Surgical approaches to congenital atresia of the external auditory canal TIMOTHY B. MOLONY, MD, and ANTONIO DE LA CRUZ, MD, New Orleans. Louisiana. and Los Angeles. California

During the past 4 years, 22 patients with congenital atresia of the external aUditory canal underwent 24 Initial operations by either an anterior or transmastold approach. No attempt at randomization was made. but the two groups were similar In number and pathology (In 14 cases approach was anterior and In 10 cases approach was transmastoid). Followup ranged from 6 months to 4 years. Hearing results were similar in the two groups (71% with air-bone gap less than 30 dB). There were no Instances of facial nerve Injury or sensorineural hearing loss. Facial nerve monitoring was used. Complications of stenosis and drainage were more common with the transmastold approach. In both groups, hearing results were accomplished with the patients' Intact osslcles or prosthetic reconstructions. Meticulous soft-tissue technique, with splitthickness grafts covering all exposed bone. Is the key to preventing stenosis. For the three cases of patients with thick. acellular atresia plates, a different approach was developed. Maintaining proper orientation during the medial dissection Is more difficUlt In these cases. Byopening the antrum primarily and Identifying the lateral canal, Ossicles. and facial nerve. an ear canal can then be created anteriorly with these landmarks In view. An Intact canal wail-like procedure Iscarried out. Although hearing results are similar. the anterior approach. because of fewer postoperative complications. Is now our procedure of choice. Proper orientation and soft-tissue technique are the keys to successful correction of the congenitally atretic ear canal. (OTOLARYNGOL HEAD NECK SURG 1990;103:991.)

Obtaining consistent results in correcting congenital atresia of the external auditory canal remains a challenging task in otology. Complications, such as stenosis, drainage, and poor hearing results, can be minimized by adhering to well-established concepts and techniques. Thorough knowledge of modern tympanoplastic methods and of temporal bone anomalies in the atretic ear is a necessity. From Kiesselbach (1883), I to Cohen and Fox (1943),2 to Pattee (1947),.1 to Bellucci 4 (I 960), numerous approaches and procedures have been tried, with varying degrees of success. At present, two generally accepted techniques are used to recon-

~------------------

From the Department of Otolaryngology (Dr. Molony). Ochsner Clinic and Alton Ochsner Medical Foundation, and the House Ear Institute (Dr. de la Cruz). Presented at the Annual Meeting of the American Academy of OtOlaryngology_Head and Neck Surgery, New Orleans. La.• Sept. 24-28. 1989. Received for publication Sept. 24. 1989: revision received June 25. 1990; accepted July 10. 1990. Reprint requests: Timothy B. Molony. MD. Ochsner Clinic. 1514 Jefferson Highway. New Orleans. LA 70121.

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struct the congenitally atretic ear canal-the anterior approach, as described by Jahrsdoerfer' in 1978 and by Mattox and Fisch" in 1985, and the transmastoid approach (with or without opening of the facial recess), as described by Bellucci," Shambaugh and Glasscock," and de la Cruz et al." (Figs. I and 2). In the past 4 years, the approach to correction of congenital atresias has changed considerably at the Otologic Medical Group. The senior author (A.D.C.) now uses the anterior approach in all atresia cases. For cases with very thick atresia plates and difficult anatomy, a modification of the anterior approach provides safer surgery and more predictable results. This report discusses and compares current methods, and describes significant modifications in technique. These modifications have made the final results more anatomically correct and more predictable. Indications, classification, and evaluation remain as discussed previously."

LITERAYURE REVIEW In 1947 Pattee.' described a technique for reconstruction of the meatus and mobilization of the stapes in cases of congenital atresia of the ear canal. This was 991

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OtolaryngologyHead and Neck Surgery

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Anterior

NOR AL

J

I I I I

,./

ATRESIA

I

!r$i i ? .I-

-==::.:-

,.

I

Transmastold

I

)

(

Anterior Tran smastoid

+

~ 0

Fig . 2. Axial anterior and transmastoid approaches.

