More Information on Rotator Cuff Surgery.
Last updated Wednesday, January 26, 2005
Figure 1 - The tendon near the deltoid is split longitudinally Figure 2 - Strong repair of the deltoid Figure 3 - Progressive supine press Figure 4 - Position of fusion Figure 5 - Rough spots are smoothed with a motorized burr Figure 6 - Minimizing tension on the repair Figure 7 - Release dividing the capsule from the glenoid Figure 8 - Tongue in groove repair Figure 9 - Drill holes in the distal tuberosity Figure 10 - Continuous passive motion Figure 11 - Progress chart Figure 12 - Consolidating split laminations of cuff Figure 13 - Active flexion as a function of cuff integrity at followup Figure 14 - Ability to perform activities of daily living as a function of cuff integrity at followup Figure 15 - Active flexion of the shoulders in which the repaired cuff was intact Introduction This is the information which might be shared with patients as they
consider rotator cuff repair. Before it can be applied to a specific
clinical situation, however, it needs to be tailored to the patient,
the problem and the surgeon.The rotator cuff The rotator cuff is composed of four tendons that blend together to
help stabilize and move the shoulder. Loss of the integrity of the
rotator cuff is a common cause of shoulder weakness. Shoulders with
large rotator cuff defects have difficulty raising the arm or rotating
it out to the side. Strong rotator cuff tissue requires a major force
to tear it. Weakened degenerative cuff tissue can be torn easily, even
while carrying out activities of daily living.Surgery or non-operative treatment? When rotator cuff tears are relatively recent and when a significant
force was required to tear the tendon, the chances of regaining
shoulder strength by rotator cuff repair surgery are good. Conversely,
when the defect is long-standing and occurred without a major injury,
the quality and quantity of tissue available for repair may not be
sufficient for the restoration of good shoulder function. Thus with
long-standing shoulder weakness from rotator cuff defects, a good try
at strengthening the remaining muscles may be worthwhile before
considering surgical repair. If surgery is undertaken, proper
postoperative care is particularly important.Who should consider this surgery? Surgical exploration and attempted cuff repair is an option for the
patient who understands the limitations of this procedure. Prompt
surgical exploration of the rotator cuff is considered for
physiologically young patients with acute tears. Repair should be
carried out before tissue loss, retraction, and atrophy occur. For
tears older than 12 months, a period of stretching and gentle
strengthening exercises can indicate the potential for nonoperative
management. Exploration is considered for patients with functionally
significant weakness from longer-standing tears refractory to
nonoperative management, provided that their expectations are realistic.
About the surgery The goal of cuff repair surgery is to improve the strength and
muscular balance of the shoulder. This operative procedure is
considered when the shoulder demonstrates weakness from a cuff defect
and when there appears to be a substantial chance of achieving a
durable functional repair. These conditions are most likely met in a
traumatic tear where a physiologically sound cuff has been torn acutely
by a substantial injury. In this situation, the quality and quantity of
tendon for repair should be excellent. By contrast, with chronic
massive degenerative tears the quantity and quality of the cuff are
less likely to be optimal for surgical repair. In this situation, the
surgeon and the patient must understand preoperatively the potential
limitations imposed by the tissue in the shoulder.
It must be remembered that there are several ways in which surgery
may worsen the function of a cuff-deficient shoulder. These need to be
reviewed before each cuff operation. The most serious is compromise of
the deltoid muscle. The deltoid may be compromised by nerve injury.
This injury may involve the intramuscular motor branches to the
anterior third of the muscle resulting from a too-distal split of the
muscle in the surgical approach. Deltoid denervation may also arise
from axillary nerve injury when searching for cuff tendons laterally
and posteriorly around the quadrangular space. Normally the deltoid has
a strong tendon of origin between its anterior and middle thirds. This
tendon attaches to the anterior lateral corner of the acromion.
Postoperative function of the deltoid may be compromised by failure to
achieve a strong reattachment of this tendon and the anterior muscle
fibers after acromioplasty. This is particularly a problem when a large
anterior acromial resection is performed requiring stretch of the
deltoid for reattachment. Failure of the anterior deltoid origin
devastates the most important motor for shoulder elevation.
