Otoplasty Flashcards

1
Q

Most otoplasty procedures are best performed e:3 years old
when most ear growth is completed

A

T

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2
Q

Simple otoplasty techniques are considered before more
complicated reconstructive procedures.

A

T

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3
Q

About 50% of newborns have an auricular deformity that persists
in 33% by 1 month old

A

T

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4
Q

50% of deformities continue to
improve over the first year of life

A

F 84% of deformities continue to
improve over the first year of life

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5
Q

prominent ears, decrease from birth to 1 year old,

A

The exception is prominent ears, which increase from birth to 1 year old, suggesting that postnatal deformation can contribute to this condition (e.g., infant sleep position may push the ear outward)

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6
Q

Half of children have a bilateral
deformity,

A

T

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7
Q

when the deformity is unilateral, the right and left sides
are affected equally. no difference in the prevalence or type of ear
deformity exists among males and females.

A

T

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8
Q

The most common type of ear anomaly

A

A helical anomaly/constricted ear is the most common disorder at birth (15%)

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9
Q

Risk factor for ear anomaly

A

Vaginal delivery and increased birth weight increase the risk of ear anomalies, likely due to forces on the ear causing deformations

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10
Q

The primary morbidity ofan ear deformity is psychosocial

A

T

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11
Q

THE IS ZERO TOLERANCE FOR EAR ASYMMETERY

A

F The ears are particularly tolerant of asymmetry because of their
lateral position over the temporal bones

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12
Q

it is most important to have
the ears as symmetrical as possible on frontal view.

A

T

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13
Q

It is important that families understand that asymmetries between the ears are common in the general
population

A

T

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14
Q

The height of the ear is 6.5 (±1) cm

A

T

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15
Q

width is 4.0 (±0.5 cm).

A

T

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16
Q

greater than 18 mm at the top of the helix and 21 mm at the midhelix.

A

Considred abnormal protrusion from the mastoid

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17
Q

some anomalies improve during the first week
of life

A

T

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18
Q

molding can be initiated from birth

A

molding should not be initiated until at least 1 week old to
allow for possible spontaneous correction

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19
Q

Ideally, molding is
started between 1 and 3 weeks old when maternal estrogens in the
child facilitate cartilage manipulation.

A

T

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20
Q

Patient can still have good respopnce from molding after 3 month

A

At 6 weeks old, estrogens in the child equal
that of an adult and ifear molding is initiated after this time, patients
are likely to have a poor response.

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21
Q

If the mother is breast-feeding,
initiation of ear molding can be attempted up to 8 to 10 weeks old

A

T

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22
Q

After 12 weeks old, ear molding give acceptable results

A

F After 12 weeks old, ear molding is not effective.

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23
Q

The ear deformity
that is most amenable to molding is a prominent ear.

A

T The antihelical
fold is recreated to set back the ear

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24
Q

A mildly constricted ear with
overhanging helical cartilage can be improved by lifting the helical
cartilage into better alignment