Fig. 1. Anterior and transmastoid approaches-lateral.

done by way of an endaural incision with a wall-down mastoidectomy. The incus and malleus were removed, leaving a mobile stapes . Split-thickness skin was used to line the cavity. No ossicular reconstruction was attempted, and results were similar to those of fenestration surgery. Also in 1947, Ombredanne? reported his results from the correction of congenital atresias by fenestration of the horizontal semicircular canal. With the advent of tympanoplasty, introduced by Wullstein' ? and Zollner, II hearing results gradually improved . Bellucci" and Crabtree" refined techniques, and described refined approaches to ossicular reconstruction and management of the cavity. Reports by Glasscock? and de la Cruz" have emphasized the safety of a transmastoid approach to identify the atresia plate and the level of the facial nerve . Hearing results with this approach are good, but occasional problems with the cavity and with late stenosis continue. Jahradoerfer' and Mattox and Fisch" have emphasized an approach to the ossicular chain by way of the atresia plate . This approach has the advantages of minimizing air-cell exposure and eliminating the drawbacks of canal walldown surgery. With no cavity to clean or drain, postoperative care is minimized. Obliteration with softtissue flaps or pate is unnecessary. Occasionally, however, this approach is technically difficult, as in

cases with a very thick atresia plate. With few landmarks in the acellular bone , orientation in these cases is difficult, and drilling and removal of the atresia plate with the ossicles intact is required . Approaching the ossicular chain by way of the atresia plate carries the potential for acoustic inner ear trauma, with subsequent sensorineural hearing loss. The approach to the atresia plate by way of the sinodural angle and mastoid antrum has the advantage of landmarks well-known to otologic surgeons. The level of the atresia plate and facial nerve is identified early in the procedure. Tympanoplasty and the creation of a new ear canal can be carried out with confidence . Acoustic trauma to the inner ear is minimized by early separation of the ossicular chain from the atresia plate . Both approaches were used in our series. Results are compared and a modification of the anterior approach is described.

SURGICAL CONSIDERATIONS At the initial visit , the patient undergoes routine audiometry, and if necessary evoked-response audiometry. Patients younger than 4 years with bilateral atresias are immediately fitted with bone-conduction aids. Patients older than 4 or 5 years with bilateral atresias and adults with unilateral atresias are considered as candidates for surgery. Computed tomographic (CT) scans with high-resolution bone programs are done in the axial

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Fig. 3. Well-pneumatized mastoid. middle ear. Normal facial nerve and inner ear.

and coronal planes . Children with unilateral atresias and evidence of cholesteatoma, infection, or very thin atresia plates are also considered surgical candidates . Bone conduction in the involved ear should average better than 45 dB . If it is worse than 45 dB, the possibility of improved hearing-aid performance with less distortion should be discussed with the patient. Good mastoid pneumatization, normal inner and middle ear morphology, adequate oval window size, and normal facial nerve anatomy visible on the CT scan indicate a good prognosis for surgical correction (Fig. 3). Patients with poor pneumatization, contracted middle ears , and absent oval window are not candidates . In cases with severe middle ear and mastoid anomalies, surgery is not recommended. These include patients with a middle ear anterior to the condyle of the mandible and those with poor pneumatization and a facial nerve anomalously passing through or directly lateral to the middle ear. These anomalies most commonly occur in the patient with Treacher Collins syndrome. Patients with bilateral atresias should undergo operation at the age of 4 to 5 years. In the patient younger than this, difficulty of postoperative care can compromise the final result. In the patient with unilateral atresia and a normal-hearing opposite ear, delay of surgery Until adulthood is recommended. If the patient, however, has very favorable anatomy-a very thin atresia plate with ecellent pneumatization and normal middle ear ossicles and facial nerve-surgery can be performed if the parents desire it. Selection of anterior or lransmastoid approach was according to surgeon pref-

erence. The initial cases were approached by way of the transmastoid approach. With encouraging initial results from the anterior approach, the remaining cases in this series were done by way of either the anterior or modified anterior approaches. APPROACHES Anterior

A postauricular incision is made. Subcutaneous tissue is elevated anteriorly to the temporomandibular joint. Care is necessary, since an anomalous facial nerve may exit the temporal bone in this area. T-shaped periosteal incisions are made and the mastoid cortex is exposed . If a remnant of the tympanic bone is present, the new ear canal is begun above it, at the level of the middle fossa dura . If no such remnant is present, drilling is begun at the level of the linea temporalis, just posterior to the glenoid fossa (Fig . 4). There are few landmarks through the atretic bone. The dissection is carried medially and anteriorly by means of cutting and with diamond burrs. The middle fossa dura is identified and followed. In all cases, the facial nerve is continuously monitored with the Nicolet NIM-2 (Nicolet Instruments , Madison, Wis.) . The anterior epitympanum is encountered, and the fused incus/ malleus mass is identified. The incus and malleus are carefully dissected away from the atresia plate. They are left intact, if possible . The horizontal facial nerve is always medial to these structures , and therefore is relatively protected . The atresia plate is removed with diamond microdrills

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OlolaryngologyHead and Neck Surgery

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Fig. 4. Anterior approach,

Skin Graft

Fascia Graft

Fig. 5. Preparation of fascia graft and skin graft.