Scarring in the humeroscapular motion interface (see Chapter 2)
between the acromion and deltoid and the cuff and humerus can restrict
humeroscapular motion, negating any benefit achieved from restoring
cuff integrity. This complication results from immobilization of the
cuff against the acromion and deltoid after surgery.
Loss of superior stability can result when the coracoacromial arch
is sacrificed without reestablishing stability with a durable cuff
repair. In this situation, deltoid contraction pulls the head of the
humerus anterior superiorly, rather than elevating it. The deltoid
becomes stretched so that the humeral head seems to be just below the
skin. Patients who lose stability and deltoid function are some of the
most unhappy we encounter after previous repair attempts. Primum non
nocere (first of all, do no harm). Surgical technique The cuff is approached though an acromioplasty incision in the skin
lines perpendicular to the deltoid fibers. This incision offers an
excellent exposure and the opportunity for a cosmetic closure,
particularly in comparison with the skin incisions parallel to the
deltoid fibers. Great care is taken to preserve the tendon fibers of
the deltoid origin to permit a strong repair. The deltoid has an
important tendon of origin between its anterior and middle thirds.
Arising from the anterior lateral corner of the acromion, this tendon
is not only the guide to exposure of the cuff, but is also the key to
reattachment of the deltoid origin at the conclusion of the surgery.
This tendon is split longitudinally for 2 cm distal to the acromion in
line with its fibers, taking care to leave some of the tendon on each
side of the split. The split is continued up over the acromion and into
the trapezius insertion. For 1 cm on either side of this split the
deltoid origin is sharply dissected off the acromion, so the strong
bony attachment fibers remain with the muscle. These fibers provide a
strong "handle" on the muscle, so a solid repair can be achieved.
Splitting the parietal layer of the bursa on the deep aspect of the
deltoid provides a view of the rotator cuff. Before a "reflex"
acromioplasty is performed, the quality and quantity of the cuff tissue
are observed to determine the likelihood of cuff reparability.
Hypertrophic bursa and scar tissue are resected to allow a good view of
the cuff tissue. We characterize cuff tears using a simple system based
on the number of tendons torn. In Type 1, only one tendon (almost
always the supraspinatus) is torn. In Type 2, two tendons (usually the
supraspinatus and infraspinatus) are torn. In Type 3, the
supraspinatus, infraspinatus and subscapularis are torn. Type 1 is
broken down into Type 1A-a partial thickness-tear, and Type 1B-the full
thickness tear confined to a single tendon. We judge the quality of the
cuff tissue in terms of its ability to hold a strong pull applied to a
suture passed through its edge. Finally, it is critical to note the
amount of tissue that has been lost. The extent of tissue loss and the
ability of the remaining tissue to hold suture are the major
determinants of cuff reparability. If there is major tissue loss and residual tendon of poor quality, it becomes evident that a robust repair cannot be performed.A smoothing operation may be performed In this situation, where primary stability from an intact cuff
cannot be restored, it is important not to perform a routine
acromioplasty, which would jeopardize the secondary stabilization
offered by the coracoacromial arch. Under these circumstances,
sacrifice of coracoacromial arch support deprives the shoulder of its
last vestige of superior stability, allowing anterosuperior "escape" of
the humeral head when elevation is attempted.
For this reason, when a strong rotator cuff repair is impossible as
a result of the limited quantity and quality of the residual cuff
tissue, we do not perform a routine acromioplasty. Instead, we perform
only a smoothing of the undersurface of the coracoacromial arch to
allow unimpeded passage of the humeral head and residual cuff beneath.
Any debris, scar, or thickened bursa in the subacromial area is
excised. It is often helpful to smooth the upper surface of the
uncovered proximal humerus, particularly if the uncovered tuberosities
are prominent or irregular.
A strong repair of the deltoid to the acromion is then carried out
(see figure). Depending on the quality of the tissues, this may be
accomplished by a side-to-side repair of the surgical split in the
deltoid tendon and trapezius fascia. Drill holes in the acromion are
used as necessary for secure reattachment. The full thickness of the
deltoid, including the deltoid side of the bursa, is incorporated in
the sutures to be certain that it does not impede smooth motion in the
humeroscapular motion interface.
A subcuticular skin closure reinforced with paper tapes provides
optimal cosmesis. The patient is returned to the recovery room with the
arm in continuous passive motion from zero to 90 degrees of flexion to
minimize the tendency to form adhesions in the humeroscapular motion
interface.
