Herman Davis and wife, Darnell Davis v. Paul A. Hatcher, Sr., M.D.

CourtCourt of Appeals of Tennessee
DecidedSeptember 9, 1996
Docket03A01-9601-CV-00016
StatusPublished

This text of Herman Davis and wife, Darnell Davis v. Paul A. Hatcher, Sr., M.D. (Herman Davis and wife, Darnell Davis v. Paul A. Hatcher, Sr., M.D.) is published on Counsel Stack Legal Research, covering Court of Appeals of Tennessee primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Herman Davis and wife, Darnell Davis v. Paul A. Hatcher, Sr., M.D., (Tenn. Ct. App. 1996).

Opinion

IN THE COURT OF APPEALS OF TENNESSEE WESTERN SECTION AT KNOXVILLE

FILED -----------------------------------------------------------------------------

September 9, 1996 HERMAN DAVIS and wife, ) DARNELL DAVIS, ) KNOX CIRCUIT ) Cecil Crowson, Jr. Appellate C ourt Clerk Plaintiffs/Appellants ) ) No. 03A01-9601-CV-00016 v. ) ) PAUL A. HATCHER, SR., M.D., ) REVERSED AND REMANDED ) Defendant/Appellee )

Laurence R. Dry, Oak Ridge, For the Appellants

T. Warren Butler, Knoxville, For the Appellees

OPINION

INMAN, Senior Judge

This malpractice action was dismissed on motion for summary judgment. It

arose from a routine prostate resection which went awry, resulting in adverse

consequences to the plaintiff. A device referred to as a resectoscope manufactured

by the Circon ACMI Ohio Manufacturing Company,1 malfunctioned while being used

by and under the control of the defendant, Dr. Paul Hatcher [hereafter, the

“defendant”]. It is not disputed that a portion of the penis of the plaintiff, Herman

Davis [hereafter, “plaintiff”], was either chemically, thermally or electrically burned

away, with disastrous results unnecessary here to be recounted.

The defendant was allegedly negligent in the care and treatment of his

contractual patient, the plaintiff, in these particulars:

1. Failing to test and inspect the resectoscope;

1 No longer in the case. 2. Failing to properly utilize the resectoscope;

3. Failing to discover that the resectoscope was improperly functioning;

4. Failing to discover the injury timely.

The defendant admitted that “Herman Davis sustained some type [of] injury

at or about the time of the procedure, but how it occurred is unknown to Dr.

Hatcher.” He denied that the injury was the proximate result of any negligent act or

omission on his part and specifically denied that he failed to test or inspect the

resectoscope or that he negligently failed to discover a malfunction.

The defendant demanded “strict proof that said injuries and disabilities did

not preexist the procedure complained of.”

He averred that he did nothing in contravention of acceptable professional

practice in the Knoxville community and alternatively “relies on the comparative

negligence of the manufacturer of the resectoscope equipment.”

On December 9, 1993, the defendant moved for summary judgment, which

he supported by the affidavit of Dr. David F. Paulson, a professor of urology at Duke

University, who testified that a “[c]areful review of the operative record does not give

any indication that the procedure was conducted outside the standards of practice.”

He further opined that “the care and treatment . . . was proper and well within the

standard of care required. The complications that occurred were not proximately

caused by any negligent act, omission or departure from the applicable standards of

care on the part of Dr. Hatcher . . . . No abnormality in the conduct of the procedure

occurred through the action of Dr. Hatcher.”

Significantly, Dr. Paulson did not address the cause of the plaintiff’s injury.

He testified, quite briefly,“that “a transurethral incision of the prostate was

conducted. Following this a midline portion of residual prostatic tissue was resected

with the electrocautery loop.”

Also supportive of the motion was the affidavit of the defendant, who testified

that “[t]wo days after the surgery, the plaintiff was found to have an unexpected

-2- condition of the central glans and meatus which appeared as a redness and

induration . . . . [which] gave the appearance of being caused by a burn in the area

where the resectoscope was in contact with the penis during the surgical

procedure.” (Emphasis added.) He testified that “more likely than not [the burn

was] caused by a defective condition of the resectoscope which was unknown and

unforeseeable by me” and that he was not negligent in any respect.

While the motion was pending, the defendant amended his answer by

alleging that the manufacturer of the resectoscope was negligent in failing to warn

him that (1) cutting loops and knives should be used only one time; (2) caustic

chemicals should be thoroughly removed from the resectoscope; (3) cutting loops

and knives were not of uniform length, which could result in “electrically charged

uninsulated parts of same to electrically charge parts of the equipment coming in

contact with patients.” The amended answer accused the manufacturer of

negligently failing to warn the University of Tennessee Memorial Hospital [where the

procedure was performed] of the importance of uniform lengths of cutting loops and

knives and the necessity for proper cleaning of the resectoscope. The defendant

also charged the hospital with negligence in (1) failing to furnish him proper

equipment, properly maintained; (2) failing to advise him of the manufacturer’s

warnings re: the safe use and care of the resectoscope; (3) furnishing him with “a

cutting knife of improper length which resulted in electrically charging portions of the

resectoscope coming in contact with the patient.”

The plaintiff responded to the motion for summary judgment by memorandum

filed March 7, 1995, exhibiting the affidavits of Dr. William Campbell, Dr. Dennis

Doblar and Dr. Cecil Morgan, Jr., all of whom had previously testified by deposition.

Dr. Campbell, a biomedical engineer, designs biomedical equipment and

teaches the use of powered biomedical equipment. He testified that he reviewed

photographs of the burn suffered by the plaintiff, all medical data, various

depositions, including that of the defendant, and expressed his opinion that the burn

-3- injury to the plaintiff was caused by electrical power from the resectoscope which

“would not otherwise have occurred had the instrument been used in accordance

with recognized biomedical engineering principles, and in accordance with

manufacturer’s recommendations.”

Dr. Doblar is a professor of anesthesiology and biomedical engineering at the

University of Alabama. He testified that he had reviewed photographs of the burn

suffered by the plaintiff, all medical data, hospital records and various depositions,

including the deposition of the defendant. He agreed with the testimony of Dr.

Campbell respecting the cause of the injury to the plaintiff and opined that the

“current escaped the instrument through a reused knife or loop or through operator

error - through the application of power while the resectoscope was on its way out of

or into the patient . . . . under the control of Dr. Hatcher.” He opined that the injury

was below the acceptable professional practice in Knoxville and that the defendant

“acted with less than or failed to act with ordinary and reasonable care in

accordance with such standard.”

Dr. Morgan, a urologist practicing in Alabama, testified that he had reviewed

all pertinent data appertaining to the injury suffered by the plaintiff and that he was

familiar with the appropriate standard of care. He further testified, “More likely than

not, Dr. Hatcher caused the burn injury . . . by using the resectoscope while it was

improperly or defectively configured, in which case he should have been aware of

that fact; or Dr. Hatcher used the instrument inappropriately.”

On the same date that the plaintiff filed his response to the motion for

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