James R. Crowley
Iryna Barvi
Jackson W. Kiser- 1Department of Molecular Imaging, Carilion Clinic, Roanoke, VA, United States
- 2Lucerno Dynamics, LLC, Cary, NC, United States
Introduction: In 2016, our center adopted technology to routinely monitor 18F-FDG radiopharmaceutical administrations. Within six months of following basic quality improvement methodology, our technologists reduced extravasation rates from 13.3% to 2.9% (p < 0.0001). These same technologists administer other radiopharmaceuticals (without monitoring technology) for general nuclear medicine procedures in a separate facility at the clinic. Our hypothesis was that they would apply 18F-FDG lessons-learned to 99mTc-MDP administrations and that 99mTc-MDP manual injection extravasation rate would be consistent with the ongoing 18F-FDG manual injection extravasation rate (3.4%). We tested our hypothesis by following the same quality improvement methodology and added monitoring equipment to measure extravasation rates for 99mTc-MDP administrations.
Results: 816 99mTc-MDP administrations were monitored during 16-month period (four 4-month periods: A, B, C, D). Period A (first four months of active monitoring) extravasation rate was not statistically different from the Measure Phase extravasation rate of the previously completed PET/CT QI Project: 12.75% compared to 13.3% (p-0.7925). Period A extravasation rate was statistically different from Period C (months 9–12) extravasation rate and Period D (months 13–16) extravasation rate: 12.75% compared to 2.94% and to 3.43% (p < 0.0001). During Period C and D technologists achieved extravasation rates comparable to the longstanding manual 18F-FDG injection extravasation rate (3.4%).
Conclusion: Our initial hypothesis, that awareness of a problem and the steps need to correct it would result in process improvement, was not accurate. While those factors are important, they are not sufficient. Our findings suggest that active monitoring and the associated display of results are critical to quality improvement efforts to reduce and sustain radiopharmaceutical extravasation rates.
Introduction
Proper administration of a diagnostic radiopharmaceutical is essential for nuclear medicine image quality and quantification (1–8). Extravasation, an incomplete delivery of a radiopharmaceutical into the venous system, can compromise imaging, the patient's ensuing care, and sometimes lead to unnecessary additional radiation dose for repeat imaging studies. In addition, large extravasations can pose radiation harm to patients (9).
Studies suggest that an average of 15% (2 to 23%) of radiopharmaceutical administrations may result in an extravasation (5, 6, 10–14), but currently there is no routine quality control to ensure complete delivery of the radiopharmaceutical into the patient's circulation. However, with adequate training and ongoing injection quality monitoring, technologists are capable of improving injection quality significantly (15) and sustaining the results by implementing ongoing monitoring (16).
In 2016, our center participated in a multicenter 18F-FDG radiopharmaceutical administration QI Project, using Define, Measure, Analyze, Improve, Control methodology (15). The goal of the Project was to monitor injection quality, use analysis of factors that contribute to extravasations to guide improvements, remeasure rates in similar number of patients, and evaluate sustainability of interventions.
A quality improvement plan (QIP) was created on the basis of the analysis of contributing factors and in discussion with each technologist participating in the study. The QIP included three components: addition of an auto-injector to provide consistent infusion and flush parameters across injections, adjustment of uptake room setup to allow for improved access to left and right arms of the patient, and peer-led refresher training for venous access and injection technique. Following the QIP the technologists reduced the extravasation rates from 13.3% (Measure Phase) to 2.9% (Control Phase) (16). The 2.9% was a combination of auto injections extravasation rate (0.6%) and manual injection extravasation rate (7.1%). Ongoing monitoring ensured continued sustainability of results and further reduced manual injection extravasation rate to 3.4%.
At our clinic, general nuclear medicine procedures were performed in a different facility than PET/CT procedures, but the technologists who performed 99mTc-MDP administrations were also the same ones who performed 18F-FDG administrations. These technologists were aware of the steps required to reduce 18F-FDG administration extravasations. As a result, we hypothesized that they would apply 18F-FDG quality improvement lessons-learned to 99mTc-MDP administrations, and the resulting 99mTc-MDP administration manual injection extravasation rate would not be statistically different from the ongoing manual injection extravasation rate (3.4%) in 18F-FDG administrations.
We tested our hypothesis by adding monitoring equipment 30 months after completing the PET/CT administration quality plan, and following quality improvement methodology, measured a baseline extravasation rate for 99mTc-MDP administrations. Our findings suggest a new hypothesis: active monitoring of radiopharmaceutical administrations is critical to ensuring radiopharmaceutical administration quality.
Materials and methods
The Institutional Review Board of Carilion has determined that quality improvement efforts for 18F-FDG do not meet the definition of research as defined by the federal government in 45 CFR 46.102(d) and therefore, no patient consent was required. No protected health information was collected or transmitted. Every patient undergoing routine 99mTc-MDP bone scans was eligible to be included in the QI methodology. Patients followed standard clinical preparations for SPECT/CT imaging and were not exposed to additional radiation during this Project.
