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About
Design:
Investigator Initiated Prospective Randomised Trial
Study Centre's:
Melbourne Private Hospital Royal Melbourne Hospital
Study Hypothesis:
Use of the SternaLock 360 will reduce the incidence of sternal motion > 2mm by absolute difference of 40% at 6 weeks of surgery compared to stainless steel wiring.
Use of the SternaLock 360 will improve bone healing and quality of recovery after surgery compared to stainless steel wiring
Study Objective:
To determine if the SternaLock 360 system reduces sternal instability, increases bone healing, and improves quality of recovery compared to stainless steel wiring of the sternum, after cardiac surgery involving median sternotomy
Inclusion Criteria:
Age ≥ 18 year old Elective cardiac surgery Primary cardiac surgical procedure No evidence of infection at time of surgery Sufficient English language to complete the Postoperative Quality of Recovery Survey
Exclusion Criteria:
Previous sternotomy (redo) Clinical sternal deformity Home locality preventing follow-up (e.g. remote regional, interstate or overseas patient)
Number of Planned Subjects:
50
Full description
Introduction/Background Information Since the inception of cardiac surgery in the early 1960s, division of the sternum has provided the superior access to cardiac structures. Cardiac surgery may involve treatment of the coronary arteries, valves or major vessels such as the ascending aorta. In children, correction of congenital malformations is also performed.
The conventional bone fixation during the 1960s was the placement of stainless steel wires around or through the sternum, predominantly as single wires which were tensioned by twisting. In the 1980s, it became fashionable for some cardiac surgeons to pass the wire twice around the bone (as would be the case repairing a fence on a farm), so-called "figure of 8" configuration and tensioning again occurring by twisting the wires. There have been no adequate studies investigating which of these two techniques may be superior.
In simple terms, bone healing is promoted by
The sternum is a connecting bone that moves in multiple planes to transfer load and position the limbs in space during every day functional tasks and respond to the demands of respiration. The healing of the sternum is in the context of many efforts by the treating physicians and physiotherapists to encourage activities that might cause distracting forces at the sternal fracture site. Additionally, simple everyday activities by the patient such as coughing, deep breathing, sneezing, transferring in and out of bed, turning over in bed and driving all lead to substantial distracting forces acting on the sternal fracture site1. External fixation is not encouraged because the patient needs to have significant chest wall movement in order to breathe and clear sputum as part of the recovery from surgery.
Also, ultrasound data suggests an additional mechanism by which sternal healing is compromised with conventional sternal wiring techniques. The shape of the sternum is complex 1. The upper part is called the manubrium to which the clavicles and first rib join, and is generally quite thick with a reasonably robust and cortex and strong marrow. By contrast, the body of the sternum which forms the majority of the sternum is thinner and the marrow is frequently less robust than for the manubrium. In both areas, the cortical bone is present superficially (anterior) and deep (posterior) with the marrow between. When sternal wires are used, and the two halves of the sternum brought together and tensioned by twisting the wires, best efforts made to ensure that the cortical bone edges on either side are opposed or well aligned (that is, that in the anterior and posterior direction that the two bone edges from either side of well opposed). Generally, this is quite well achieved, but not always. Yet, even with ultrasound studies performed 1 or 2 days after surgery, the alignment between the anterior cortical bone edge on either side is lost as detected by the cortical bone of one side overriding the cortical bone of the other side.
The implications of this ultrasound finding are twofold
Consequences of poor sternal healing: Patients may feel movement of the sternum and that may limit their activity. However, chronic sternal instability is associated with pain 2, which may in turn affect other aspects of daily living, require long term medications and predispose to depression.
SternaLock 360 system The SternaLock 360 system is a band and plating system designed to improve sternal stability. 3 bands surround the sternum to oppose the bones (like wires), but an additional 3 plate system prevents anterior posterior displacement and provides a rigid fixation. CT scan follow up shows improved bone healing at 3 months after surgery compared to conventional wires, but the CT scan is a poor measurement of dynamic movement. Quality of recovery and functional status has not been adequately studied.
