Hopkins v. Silber

785 A.2d 806, 141 Md. App. 319
CourtCourt of Special Appeals of Maryland
DecidedNovember 29, 2001
Docket1159, Sept. Term, 2000
StatusPublished
Cited by4 cases

This text of 785 A.2d 806 (Hopkins v. Silber) is published on Counsel Stack Legal Research, covering Court of Special Appeals of Maryland primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Hopkins v. Silber, 785 A.2d 806, 141 Md. App. 319 (Md. Ct. App. 2001).

Opinion

KRAUSER, Judge.

Appellant, Howard Hopkins, filed a complaint in the Circuit Court for Baltimore City, alleging that he had been the subject of two negligently performed penile implant surgeries: the first was performed by appellee, Stanley R. Silber, M.D., and the second by Horst K. Schirmer, M.D. A jury found both doctors negligent and awarded appellant $15,000 in past medical expenses and $20,000 in non-economic damages.

Although the jury rejected appellees’ defense of contributory negligence, it nonetheless found that appellant, by his post-surgery conduct, had negligently contributed to the injuries he sustained. This finding, appellant claims, unfairly depressed the amount of non-economic damages the jury awarded because, according to appellant, the issue of contributory negligence should not have been submitted to the jury in the first place. For that reason, among others, appellant now seeks a new trial solely on the question of non-economic damages. Because of a post-trial settlement of his claim against Dr. Schirmer, this appeal only involves appellant’s claim against Dr. Silber. In turn, Dr. Silber has filed a cross-appeal against appellant, claiming that the circuit court should have set aside *324 the verdict because the jury found contributory negligence, if only as to damages.

The specific issues presented by appellant 1 are:

I. Whether the circuit court erred in permitting the issue of contributory negligence to go to the jury.
II. Whether the circuit court erred in instructing the jury that appellant had a duty to reduce his injuries.
III. Whether the circuit court erred in instructing the jury on intervening superseding causes.
IV. Whether the circuit court erred in failing to grant appellant’s motion for a mistrial after appellee made a “golden rule” argument to the jury.

In his cross-appeal, appellee raises, as noted earlier, only one issue:

Whether the circuit court erred in failing to set aside the verdict and award of damages in favor of appellant because the jury found contributory negligence.

For the reasons that follow, we shall affirm the judgment of the circuit court.

FACTS

Appellant developed prostate cancer, requiring the surgical removal of his prostate gland and radiation treatment. As a result of the radiation treatment, appellant became impotent and consulted appellee, Stanley R. Silber, M.D. Appellee recommended at first a prescription drug, then a vacuum pump, and finally, penile injections. When these measures failed to cure the problem, appellee suggested penile implants, and appellant agreed.

On January 2, 1996, appellee surgically implanted two prostheses in appellant’s penis. After surgery, Dr. Silber instructed appellant to refrain from sex for “five or six weeks,” and to keep his penis in an upright position and in an erect *325 state until it healed from the surgery. He further instructed appellant to return periodically to appellee’s office for an examination to determine whether he could resume sex. As instructed, appellant returned to appellee’s office on January 11, January 19, and February 2 of 1996. But, in disregard of appellee’s instructions, appellant “tr[ied] to have sex” six different times before the recommended waiting period had expired.

Four weeks after surgery, appellant’s post-operative pain “had subsided somewhat,” leaving him with a “small amount of pain.” At his February 2 appointment with appellee, however, appellant informed appellee that he could not deflate his implants. They failed to function, according to appellant, as appellee had promised they would.

Unhappy with his penile implants, appellant canceled his sixth week appointment with appellee, scheduled for February 16. He thereupon made an appointment to see Horst Schirmer, M.D., later to be named appellee’s co-defendant. On February 23, 1996, appellant met with Dr. Schirmer. At that consultation, appellant informed Dr. Schirmer that two prostheses had been implanted in his penis and that he was unable to deflate them. He also complained that “the prosthesis on the right side was pressing on the skin just behind the penis glans, the bulb on the end of the penis.” It was, according to appellant, “quite painful.”

Dr. Schirmer examined appellant and found ischemia 2 on the right side of appellant’s penis. Dr. Schirmer informed appellant that the prosthesis on the right side of his penis was too long and that it was causing the ischemia by “putting too much pressure on the penis and starving the tissue in that area from getting blood.” There was a danger, Dr. Schirmer explained, that the implant would extrude through the tissue “out to the skin.” He therefore recommended that the implant be removed. Until that could be done, Dr. Schirmer *326 suggested relieving “some of the pressure off of the right device by sticking a needle in the cylinder on the right side and pulling fluid out.” Appellant agreed.

When appellant returned to his office, Dr. Schirmer performed that procedure but to no avail; appellant’s penis remained erect and, according to appellant, “painful and swollen.” Dr. Schirmer then advised appellant that the implants should be removed and replaced with, what he described as “malleable rods.” The implants were removed, and the rods implanted in May, 1996.

After surgery, however, the implant on the right side of appellant’s penis broke through the right corporal body 3 inside his penis, requiring removal of the implant. The removal was performed by Harold J. Alfert, M.D., at Johns Hopkins Hospital in November of 1996. After removing the device, Dr. Alfert showed it to appellant. It was not a malleable rod, but, according to appellant, a “rubbery device,” known as a “sizer,” and, on the side of that device, were imprinted the words “not for implant.” 4 Dr. Alfert did not remove the malleable rod that Schirmer had implanted on the left side of appellant’s penis.

Following the removal of the sizer, Dr. Alfert' referred appellant to Arthur Burnett, M.D. Dr. Burnett met with appellant and discussed with him the risks of undergoing another penile prosthesis surgery. The risks, according to Dr. Burnett, included “device infection, erosion, malfunction, [and the] need for replacement.” Dr. Burnett also informed appellant that “repeated penial prosthesis surgeries can be more *327 problematic in terms of risks.” “The concern,” he explained, “is that some of the penial tissues with scarring and perhaps poor circulation [may not] hold the device.... ” And he stated that “the risk of device failure for repeated surgeries are higher.”

A pre-surgical consultation with Dr. Burnett was scheduled as appellant appeared “inclined to proceed ahead with penial prosthesis surgery.” At that consultation, Dr.

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Bluebook (online)
785 A.2d 806, 141 Md. App. 319, Counsel Stack Legal Research, https://law.counselstack.com/opinion/hopkins-v-silber-mdctspecapp-2001.