3–9). Miller did, however, have an active hepatitis B infection at that time. On May 19, 2010, two days after Miller’s provider tested his hepatitis C viral load

but one day before the prison received those test results, Miller saw an infection control nurse. During that visit, the nurse (1) educated Miller about hepatitis C and the possibility for treatment; (2) obtained Miller’s signed consent to receive hepatitis C treatment and to participate in the chronic care clinic; and (3) administered the first of three doses of the Twinrix vaccine for hepatitis A and hepatitis B. (Wexford Med. Rs. at DPSCS000170–72).

Miller received the second and third dose of the Twinrix vaccine on June 9, 2010, and November 19, 2010, respectively. (Id. at DPSCS0000175, DPSCS000220). 2. Miller’s Initial Gastrointestinal Bleeding In late February 2012, Miller had his first episode of bleeding esophageal varices.

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Charette v. Wexford Health Sources Inc., Counsel Stack Legal Research, https://law.counselstack.com/opinion/charette-v-wexford-health-sources-inc-mdd-2023.