Looney v. Moore

Citation886 F.3d 1058
Decision Date30 March 2018
Docket NumberNo. 15-13979,15-13979
Parties Billy Ryan LOONEY, etc., et al., Plaintiffs, Christian Lewis, by and through his parents, Bernita Lewis and Earnest Thomas, Dreshan Collins, by and through his mother, Sharrissa Cook, Jaylen Malone, by and through his mother, Nikida Sellers, Plaintiffs–Appellants, v. Sheila D. MOORE, Director of the Office of the University of Alabama Institutional Review Board, Ferdinand Urthaler, M.D., Chairman of the University of Alabama Institutional Review Board, Waldemar A. Carlo, M.D., in his individual capacity, Masimo Corporation, Dr. John Carpenter, in his individual capacity, et al, Defendants–Appellees, Individual Members of the University of Alabama Institutional Review Board, THE, etc., et al., Defendants.
CourtUnited States Courts of Appeals. United States Court of Appeals (11th Circuit)

Reginald D. McDaniel, Attorney, Birmingham, AL, Alan Carl Milstein, Michael J. Dube, Sherman Silverstein Kohl Rose Podolsky, PA, Moorestown, NJ, for PlaintiffsAppellants.

Jay Michael Ezelle, Walter W. Bates, Cole Robinson Gresham, Sybil Vogtle Newton, William S. Starnes, Jr., Starnes Davis Florie, LLP, Birmingham, AL, for DefendantsAppellees SHEILA D. MOORE, FERDINAND URTHALER, WALDEMAR A. CARLO.

Joseph R. Re, Joseph S. Cianfrani, Cameron Jahansouz, Stephen C. Jensen, Payson J. Lemeilleur, Knobbe Martens Olson & Bear, LLP, Irvine, CA, Ivan B. Cooper, Enrique Jose' Gimenez, Adam K. Peck, Lightfoot Franklin & White, LLC, Birmingham, AL, for DefendantAppellee MASIMO CORPORATION.

Jay Michael Ezelle, Cole Robinson Gresham, Sybil Vogtle Newton, Starnes Davis Florie, LLP, Birmingham, AL, for DefendantAppellee JOHN CARPENTER.

Jay Michael Ezelle, Sybil Vogtle Newton, Starnes Davis Florie, LLP, Birmingham, AL, for DefendantsAppellees MARY HILLIARD, RICHARD PARKER, WILLIAM BLACKERBY, MARGUERITE KINNEY, MARILYN DOSS, CHARLES BOSWELL, DENISE BALL.

Before WILSON, and JULIE CARNES, Circuit Judges, and HALL,* District Judge.

JULIE CARNES, Circuit Judge:

Through their parents, Plaintiffs DreShan Collins, Christian Lewis, and Jaylen Malone brought claims against Defendants for harms allegedly visited on Plaintiffs when the latter were enrolled in a clinical study while being treated for health issues accompanying their premature births. Defendants fall into three groups: (1) Dr. Carlo, the physician who designed and ran the study; (2) Internal Review Board (IRB) physicians who approved the study and the informed consent materials; and (3) Masimo Corporation, which manufactured medical equipment used in the study.

Plaintiffs brought claims against the various Defendants for negligence, negligence per se, breach of fiduciary duty, products liability, and lack of informed consent. The district court granted summary judgment on all claims. Like the district court, we conclude that Plaintiffs have failed to establish that participation in the clinical study caused any injuries, which means that, under Alabama law, the negligence, negligence per se, breach of fiduciary duty, and products liability claims were properly dismissed.

Alabama law has not directly addressed the viability of the claim alleging lack of informed consent. At issue is whether a plaintiff who claims that he did not give informed consent to medical treatment provided as part of a clinical study must show that he was injured as a result of that treatment. Based on our review of analogous Alabama caselaw, we conclude that Alabama law requires that there be an actual injury caused by the treatment. Accordingly, because Plaintiffs have failed to establish that their lack of informed consent caused any actual injuries, the district court appropriately granted summary judgment to Defendants on these claims as well.

I. BACKGROUND
A. Factual Background

The University of Alabama at Birmingham was the lead study site for a national clinical research trial known as the Surfactant, Positive Pressure, and Oxygenation Randomized Trial ("SUPPORT"). Designed by Dr. Carlo and approved by the IRB Defendants, the SUPPORT study was created to analyze the effects of differing oxygen saturation

levels on premature infants. At the time of the study, it was nationally accepted (and neither party contests) that the recognized standard of care was to keep the oxygen saturation levels of low-birth-weight infants at between 85% and 95%. This standard notwithstanding, it was also known that a prolonged period of high oxygen saturation can result in oxygen toxicity, which leads to an increased risk of "retinopathy of prematurity."1 On the other hand, a prolonged period of low oxygen saturation can result in neuro-developmental impairment and death. Given the difficulties of calibrating the optimal oxygen range, the SUPPORT study sought to determine whether, within the accepted standard of care, there was a more precise range of oxygen saturation that would better reduce the risk of exposing an infant to either too much or too little oxygen.

The SUPPORT study randomly divided eligible and enrolled premature infants into two groups. One group was to be kept at an oxygen saturation

level between 85–89%, which is the low end of the standard-of-care range, while the other would be kept at an oxygen saturation level between 90–95%, which is the high end of that range. Further, to ensure double-blind data collection, the study would employ specialized oximeters (manufactured by Masimo) that would "mask" to an onlooker the true oxygen saturation levels of the infants. The oximeters would, however, signal an alarm whenever an infant's oxygen level strayed below 85% or above 95%.

