Chavez v. Parkview Episcopal Medical Center

32 P.3d 609, 2001 Colo. J. C.A.R. 3250, 2001 Colo. App. LEXIS 996, 2001 WL 693896
CourtColorado Court of Appeals
DecidedJune 21, 2001
Docket00CA739
StatusPublished
Cited by5 cases

This text of 32 P.3d 609 (Chavez v. Parkview Episcopal Medical Center) is published on Counsel Stack Legal Research, covering Colorado Court of Appeals primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Chavez v. Parkview Episcopal Medical Center, 32 P.3d 609, 2001 Colo. J. C.A.R. 3250, 2001 Colo. App. LEXIS 996, 2001 WL 693896 (Colo. Ct. App. 2001).

Opinion

Opinion by

Chief Judge HUME.

Defendant, Parkview Episcopal Medical Center (Parkview), appeals the judgment entered on a jury verdict in favor of plaintiff, Elsie Bernice Chavez, on her negligence claim against Parkview. We affirm.

Plaintiff received an over-infusion of Demerol, a narcotic, following shoulder surgery at Parkview in 1995. The over-infusion occurred when the Demerol escaped from the syringe in a Patient Controlled Analgesia (PCA) pump, an apparatus which permits the patient to self-administer intravenous pain medication. As a result of this event, plaintiff, a licensed practical nurse, suffered mild global brain damage and is unable to continue in her occupation or in her training to become a registered nurse.

Baxter Healthcare Corporation (Baxter) manufactured both the PCA pump and the plastic tubing extension set used in the incident. Although Baxter produced several models of extension sets that incorporated anti-siphon valves, the model Parkview purchased did not possess that feature.

Plaintiff sued both Parkview and Baxter, but entered into a settlement agreement with Baxter. Parkview then designated Baxter as a nonparty at fault. Parkview also later attempted to designate the syringe manufacturer, Becton Dickinson (B-D), as a nonparty *611 at fault, but the court denied the motion as untimely and lacking merit.

At trial, plaintiff proceeded on the theories that the Parkview nurse incorrectly loaded the syringe and that Parkview negligently failed to utilize an extension set with an anti-siphon valve. The jury found for plaintiff, awarding past and future noneconomic damages totaling $325,000 and past and future economic damages totaling $475,000. The jury apportioned fifty-five percent fault to Baxter and forty-five percent fault to Park-view, resulting in the judgment against Park-view for the principal amount of $360,000 plus prejudgment interest and costs.

I.

Parkview argues that the trial court erred by denying its request to designate B-D as a nonparty at fault and also by granting plaintiff's motion in limine to exclude any evidence that the over-infusion was caused by a defective syringe. We perceive no error.

Parkview concedes that evidentiary rulings are reviewed on an abuse of discretion standard and are reversible only if they are manifestly arbitrary, unreasonable, or unfair. Hock v. New York Life Ins. Co., 876 P.2d 1242 (Colo.1994).

A.

Section 18-21-111.5(8)(a), C.R.98.2000, allows evidence of nonparty fault to be considered, providing that the following requirements set forth in § 18-21-111.5(8)(b), C.R.S.2000, are met.

Negligence or fault of a nonparty may be considered if the claimant entered into a settlement agreement with the nonparty or if the defending party gives notice that a nonparty was wholly or partially at fault within ninety days following commencement of the action unless the court determines that a longer period is necessary. The notice shall be given by filing a pleading in the action designating such nonparty and setting forth such nonparty's name and last-known address, or the best identification of such nonparty which is possible under the circumstances, together with a brief statement of the basis for believing such nonparty to be at fault. Designation of a nonparty shall be subject to the provisions of section 18-17-102.

Here, the trial court determined that Parkview was untimely in attempting to designate B-D as a nonparty some seven months after the case was initiated and that it also failed to provide a brief statement describing the basis for fault. In addition, the court found that the information concerning B-D's potential fault was previously available to Parkview and that Parkview had discarded the syringe following the incident. Although Parkview argues on appeal that plaintiff's changing theory of lability justified its late designation of B-D, the trial court found that plaintiffs amended complaint did not justify the late designation, because Parkview conceded that it contained no new allegations. Given these facts, we perceive no error in the court's determination.

B.

Nonetheless, Parkview contends that, even if the trial court properly denied its motion to designate B-D as a nonparty, the court erred by refusing to admit evidence that a failure of the syringe manufactured by B-D may have caused plaintiff's over-infusion. We do not agree.

We note initially that Parkview destroyed the syringe involved in this incident without inspecting it, but did inspect the same model syringe, which had been used in a later siphoning incident involving the same nurse, and found nothing wrong with it. Further, no Parkview expert stated that syringe failure was a probable cause of the siphoning. See CRE 702; Thirsk v. Ethicon, Inc., 687 P.2d 1315 (Colo.App.1983)(medical opinion is admissible if founded on reasonable medical probability). Thus, it does not appear that there was evidence of syringe failure.

Although Parkview relies upon Thirsk v. Ethicon for the proposition that a defendant may present evidence of other possible causes of the plaintiff's injury in order to counter the plaintiff's causation evidence, that case was decided before the General Assembly enacted § 18-21-111.5(8)(a). Nor *612 does Staley v. Bridgestone/Firestone, Inc., 106 F.3d 1504 (10th Cir.1997), persuade us otherwise, because there the Tenth Circuit merely approved the trial court's discretionary ruling allowing evidence that a nondesig-nated nonparty was the purported sole cause of the injury.

Here, even if evidence of syringe failure existed, plaintiff also alleged that Parkview was negligent in failing to use anti-siphon tubing, and Parkview actively sought apportionment of negligence or fault among itself, Baxter, and B-D. Furthermore, the record indicates that the trial court stated that it would allow Parkview to provide evidence of a sole cause other than its own negligence. Thus, Parkview was not entirely foreclosed from presenting evidence of other causes.

In Thompson v. Colorado & Eastern Railroad Co., 852 P.2d 1328, 1330 (Colo.App.1993), a division of this court held that

a court may not allow the finder of fact to consider the negligence or fault of a non-party unless such issue has been properly raised by the defendant in a pleading which complies with the requirements of § 18-21-111.5(8), C.R.S.. ...

Following that rule, and under these circumstances, we perceive no abuse of discretion in the court's decision to exclude the evidence.

IL.

Parkview also argues that the trial court erred in excluding evidence of a notice Baxter sent in January 2000 reporting siphoning incidents and directing that only anti-siphon extension sets be used with the PCA pump. Again, we perceive no reversible error.

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Bluebook (online)
32 P.3d 609, 2001 Colo. J. C.A.R. 3250, 2001 Colo. App. LEXIS 996, 2001 WL 693896, Counsel Stack Legal Research, https://law.counselstack.com/opinion/chavez-v-parkview-episcopal-medical-center-coloctapp-2001.