Pogue v. Goodman

638 S.E.2d 824, 282 Ga. App. 385, 2006 Fulton County D. Rep. 3476, 2006 Ga. App. LEXIS 1396
CourtCourt of Appeals of Georgia
DecidedNovember 14, 2006
DocketA06A1523
StatusPublished
Cited by8 cases

This text of 638 S.E.2d 824 (Pogue v. Goodman) is published on Counsel Stack Legal Research, covering Court of Appeals of Georgia primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Pogue v. Goodman, 638 S.E.2d 824, 282 Ga. App. 385, 2006 Fulton County D. Rep. 3476, 2006 Ga. App. LEXIS 1396 (Ga. Ct. App. 2006).

Opinion

Bernes, Judge.

In this medical malpractice action, Rebecca Pogue and John Pogue appeal from the trial court’s grant of summary judgment to the *386 appellees Michael Louis Goodman, M.D., and Richardson & Goodman Neurosurgical Associates, P.C., on the grounds that the statute of limitation had expired. For the reasons that follow, we affirm.

On review from the grant of summary judgment, we conduct a de novo review of the law and evidence to determine whether there exists a genuine issue of material fact, viewing the evidence in the light most favorable to the nonmovant. Taylor v. S & W Dev., 279 Ga. App. 744 (632 SE2d 700) (2006). So viewed, the record reflects that Dr. Goodman performed surgery on Ms. Pogue on August 14, 2001. On that date, Dr. Goodman removed a morphine pain pump that he had inserted in Ms. Pogue approximately six years earlier and inserted a new one. The new pain pump was implanted in a pouch of skin embedded in Ms. Pogue’s abdominal wall. A drug delivery catheter, which Dr. Goodman inserted into Ms. Pogue’s spine and threaded up her spinal canal, was attached to the pump. The pump and the attached catheter were intended to deliver a constant dose of medication into Ms. Pogue’s spinal canal and relieve the pain Ms. Pogue had been experiencing in her lumbar spine.

According to Dr. Goodman, his practice as to morphine pumps was to advance the end of the catheter to at least the level of the mid-thoracic spine in order to maximize pain relief for his patients and also to reduce the risk that the catheter would be pulled out of the spinal canal during normal patient movement. During his deposition, Dr. Goodman admitted that a radiologist who had reviewed Ms. Pogue’s post-surgery x-ray noted that the x-ray did not disclose the end location of the catheter and recommended additional x-rays to determine its location. However, Dr. Goodman believed that because narcotic pain medication rapidly diffuses through spinal fluid, the specific height of the distal end of the catheter was immaterial so long as it reached the mid-thoracic region.

Almost immediately after the August 14, 2001 surgery, Ms. Pogue began to experience symptoms that she believed were related to the new pain pump system. She reported that she felt “fuzzy-headed” and fell asleep at random times of the day while doing everyday activities. She indicated that she believes that one such episode caused her to have an accident while driving in November 2001. She also did not experience the same level of pain relief that she had attained with her first morphine pump system. Ms. Pogue testified that the frequency of these events increased over time, and she believed that the episodes seemed to worsen as the dosage of her medication was increased.

At some point after the surgery, Ms. Pogue began seeing a new pain physician. In October 2003, her new physician became concerned about the insufficiency of Ms. Pogue’s pain relief and performed a procedure to evaluate the pain pump system. The procedure *387 revealed that the drug delivery catheter that Dr. Goodman had implanted traveled the length of her spinal canal such that the end actually reached into her cranial cavity.

Ms. Pogue subsequently consulted with another physician who agreed that the tip of the catheter was too high in the spinal canal and recommended the insertion of a new catheter at a different location in the spine. The physician concluded that actual removal of the catheter could cause life-threatening complications and so instead recommended that the catheter be disconnected from the pain pump but not removed, and that a replacement catheter be inserted lower in the canal. Following this advice, Ms. Pogue underwent surgery late in 2003. Since that time, her symptoms of being “fuzzy-headed” and randomly falling asleep have resolved, and her pain relief has improved.

Appellants filed the instant medical malpractice complaint against Dr. Goodman and his practice on August 6, 2004, nearly three years after Dr. Goodman performed the surgery at issue, but less than a year after the test revealed that the catheter had extended into her cranial cavity. In her complaint, Ms. Pogue alleges that Dr. Goodman negligently placed a “foreign object” into her spine and cranial cavity. She also alleges that he then fraudulently concealed the alleged negligent placement of the catheter by intentionally withholding from her information that the catheter had been misplaced. Mr. Pogue asserted a claim for loss of consortium.

The trial court granted appellees’ motion for summary judgment after finding that the relevant statute of limitation had expired. Appellants contend the trial court erred in granting appellees’ motion for two reasons. We will address each in turn.

1. Appellants first argue that the catheter constituted a foreign object as contemplated by OCGA § 9-3-72 and that the statute of limitation therefore did not expire until one year following the date of appellants’ discovery of the foreign object. 1

Generally, a medical malpractice action must be brought within two years of the date on which the injury arising from a negligent act occurred. OCGA§ 9-3-71 (a). However, OCGA§ 9-3-72 sets forth the following exception to the two-year limitation:

The [two-year statute of limitation for medical malpractice actions] shall not apply where a foreign object has been left in a patient’s body, but in such a case an action shall be *388 brought within one year after the negligent or wrongful act or omission is discovered. For the purposes of this Code section, the term “foreign object” shall not include a chemical compound, fixation device, or prosthetic aid or device.

We have interpreted the term “foreign object” to include only those objects that are inadvertently left within a patient’s body. See Shannon v. Thornton, 155 Ga. App. 670 (272 SE2d 535) (1980). Where “an object is purposely placed in a body[,] it cannot be said to have been ‘left,’ which, in the context of the statute, connotes a non-purposeful act.” (Punctuation omitted.) Id. See also Ringewald v. Crawford W. Long Mem. Hosp., 258 Ga. 302, 304 (2) (368 SE2d 490) (1988) (recognizing that a bulldog clamp left in a patient’s body constitutes a “foreign object” under OCGA § 9-3-72 because the physician had not intended to leave it in the patient’s body following the surgical procedure), overruled on other grounds, Spivey v. Whiddon, 260 Ga. 502 (397 SE2d 117) (1990).

Here, the undisputed evidence showed that Dr. Goodman intentionally placed the catheter in Ms. Pogue’s body for the purpose of relieving her pain. It cannot be said that the catheter in this case is a “foreign object” inadvertently “left” in Ms. Pogue’s body. Compare Ivey v. Scoggins, 163 Ga. App.

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Bluebook (online)
638 S.E.2d 824, 282 Ga. App. 385, 2006 Fulton County D. Rep. 3476, 2006 Ga. App. LEXIS 1396, Counsel Stack Legal Research, https://law.counselstack.com/opinion/pogue-v-goodman-gactapp-2006.