Crooks v. Keene

10 Mass. L. Rptr. 56
CourtMassachusetts Superior Court
DecidedMarch 26, 1999
DocketNo. 952323
StatusPublished

This text of 10 Mass. L. Rptr. 56 (Crooks v. Keene) is published on Counsel Stack Legal Research, covering Massachusetts Superior Court primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook
Crooks v. Keene, 10 Mass. L. Rptr. 56 (Mass. Ct. App. 1999).

Opinion

Kottmyer, J.

INTRODUCTION

Plaintiffs bring this action against defendants Drs. Maura Keene (“Keene”), Diane Amsterdam (“Amsterdam”), Walter Glaser, and Mary E. Annarella (“An-narella") for negligence in failing to diagnose and treat Anne Grenadier-Terault (“Grenadier-Terault”). Plaintiffs also assert claims against SmithKline Beecham Clinical Laboratories (“SmithKline”), Northeast Per-manete Medical Group, P.C., and Carlson Pathology Associates (“Carlson") based on vicarious liability. Defendants SmithKline and Carlson now move for summary judgment. For the following reasons, their motions for summary judgment are DENIED.

BACKGROUND

The facts, viewed in the light most favorable to plaintiffs, are as follows. On November 15, 1993, Amsterdam collected a Pap smear from Grenadier-Terault which he then sent to the SmithKline laboratory in Waltham, Massachusetts (“the Laboratory”) for interpretation. On December 1, 1993, a cytotechnologist employed by SmithKline who had reviewed the slide referred it to Annarella, a pathologist who was also the Medical Director of the Laboratory. Annarella incorrectly read the slide as being within normal limits. Plaintiffs allege Annarella negligently interpreted the slide and that SmithKline and Carlson are vicariously liable for her negligence.

• On September 1, 1993, Annarella and Carlson had executed an employment agreement (the “Employment Agreement”) wherein Carlson agreed to employ Annarella as a Senior Pathologist. The Employment Agreement provided that Annarella would serve as Medical Director of the Laboratory and provide [pathology] services at the Laboratory. The Employment Agreement further provided that Annarella would provide pathology and administrative services to Brockton Hospital. Carlson reserved the right to designate other locations at which Annarella would provide pathology services. The Employment Agreement provided that Annarella would perform all her duties under the supervision and direction of the President of Carlson Pathology, who was also a pathologist. In the Employment Agreement, Annarella agreed that she would not undertake additional professional obligations without consent of the President of Carlson Pathology. Carlson had the right to terminate An-narella for cause relating to patient care or if Carlson ceased to provide services to the Laboratory. The Employment Agreement expressly provided that An-narella would provide services under the agreement in accordance with SmithKline’s qualify assurance standards and its bylaws, rules and regulations, as well as all applicable regulations and laws.

Annarella divided her time between Brockton Hospital and the Laboratory which are not related entities. Annarella believed she was an employee of Carlson. Her superior at Carlson was Dr. Carlson, but she did [57]*57not consider Dr. Carlson her superior with respect to what she did at SmithKline. Carlson paid Annarella’s salary. Her salary did not depend upon the number of slides she reviewed at SmithKline. Carlson provided Annarella fringe benefits including vacation time, continuing education leave, sick leave, and holidays and procured professional liability insurance covering her. Carlson set charges, billed, and collected fees for services rendered by Annarella at the Laboratory and at Brockton Hospital.

In the Employment Agreement, Annarella agreed to provide services to SmithKline pursuant to any oral and written agreements between Carlson and Smith-Kline. Sometime before December 1993, when An-narella reviewed Grenadier-Terault’s slide, Carlson and SmithKline had orally agreed that Carlson would provide SmithKline pathology services and the services of a Medical Director. Carlson’s designation of a physician to serve as Medical Director and provide pathology services was subject to SmithKline’s approval. SmithKline did approve the selection of An-narella.

On March 1, 1994, Carlson and SmithKline executed a written agreement, which covered the same services (the “SmithKline-Carlson Agreement”). In the SmithKline-Carlson Agreement, Carlson agreed to provide a qualified pathologist to act as Medical Director of the Laboratory and to review slides. The Medical Director maintained quality control measures and assured that the Laboratory complied with all SmithKline’s policies and procedures, as well as all federal, state, and local laws, rules, and regulations. The Medical Director reviewed and inspected all tech-nics and testing performed in the laboratory.

As Medical Director, Annarella had an office at the Laboratory, SmithKline writing tablets with her name printed on them, and SmithKline business cards. Annarella’s name appeared on all Laboratory reports. SmithKline’s laboratory organization chart also listed Annarella as a pathologist. SmithKline required An-narella to follow and enforce policies and procedures contained in its cytopathology handbooks. SmithKline’s policies and procedures required a pathologist to review certain categories of slides. Grenadier-Terault’s slide fell within such a category because a cytotechnologist marked Anne Grenadier-Terault’s Pap smear as having squamous and endocervical cells. Annarella reviewed Grenadier-Terault’s slide in her capacity as pathologist. SmithKline billed and received payment from Grenadier-Terault (or her insurer) for Annarella’s review of Grenadier Terault’s pap smear.

Annarella spent approximately twenty hours per week at SmithKline. She spent the majority of her time interpreting slides. SmithKline provided all necessary laboratory equipment and supplies. Annarella reported her results in accordance with SmithKline’s reporting system. The system employed by Annarella to mark slides was the system used by SmithKline. She used SmithKline’s diagnostic form in reading slides and SmithKline’s standardized codes. Several times each day Annarella consulted with SmithKline’s cytology supervisor or senior technician about findings and, on occasion, consulted with Dr. Carlson about a particular slide.

Pursuant to Chapter 111D, §4 of the Massachusetts General Laws, SmithKline was required to have a clinical laboratory license to operate the Laboratory. On October 1, 1991, the Massachusetts Department of Public Health (the “Department”) granted SmithK-line a full clinical laboratory license effective as of February 28, 1992. Annarella practiced clinical pathology at the Laboratory under SmithKline’s clinical laboratory license.

The Massachusetts licensing scheme requires all clinical laboratories to appoint a clinical laboratory director. The director is responsible for the direction of the technical and scientific operation of the laboratory. G.L.c. 111D, §7.3 The regulations provide that “the owner and director shall, if different persons, be jointly and severally responsible for the operation of the laboratory in compliance with [regulatory and statutory requirements].” 105 CMR 180.041(E).

The regulations establish minimum standards of quality assurance all licensed clinical laboratories must follow. The laboratory must make its procedure manual readily available, at all times, in the work area of personnel examining specimens. The manuals must contain complete descriptions and instructions for all automated and manual test procedures including the analytical methods to be used, the control and calibration procedures, and the available literature references. Id. 180.255.

The regulations further require the laboratory to establish procedures for conducting screening tests.

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Bluebook (online)
10 Mass. L. Rptr. 56, Counsel Stack Legal Research, https://law.counselstack.com/opinion/crooks-v-keene-masssuperct-1999.