II. Definitions
- Stuttering
- Involuntary dysfluency in verbal expression
- Persistent Stuttering
- Stuttering that lasts beyond age 7 years
III. Epidemiology
- Genetic component (from twin studies)
-
Prevalence
- Childhood-Onset Fluency Disorder: 5-10% of preschoolers
- Children under age 10 years: 1.4% (66% are boys)
- Adults: <1% (80% are men)
IV. Pathophysiology
- Fluent speech requires CNS complex coordination of respiratory, laryngeal and articulatory Muscles
- Preschool children normally display speech disfluency as they are learning to speak
- Those with Childhood-Onset Fluency Disorder display CNS imaging changes affecting speech related pathways
- Requires concious monitoring by those who Stutter, in contrast to unconscious fluent speech
V. Signs
- Involuntary dysfluency
- Repeated sounds, syllables or words
- Speech blocks
- Prolonged pauses between words
- Associated compensatory behaviors
- Eye blinking
- Jaw jerking
- Provocative Factors
- Stressful circumstances
- Public speaking
VI. Types
- Developmental Stuttering (80% of cases)
- Stuttering occurs at begining of words
- Prominent secondary behaviors
- Onset at age 3-8 years and resolves within 4 years in 75% of cases
- Neurogenic Stuttering
- Acquired Stuttering due to neurologic Trauma (e.g. Cerebrovascular Accident, Head Trauma)
- Psychogenic Stuttering (rare)
VII. Differential Diagnosis
- Stutter-like Dysfluency
- Dysthymic phonation
- Blocks (unable to articulate)
- Broken words ("I am sp.....eaking")
- Prolonged sounds ("ssssssugar")
- Partial word repetition ("my ddddd dad is here.")
- Single word repetitions ("I think I think..." or "she she she")
- Dysthymic phonation
- Interjections (e.g. "um")
- Incomplete phrase ("He is - oh where is he")
VIII. Grading
- Normal Stuttering
- Onset age 1.5 to 3 years old
- Repeated syllables and sounds at the begining of sentences
- Children have no awareness of their Stuttering
- Mild Stuttering
- Onset age 3 to 5 years old
- Similar to normal Stuttering but more frequent, associated with secondary behaviors
- Severe Stuttering
- Onset age 1-7 years
- Stuttering occurs in most phrases and sentences
IX. Management
- Refer Mild and Severe Stuttering to Speech Pathology
- Early interventions are most effective (plastic brain) and less likely to develop complications (see below)
- Stutter-like Dysfluency (see differential diagnosis above)
- Parental concerns regarding child's speech
- Persistent dysfluency >12 months
- Worsening dysfluency
- Best therapies focus on reducing, not eliminating Stuttering
- Decrease Stuttering to less than half the prior events (and ideally to where the child and others do not notice)
- Decrease secondary behaviors and mannerisms (e.g. facial expressions, word avoidance)
- Speech pathology sessions are typically with both parent and child
- Parent learns interventions to practice with their child
- Medications are ineffective in Stuttering
- Devices (Contremporary Stuttering devices, Fluency-shaping mechanisms)
- Example: Delayed auditory feedback device (slows speaking rate)
- Behavioral Techniques
- Provide relaxed environment that allows child enough time to speak without hurrying
- Parents and teachers praise fluent speech
- Ocasionally acknowledge and correct Stuttering in a gentle non-judgemental way
- Examples of feedback: Noting either bumpy or fluid speech
X. Complications
- Decreased self esteem and negative Perception by others
- Word avoidance and mannerisms (e.g. facial expressions during Stuttering)
- Social withdrawal
- School difficulties and difficulty completing education
- Unemployment or impeded career advancement
- Anxiety Disorder (including social anxiety)
XI. Prognosis
- Most Stuttering (65-87%) resolves by age 7 years with or without treatment
XII. Resources
- American Board of Fluency and Fluency Disorders
- American Speech-Language-Hearing Association (ASHA)
- National Stuttering Association
- Stuttering Foundation of America
XIII. References
- Moore and Jefferson (2004) Handbook Psychiatry , 2nd ed, Chap. 20
- Simms in Kliegman (2007) Nelson Pediatrics, 18th ed., Chap. 32
- Prasse (2008) Am Fam Physician 77(9): 1271-8 [PubMed]
- Sander(2019) Am Fam Physician 100(9): 556-60 [PubMed]
- Costa (2000) CMAJ 162(13):1849-55 [PubMed]