Fig. 6. Mealoplasty,

and curettes to completely expose the ossicles. Care must be taken on dissction of the inferior and posterior aspect, since the aberrant facial nerve often passes laterally through the atresia plate in this area. The ossicular chain is left intact if complete. Identification of the stapes may be difficult because of overhanging or anomalousfacial nerve anatomy. Mastoid air-cell exposure is avoided if possible. A new ear canal approximately 11/ 2 times normal size is created. A 20- X IS-mm oval of temporalis fascia is cut to fashion a tympanic membrane graft. Small 3- x 6-mm "tabs" are cut in the anterior and superior aspects of the graft (Fig. 5). The new tympanic membrane is grafted with the fascia to either the lateral surface of the intact ossicular chain or with prosthetic partial ossicular replacement prosthesis (PORP) or total ossicular replacement prosthesis (TORP) covered with onlayed cartilage. The "tabs" are placed medially into the protympanum and epitympanum. A 0.012-inch split-thickness skin graft. 6 x 6 ern, is taken from the abdomen or thigh. One edge of the graft is cut in a zig-zag fashion approximately l.S-cm deep. The new ear canal is circumferentially lined with the split-thickness skin, with the zigzags totally overlapping the reconstructed eardrum.

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VOlume103 Number 6 December 1990

Surgical approaches to congenital atresia of the external aud itory canal

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.Skln Graft Tr nsm

toid Appro ch

.. , ,



I

"

,

.. . '

Fascia Graft

Fig. 7. Placement of fascia and skin grafts.

Fig. 8. Transmastold approach.

All bone in the ear canal should be covered. There should be 2 to 3 cm of excess skin laterally to line the soft tissue meatoplasty. A single layer of antibioticsoaked Gelfoam is used to hold the skin and fascia of the new eardrum in place. A disc ofO.040-inch silicone rubber is placed over this . Next, 1.5 x 6 em gauze strips impregnated with Vaseline (Sherwood Medical CO./Hospital Products D, Greenwich, Conn.) are placed in the canal lateral to the silicone rubber to make a rosebud dressing. The center is filled with small Vaseline-impregnated gauze pieces. Meatoplasty is then performed, and skin and subcutaneous cartilage and tissue are removed in a 2-cm diameter area over the new meatus (Fig. 6). The ear is turned and the skin of the canal is brought through the meatoplasty. The skin graft is attached circumferentially to the meatal skin with absorbable sutures (Fig. 7). The soft tissue of the meatus should be completely lined . The meatus is packed open widely with a rolled-up strip of Vaselineimpregnated gauze. The postauricular incision is then closed. Tran_mastold

A postauricular incision is made and continued down to the mastoid cortex. Soft tissue is elevated anteriorly, and the glenoid fossa is explored. Dissection is begun at the level of the linea temporalis, well posterior to the

temporomandibular joint. The sinodural angle is identified and followed medially to the antrum. The facial nerve is monitored continuously with the Nicolet NIM2. The lateral semicircular canal and the atresia plate are identified. The atresia plate is carefully removed. At this point incudostapedial joint separation if possible , is recommended to prevent acoustic trauma to the inner ear. Mastoid air-cell exenteration, with lowering of the facial ridge to the level of the facial nerve, is then carried out (Fig. 8). If the ossicles are intact, the temporal is fascia is grafted directly to them. If not, reconstruction is done with a PORP or TORP, with cartilage overlay followed by mastoid air-cell obliteration with soft-tissue flaps or bone pate, meatoplasty, and canal skin grafting as described previously. Anterior Approach Modlftcatlon

In patients with thick, bony atresia plates, orientation in the anterior approach is often difficult during the medial dissection . These patients typically have few air cells , making this approach particularly challenging (Fig . 9). Dissection too far in either the inferior or posterior direction risks inadvertent carotid, lateral canal, or facial nerve injury. Orientation can be achieved in these cases with initial posterior dissection and an-

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OtolaryngologyHead and Neck Surgery

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Fig. 9. Thick atresia plate .