The postoperative management must be tailored by the surgeon to
match the patient and the surgery. Often, the patient is taught passive
mobilization of the shoulder to 140 degrees of elevation and 40 degrees
of external rotation and is discharged when these goals are achieved
comfortably. Light use of the shoulder with the arm at the side is
allowed as comfort permits. Sling immobilization is unnecessary.
Strengthening of the deltoid and residual cuff muscles is started six
weeks after surgery. The best exercise we have found for optimizing
active elevation is the progressive supine press (see figure). In this
exercise small increments are used to train the remaining muscles to
optimal advantage. Note that the scapular muscles are also put to work
in these exercises. When a massive cuff defect coexists with a detached, denervated, or
dysfunctional deltoid, the shoulder is without effective glenohumeral
motors.Salvage option Under these circumstances, a glenohumeral arthrodesis provides a
salvage option. By securing the humeral head to the scapula, the
scapular motors can be used to power the humerus through a very limited
range of humerothoracic motion. We prefer a fusion technique which
preserves all remaining deltoid function, and which uses decortication
of the humerus and glenoid, 6.5 mm compression screws across the joint,
with or without a neutralization plate from the scapular spine across
the joint and down the humeral shaft.
The best candidates for this procedure are those patients with:
- permanent and severe weakness due to loss of cuff and deltoid function;
- a good understanding of the limitations and potential complications of a shoulder fusion;
- intact scapular motors;
- good motivation; and
- minimal complaints of pain.
To establish the limitations of shoulder fusions, we studied the
humerothoracic motion of twelve patients who had glenohumeral
arthrodeses at least two years prior to the time of study. Elevation in
the plus 90 degrees (anterior sagittal) plane averaged 47 degrees.
Elevation in the minus 90 degrees (posterior sagittal) plane averaged
22 degrees. External rotation averaged 9 degrees and internal rotation
46 degrees. These ranges of motion were similar to the scapulothoracic
motion measured in normal subjects. Only one of the patients could
reach his hair without bending his neck forward, only five could reach
their perineum, six could reach the back pocket, seven the opposite
axilla, and ten the side pocket.
We studied normal in vivo shoulder kinematics to predict the
functions which would be allowed by various positions of glenohumeral
arthrodesis, assuming that the scapulothoracic motion would remain
unchanged. Using the normal scapulothoracic motions we were able to
model the functional effects of fusion positions (reported in relation
to the thorax). We found that activities of daily living could be best
performed if the joint was fused in 15 degrees of flexion, 15 degrees
of abduction, and 45 degrees of internal rotation. This position of
fusion with a low angle of elevation and relatively high degree of
internal rotation facilitated reaching the face, opposite axilla, and
perineum (see figure). However, all positions represented major
compromises of normal function. If inspection of the cuff at surgery reveals good quality tissue in
sufficient quantity for a robust repair, primary glenohumeral stability
from concavity compression can usually be restored.Standard anteroinferior acromioplasy Thus, a standard anteroinferior acromioplasty is performed to
improve exposure and to protect the repair from abrasion. A flexible
osteotome is directed so that the anterior undersurface of the acromion
is resected in the same plane as the posterior acromion. Rough spots
are smoothed with a motorized burr (see figure 5).
The goal of repair is a strong fixation of the tendon to the humerus
under normal tension with the arm at the side. The desired attachment
site is at the sulcus near the base of the tuberosity. This goal is
facilitated by using three stages of sequential release. These releases
are required because the cuff is usually retracted and because tissue
is lost in chronic cuff disease. Unless these releases are carried out,
increased tension in the repaired tendon will predispose to tightness
of the glenohumeral joint and will additionally challenge the repair
site. The humeral head is rotated to present the different margins of
the cuff defect through the incision, rather than enlarging the
exposure to show the entire lesion. The deep surface of the cuff is
searched for retracted laminations. All layers of the cuff are
assembled and tagged with sutures.
