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Beyond Ear Molding: Microtia, Hearing Function & Future Horizons

Author Ashton Steed covers Beyond Ear Molding: Microtia, Hearing Function & Future Horizons on BackTable ENT

Ashton Steed • Updated Sep 30, 2025 • 31 hits

Infant ear molding is an effective way to reshape minor auricular deformities during the early weeks of life. However, it is limited in its uses and cannot improve significant deformities such as microtia or those seen in broader syndromic conditions. These children often require early hearing assessments, multidisciplinary planning, and staged reconstruction to address both functional and aesthetic needs
In this article, we explore insights shared by Dr. Jason Qian on the BackTable ENT Podcast, focusing on what happens when ear molding alone is not enough. The discussion highlights how careful physical exam and newborn screening guide candidacy, why microtia requires early identification and multidisciplinary care, and how syndromic patients often need broader craniofacial planning. Emerging technologies such as bone conduction implants also offer new opportunities for hearing restoration, but these must be timed thoughtfully within a child’s overall treatment plan.
This article features excerpts from the BackTable ENT Podcast. You can listen to the full episode below.

The BackTable ENT Brief

• A thorough newborn ENT exam, including photo documentation, helps determine candidacy for ear molding and rules out more complex anomalies such as microtia or syndromic conditions


• Minor irregularities may improve with growth, while significant deformities and motivated families are better candidates for molding


• Molding is most effective when started before six weeks of age while neonatal cartilage remains soft


• Ear molding cannot address absent cartilage or skin in microtia, which requires staged surgical reconstruction and coordinated hearing management


• Syndromic patients, such as those with hemifacial microsomia, often require multidisciplinary care to plan craniofacial and hearing interventions over time


• Advances in bone conduction implants like Osia and Sentio are expanding hearing options for children with syndromic conditions, but these must be carefully timed with craniofacial surgeries

Beyond Ear Molding: Microtia, Hearing Function & Future Horizons

Table of Contents

(1) Physical Exam & Assessment

(2) The Window for Ear Molding

(3) When Ear Molding Isn’t Enough

Physical Exam & Assessment

Evaluation of an infant referred for ear molding begins with a comprehensive newborn ENT exam. Careful assessment of ear appearance and function, along with photo documentation for before-and-after comparison, helps guide candidacy and counseling. A key step is ruling out microtia or syndromic conditions, which represent more complex anomalies that will not respond to molding and require additional treatment. Comparison with the contralateral ear provides a useful reference, with the goal not being perfect symmetry but rather guiding the affected ear toward a more typical appearance.
Not every minor irregularity requires intervention. Subtle rim flattening or mild asymmetry may improve with growth over the child’s life, particularly if families are not very concerned. By contrast, more significant deformities, paired with strongly motivated parents, make the best candidates for molding.

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[Dr. Gopi Shah]:
In terms of your physical exam, take me through your physical exam. Are you doing photos? Do you photo-document as well?

[Dr. Jason Qian]: That's a great question. The physical exam for these, other than my general newborn ENT exam, if they do have a typical contralateral ear, I'm really looking at that. If the parents have bilateral concerns and we're putting on the bilateral molds, then there's not necessarily one that we're trying to create symmetric-- I guess it's similar to how you would think about an otoplasty, but in a newborn, I am actively trying to be better at taking photos because a lot of times you come in, you're starting the counseling, you're examining the baby. A lot of times, I have the baby on the bed and the medical assistant is holding the head, and I just start molding right away.

[Dr. Gopi Shah]:
Yes. Okay. The babies in your clinic, which babies are good candidates for your molding and which babies would you say, "You know what, this is something that we can observe. It should get better with time"?

[Dr. Jason Qian]:
I think having one of the obvious, more named auricular anomalies are good candidates. Then, a lot of times, it comes down to the parent motivation. I do now get some patients in my clinic where the pediatrician sent them just because they were like, "The helical rim looks a little bit flat. I think you should get it checked out." The parents aren't really that bothered by it. If the parents aren't bothered, and it is pretty subtle to me because newborn ears are a little bit weird looking, unless it's one of those really obvious ones, I tend to just be really realistic. It's like, "I think this isn't something we can have a huge improvement on." If the parents aren't also super motivated, then we're good to-- They're like, "I just want to be here to have it checked out. Just want to be reassured. If you don't think there's an issue, we don't have an issue," those I won't mold.

