Difference between revisions of "Myotonic muscular dystrophy"
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There are two types of myotonic dystrophy caused by two mutations in two distinct gene loci: myotonic dystrophy types 1 and 2. Type 1 is a multisystem disease affecting the musculoskeletal system, the heart, the respiratory system, the central nervous system and the endocrine system. Type 2 has similar manifestations, but is less severe. | |||
Muscle weakness begins distally and progresses proximally, with muscle wasting developing over time. | |||
==Anesthetic implications<!-- Briefly summarize the anesthetic implications of this comorbidity. -->== | ==Anesthetic implications<!-- Briefly summarize the anesthetic implications of this comorbidity. -->== | ||
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===Intraoperative management<!-- Describe how this comorbidity may influence intraoperative management. -->=== | ===Intraoperative management<!-- Describe how this comorbidity may influence intraoperative management. -->=== | ||
Succinylcholine produces exaggerated contractures severe enough to impair ventilation, and can make intubation/ventilation very difficult. May have enhanced response to NDNMBs due to chronic myopathy. Neostigmine may provoke myotonia. Peripheral nerve stimulators may provoke myotonia. | |||
The generally preferred option for induction is RSI with rocuronium and eventual reversal with sugammadex. | |||
===Postoperative management<!-- Describe how this comorbidity may influence postoperative management. -->=== | ===Postoperative management<!-- Describe how this comorbidity may influence postoperative management. -->=== | ||
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==Pathophysiology<!-- Describe the pathophysiology of this comorbidity. Add subsections as needed. -->== | ==Pathophysiology<!-- Describe the pathophysiology of this comorbidity. Add subsections as needed. -->== | ||
Myotonic dystrophy is theorized to be caused by an abnormality in the intracellular adenosine triphosphate system, causing a failure of calcium to return to the sarcoplasmic reticulum and hence a myotonic response (delayed relaxation of skeletal muscle after voluntary contraction). | |||
==Signs and symptoms<!-- Describe the signs and symptoms of this comorbidity. -->== | ==Signs and symptoms<!-- Describe the signs and symptoms of this comorbidity. -->== | ||
MSK: Myotonic responses to voluntary movement. | |||
Respiratory: Pulmonary function test reveals restrictive lung disease pattern due to contractures of intercostal muscles. Ventilatory response to hypoxia and hypercarbia is impaired. Patients are predisposed to developing pneumonia due to reduced lung volume and ineffective cough mechanism. Patients are especially sensitive to the respiratory depressant effects of common anesthetic medications | |||
Endocrine: insulin resistance | |||
Cardiac: defects in cardiac conduction | |||
CNS: neuropsychiatric impairment | |||
HEENT: Cataracts, frontal balding in males | |||
GU: Testicular atrophy. | |||
Gyn: High incidence of OB complications including polyhydramnios, breech, premature labor, impaired cervical dilation, uterine atony, retained placenta, postpartum hemorrhage. Symptoms are exacerbated by pregnancy due to elevated progesterone levels. | |||
==Diagnosis<!-- Describe how this comorbidity is diagnosed. -->== | ==Diagnosis<!-- Describe how this comorbidity is diagnosed. -->== | ||
Latest revision as of 03:02, 22 July 2022
| Anesthetic relevance |
High |
|---|---|
| Anesthetic management |
Induce with RSI with roc and reverse with sugammadex. Sux, roc, and neostigmine may produce atypical responses. |
| Specialty |
MSK |
| Signs and symptoms | |
| Diagnosis | |
| Treatment | |
| Article quality | |
| Editor rating | |
| User likes | 0 |
There are two types of myotonic dystrophy caused by two mutations in two distinct gene loci: myotonic dystrophy types 1 and 2. Type 1 is a multisystem disease affecting the musculoskeletal system, the heart, the respiratory system, the central nervous system and the endocrine system. Type 2 has similar manifestations, but is less severe.
Muscle weakness begins distally and progresses proximally, with muscle wasting developing over time.
Anesthetic implications
Preoperative optimization
Intraoperative management
Succinylcholine produces exaggerated contractures severe enough to impair ventilation, and can make intubation/ventilation very difficult. May have enhanced response to NDNMBs due to chronic myopathy. Neostigmine may provoke myotonia. Peripheral nerve stimulators may provoke myotonia.
The generally preferred option for induction is RSI with rocuronium and eventual reversal with sugammadex.
Postoperative management
Related surgical procedures
Pathophysiology
Myotonic dystrophy is theorized to be caused by an abnormality in the intracellular adenosine triphosphate system, causing a failure of calcium to return to the sarcoplasmic reticulum and hence a myotonic response (delayed relaxation of skeletal muscle after voluntary contraction).
Signs and symptoms
MSK: Myotonic responses to voluntary movement.
Respiratory: Pulmonary function test reveals restrictive lung disease pattern due to contractures of intercostal muscles. Ventilatory response to hypoxia and hypercarbia is impaired. Patients are predisposed to developing pneumonia due to reduced lung volume and ineffective cough mechanism. Patients are especially sensitive to the respiratory depressant effects of common anesthetic medications
Endocrine: insulin resistance
Cardiac: defects in cardiac conduction
CNS: neuropsychiatric impairment
HEENT: Cataracts, frontal balding in males
GU: Testicular atrophy.
Gyn: High incidence of OB complications including polyhydramnios, breech, premature labor, impaired cervical dilation, uterine atony, retained placenta, postpartum hemorrhage. Symptoms are exacerbated by pregnancy due to elevated progesterone levels.