1

Modified Anterior Appro ch

(Fig. 10). The lateral canal can be used as a landmark to indicate depth and anterior-posterior and superiorinferior directionality, thus expediting the dissection . An intact canal wall-like procedure is carried out. Tympanic membrane grafting, meatoplasty, ossiculoplasty and ear canal grafting are carried out as described previously. CASE REPORT: MODIFIED ANTERIOR APPROACH

Fig. 10. Modified ante rior approach.

trotomy to identify the levels of the lateral canal, facial nerve, and atresia plate. A new ear canal can then be created anteriorly by drilling just posterior to the glenoid fossa and following the tegmen mastoidum medially

A 16-year-old boy had a right- sided congenital atresia of the ear canal, with a grade II microtia on that side and a rudimentary blind-sac ear canal. His left auricle and ear canal were normal. He had normal hearing on the left and a bone conduction level of 15 dB on the right , with an air conduction level of 42 dB . CT scanning indicated a very thick atresia plate and a well-pneumatized mastoid on the right (Fig. II) . Facial nerve anatomy and middle ear were normal. The right ear was approached by postauricular incis ion . A short vascular strip was made in the rudimentary ear canal and the ear was reflected forward. Drilling was begun in the ear canal at the anterior and superior aspect . Solid bone that was quite thick and acellular was encountered. There were no visible landmarks to follow . At this point attention was turned to the mastoid , where drilling was begun posteriorly and the sinodural angle was identified . The dissection was continued medially and the antrum was entered . The lateral semicircular canal was identified , the facial recess was opened. and the facial nerve was identified . With these landmarks in view . attention was directed to the ear canal. where the atresia plate was then removed. The epitympanum and the fixed, fused ossicular mass were identified . With diamond burrs, bone

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VOlume103 Number 6 December 1990

Surgical approaches to congenital atresia of the external auditory canal

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Fig. 11. Reported case. Thick atresia plate, pneumatized mastoid.

Over the cssicular mass was carefully removed to expose the middle ear. Stapes mobility could not be determined because of the size and position of the ossicular mass. Removal of this mass revealed a mobile stapes. The middle ear was filled with Gelfoam, and a PORP was placed over the stapes with atresiaplate cartilagecovering the platform. Temporalis fascia Was used as a tympanic membrane overlay graft with a "tab" into the protympanum. Split-thickness skin was used to line the new ear canal. Gelfoam was packed lateral to the graft, followed by a disc of silicone rubber. Antibiotic-impregnated gauze was used to fill the new ear canal. Meatoplasty was carried out by incising a 2-cm circle in the skin and deep soft tissue lateral to the newly created bony meatus. Ear canal skin graft was brought out through the meatus and attached laterallyto the meatoplastyedge with absorbablesutures. The postauricular incision was closed after a wedge had been incised to retract the auricular remnant posteriorly and superiorly.The postoperativecourse was uneventful. When seen 6 months after surgery, the patient had a well-formed ear canal, with an air-bone gap of 13 dB and a speech reception threshold (SRT) of 25 dB.

METHODS AND RESULTS From 1984 to 1988, 86 patients with congenital atresia of the external auditory canal were evaluated at the Otologic Medical Group. Charts were reviewed retrospectively for data on first visit, surgical procedure, postoperative results, and complications. Surgical correction was recommended in 39 cases. From the 22 patients who underwent surgical correction, results are available in 24 ears (Table I). No

patients were unavailable for followup. There were 15 male and 7 female patients, aged 4 to 61 years. Fifteen patients had unilateral atresias and 7 had bilateral atresias. Average preoperative air-bone gap was 51 dB. Average preoperative SRT was 65 dB. Of 15 right ears and 9 left ears, 10 initial procedures were performed by way of a trans mastoid approach. Fourteen were performed by way of an anterior approach, with three of these through the modified anterior approach. Length of followup ranged from 6 months to 4 years. Success in this series is defined as a closure of the air-bone gap to within 30 dB at the last follow-up examination. Results are also reported for closure of the air-bone gap to within 20 dB. Of the 24 initial surgical procedures, 17 were eventually classified as successful, with 71 % of the patients having air-bone gaps of less than 30 dB and 50% having air-bone gaps of less than 20 dB (Table 2). SRT in the larger group ranged from 20 to 50 dB, with an average SRT of 31 dB. There were no instances of sensorineural losses. Six of the 10 transmastoid operations and 11 of the 14 anterior operations were successful. Fourteen of the 24 ears were reconstructed to their intact ossicular chain; nine of these reconstructions were successful (Table 3). Seven of eight prosthetic reconstructions were successful. In two cases, reconstruction was not performed. There were no cases of postoperative facial weakness. There were seven failures in this series. Three cases