Publishing the results of the study in the New England Journal of Medicine, the study authors concluded that infants in the high-oxygen group were more likely to be diagnosed with retinopathy

while infants in the low-oxygen group were more likely to die. There was no statistically significant difference in the incidence of neuro-developmental impairments between the high and low groups.

To enroll in the study, Plaintiffs' guardians had to execute informed consent documents that were drafted and approved by Defendants. After the study's completion, however, the Department of Health and Human Services authored a letter questioning whether these informed consent documents had properly disclosed all of the risks associated with enrollment in the SUPPORT study.

B. Procedural History

Plaintiffs filed the operative Fifth Amended Complaint in the United States District Court for the Northern District of Alabama asserting claims against Defendants for negligence, negligence per se, breach of fiduciary duty, products liability, and lack of informed consent. Plaintiffs allege that they suffered serious injuries as a result of their participation in the study. Specifically, Plaintiffs Lewis and Malone were assigned to the low-oxygen group, with prolonged periods of low oxygen saturation

being associated with neuro-developmental impairment and death. Fortunately, neither infant died, but they did develop neurological issues. Plaintiff Collins was assigned to the high-oxygen group, with prolonged high-oxygen saturation being associated with retinopathy, which can lead to blindness. Plaintiff Collins did develop retinopathy, but fortunately he did not suffer permanent vision loss.

Following discovery, Defendants moved for summary judgment asserting that, based on the undisputed material facts, Plaintiffs had failed to demonstrate that participation in the SUPPORT study had caused the injuries alleged in the Complaint. The district court agreed that Plaintiffs had failed to prove that their injuries were caused by participation in the SUPPORT study, as opposed to being a consequence of their premature births, and the court granted summary judgment to Defendants.

II. STANDARD OF REVIEW

"We review de novo the district court's grant of summary judgment." Greenberg v. BellSouth Telecomms., Inc. , 498 F.3d 1258, 1263 (11th Cir. 2007). Summary judgment is appropriate "if the pleadings, depositions, answers to interrogatories, and admissions on file, together with the affidavits, if any, show there is no genuine issue as to any material fact and that the moving party is entitled to judgment as a matter of law." Fed. R. Civ. P. 56. Viewing the evidence in the light most favorable to the nonmoving party, "[t]here is a genuine issue of material fact if the nonmoving party has produced evidence such that a reasonable factfinder could return a verdict in its favor." Greenberg , 498 F.3d at 1263 (quoting Waddell v. Valley Forge Dental Assocs., Inc. , 276 F.3d 1275, 1279 (11th Cir. 2001) ).

III. DISCUSSION

We agree that under applicable Alabama law, and taking all inferences in the light most favorable to Plaintiffs, Plaintiffs have failed to show that enrollment in the SUPPORT study caused their injuries. And although Alabama law has not squarely addressed whether the absence of an actual physical injury caused by the SUPPORT study dooms Plaintiffs' claims based on Defendants' failure to obtain Plaintiffs' informed consent to participate in that study,2 we conclude that it does. We first discuss the causation issue before turning to the informed consent claims.

A. Plaintiffs Have Presented Insufficient Evidence that the SUPPORT Study Caused Plaintiff's Alleged Injuries

The Alabama Supreme Court has made clear that, "to present a jury question, the plaintiff in a medical-malpractice action must adduce some evidence indicating that the alleged negligence (the breach of the appropriate standard of care) probably caused the injury. A mere possibility is insufficient."3 Cain v. Howorth , 877 So.2d 566, 576 (Ala. 2003) (alterations omitted; emphasis in original) (quoting Rivard v. Univ. of Alabama Health Servs. Found., P.C. , 835 So.2d 987, 988 (Ala. 2002) ); see also Lyons v. Walker Reg'l Med. Ctr. , 791 So.2d 937, 942 (Ala. 2000) ; Golden v. Stein , 670 So.2d 904, 907 (Ala. 1995). The district court concluded that Plaintiffs had failed to show that it was their participation in the...

To continue reading

Request your trial
39 cases
  • United States v. Mosquera
    • United States
    • United States Courts of Appeals. United States Court of Appeals (11th Circuit)
    • March 30, 2018
  • Quashen v. Carnival Corp.
    • United States
    • U.S. District Court — Southern District of Florida
    • December 17, 2021
    ...Carnival's medical staff and summary judgment is, therefore, proper as to Counts IV and V of the Amended Complaint. Looney v. Moore , 886 F.3d 1058, 1065 (11th Cir. 2018) (explaining the standards for medical malpractice).III. CONCLUSIONAccordingly, UPON CONSIDERATION of the Motion, the per......
  • Marocchini v. Brown
    • United States
    • U.S. District Court — Southern District of Alabama
    • September 27, 2021
    ...that under an informed consent claim, Alabama law requires that there be an actual injury caused by the treatment. Looney v. Moore, 886 F.3d 1058, 1060-61 (11th Cir. 2018). Notably, the Court distinguished between a no-consent claim which is analogous to a battery claim and an informed cons......
  • Marocchini v. Brown
    • United States
    • U.S. District Court — Southern District of Alabama
    • September 27, 2021
    ...identified injury. The informed consent analysis discussed above was shortened to two prongs. As explained by the Eleventh Circuit in Looney v. Moore: ... in describing the elements necessary to prove an informed consent claim, Alabama law appears not to include as an element proof of an in......
  • Request a trial to view additional results

VLEX uses login cookies to provide you with a better browsing experience. If you click on 'Accept' or continue browsing this site we consider that you accept our cookie policy. ACCEPT