I would say the vast majority that are coming into my practice are very parent-driven, that, "I've looked this up. This is something I want molded. I'm very concerned about it." Setting the expectation with parents about what our outcomes are going to be, and then I'm happy to try this with them. I make no guarantees that it's going to look exactly how they want it to. Most parents, they just want it a little bit better. It's actually easy that way because you take the molds off, and with most cases, it looks a little bit better or a lot better. Parents are very happy, and they're like, "Thank you for doing this," and they're on their way.

Listen to the Full Podcast

Ear Molding for Infants with Dr. Jason Quian on the BackTable ENT Podcast
Ep 213 Ear Molding for Infants with Dr. Jason Quian
00:00 / 01:04

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The Window for Ear Molding

Timing remains critical for initiating ear molding. Neonatal cartilage remains soft and pliable under maternal estrogen influence for only a short period, with the most effective molding achieved before six weeks of age. For this reason, many practices prioritize these referrals and adjust schedules to accommodate newborns quickly.
The initial visit is also an opportunity to screen for associated conditions. Confirming a passed newborn hearing screen at birth, evaluating for microtia, and identifying syndromic features all help determine whether ear molding is appropriate. A thorough first evaluation ensures the right patients receive molding, while those with more complex needs are directed to appropriate workup and management.

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[Dr. Jason Qian]:
The younger the child is when we put the device on, the better the long-term outcome. Practically speaking, a lot of times our referrals are coming in the first or second week of life. The clinic rearranges the schedule to have them added on. I'm seeing them Week 3, 4, 5. There is that practical aspect. The clinic knows that these patients need to see me before six weeks. The earlier, the better, if possible.

[Dr. Gopi Shah]:
Just going back to that initial visit, is there anything specific as part of your history? Are there any risk factors that you're asking about, whether it's during the pregnancy or delivery?

[Dr. Jason Qian]:
Yes. The big thing for me is really the hearing, did they pass their newborn hearing screen? Newborn ears are sometimes hard to really even make sense. Like, is this a Grade 1 microtia, or does it just like look a little bit weird? If it is on the microtia spectrum, of course, we do want to. That's a whole other conversation in itself. It's really important to capture any conductive hearing loss and intervene early on. If they're passing their newborn hearing screen, the other thing would be, are there any other big syndromic features that make us concerned.

With the microtia kids, I like to make sure that they have a renal ultrasound because there has been an association between renal anomalies and microtia. One of the thoughts there is that the kidneys and the ears, they develop at the same gestational age. That's one of the reasons for the association. Outside of that, family history, although for the ear molding candidates, there's not always a good family history when it comes to lop ear, a lot of times, prominent ear, you can see it in the parents.

Then I do an ear exam. I don't know about you, though, but when I do a newborn otoscopy, I see an eardrum, but it's usually really floppy and gray. It's not like I'm seeing great landmarks to begin with. If you pass a newborn hearing and you have an eardrum, I'm like, "You're good for now."

When Ear Molding Isn’t Enough

While ear molding can make a lasting difference for infants with minor auricular deformities, it has clear limits. For children with microtia where there is a deficiency of cartilage or skin, molding cannot create what is not there. These patients often require staged surgical reconstruction in partnership with craniofacial and plastic surgery teams. Because microtia is frequently associated with middle ear and canal anomalies, early referral is essential not just for appearance but also for identification and early intervention for hearing loss.
Syndromic patients add another layer of complexity. Conditions such as hemifacial microsomia may involve broader craniofacial differences requiring jaw reconstruction or other interventions. In these cases, ear reconstruction must be timed carefully within the overall surgical plan and timing with the child’s growth. Surgical options for hearing loss in these children now include bone conduction implants, such as Osia and Sentio, which have expanded options and may allow near-normal hearing levels at younger ages. Even so, their use must be coordinated with planned craniofacial surgeries, which further highlights the importance of a multidisciplinary team for these complex patients.