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998 MOLONY and

OtolaryngologyHead and Neck Surgery

D! LA CRUZ

Table 1. Case descriptions

Patient

Age (yr)

6

2

3

14

Op side

Atresia

Pathology

Procedure

L

81

Pneumatized, soft-tissue stenosis. FN over OW Pneumatized, 5 rnrn atresia plate, hypoplastic malleus, normal ME Left -~ pneumatized; normal ME, FN, OW; 3 mm atresia plate: fixed stapes pneumatized; Right normal ME, FN, OW: 3 mm atresia plate: fixed stapes Pneumatized, no plate anterior FN, narrow ME, abnormal ossicles Pneumatized; normal ME, FN, OW; cholesteatom a medial to mid canal Pneumatized; bony canal stenosis: normal ME, ossicles, FN Bony canal stenosis, soft-tissue atresia, normal ME Pneumatized, thin atresia plate, ME normal Pneumatized; thin bony plate; normal FN, ME Pneumatized, normal ME, malformed ossicles Drainage, softtissue stenosis, 4 mm atresia plate. cholesteatoma in ME staoes Pneumatized; normal OW. ME. FN: thick atresia plate

ANT

R

UNI

L

BI

6 R

4

5

6

7

61

17

20

16

R

R

R

L

BI

UNI

UNI

UNI

UNI

8

12

R

UNI

9

14

L

UNI

10

18

R

UNI

11

7

12

25

L

R

BI

UNI

Reconstruction

Result [preop. AC, postop. AC/BC (ABGll*

New OW with stapes prosthesis

70,45/20

ANT

To ossicles

55, 36/10 (26)

ANT

Stapes prosthesis, incus to OW

72,47/20

Stapes prosthesis, Incus to OW

72,47/20

To ossicles. secend procedure with TORP

83,41/26

To ossicles: removal of cholesteatoma

58,24/10

To ossicles

65,45/25

ANT

ANT

ANT

ANT

Comments

(25)

(27)

(27)

(15) late fixation

2 proce-

cures. corrected With TORP at 1 year

(14)

(20)

ANT

To ossicles

72, 69/25 (44)

ANT

To ossicles

66,59/18 (41)

ANT

To ossicles

54,39/9 (20)

ANT

To ossicles

69, 69/20 (49)

Modified ANT

Modified ANT

Staged with TORP

To ossicles

60, 22110 (12)

Lateralized graft

Lateralized graft

Failure, unknown cause Staged with TORPsecond procedure

100, 65/54 (11 )

Op, Side operated on: AC, air conduction. BC, bono conoucncn: BI, [)ilateriJl Ow. oval Window, ANI, anterior, UNI, unilateral, ME, rniodle ear, EAC, external aUditory canal. TRANS, transmastoid. 'Pure-tone average, American National Standards Institute (1969)

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VOlume 103 Number6 December 1990

Surgical approaches to congenital atresia of the external auditory canal

999

Table 1. Case descriptions-(cont)

Patient

Age (yrl

Op side

Atresia

13

16

R

UNI

14

10

L

BI

-

15

5

R

BI

16

5

L

BI

17

18

R

UNI

18

18

L

UNI

19

26

R

UNI

20

30

R

UNI

21

18

R

UNI

5

R

BI

6

L

BI

22

Pathology Pneumatized thick atresia plate. normal FN. ME Pneumatized: no ear canal, 2 rnm atresia plate: normal FN. ME: cholesteotoma in ME Pneumatized: normal ME, FN

Result [preop. AC. postop. AC/BC (ABGIl*

Procedure

Reconstruction

Modified ANT

PORP

38,29/16 (13)

To ossicles

47. 38/20 (18)

TRANS

TRANS

None

60, 60/20 (40)

Pneumatized. 12 rnrn bony plate, abnormal FN (over OW) Pneumatized; soft tissue in EAC: normal ME. FN

TRANS

None

65.65/15 (50)

TRANS

To ossicles

66, 24/4 (20)

Pneumatized: 4 mm atresia plate; normal FN. ME Pneumatized: normal ME, FN

TRANS

To ossicles

69, 50/31 (19)

TRANS

To ossicles

77.67/20 (47)

TRANS

To ossicles

65,30/15 (15)

TRANS

To ossicles

80, 65/35 (30)

Pneumatized; normal ME, FN

TRANS

PORP

59 49/6 (43)

Borderline pneumatization, lateral FN

TRANS

PORP

59,17/1 (16)