For 30 months after completion of the 18F-FDG quality improvement project we did not actively monitor the quality of 99mTc-MDP administrations. We then introduced a Lara® System (Lucerno Dynamics, Cary, NC) designed for capturing 99mTC emissions to help clinicians determine the quality of MDP administrations. The Lara® System is comprised of gamma scintillating sensors, adhesive pads, a reader, and software (Figure 1). After technologists gain venous access, they place the sensors on the injection arm and in a mirrored location on the other arm. The sensors identify the presence of excess radiopharmaceutical near the injection site and are connected to a reader that provides real-time display of activity in each arm. The reader also stores data and later transmits the recorded scan to a server for processing of time-activity curves (TACs).
Figure 1. The Lara System consists of 2 scintillating sensors, 2 adhesive pads, reader, docking station and software. Sensors are placed on injection and reference arm of the patient. Real-time counts are visible on reader's display.
Bone SPECT images were acquired with a Siemens Intevo Bold (Siemens Medical Solutions USA, Inc.) after standard injected activity of 25mCi 99mTc-MDP using a LEHR collimator and matrix size of 256 × 256 with a zoom of 1. SPECT data were acquired using 30 views in a noncircular (body contour) orbit with an acquisition time of approximately 20 s per view. For CT Acquisition, data were acquired using 130 kVp with CareDose 4D and pitch of 1.5 and detector settings of 16 × 1.2 mm with 3 mm slice thickness.
Statistical analysis
Statistical analysis was performed using the JMP 16.0 statistical software package (SAS). Unadjusted extravasation rates were calculated by dividing the number of extravasations by the number of injections. The Fisher's Exact test and Two Sample Test were used to compare increase or decrease in extravasation rates in groups before and during active monitoring. All statistical tests were 2-sided, and a threshold P value of less than 0.05 was considered statistically significant for rejection of the null hypothesis. Chi-square test was used to identify contributing factors in each period as well as to identify whether the difference in extravasation rates among those factors is statistically significant.
Results
Data were collected on 816 administrations during 16-month period and the extravasation rate was found to be 7.84%. A closer examination of the 16-month (four 4-month periods: A, B, C, D) and potential contributing factors revealed that a significant reduction in extravasation rate had occurred over these periods (Figure 2).
Figure 2. Extravasation rate reduction during four periods.
Period A (first four months of active monitoring) extravasation rate was not statistically different from the Measure Phase extravasation rate of the previously completed PET/CT QI Project: 12.75% compared to 13.3% (p-0.7925). Periods C (months 9–12) and D (months 13–16) extravasation rates were statistically lower than period A extravasation rate: 2.94% and 3.43% (p < 0.0001) compared with 12.75%. After analyzing contributing factors and implementing improvements, technologists achieved extravasation rates during Period C and D comparable to the longstanding manual 18F-FDG injection extravasation rate (3.4%).
Our contributing factors analysis suggests that during Period A, injection site location, venous access technique, and needle size, were associated with higher extravasation rates (Table 1). Further analyses suggest that when technologists stopped using the venous access technique of straight sticks (Table 2) and 23-gauge needles (Table 3), those factors were no longer associated with extravasation rates in Period D.
Table 1. Period A contributing factors.
Table 2. Straight stick extravasation rate compared to IV access technique extravasation rate.
Table 3. 23-Gauge needle extravasation rate compared to other needle gauge extravasation rates.
Discussion
Our hypothesis that problem awareness and solution availability from the previously completed quality improvement project would result in radiopharmaceutical administration process improvement was not accurate. While those factors are important, they are not sufficient. At our center, active monitoring and the associated display of results have proven to be critical to quality improvement efforts to reduce and sustain radiopharmaceutical extravasation rates. Active monitoring provides information necessary to determine contributing factors and when combined with active management review of displayed results, leads to improved administration quality. Our findings related to active monitoring are also supported by another center's quality improvement results1.
While ongoing active monitoring may be necessary for sustained quality administrations, it has many other implications.
Regulatory implications
In 2020 members of nuclear medicine community had an opportunity to share their position on diagnostic extravasations with the Nuclear Regulatory Commission (NRC). The NRC had requested public comments on a petition to eliminate an internal NRC policy that exempts extravasations from medical event reporting, even if the extravasation's absorbed tissue dose exceeded the reporting limit. As part of the request for public comments, the NRC asked: “Do you expect that monitoring for extravasation and reviewing the results would improve radiopharmaceutical administration techniques at medical use licensee facilities?” The leaders of the Society of Nuclear Medicine and Molecular Imaging (SNMMI), the organization that provides guidelines and standards for molecular imaging and nuclear medicine practice, stated that regular in-service education of those individuals who administer radiopharmaceuticals was important, but that “monitoring is not expected to improve administration techniques”2. Our findings and the well-documented “observer effect” experienced by our technologists suggest the opposite: monitoring will improve administration techniques.
