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motion may be without clinical significance. Further,

Roy et al. showed that laryngoscopic findings are not

consistent from case to case, even in experimentally

induced isolated unilateral superior laryngeal nerve

palsy, a condition probably more homogeneous than that

which presents clinically.

17

Respondents identified defi-

cits of gross motion as having the highest positive pre-

dictive value for VFP, despite reporting heavy reliance

on stroboscopic examination in practice. This may reflect

merely that stroboscopy is the standard clinical exami-

nation for patients with a voice complaint in the special-

ized practices of these physicians rather than the use of

examination under stroboscopic light to identify VFP.

Mucosal wave phase asymmetry was deemed the most

useful stroboscopic sign, ranking only fifth in order of

preference despite a report that identified it as correlat-

ing very well with LEMG abnormalities.

7

Stroboscopic

signs (phase, amplitude, and frequency) were also

marked by the greatest divergence of opinion regarding

significance, as reflected by the standard error. The few

signs that have been the subject of systematic analysis

in the literature, namely arytenoid rotation

8

and unilat-

eral ventricular fold hyperfunction,

6

were not regarded

as among the most useful. Reports have proposed a rela-

tionship between contact lesions

9,10

and vocal fold pseu-

docysts

11

and VFP. Despite this, respondents thought

that the potential for VFP to be present when such

lesions were identified was very low.

Overall, this investigation reveals that paresis is fre-

quently diagnosed and appears to be a significant clinical

entity in laryngology practices. Diagnosis appears to be

made on the basis of qualitative findings on laryngoscopy,

principally deficits of gross vocal fold motion. Although

stroboscopy is widely used, stroboscopic signs are not con-

sidered the most reliable signs to identify VFP. Electro-

physiologic testing is not used often. Plainly, there exists

no clear consensus on how the diagnosis of VFP should be

made in a given patient, and establishing one will be a

challenge in the absence of tests or findings that are both

reasonably specific and sensitive. Under these circum-

stances, and given the frequency of asymmetric motion in

the larynx, VFP is at risk of being diagnosed uncritically

when no other obvious reason for a patient’s complaint is

evident to the examiner.

The survey format is subject to substantial recall

bias and may give a false impression—likely falsely ele-

vated—of the prevalence of paresis. This survey explic-

itly did not distinguish between superior laryngeal nerve

paresis and recurrent laryngeal nerve paresis, fre-

quently separated in the literature, which may have

caused surveyed physicians to assign less positive pre-

dictive value to the signs under consideration than a

more specific diagnosis. Reasons for the relatively rare

use of LEMG were not investigated; these may have lit-

tle to do with reservations regarding LEMG utility. Most

importantly, the format of the survey necessarily does

not well reflect the method of diagnosis of VFP in clini-

cal practice. Such a diagnosis is rarely made on the basis

of a single element of the evaluation or a single sign con-

sidered by itself, but depends on an educated critical

synthesis of the clinical evidence. Physicians may form

an impression of the likelihood of a given diagnosis

based on the history, which then informs the physical

examination. In fact, the perceived likelihood of VFP

based on symptoms and clinical evolution of the com-

plaint may significantly affect the perceived positive pre-

dictive value of a given laryngoscopic sign. Despite these

limitations, this data may form a useful basis for further

consideration of this challenging topic.

CONCLUSION

Surveyed laryngologists diagnose VFP frequently,

relying principally on laryngeal strobovideolaryngoscopy

to make the diagnosis. Among laryngoscopic signs, gross

motion abnormalities were judged to have the highest

positive predictive value for VFP, followed by abnormal-

ities in the mucosal wave. Opinion varied most about

the importance of these. LEMG was infrequently used to

assess for VFP and was considered to have only moder-

ate sensitivity for the diagnosis. Given the perceived

clinical importance of VFP, directed investigation is nec-

essary to refine diagnostic accuracy.

BIBLIOGRAPHY

1. Sulica L., Vocal Fold Paresis: An Evolving Clinical Concept.

Curr Otorhi-

nolaryngol Rep

2013;1:158–162.

2. Koufman JA, Postma GN, Cummins MM, Blalock PD. Vocal fold paresis.

Otolaryngol Head Neck Surg

2000;122:537–541.

3. Heman-Ackah YD, Barr A. Mild vocal fold paresis: understanding clinical

presentation and electromyographic findings.

J Voice

2006;20:269–281.

4. Rubin AD, Praneetvatakul V, Heman-Ackah Y, Moyer CA, Mandel S,

Sataloff RT. Repetitive phonatory tasks for identifying vocal fold paresis.

J Voice

2005;19:679–686.

5. Simpson CB, Cheung EJ, Jackson CJ. Vocal fold paresis: clinical and elec-

trophysiologic features in a tertiary laryngology practice.

J Voice

2009;

23:396–398. doi:

10.1016/j.jvoice.2007.10.011.

6. Belafsky PC, Postma GN, Reulbach TR, Holland BW, Koufman JA. Muscle

tension dysphonia as a sign of underlying glottal insufficiency.

Otolaryn-

gol Head Neck Surg

2002;127:448–451.

TABLE III.

Respondent Opinion Regarding Positive Predictive Value of

Laryngoscopic Findings in VFP.

Examination finding

Average % Error

r

Slow/sluggish motion

74.9

3.0 22.8

Decreased VF adduction

67.3

3.5 26.7

Decreased VF abduction

65.4

3.4 26.1

Decreased VF tone

61.1

3.5 26.3

Asymetric MW phase

60.2

4.1 31.3

Hemilarynx atrophy

60.1

4.0 30.8

Unilateral supraglottic hyperfunction

58.9

3.9 29.4

Glottic insufficiency

55.4

3.5 26.8

Asymetric MW amplitude

51.7

4.2 31.7

Asymetric MW frequency

48.6

4.0 30.6

VF height difference

43.5

3.8 28.6

Impairment of arytenoid rotation

42.9

3.6 27.8

Glottic axis deviation

41.3

3.8 29.3

Bilateral supraglottic hyperfunction

32.0

3.3 25

Presence of contact lesion

27.3

2.4 18.1

Presence of pseudocyst

22.3

2.8 21.4

MW

5

mucosal wave; VF

5

vocal fold; VFP

5

vocal fold paresis.

Laryngoscope 125: April 2015

Wu and Sulica: Paresis Survey

28