ACE Report Cover
No radiographic or clinical benefit of patient specific instrumentation in TKA
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Language
Download Download Download
Download
Cite this Report Cite this Report Cite this Report
Cite
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favorites
Translate this  ACE Report Translate this  ACE Report Translate this  ACE Report
Language
Download Download Download
Download
Cite this Report Cite this Report Cite this Report
Cite
Add to Favorites Add to Favorites Add to Favorites Remove from Favorites Remove from Favorites Remove from Favorites
+ Favorites
ARTHROPLASTY
No radiographic or clinical benefit of patient specific instrumentation in TKA .
Verified
This report has been verified by one or more authors of the original publication.
High Impact
This study has been identified as potentially high impact. OE's AI-driven High Impact metric estimates the influence a paper is likely to have by integrating signals from both the journal in which it is published and the scientific content of the article itself. Developed using state-of-the-art natural language processing, the OE High Impact model more accurately predicts a study's future citation performance than journal impact factor alone. This enables earlier recognition of clinically meaningful research and helps readers focus on articles most likely to shape future practice.

OrthoEvidence Journal (OE Journal) - ACE Report

OE Journal. 2016;4(22):3 Acta Orthop. 2016 Aug;87(4):386-94

21 studies evaluating the use of patient-specific instrumentation in total knee arthroplasty were included in this meta-analysis and systematic review. Pooled analyses demonstrated no significant difference between patient-specific instrumentation systems and conventional instruments in the incidence of excessive malalignment (>3 degrees deviation) in hip-knee-ankle angle. Additionally, the incidence of femoral component outliers in the coronal, sagittal, and axial planes, and tibial component outliers in the sagittal plane did not significantly differ, while tibial component outliers in the coronal plane occurred significantly more often with patient-specific instrumentation. No significant differences were found in short-term (3-month) clinical outcome measures. Two analyses which did favour patient-specific instrumentation were a lower number of surgical trays required during the procedure and shorter length of stay.


Publication Funding Details +
Funding:
Not Reported
Conflicts:
None disclosed

Risk of Bias

9/10

Reporting Criteria

19/20

Fragility Index

N/A

Were the search methods used to find evidence (original research) on the primary question or questions stated?

Was the search for evidence reasonably comprehensive?

Were the criteria used for deciding which studies to include in the overview reported?

Was the bias in the selection of studies avoided?

Were the criteria used for assessing the validity of the included studies reported?

Was the validity of all of the studies referred to in the text assessed with use of appropriate criteria (either in selecting the studies for inclusion or in analyzing the studies that were cited)?

Were the methods used to combine the findings of the relevant studies (to reach a conclusion) reported?

Were the findings of the relevant studies combined appropriately relative to the primary question that the overview addresses?

Were the conclusions made by the author or authors supported by the data and or analysis reported in the overview?

How would you rate the scientific quality of this evidence?

Yes = 1

Uncertain = 0.5

Not Relevant = 0

No = 0

The Reporting Criteria Assessment evaluates the transparency with which authors report the methodological and trial characteristics of the trial within the publication. The assessment is divided into five categories which are presented below.

4/4

Introduction

4/4

Accessing Data

4/4

Analysing Data

4/4

Results

3/4

Discussion

Detsky AS, Naylor CD, O'Rourke K, McGeer AJ, L'Abbé KA. J Clin Epidemiol. 1992;45:255-65

The Fragility Index is a tool that aids in the interpretation of significant findings, providing a measure of strength for a result. The Fragility Index represents the number of consecutive events that need to be added to a dichotomous outcome to make the finding no longer significant. A small number represents a weaker finding and a large number represents a stronger finding.

Why was this study needed now?

Patient-specific instrumentation (PSI) for component implantation in total knee arthroplasty is a recently-developed technology, with a number of randomized controlled trials performed investigating the systems of major orthopaedic device companies. PSI systems were designed to improve component alignment in these procedures, though conclusions on efficacy from previous studies vary widely. A synthesis of the literature was therefore needed to assess the current status of the role of PSI in TKA procedures.

What was the principal research question?

In total knee arthroplasty, are there any significant differences in radiographic alignment accuracy of component placement, perioperative parameters (blood loss, operative time, etc), and patient-reported outcome measures between patient-specific instrumentation and conventional instrumentation?