The unique design of the SternaLock 360 system, is that it combines a
Pilot Data Our research group is experienced in assessing sternal motion with ultrasound 4. We have conducted sternal ultrasound measurements of sternal motion after surgery as part of clinical follow up.
Over all the SternaLock 360 results in a far greater rigid fixation as noted at the time of surgical implantation. Subsequent pilot ultrasound studies performed during dynamic distracting forces (such as coughing) reveal reduced or absent movement at the fracture site and better preservation of fracture alignment. Ultrasounds have been performed at varying intervals from Day 1 post-operative to 6 weeks post-operative, and ultrasounds of sternal wire fixation have been performed at varying intervals after 10 months post-operative. Our observations are that fewer than 10% of patients who have received the SternaLock 360 have had motion >2 mm, whereas patients with conventional wiring have motion > 2 mm in more than 50%.
Evidence Gap The SternaLock 360 is an effective system for closing the sternum. There are few comparative data investigating bone healing with CT scans, but the CT alone is a poor indicator of sternal instability. There is no long term comparative data on sternal micro motion, or quality of recovery outcomes to identify whether the SternaLock 360 system will improve patient centred outcomes over and above improved bone healing.
Study Objectives Hypothesis Use of the SternaLock 360 will reduce the incidence of sternal motion > 2mm by absolute difference of 40% at 6 weeks of surgery compared to stainless steel wiring.
Use of the SternaLock 360 will improve bone healing and quality of recovery after surgery compared to stainless steel wiring.
Study Aims To determine if the SternaLock 360 system reduces sternal instability, increases bone healing, and improves quality of recovery compared to stainless steel wiring of the sternum, after cardiac surgery involving median sternotomy.
Randomisation The randomization sequence will be produced using a computer generated randomization sequence, in unequal blocks. Concealment will be by placing the card containing the allocation information in double opaque sealed envelopes, and concealment will be maintained until after recruitment and the patients is admitted to the operating theatre. The treating surgical team will then open the envelopes to reveal the allocation after (1) weaning from cardiopulmonary bypass and (2) final confirmation from the treating surgeon that the patient is suitable to be randomised.
Statistical Methods Participants who are scheduled for cardiac surgery will be screened and recruited from the cardiac surgery operation lists, surgeon's clinics and pre-operative ward.
The initial contact will be made in person during the first contact session prior to surgery. In-patients scheduled for cardiac surgery will be screened on the ward.
Medical histories will be reviewed and screened for participant suitability and eligibility. Once the patient's medical history has been reviewed and the patient's eligibility has been confirmed, the patient is then approached by the research staff member and the process of informed consent will proceed.
Power Calculation and Study Size Sample size estimates are based on the primary outcome of sternal motion > 2 mm at any location at 6 weeks after surgery. From pilot data, fewer than 10% of patients who have received the SternaLock 360 have had motion >2 mm, whereas patients with conventional wiring have motion > 2 mm in more than 50%. Based on a Fischer's Exact test, Alpha of 0.05, power of 80% and two-tailed design, 25 participants are required in each group to detect a difference of 50% to 10% between groups, favoring the SternaLock 360 system. The sample size will increase to 26 in each group to account for an estimated 5% dropout rate. The total number will be 52 participants.
Statistical Methods To Be Undertaken The primary endpoint will be assessed using the Chi Squared test on the incidence of sternal motion > 2 mm at 6 weeks after surgery.
Postoperative Quality of Recovery Variables of "recovery" are dichotomized to "recovered" or "not recovered" based on whether they have returned to their baseline (preoperative) values or a better result than their preoperative values; at each of the time points when measurements are performed. A tolerance factor is included in the scoring of cognitive recovery to allow for performance variability 6. The secondary outcomes of recovery over time, analysis will be performed using the a general linear mixed model to investigate group differences over time.
Continuous data will be analyzed using independent samples t test, or repeated measures analysis of variance (RM ANOVA). A P[Symbol]0.05 will define statistical significance.
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50 participants in 2 patient groups
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Data sourced from clinicaltrials.gov
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