Griffin, Lisa v. Foley, Robert K.

CourtCourt of Appeals for the Seventh Circuit
DecidedSeptember 4, 2008
Docket07-2689
StatusPublished

This text of Griffin, Lisa v. Foley, Robert K. (Griffin, Lisa v. Foley, Robert K.) is published on Counsel Stack Legal Research, covering Court of Appeals for the Seventh Circuit primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Griffin, Lisa v. Foley, Robert K., (7th Cir. 2008).

Opinion

In the

United States Court of Appeals For the Seventh Circuit ____________

No. 07-2689

L ISA G RIFFIN and M ICHAEL W. G RIFFIN,

Plaintiffs-Appellants, v.

R OBERT K. F OLEY, M.D., Defendant-Appellee. ____________ Appeal from the United States District Court for the Southern District of Indiana, Evansville Division. No. 05 C 15—Richard L. Young, Judge. ____________

A RGUED F EBRUARY 28, 2008—D ECIDED S EPTEMBER 4, 2008 ____________

Before F LAUM, M ANION, and E VANS, Circuit Judges. M ANION, Circuit Judge. As a result of a car accident, Lisa Griffin had to undergo back surgery, which Dr. Robert Foley performed. After complications arose from the surgery, Lisa and her husband Michael filed this diversity suit against Foley in the district court alleging medical malpractice. The case went to trial, and a jury returned a verdict in favor of Foley. The Griffins appeal, raising 2 No. 07-2689

several challenges to the trial court’s procedural handling of their case. We affirm.

I. On June 11, 1994, while traveling through Georgia, the Griffins’ minivan was struck in the rear by a pickup truck. As a result of the collision, Lisa Griffin (“Lisa”) sustained severe injuries, including a burst fracture1 at the L1 verte- bra. Lisa was flown to Evansville, Indiana, where, on June 14, 1994, orthopedic surgeon Dr. Robert Foley per- formed both a laminectomy 2 and a spinal fusion on her back. During the operation, Foley used an internal fixation device consisting of rods and hooks to keep Lisa’s back in place. He then combined the bone he took from Lisa’s lamina with coralline hydroxyapatite, a bone graft substitute made of coral reef that goes by the trade name Pro Osteon. Although the Food and Drug Adminis- tration had approved Pro Osteon as a bone graft sub- stitute to fill holes in bone, the FDA had not specifically

1 A burst fracture, or axial compression, is a “fracture of a vertebra by excessive vertical force, so that pieces of it move out in horizontal directions, often injuring the spinal cord.” Dorland’s Illustrated Med. Dictionary 708 (29th ed. 2000). 2 A laminectomy is the surgical removal of one or more pieces of bone from the lamina, a part of the posterior structure of a vertebra, in order to relieve the pain caused by pressure on a nerve being compressed by bones in the spine. Am. Med. Ass’n, Complete Med. Encyclopedia 768 (2003) (hereinafter “Encyclo- pedia”). No. 07-2689 3

approved it for use as a bone graft extender in spinal fusions. Foley placed the mixture at the fracture site as a bone graft and completed the surgery. Foley continued to see Lisa in follow-up visits after the surgery. While at trial the parties disputed the relative success of the surgery, it was undisputed that, in October 1994, x-rays of Lisa’s back showed increased kyphosis 3 in her spine, a recognized complication of spinal fusion surgery. The kyphosis made the rods and hooks from the fixation device conspicuous underneath her skin, so on May 16, 1995, Foley performed a second surgery on Lisa to remove the internal fixation device. However, a later x-ray taken in March 1996 showed further kyphosis in Lisa’s spine. At this point, Foley recommended addi- tional surgery—the parties disputed the nature of the surgery recommended—which Lisa declined. Later on, the failure of the back fusion to achieve a union (another recognized complication of fusion surgery) became evi- dent. When Foley ought to have been aware of that fact and how he should have reacted were vigorously con- tested at trial. As a result of her back, Lisa is now perma- nently disabled and unable to work. The Griffins initiated this medical malpractice suit against Foley on June 11, 1998. Pursuant to Indiana law,4 they first filed a proposed complaint with the Indiana Department of Insurance alleging that Foley was

3 Kyphosis is an “abnormal and excessive outward curvature of the vertebrae in the upper spine.” Encyclopedia 764. 4 See Ind. Code § 34-18-8-4. 4 No. 07-2689

negligent because, among other things, he used Pro Osteon as a bone graft substitute in Lisa’s spine surgery when it was not FDA-approved for that use and had no therapeutic benefit as a bone graft substitute in spinal fusion surgery. The Department of Insurance assembled a medical review panel to review the case.5 After the case languished before the panel for over six years, the panel issued a one-sentence opinion: “The evidence does not support the conclusion that the defendant failed to meet the applicable standard of care as charged in the com- plaint.” 6 The Griffins then took their case to federal court in January 2005. Trial was scheduled for October 10, 2006, and the case management plan approved by both parties and the district court gave the Griffins until April 18, 2006, and Foley 60 days thereafter, to submit the expert witness reports required by Federal Rule of Civil Proce- dure 26.7 On April 18, 2006, the Griffins filed Rule 26

5 See Ind. Code § 34-18-10-1 et seq. 6 Under Indiana law, an opinion by a medical review panelist is not conclusive of the issue of liability. Ind. Code § 34-18-10-23. However, that statute also provides that “either party, at the party’s cost, has the right to call any member of the medical review panel as a witness. If called, a witness shall appear and testify.” Id. 7 Federal Rule of Civil Procedure 26(a)(2)(A) requires a party to “disclose to the other parties the identity of any witness it may use at trial to present evidence under Federal Rule of (continued...) No. 07-2689 5

reports for their experts: Dr. Lawrence Weis, Dr. Robert Lieberson, Dr. Timothy Lalk, and Professor John Navin. After the Griffins filed their expert witness reports, Foley noticed Navin’s deposition for April 28, 2006. Three days prior to the deposition, the Griffins’ counsel served notice that he would be videotaping Navin’s deposition for purposes of trial. 8 In response, Foley filed a motion for a protective order seeking to preserve the opportunity to cross-examine Navin for purposes of trial at a later date. In that motion, Foley asserted that the Griffins’ counsel had refused to produce Navin at a later date to allow the defense to cross-examine him for purposes of trial. The magistrate judge assigned to the case granted Foley’s motion, stating in its order that Navin must appear for his previously noticed discovery deposition

7 (...continued) Evidence 702, 703, or 705.” Along with the disclosure of the identity of its experts, a party must also submit a written report, “prepared and signed” by the expert, which contains (among other things) “a complete statement of all opinions the [expert] will express and the basis and reasons for them.” Fed. R. Civ. P. 26(a)(2)(B). “Absent a stipulation or a court order,” these expert disclosures must be made either 90 days before trial or, “if the evidence is intended solely to contradict or rebut evidence on the same subject matter identified by another party under Rule 26(a)(2)(B),” 30 days after the other party’s disclosure. Id. 26(a)(2)(C). 8 Federal Rule of Civil Procedure 30(b)(3)(A) allows for audio- visual recording of a deposition.

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