A

T

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25
A Stahl deformity can be corrected by flattening the abnormal crus.
T
26
many parents decide to correct an ear anomaly when the child is between 3 and 4 years old why?
Because long-term memory and self-esteem begin to form at approximately 4 year old At this time, the ear has achieved 85% of its size and the risk of scar limits ear growth is reduced the ear is larger to facilitate the procedure and (2) it is not urgent to intervene before this time
27
Most ear growth is completed by 6 years old
T
28
data have shown that operating on ears before 3 years old does not inhibit growth
T
29
I prefer to wait until at least 3 years old because (1) the ear is larger to facilitate the procedure and (2) it is not urgent to intervene before this time because memory and self-esteem have not yet formed
T
30
An advantage of early intervention
is that children tolerate the procedure more favorably than older patients who are more anxious about the operation and are busier with activities such as sports and school
31
Children between 5 and 8 years old typically are bothered by a deformity, but fear of the operation outweighs their desire to improve their appearance
T
32
At 9 to l0 years old, the child's interest in correcting the anomaly begins to outweigh the anxiety about the operation.
T
33
Approximately 5% of the population has a prominent ear caused by an absent or weak antihelical fold and/or overgrown concha
T
34
Most patients patient will have a normal antihelix and only require a procedure on the concha.
F Most patients will require recreation of the antihelical fold and setback of the concha. Rarely, a patient will have a normal antihelix and only require a procedure on the concha
35
all patients will need to have the upper and/or middle third of the ear setback
T
36
All of the patients in my practice will benefit from having their lobule setpack as well.
T
37
Three-fourths of patients in my experience undergo bilateral setback otoplasty, whereas one-fourth of individuals have prominence of only one ear.
T
38
There is no need for antibiotics in otoplasty
F one dose of intraoperative antibiotics because I am placing permanent foreign bodies (merseline sutures) and exposing cartilage
39
No need to excise skin in otoplasty
F skin excision necessary because it facilitates the procedure by enhancing exposure, and once the ear is set back, there is sufficient skin to reapproximate.
40
recreation of the antihelical fold by wich technique
(1) placement of scapha-concha sutures (Mustarde technique), (2) cartilage scoring (Stenstrom technique)
41
I prefer scapha-concha sutures because it gives greater control and more predictability compared to scoring the cartilage
T
42
scoring the cartilage can cause damage to the cartilage and contour abnormalities
T
43
scoring may be considered as an adjunct to weaken the cartilage to facilitate its bending during the placement of sutures.
T
44
On front view, the antihelix should have a gentle curve and the helix should be visible behind the antihelix
T
45
measure the distance from the most superior point of the helix to the mastoid and achieve a distance of 15 mm (±3 mm). after correction
T
46
If superior third remains prominent despite scapha-concha sutures
In this situation, one or two sutures can be placed from the scapha to the temporal fascia or conchal cartilage Alternatively, scapha and helical cartilage can be excised
47
Middle Third correction
Options to set back the middle third of the ear include excision of concha or concha-mastoid sutures (Furnas technique)
48
cartilage excision is not preferred because it distorts the concha
F cartilage excision preferred because it reduces the risk of recurrence and weakens the area to facilitate the antihelix contour provided by the scapha-concha sutures.
49
suturing the hard cartilage to the weak mastoid fascia/periosteum has an increased risk of recurrence of prominence because of suture dehiscence and/or stretching of tissue
T
50
An approximately2.0 to 2.5 cm long piece ofsuperior conchal cartilage is removed just below the scapha-concha sutures
T
51
the width ofthe area can be2 to 7 mm
T
52
If more than a 15 mm width of cartilage is removed, then it is possible that the excess skin anteriorly might be bothersome to the patient and require excision
F If more than a 7 mm width of cartilage is removed,
53
Care must be taken to not overcorrect the middle third of the ear to prevent a telephone deformity
T
54
Lobule prominence is present in approximately one-fourth of patients and is often not appreciated preoperatively.
T
55
If the lobule remains prominent after setting back the superior and middle third of the ear What you will do?
first place a aMersilene suture through the area of the tail of the helix to the base of the conchal bowl. Another option is to extend the conchal cartilage excision inferiorly. A posterior lobule skin excision also can be performed. Finally, a suture can be placed from the posterior lobule to the conchal cartilage
56
The goal is to prevent the appearance of a hockey stick appearance of the ear.
T
57
the superior distance of the helix to the mastoid must be 15 (±3 mm) and the middle distance 18 (±3 mm).