By applying traction to these sutures, the cuff is mobilized
sequentially as necessary to allow the torn tendon edge to reach the
desired insertion at the base of the tuberosity. First, the
humeroscapular motion interface is freed between the cuff and the
deltoid, acromion, coracoacromial ligaments, coracoid, and coracoid
muscles. Next, the coracohumeral ligament/rotator interval capsule is
sectioned around the coracoid process to eliminate any restriction to
the excursion of the cuff tendons and to minimize tension on the repair
during passive movement (see figure 6). This release of the
coracohumeral ligament and rotator interval capsule also contributes to
the comfort and ease of motion after the surgical repair by minimizing
the capsular tightening effect of cuff repair. At this point the ease
with which the cuff margins can be approximated to their anatomic
insertion at the base of the tuberosity is evaluated. If good tissue
cannot reach the sulcus, the third release is carried out. This release
divides the capsule from the glenoid just outside the glenoid labrum
(see figure 7), allowing the capsule and tendon of the cuff to be drawn
further laterally toward the desired tuberosity insertion without
restricting range of motion.
After the necessary releases have been completed, a judgment is made
concerning the site at which the cuff can be implanted into the bone
without undue tension while the arm is at the side. Ideally, the site
of implantation will be in the sulcus at the base of the tuberosity. In
large cuff defects, a somewhat more medial insertion site may be
necessary. Often, when a medial insertion site is required for a large
cuff defect, the new insertion lies in an area where the articular
cartilage has been damaged by abrasion against the undersurface of the
acromion.
The repair is accomplished as a tongue in groove (see figure 8),
with the cuff tendon drawn into a trough near the tuberosity, providing
a smooth upper surface to glide beneath the acromion. This groove
provides the additional advantage that if some slippage occurs in the
suture fixation of the cuff to bone, contact between the tendon and
bone is not lost. Nonabsorbable sutures passed through the tendon
margin are then passed through drill holes in the distal tuberosity
(see figure 9) so that the knots will not catch beneath the acromion.
The knots are tied over the tuberosities so that they will lie out of
the subacromial space. If there is a longitudinal component to the
tear, it is repaired side-to-side with the knots buried out of the
humeroscapular motion interface. The repair is checked throughout a
range of motion to 140 degrees of elevation and 40 degrees of external
rotation to assure that it is strong, it is not under excessive
tension, and it will permit smooth subacromial motion. If additional
resection of the undersurface of the acromion is required to allow
smooth passage of the repaired tendon, it is performed at this time.
After a careful and robust deltoid repair using nonabsorbable
sutures and cosmetic skin closure, the patient is returned to the
recovery room.
The postoperative management must be tailored by the surgeon to the
patient and the procedure. We often place the affected arm in zero to
90 degrees of continuous passive motion (see figure 10). Immediate
postoperative motion is valuable because there is a tendency for
scarring between the raw undersurface of the acromion and the upper
aspect of the rotator cuff or proximal humerus. Immediate postoperative
continuous passive motion is facilitated if the surgery is performed
under a brachial plexus block, which provides analgesia for up to 18
hours after surgery. Continuous passive motion is continued for up to
48 hours after surgery but does not appear to be necessary after that.
The patient is expected to perform passive exercises in flexion and
external rotation. Before discharge, the patient should be able to
attain comfortably 140 degrees of passive flexion and 40 degrees of
passive external rotation. A progress chart mounted on the patient's
wall helps to document progress toward these discharge goals (see
figure 11).
Postdischarge management must consider the magnitude of the tear and
the strength of the repair. It is unlikely that the repair will have
substantial strength until at least three months after surgery. As is
the case with repairs of the anterior cruciate ligament, major cuff
repairs may require six to twelve months to regain useful strength.
Thus, in the first several postoperative months, the emphasis is placed
on maintaining passive motion and avoiding loading of the repair. Partial thickness defects of the cuff may manifest clinically as the
inability to use the cuff forcefully against resistance, by pain on
isometric abduction or external rotation (a positive "tendon sign"), or
by crepitance with rotation of the partially elevated arm (a positive
"abrasion sign").Partial defects These partial defects are more likely to be associated with shoulder
stiffness than larger full thickness defects, because the larger
defects in the cuff provide the equivalent of a capsular release.
Nonoperative management must emphasize stretching in internal rotation,
cross-body adduction, and elevation. When a comfortable normal range of
passive motion is reestablished, gentle progressive strengthening of
the cuff muscles is instituted. An emphasis is always placed on gentle
and comfortable progress of this rehabilitation program.
