Terrence J. Mullan, Apps. v. North Cascade Cardiology, Pllc, Res.

CourtCourt of Appeals of Washington
DecidedMay 28, 2013
Docket68513-9
StatusUnpublished

This text of Terrence J. Mullan, Apps. v. North Cascade Cardiology, Pllc, Res. (Terrence J. Mullan, Apps. v. North Cascade Cardiology, Pllc, Res.) is published on Counsel Stack Legal Research, covering Court of Appeals of Washington primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Terrence J. Mullan, Apps. v. North Cascade Cardiology, Pllc, Res., (Wash. Ct. App. 2013).

Opinion

IN THE COURT OF APPEALS FOR THE STATE OF WASHINGTON

TERRENCE J. MULLAN, individually, No. 68513-9-1 and as Personal Representative of the Estate of DANA MULLAN, and for DIVISION ONE c —-u

MATTHEW D. MULLAN, a minor, MICHAEL P. MULLAN, a minor, and o

CHRISTOPHER R. MULLAN, a minor, ro CO

Appellants, T* OCT-'

\

UNPUBLISHED OPINION NORTH CASCADE CARDIOLOGY, PLLC, a Washington professional limited liability company; ANDREW and JANE DOE COLETTI, a marital community; and ST. JUDE MEDICAL, INC., a Minnesota corporation,

Respondents. FILED: May 28. 2013

Spearman, A.C.J. — The Estate of Dana Mullan appeals the trial court's

dismissal of its claims against Ms. Mullan's health care providers and the company

that manufactured her pacemaker. Finding no questions of fact exist regarding

proximate cause, we affirm the trial court.

FACTS

Dana Mullan was diagnosed with a congenital heart condition in November

1989. In May 1994, Ms. Mullan underwent surgery and had a pacemaker implanted. The pacemaker was manufactured by St. Jude Medical, Inc. The user manual for the No. 68513-9-1/2

pacemaker includes a discussion of battery longevity and recommended replacement

time. The recommended replacement time for Ms. Mullan's pacemaker, which is

shown on the device as "Elective Replacement Indicator" (ERI), occurs when the

available battery voltage decreases from a maximum capacity of 2.8 volts to

approximately 2.4 volts. By contrast the "end of life" (EOL) for the battery is defined

as "the point in time when the device's pulse amplitude reduces to approximately 50

percent of the programmed value. EOL occurs when the available battery voltage has

decreased to 2.2 volts." Clerk's Papers (CP) at 83.

On September 11, 2008, Ms. Mullan's doctor, Andrew Coletti of North

Cascade Cardiology, examined Ms. Mullan after a registered nurse, Maria Healey,

had "interrogated"1 Mullan's pacemaker. Healey faxed the information she obtained

from the interrogation to a St. Jude representative who opined that, based on the

data provided by Healey, the pacemaker had approximately five to six months before

it needed to be replaced. Healey relayed this information to Ms. Mullan.

About one month later, on October 12, 2008, Ms. Mullan died. An autopsy

concluded that the cause of death was cardiac arrhythmia. Ms. Mullan's pacemaker

was "explanted," i.e. removed, during the autopsy and testing done at that time put

the battery voltage at 2.14V, or below the level indicating EOL. Thereafter, the

pacemaker was sent to St. Jude for further testing. St. Jude determined the

pacemaker was functioning normally and was not at the EOL stage. It explained that

Interrogating a pacemaker refers to wirelessly measuring readings from the pacemaker. No. 68513-9-1/3

because the initial testing was "performed outside of the body at a colder

temperature, [it was] not reflective of actual device performance at body

temperature." CP at 268. Ms. Mullan's Estate, asked St. Jude for the test results,

which St. Jude provided on August 17, 2009.

In July 2011, about three years after Mullan died, the Estate filed a complaint

for wrongful death against St. Jude, Coletti, Healey, and North Cascade Cardiology

(the healthcare defendants). St. Jude and the health care defendants moved for

summary judgment. The court granted both motions. The Estate appeals.

DISCUSSION

Standard of Review. In general, the moving party on summary judgment bears

the initial burden of showing the absence of an issue of material fact. Young v. Key

Pharm.. Inc., 112 Wn.2d 216, 225, 770 P.2d 182 (1989). Amoving defendant may

meet the initial burden by "'showing'—that is, pointing out to the [trial] court—that

there is an absence of evidence to support the nonmoving party's case." Young. 112

Wn.2d at 225 n.1, (quoting Celotex Corp. v. Catrett, 477 U.S. 317, 325, 91 L.Ed.2d

265, 106 S.Ct. 2548 (1986)). Where a plaintiffs response to the motion "'fails to make

a showing sufficient to establish the existence of an element essential to that party's

case, and on which that party will bear the burden of proof at trial,'" the trial court

should grant the motion. ]d. at 225 (quoting Celotex Corp.. 477 U.S. at 322.

This court reviews summary judgments de novo, Michael v. Mosouera-Lacv,

165 Wn.2d 595, 601, 200 P.3d 695 (2009), and must consider all facts submitted and No. 68513-9-1/4

all reasonable inferences from the facts in the light most favorable to the nonmoving

party. Yakima Fruit & Cold Storage Co. v. Central Heating & Plumbing Co.. 81 Wn.2d

528, 530, 503 P.2d 108 (1972) (citation omitted).

Dismissal of claim against St. Jude. The Estate alleged St. Jude was negligent

in that it: "failed to exercise ordinary care in providing current, accurate, and timely

technical assistance to Dana Mullan's health care providers with regard to the useful

safe life of the battery" for her pacemaker. CP at 4. Negligence requires proof of four

elements: (1) the existence of a duty to the person alleging negligence; (2) breach of

that duty; (3) resulting injury; and (4) proximate cause between the breach and the

injury. American Commerce Ins. Co. v. Enslev. 153 Wn. App. 31, 42, 220 P.3d 215

(2009) (citing Hutchinsv. 1001 Fourth Ave. Assocs., 116 Wn.2d 217, 220, 802 P.2d

1360 (1991)). Among other things, St. Jude argues there is no evidence that any of

its acts proximately caused Ms. Mullan's death. We agree.

St. Jude's motion to dismiss puts the Estate to its proof on the element of

proximate cause. In support of the motion to dismiss, St. Jude provided expert

testimony indicating that its pacemaker was functioning properly, and that the

pacemaker was not the cause of Ms. Mullan's death:

5. The analysis conclusion was: "ERI caused by a normal depletion of the battery. The implant duration was approximately 14.4 years." 6. Such a conclusion does not mean that the battery improperly depleted, or that the battery was completely depleted and not working. Just the contrary. The foregoing analysis shows that the battery was continuing to deplete as it continued to work and age. The analysis also concluded that the battery No. 68513-9-1/5

(and the entire device) was working normally and as it would be expected to work at this stage of its cycle.

7. The conclusions and findings regarding the battery longevity of this device are also well within the standards and parameters set forth in the User Manual for this device that has been approved by the FDA.

8. According to the User Manual, this device, depending on its programming and on the patient's physiology, could have lasted additional months properly providing therapy beyond the point of ERI prior to being fully depleted.

9.

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