Quality improvement implications
Measurement and identification of contributing factors are critically important for process improvement. Nuclear medicine extravasation rates have been difficult to measure without active monitoring. These measurement difficulties are related to a few factors. When extravasated, the small injection volumes of non-vesicant radiopharmaceuticals do not cause immediate, visible changes to the overlying skin near the injection site, nor immediate pain to patients. Additionally, injection sites are routinely outside of the standard imaging field of view for non-MDP injections (10). When diagnostic extravasations go undetected, and centers do not understand contributing factors, administration quality is difficult to improve. Active monitoring enables measurement and provides public feedback specific to technologist/technologist teams based on analyses of contributing factors, leading to process improvement efforts.
Dosimetric implications
Routine diagnostic procedures, including bone scans, are often viewed as low risk to patients. However, recent findings show that large extravasations of diagnostic radiopharmaceuticals can result in high doses to the tissue leading to adverse tissue reactions (9, 17). In such cases timely measurements of radioactivity can protect both patients and institutions, assisting in determining the need for repeat imaging and patient follow-up. In order to assess absorbed dose to tissue, the following factors are important: initially extravasated activity, emission types and energies, the mass of affected tissue, and the rate of biological clearance (9). Active monitoring promptly identifies extravasations that require dosimetry. It also helps to determine biological clearance and initially extravasated activity (9). Active monitoring can reveal patient- or procedure-specific insights. For example, due to the chemical properties of 99mTc-MDP, biological clearance can be limited. Additionally, extravasations of 99mTc-MDP, which is commonly injected using a straight stick with no saline flush, can result in a small volume of highly concentrated radiopharmaceutical.
Precision medicine implications
Precision medicine is becoming more important in radiology and nuclear medicine. Variability in clinical interpretation of images limits progress toward precision medicine. Extracting reproducible, quantitative standardized uptake value (SUV) results from scans is important in reducing variability and becoming an expected performance measure (18). Obtaining accurate SUV measures requires attention to all potential sources of variance. Extravasation can be a major source of variance. Active monitoring of injection quality can reduce this variance.
Theranostic implications
The use of radiotherapy is growing worldwide. These therapies typically require administrations of high activity alpha- and beta-emitting energies. Often times these therapies use isotopes with longer half-lives which increase their effectiveness. Many radiotherapeutic procedures do not include imaging until the following day or days. As a result, an extravasation of administered activity can go undetected and result in a high absorbed dose to tissue (19, 20). Active monitoring of the radiotherapeutic administration raises technologist awareness and allows immediate application of mitigation strategies to minimize absorbed dose to tissue.
Conclusions
Our initial hypothesis that awareness of a problem and the steps needed to correct would result in process improvement was incorrect. In our center, technologists trained in QI methodology had not applied lessons-learned from their 18F-FDG PET/CT QI Project to 99mTc-MDP administrations. However, by requiring active monitoring and displaying results, the trained technologists determined contributing factors and reduced extravasation rates significantly. These findings are consistent with our previous experience in PET/CT QI findings from another center, and the well-known observer effect phenomenon. These findings also suggest that centers that want to improve their radiopharmaceutical extravasation rates can benefit by implementing active monitoring.
Data availability statement
The original contributions presented in the study are included in the article/Supplementary Material, further inquiries can be directed to the corresponding author.
Ethics statement
The studies involving human participants were reviewed and approved by Carilion Clinic Institutional Review Board. Written informed consent from the patients/participants OR patients/participants legal guardian/next of kin was not required to participate in this study in accordance with the national legislation and the institutional requirements.
Author contributions
JRC contributed to data collection, interpretation, and preparation of the manuscript. IB contributed to data analysis and preparation of the manuscript. JWK contributed by obtaining, analyzing, interpreting patient data, and preparation of the manuscript. All authors contributed to the article and approved the submitted version.
Conflict of interest
JRC and JWK report non-financial support from Lucerno Dynamics during QI Project. IB is employee of Lucerno Dynamics, the manufacturer of the Lara System described in this manuscript. No other potential conflicts of interest relevant to this article exist.
Publisher's note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Footnotes
1Allison Fulp, Shane Masters, Anita Thomas, Jean-Luc Urbain, Jonathan Richardson, Paige Bennett. Improving the quality of PET radiopharmaceutical injections: Our lessons learned. Wake Forest School of Medicine at SNMMI Annual Meeting. Available at: https://lucerno.com/wp-content/uploads/2023/02/WFU_Poster.pdf
2Available online at: https://www.regulations.gov/comment/NRC-2020-0141-0428.
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Keywords: extravasations, 18F-FDG, 99mTc-MDP, quality improvement, infiltrations
Citation: Crowley JR, Barvi I and Kiser JW (2023) Active monitoring improves radiopharmaceutical administration quality. Front. Nucl. Med. 3:1126029. doi: 10.3389/fnume.2023.1126029
Received: 17 December 2022; Accepted: 16 February 2023;
Published: 7 March 2023.
Edited by:
David Townsend, National University of Singapore, SingaporeReviewed by:
Nikolaos Papathanasiou, General University Hospital of Patras, GreeceYoichi Shimizu, Kyoto University, Japan
© 2023 Crowley, Barvi and Kiser. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Jackson W. Kiser andraXNlckBjYXJpbGlvbmNsaW5pYy5vcmc=
Specialty Section: This article was submitted to Radiopharmacy and Radiochemistry, a section of the journal Frontiers in Nuclear Medicine