T
58
These measurements should have a difference of <2 mm between the ears to ensure adequate symmetry.
T
59
Patients then are instructed to wear a soft headband at night for 1 weeks postoperatively
F Patients then are instructed to wear a soft head band at night for 6 weeks postoperatively
60
Six weeks postoperatively scar tissue is strong enough to maintain the shape of the ear.
T
61
spectrum of constricted (e.g., lop, cup) ear
(1) lidding of the helix, (2) prominence, and/or (3) reduced size from deficient structures.
62
Minor deformities of the helix in cryptocia can be improved with simple excisions
T
63
Moderately constricted ears that contain a sufficient amount of structures may be improved using techniques employed for prominent ear deformities
T
64
the primary morbidity of a constricted ear is that it is small.
F the primary morbidity of a constricted ear is that it is prominent.
65
If the ear is set back by strengthening the antihelical fold and placing sutures from the cartilage to the mastoid and temporal fascia to lengthen the vertical dimension of ear, the appearance of the child can be significantly improved
T
66
Severely constricted ears that approximate conchal-type microtia require partial or total auricular construction using cartilage grafts
T
67
Patients with cryptotia have a superior helix that is attached to the postauricular skin without a sulcus
T
68
tissue expansion can be used in cryptosia
T
69
STAHL DEFORMITY cause psychosocial morbidity
Usually, the anomaly is minor and does not cause psychosocial morbidity
70
Operative intervention may be indicated to treat a severe deformity
T
71
Patients with Stahls ear always have prominent ear
Occasionally, patients may have a prominent ear deformity as well requiring setback otoplasty techniques.
72
Accessory cartilage in the preauricular area is the most common ear anomaly.
T
73
Indication of Accessory cartilage removal under GA
If an infant has a large lesion with a wide cartilage base that cannot be easily excised and closed Patients who present after 12 months old as well are managed in the operating room because it is difficult to restrain the child in the clinic.
74
The scar of split ear lope can be re-pierced 3 months later when it has achieved its maximal strength.
T
75
The advantages ofrepiercing along the scar
that the scar is camouflaged and if the earring pulls through again, a second scar is not formed.
76
The disadvantage of piercing the scar
is thatit is not as strong as the adjacent lobule and thus has a higher risk of pulling through again
77
The ear lobe has a greater risk of forming keloid scars from piercings, compared to other parts of the ear
T
78
Small lesions can be treated with pressure only.
T
79
The pressure device is worn at night when sleeping
T
80
A pressure earring is a good first-line intervention for minor keloids in young children who are less tolerant of undergoing a corticosteroid injection in the clinic
T
81
without close follow-up and the use of postoperative compression and corticosteroid injections, the keloid will return and can be worse
T
82
After rcsccting the keloid, the patient wears a pressure earring beginning 2 weeks following the procedure at night
T
83
Four weeks postoperatively, the patient returns for monthly evaluations and possible corticosteroid injections. After 6 months, the patient follows up as needed
T
84
he lobule can be constructed using staged skin flaps from the adjacent neck, or by placing a conchal cartilage graft
T
85
using cartilage gives the most favorable outcome
T
86
Rarely, a skin abrasion or full-thickness wound can occur with ear molding;
T
87
The most common aesthetic ear surgery complication
most common problem is an unfavorable "cosmetic" outcome
88
Infection, hematoma, extrusion of sutures, or wound dehiscence is uncommon
T
89
the primary goal is to improve their appearance on frontal view
T
90
the simplest technique often is preferred.
T
91
Ear molding may correct all anomalies during the neonatal period.
F Ear molding may correct some anomalies during the neonatal period.
92
Ear abnormalities can be broadly separated into malformations (absence of part of the ear) or deformations (fully developed ear but misshapen).
T
93
1be axis of the ear is angled approximately 20° more posterior than a vertical line.
T
94
The top of the helix is at the level of the eyebrow and the lobule is at the base of the columella
T
95
The ear deformity that is most amenable to molding
a prominent ear. The antihelical fold is recreated to set back the ear mildly constricted ear with overhanging helical cartilage can be improved by lifting the helical cartilage into better alignment A Stahl deformity can be corrected by flattening the abnormal crus.
96
Timing of intervention falls into three categories: infancy, 3 to 4 years old, and late childhood or adolescence
T
97
Simple excisions of excess structures can be performed during infancy with local anesthesia as early as 4 to 6 weeks old.
T
98
Occasionally, the helical cartilage may be significantly deformed and require scoring, sutures, and/or grafts to improve its shape in cryptia
T
99
Rarely, a patient can have an absent lobule on the spectrum of microtia
T