Study Characteristics +
Data Source:
MEDLINE and EMBASE were searched for relevant articles published up to May 28 2015.
Index Terms:
Keyword terms included: "knee arthroplasty", "knee replacement", "patient match", "patient specific", and "custom".
Study Selection:
Eligibility criteria included: a randomized or quasi-randomized controlled trial design; enrolled patients requiring total knee arthroplasty; and allocated patients to treatment with either patient-specific instrumentation or conventional intra- and extramedullary guides. The selection was performed independently by two reviewers, with disagreement resolved through discussion. A total of 21 studies. with data sampled from 1587 procedures, were selected for final inclusion.
Data Extraction:
Data extraction was performed by a single reviewer.
Data Synthesis:
Statistical analysis was performed using Review Manager software (RevMan 5.3). Continuous outcomes were expressed as weighted mean differences, and dichotomous outcomes as risk ratios, both with 95% confidence intervals. All analyses were performed under both a fixed-effects and random-effects model. Heterogeneity was assessed using the I-squared (I^2) statistic.
What were the important findings?
  • There was no significant difference in the incidence of outliers in hip-knee-ankle angle (>3deg deviation from neutral) overall between patient-specific and conventional instruments (13 studies; RR 1.02 [95%CI 0.82-1.27]; p=0.86), or when specific products (PSI-Zimmer, Signature-Biomet, TruMatch-DePuy, Visionaire-Smith & Nephew) were analyzed as subgroups (all p>0.05).
  • There was no significant difference between groups in the incidence of femoral component outliers in the coronal plane (11 studies; RR 0.81 [95%CI 0.6-1.09]). The incidence of tibial component outliers in the coronal plane was significantly higher among patient specific groups (11 studies; RR 1.64 [95%CI 1.12-2.42]).
  • There were no significant differences between groups in the incidence of outliers in the sagittal plane of either the femoral component (8 studies; RR 0.97 [95%CI 0.82-1.15]) or the tibial component (8 studies; RR 1.47 [95%CI 0.97-2.23]).
  • There was no significant difference between groups in the incidence of femoral component rotational outliers (6 studies; RR 0.80 [95%CI 0.52-1.23]).
  • No significant difference between patient-specific and conventional instrumentation groups was observed in operative time (12 studies; MD -0.90min [95%CI -4.78, 2.98]; p=0.65) or tourniquet time (3 studies; MD -6min [95%CI -21.2, 10.1]). No significant differences were observed in analyses of intra-, postoperative, and total perioperative blood loss.
  • The length of hospital stay was shortened by 8 hours (95%CI 3.1-12.5) following the use of patient-specific instrumentation versus conventional instrumentation.
  • Two studies demonstrated a significantly lower use of surgical trays (MD 4 trays [95%CI 2.58-5.61]) with patient-specific versus conventional instrumentation.
  • No significant differences between groups were observed in patient-reported outcome measures at 3 months, including Knee Society Scores and Oxford Knee Scores.
What should I remember most?

In total knee arthroplasty, the use of patient-specific instrumentation did not significantly reduce the incidence of malalignment overall, or of individual components in the coronal, sagittal, and axial planes. In fact, the incidence of tibial component outliers in the coronal plane was significantly higher following TKA with patient-specific instrumentation. No significant differences were observed in analyses of operative time, blood loss, or short-term clinical outcome. Advantages with the use of patient-specific instrumentation were noted concerning the number of surgical trays during the procedure, as well as in length of hospital stay.

How will this affect the care of my patients?

The results of this study suggest that there is no radiographic or clinical advantage to the use of patient-specific instrumentation in total knee arthroplasty, and in fact may compromise alignment of the tibial component. Benefits of patient-specific instrumentation appear limited to parameters of resource consumption, as evidenced by the analyses on surgical trays and the short, but significant, reduction in hospital stay. An economic analysis is needed to determine if these improvements in efficiency off-set the cost of the patient-specific instrumentation technology itself, as well as the preoperative imaging required to make the technology.

DISCLAIMER

This content found on this page is for informational purposes only and is not intended to be a substitute for professional medical advice, diagnosis, or treatment. If you require medical treatment, always seek the advice of your physician or go to your nearest emergency department. The opinions, beliefs, and viewpoints expressed by the individuals on the content found on this page do not reflect the opinions, beliefs, and viewpoints of OrthoEvidence.

0 of 4 monthly FREE articles unlocked
You've reached your limit of 4 free articles views this month

Access to OrthoEvidence for as little as $1.99 per week.

Stay connected with latest evidence. Cancel at any time.
  • Critical appraisals of the latest, high-impact randomized controlled trials and systematic reviews in orthopaedics
  • Access to OrthoEvidence podcast content, including collaborations with the Journal of Bone and Joint Surgery, interviews with internationally recognized surgeons, and roundtable discussions on orthopaedic news and topics
  • Subscription to The Pulse, a twice-weekly evidence-based newsletter designed to help you make better clinical decisions
Upgrade
Welcome Back!
Forgot Password?
Start your FREE trial today!

Your account will be affiliated with
and includes free access to OrthoEvidence


OR
Forgot Password?

OR
Please check your email

If an account exists with the provided email address, a password reset email will be sent to you. If you don't see an email, please check your spam or junk folder.

For further assistance, contact our support team.

Please login to enable this feature

To access this feature, you must be logged into an active OrthoEvidence account. Please log in or create a FREE trial account.

Translate ACE Report

OrthoEvidence utilizes a third-party translation service to make content accessible in multiple languages. Please note that while every effort is made to ensure accuracy, translations may not always be perfect.

How to cite this ACE Report

OrthoEvidence. No radiographic or clinical benefit of patient specific instrumentation in TKA. OE Journal. 2016;4(22):3. Available from: https://myorthoevidence.com/AceReport/Show/no-radiographic-or-clinical-benefit-of-patient-specific-instrumentation-in-tka

Copy Citation
Please login to enable this feature

To access this feature, you must be logged into an active OrthoEvidence account. Please log in or create a FREE trial account.

Premium Member Feature

To access this feature, you must be logged into a premium OrthoEvidence account.

Share this ACE Report