In many respects, the treatment of a partial cuff tear is analogous
to the treatment of a partial Achilles tendon tear or tennis elbow. The
functional deficits are likely to be related to tension on a partially
torn tendon. Treatment requires first stretching and then gentle
strengthening. Surgery is usually considered only if symptoms persist
in spite of regaining normal passive motion and if the patient is
prepared for an extended recovery period.
In planning surgical management for refractory problems from partial
thickness tears, it must be determined if the patient's functional
deficits are related to tension on a partially torn tendon as indicated
by a positive tendon sign. In this case, completion of the detachment
and reattachment, as for a full thickness tear, may be necessary. This
procedure will tighten the shoulder and is not a suitable treatment for
a contracted shoulder. Alternatively, the symptoms may be related to
secondary subacromial abrasion from the slight superior instability
resulting from the tendon defect as well as the associated thickening
of the intervening bursa. Under these circumstances the abrasion sign
(rotating the partially elevated arm beneath the coracoacromial arch)
should reproduce the patient's symptoms. In the second instance, an
anterior inferior acromioplasty and bursal resection may be of benefit
as long as normal shoulder flexibility has been restored to eliminate
the effect of a tight posterior capsule. Anterior acromioplasty does
not treat shoulder stiffness, which must be eliminated by exercises or
by surgical releases.
The decision to complete a partial thickness cuff defect may be
influenced by surgical findings. The thickness of the cuff can be
determined at acromioplasty by inspection for superior surface defects.
For deep surface or intratendinous lesions the cuff thickness is
determined by palpation, by injecting saline or dilute methylene blue
solution in the joint, or by using a depth gauge or calibrated nerve
hook. A tenotomy can also be performed in the most suspicious area
along the line of the tendon fibers to explore the full thickness of
the tissue. If, as is usually the case, the defect is near the anterior
insertion of the supraspinatus, a longitudinal tenotomy and capsulotomy
are performed along the anterior aspect of the supraspinatus in the
rotator interval capsule. This cut is then extended at right angles
posteriorly through the partially detached cuff at its insertion to the
greater tuberosity, turning back the flap of cuff until tendon of full
thickness is encountered. Next an attempt is made to retrieve and
consolidate any split laminations of cuff which may have retracted
medially (see figure 12). These are usually on the deep articular
surface where the cuff lesion begins and may have retracted medially up
to 1 cm. Release of the coracohumeral ligament and rotator interval
capsule from the base of the coracoid will minimize tension on the
repair. Then the full thickness defect is repaired in the manner
previously described. The shoulder is then put through a full range of
motion to verify that the acromioplasty is adequate to protect the
repaired tendon from acromial abrasion.
Postoperative management is tailored by the surgeon for the patient, but often is the same as for the full thickness defects. Patients are usually pleased with the results of cuff surgery. Yet it
may be difficult to determine what aspect of the treatment program is
responsible for the improvement.Cuff integrity and quality of result of surgery It is known that many patients with deficient cuffs are surprisingly
comfortable and functional and, therefore, never undergo surgery. It is
also known that the tissue encountered at surgery is not infrequently
insufficient to allow a durable repair, yet the patient is improved
after surgery. These observations bring up the question of the
relationship of cuff integrity to the quality of the result after cuff
surgery. To help answer this question, we undertook a study of 105 of
our own surgical repairs of chronic rotator cuff tears in 89 patients
at an average of five years postoperatively. The patients' ages at the
time of repair averaged 60 years (range 32 to 80). Eighty-six (82%) of
the shoulders had no prior attempt at repair of the cuff.
In all of the surgeries an anterior-inferior acromioplasty was
carried out. The involved tendon or tendons were mobilized as
necessary. A bony trough was created in the humerus to reattach the
mobilized tendons. The site of reattachment was usually in the sulcus
adjacent to the humeral articular surface. In some cases the trough was
placed somewhat more medially, if after mobilization the tendons did
not reach their original anatomic attachment without undue tension when
the arm was at the side. The cuff was protected from active use for
three months postoperatively.
We correlated the functional result with the integrity of the cuff,
as determined by expert ultrasonography. Expert ultrasonography was
selected because of its superior accuracy to cost ratio and
practicality.