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[Dr. Jason Qian]:
With the isolated ear molding, like a lot of cases, if there's no other concerns with hearing or no other craniofacial concerns, it's just a standalone thing, again, I always offer to these parents, "If this is something that you're still unhappy with at age five, you're happy to come back to see me," I do otoplasty. That's a need within our group that I have the training, and I'm happy to fill. Most of that conversation is happening for the kids who are beyond the window, who then get referred to me. It's more of, "We'll see what happens. There's nothing to do now, but come back to see me."

When it does get a bit more complicated, like microtia, I do collaborate. I do the hearing for microtia. That's a whole other conversation, because with the microtia, that's an external ear issue, but very often comes with canal and middle ear anomalies and conductive hearing loss. It's a really big effort, not only surgically to do the microtia, but also with the wound care afterwards and the coordination with the hearing. I do collaborate with our craniofacial clinic and plastic surgery for total auricular reconstruction, which is what you would need for most cases of microtia.

Now, the landscape; it's a really interesting time because my primary concern, especially early in life with the microtia kids, is the hearing. The goal is, and anyone who sees ear molding, you have to identify, "Well, this is not moldable and actually this is going down microtia pathway." We have to get them plugged in. The goal is to identify any conductive hearing loss and get a soft band conduction hearing aid on by six months. Historically, the hearing reconstruction would be a canalplasty for stenosis or atresiaplasty for atresia. Now, I still offer canalplasty for stenosis and OCR if they are a good candidate. I use a modification of the Jahrsdoerfer score.

For me, it's really important to have that stapes. Traditionally, they teach us that the stapes counts for two points in the Jahrsdoerfer score, but if there's no stapes, it's a no-go for me. Without getting too much into that, I'll still offer the canalplasty for certain kids with stenosis and OCR for hearing. Atresiaplasty is very controversial. There's a very high complication rate of creating a hole out of nothing and doing circumferential skin grafts that can't self-clean itself, and it's like a lifetime commitment to seeing an otologist. Even the most experienced atresia surgeons, the best outcomes are expected to be still around a 20 to 30 decibel loss.

Now we're in an exciting time where we have these bone conduction implants. Osia, made by Cochlear corp is right now the most popular bone conduction implant. It recently, in the past couple of months, was FDA-approved down to age five, which is around the earliest time that you start thinking about doing a microtia reconstruction. There's also now a competitor on the market called Sentio, made by Oticon. Now Oticon makes the Ponto hearing aid device, which is really popular because it has a huge range and great sound quality. I understand they're doing FDA trials to approve the Sentio down to age three.

This is a big game changer for atresia because it can give normal levels of hearing. In the microtia world, historically, the hearing has come during or after the auricular reconstruction. Even with these implants, it would still come during or after because monopolar cautery is contraindicated. Raising any flap, you wouldn't want to do with an Osia or a Sentio in. Although there are some plastic surgeons out there that say they do and it's fine, but it's not. It's just not. We're seeing those patients afterwards and the devices are all wonky. There are ways now to raise the flap with a harmonic scalpel blade, which is not monopolar cautery. It is an interesting time now that I'm sure we'll see some groups try to implant before auricular reconstruction, but it is a big coordinated effort.

Then again, for the kids who have not isolated microsia, but if they do have very severe hemifacial microsomia, they'll need a mandible later, that's plastics for us here. We have to make sure that we're not going to do anything with a hearing and putting an implant in if they're like, "No, we're going to do a mandible after, so there's no point in putting it in now." Being involved with the craniofacial clinic is important in some cases.

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Podcast Contributors

Dr. Jason Qian discusses Ear Molding for Infants on the BackTable 213 Podcast

Dr. Jason Qian

Dr. Jason Quian is a pediatric otolaryngologist at Rady Children's Hospital in San Diego, California.

Dr. Gopi Shah discusses Ear Molding for Infants on the BackTable 213 Podcast

Dr. Gopi Shah

Dr. Gopi Shah is a pediatric otolaryngologist and the co-host of BackTable ENT.

Cite This Podcast

BackTable, LLC (Producer). (2025, March 4). Ep. 213 – Ear Molding for Infants [Audio podcast]. Retrieved from https://www.backtable.com

Disclaimer: The Materials available on BackTable.com are for informational and educational purposes only and are not a substitute for the professional judgment of a healthcare professional in diagnosing and treating patients. The opinions expressed by participants of the BackTable Podcast belong solely to the participants, and do not necessarily reflect the views of BackTable.

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