Pneumatized; deformed ossicles: normal ME. FN Pneumatized; normal ME, FN; abnormal ossicles

showed varying degrees of lateralization and stenosis 30-dB air-bone gap)

Ossicular Chain

TORP

PORP

Piston

9 5

2

o

2 1

o

Table 4. Complications Failure Laterallzalion Stenosis Drainage unknown

Transmastoid Anterior Modified anterior

2

3

2

o o

o

o

3

o o

1 1

o

revision cases for lateralization and stenosis were done by way of an initial transmastoid approach. Treatment for stenosis consists initially of repeated dilatations of the ear canal with expandable wicks and steroid! antibiotic drops. Two of the revisions were successful in maintaining a patent meatus, with a good hearing result. One patient required three operations. Of the total of 24 initial cases, one in four patients underwent more than one operation.

DISCUSSION Results from this series indicate that the anterior and transmastoid approaches yield 79% and 60% success rates, respectively. The modified anterior approach combines the advantages of early identification of surgical landmarks with the good anatomic and functional results of the anterior approach. At present, ossicular reconstruction with the patient's intact ossicular chain is preferred to reconstruction with prosthetic ossicles. Although five of the seven failures were reconstructed with intact ossicles, it appears that failure was caused more by graft and ear canal healing problems than by ossicular problems. With current techniques, extrusion of the prosthetic ossicles is expected in less than 5% of cases; follow-up study in this series has not been long enough to comment on this factor. In three of four cases, closure of air-bone gaps to within 30 dB can be expected. Closure to within 20 dB

3

No reconstruction

o 2

can be expected in 50% of cases. There were no instances of facial nerve injury or sensorineural losses. The advent of continuous facial nerve monitoring has made operating on ears with congenital atresia of the external auditory canal safer, and gives the surgeon an extra measure of confidence. One of four patients required more than one operation. As in our previous report, x lateralization and stenosis were the most common causes of failure. Lateralization of the graft can occur with either procedure. Stenosis occurred more frequently with the transmastoid approach.

CONCLUSIONS Three of four patients undergoing surgery to correct conductive hearing loss in congenital atresia of the ear canal should experience signiticant improvement in hearing levels. Either a transmastoid or an anterior approach can be used, with similar hearing results. Postoperative problems of stenosis and drainage are more common with the transmastoid approach. The anterior approach is more difficult in an ear with a thick and acellular atresia plate, but it can be accomplished with confidence by initial identification of landmarks through the antrum, and by continuous facial nerve monitoring. The anterior approach or its modification, with fewer healing and drainage problems, is currently our procedure of choice in cases of surgically correctable congenital atresia of the ear canal. Meticulous soft-tissue technique with skin covering all exposed bone, adequate meatoplasty, and accurate graft placement are the keys to surgical correction of the congenitally atretic ear canal. We would like to thank Diane Knutsen from the House Ear Institute. Barbara Lynch and Marion Stafford of Medical Editing, and Barbara Seide of Medical Illustrations. Alton Ochsner Medical Foundation.

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Volume 103 Number 6 December 1990

Surgical approaches to congenital atresia of the external auditory canal

REFERENCES

I. Fraser JS. Maldcvelopments of the auricle. external acoustic meatus and middle ear; microtia and congenital meatal atresia. Arch Otolaryngol 1931; n: 1-27. 2. Cohen L. Fox SL. Atresia of external auditory canal. Arch Otolaryngol 1943;38:338-46. Transactions of the Annual Meeting of the American Laryngological Rhinological & Otological Society 1943; 136-49. 3. Pattee GL. An operation to improve hearing in cases of congenital atresia of the external auditory meatus. Arch Otolaryngol 1947;45:568-80. 4. Bellucci RJ. The problem of congenital auricular malformation. I. Construction of the external auditory canal. Trans Acad Ophthalmol 0101 1960:64:840-52. 5. Jahrsdoerfer RA. Congenital atresia of the ear. Laryngoscope I978;8lHsuppl 13):I -48. 6. Mattox DE. Fisch U. Surgical correction of congenital atresia of the ear. OTOLARYNGOL HEAD NECK SL'RG 1986;94:574-7.

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7. Shambaugh em Jr. Glasscock ME III. Surgical correction of congenital malformations of the sound-conducting system. In: Shambaugh GE Jr. Glasscock ME III. cds. Surgery of the car. Philadelphia. WB Saunders Co. I

Surgical approaches to congenital atresia of the external auditory canal.

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