We characterized the status of the cuff at surgery and at follow-up
in terms of the integrity of the different tendons. No patient who had
a partial thickness tear repaired had a full thickness retear. In 80
percent of shoulders with repaired full-thickness supraspinatus tears,
the cuff was found to be intact at follow-up. Only 57 percent of cuffs
that had tears involving both the supraspinatus and infraspinatus were
intact at an average follow-up of six years. Less than one-third of the
cuffs which had tears involving all three major tendons were intact
after repair at an average of four years of follow-up. It is evident,
therefore, that the rotator cuff is more likely to develop a secondary
defect after the repair of a large tear. This may be a reflection of
the age of the patient, the quality of the tissue, the quantity of
tissue, the effect of tendon mobilization on tendon viability, or the
greater difficulty in getting healthy tendon securely implanted in bone
when there is a major deficiency in the cuff.
Patients were generally satisfied with the results of surgery, even
when expert sonography showed that the cuff was no longer intact. This
result indicates that patient satisfaction is not a reliable indication
of cuff integrity.
Shoulders with intact repairs at follow-up had the greatest range of
active flexion as compared to those with large recurrent defects (see
figure 13). These patients also demonstrated the best function in
activities of daily living. Where the cuff was not intact, the degree
of functional loss was related to the size of the recurrent defect (see
figure 14). These results indicate that integrity by ultrasound
correlates with cuff function.
Patients with intact repairs of large tears had just as good
function as did those with intact repairs of small tears. We found an
overall greater incidence of recurrent defects in shoulders with repeat
repairs. However, shoulders with intact cuffs after repeat repairs
functioned as well as did those with intact primary repairs (see figure
15).
From this study we concluded that the integrity of the rotator cuff
at follow-up (and not the size of the tear at the time of repair) is
the major determinant of the outcome of surgical repair. An intact
repair of a recurrent tear is likely to yield a result comparable to
that of an intact repair of a primary tear. Likewise, intact repairs of
large tears yield results comparable to intact repairs of small tears.
The chances of the repair of a large tear remaining intact, however,
are not as good as those for a small tear. Older patients tended to
have larger tears and to have a higher incidence of recurrent defects. These are typical instructions given to a patient after a rotator cuff
repair. However, the program will vary with the surgeon, the patient
and the repair. If you have had such a repair, only your surgeon can
give you instructions on the postoperative management. Do not do any
exercises after surgery except after consultation with your physician.Healing period After a cuff repair, the tissue remains quite weak until your body has
time to complete the bonding of the tissue to bone. This may require as
much as six months. Use of the arm before the healing is complete can
cause the repair to fail. On the other hand, immobilizing the shoulder
for a long period of time to protect the repair can cause shoulder
stiffness. For these reasons, careful postoperative rehabilitation is
an essential part of your surgery. Because each patient and each
surgery are different, it is essential that the postoperative
management be tailored by the surgeon to meet the patient's individual
situation.Rehabilitation program There are two aspects of the rehabilitation program: preventing unwanted scar formation and protecting the repair.
Protect your repair by being careful that your arm does not
participate in lifting, pushing, or pulling and that it is not raised
away from the side under its own power. Unless we tell you otherwise,
you may use your hand for typing or writing as long as the elbow is
kept at your side. Raising the arm even a small amount places demands
on your repair and should be avoided. We will tell you how long these
restrictions need to be in effect. During this time you should not
drive!
While your shoulder is healing, passive motion is necessary to
prevent unwanted scar tissue formation. Passive motion means that the
shoulder is moved, but not under its own power. These exercises must be
comfortable for you--if you have problems doing them comfortably, let
your doctor or therapist know. Your operated shoulder is moved by your
other hand while the muscles of the operated shoulder are completely
relaxed. You can move your shoulder passively by standing up and
bending over at the waist, allowing the operated arm to dangle down in
a relaxed way. Passive motion is also easily done while you are lying
on your back. Grasp the arm of your operated shoulder with the opposite
hand and slowly help the arm up to a vertical position and then over
your head (see figure 16). On lowering it back down you will need to
concentrate on keeping the operated shoulder completely relaxed.
A second exercise is performed while you are lying down with both
your elbows bent to a right angle. Using a cane or dowel or yardstick,
gently push the wrist of the operated shoulder out to the side while
keeping your elbow at the side (see figure 17).
These precautions against active use and the passive motion
exercises are continued until your surgeon tells you it is time to
start the next phase of exercises. Please do not change your program
just because it seems time to do so. If you have any questions, please
let your doctor know.
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