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I n t e r n a t i o n a l C o n f e r e n c e o n

Nuclear Medicine &

Radiation Therapy

Journal of Medical Physics and Applied Sciences

ISSN: 2574-285X

O c t o b e r 0 1 - 0 2 , 2 0 1 8

S t o c k h o l m , S w e d e n

Nuclear Medicine & Radiation Therapy 2018

Page 30

Biography

Christopher J Palestro has pioneered the use of combined

labelled leukocyte/bone marrow imaging for diagnosing os-

teomyelitis. He has authored or co-authored more than 150

peer reviewed articles, nearly 100 book chapters and review

articles. He serves on the Editorial Boards of Radiology,

Journal

of Nuclear Medicine and Quarterly Journal of Nuclear Medicine

and

Molecular Imaging

. He is Co-chair of the Society of Nucle-

ar Medicine and Molecular Imaging’s Working Group for the

Tc-99m and In-111 Labeled Leukocyte Procedure Standards/

Guidelines and Chair of the Appropriate Use Criteria Commit-

tee for Inflammation and Infection. He is a Former Chair of the

American Board of Nuclear Medicine. In 2013, he received the

Presidential Distinguished Educator Award from the Society of

Nuclear Medicine andMolecular Imaging. In 2017, he was elect-

ed as Fellow of the Society of Nuclear Medicine and Molecular

Imaging, one of that organization’s most prestigious awards.

palestro@northwell.edu

Labelled leukocyte/bone marrow

imaging for diagnosing infection of

recently implanted lower extremity

arthroplasties

Christopher J Palestro

1

, C Love

2

, G G

Tronco

1

, K K Bhargava

1

and K J Nichols

1

1

Donald & Barbara Zucker School of Medicine, USA

2

Albert Einstein College of Medicine, USA

Christopher J Palestro et al., J. med phys & appl sci 2018, Volume: 3

DOI: 10.21767/2574-285X-C1-001

D

iagnosing lower extremity prosthetic joint infection during the first year after

implantation, when up to two thirds of these infections occur, is challenging.

Pain usually is present, fever is variable. Leucocytosis is a poor predictor of

infection. C-reactive protein remains elevated for up to three weeks. Erythrocyte

sedimentation rate can remain elevated for up to one year. Joint aspiration with

culture, the definitive preoperative diagnostic procedure, is specific, sensitivity is

variable. Plain radiographs lack sensitivity and specificity. Data on radionuclide

imagingduringtheearlypostoperativeperiodarelimited.Thebonescancanexclude

infection. It is a good rule out test, but cannot rule in infection.

67

Ga accumulates

in normally healing surgical incisions and in aseptic inflammation. With an overall

accuracy of 60%-80%, there is little role for this radiopharmaceutical in prosthetic

joint infection. Data about diagnosing prosthetic joint infection with

18

F-FDG in

the early post-operative period are scant; uptake of this radiopharmaceutical in a

variety of postoperative settings for variable time periods, however, is well known.

111

In labelled leukocytes do not accumulate in normally healing surgical wounds

and combined with bone marrow imaging is about 90% accurate for diagnosing

prosthetic joint infection. We reviewed combined labelled leukocyte/marrow

imaging performed on 40 lower extremity arthroplasties implanted within one year

before imaging, including 15 implanted within 3 months prior to imaging. Imaging

results were compared to final diagnoses, which were surgically, microbiologically

and histopathologically confirmed. 28/40 arthroplasties were infected including

10/15 imaged within three months after implantation. Sensitivity, specificity and

accuracy were 96%, 92%, 95% respectively for all 40 arthroplasties and 100%, 80%,

93% respectively for 15 arthroplasties imaged within 3 months after implantation.

Results are comparable to those reported for diagnosing prosthetic joint infection

in general and indicate that during the first year after implantation, when evolving

postoperative changes can confound diagnostic test results, labelled leukocyte/

marrow imaging accurately diagnoses lower extremity prosthetic joint infection.