Exam 31: Cardiopulmonary Assessment and Care of Patients With Neuromuscular Disease
Exam 1: The Patient Interview13 Questions
Exam 2: The Physical Examination14 Questions
Exam 3: The Pathophysiologic Basis for Common Clinical Manifestations12 Questions
Exam 4: Pulmonary Function Testing13 Questions
Exam 5: Blood Gas Assessment14 Questions
Exam 6: Assessment of Oxygenation14 Questions
Exam 7: Assessment of the Cardiovascular System13 Questions
Exam 8: Radiologic Examination of the Chest14 Questions
Exam 9: Other Important Tests and Procedures14 Questions
Exam 10: The Therapist-Driven Protocol Program11 Questions
Exam 11: Respiratory Insufficiency, Respiratory Failure and Ventilatory Management Protocols10 Questions
Exam 12: Recording Skills and Intra-Professional Communication11 Questions
Exam 13: Chronic Obstructive Pulmonary Disease, Chronic Bronchitis and Emphysema18 Questions
Exam 14: Asthma17 Questions
Exam 15: Cystic Fibrosis21 Questions
Exam 16: Bronchiectasis20 Questions
Exam 17: Atelectasis18 Questions
Exam 18: Pneumonia, Lung Abscess Formation, and Important Fungal Diseases38 Questions
Exam 19: Tuberculosis18 Questions
Exam 20: Pulmonary Edema18 Questions
Exam 21: Pulmonary Vascular Disease: Pulmonary Embolism and Pulmonary Hypertension19 Questions
Exam 22: Flail Chest16 Questions
Exam 23: Pneumothorax17 Questions
Exam 24: Pleural Effusion and Empyema15 Questions
Exam 25: Kyphoscoliosis16 Questions
Exam 26: Cancer of the Lung, Prevention and Palliation16 Questions
Exam 27: Interstitial Lung Diseases17 Questions
Exam 28: Acute Respiratory Distress Syndrome19 Questions
Exam 29: Guillain-Barré Syndrome17 Questions
Exam 30: Myasthenia Gravis20 Questions
Exam 31: Cardiopulmonary Assessment and Care of Patients With Neuromuscular Disease19 Questions
Exam 32: Sleep Apnea17 Questions
Exam 33: Newborn Assessment and Management16 Questions
Exam 34: Pediatric Assessment, Protocols, and Pals Management9 Questions
Exam 35: Meconium Aspiration Syndrome16 Questions
Exam 36: Transient Tachypnea of the Newborn17 Questions
Exam 37: Respiratory Distress Syndrome19 Questions
Exam 38: Pulmonary Air Leak Syndrome17 Questions
Exam 39: Respiratory Syncytial Virus Infection Bronchiolitis15 Questions
Exam 40: Chronic Lung Disease of Infancy16 Questions
Exam 41: Congenital Diaphragmatic Hernia17 Questions
Exam 42: Congenital Heart Disease11 Questions
Exam 43: Croup and Croup-Like Syndromes: Laryngotracheobronchitis, Bacterial Tracheitis, and Acute Epiglottitis15 Questions
Exam 44: Near Drowningwet Drowning13 Questions
Exam 45: Smoke Inhalation, Thermal Injuries, and Carbon Monoxide Intoxication18 Questions
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Which of the following areas involved in a stroke will cause sensory and motor impairment of the lower extremities?
Free
(Multiple Choice)
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Correct Answer:
A
Which of the following is disease in which patients may have facial wasting, hypotonia, an arched palate with progressive weakness that begins in the distal muscles?
Free
(Multiple Choice)
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Correct Answer:
C
Tissue plasminogen activator (TPa) should be administered within ________ of the onset of stroke symptoms.
Free
(Multiple Choice)
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(83)
Correct Answer:
A
Management of a traumatic spinal cord injury below the level of C5 involves:
1) prompt assessment to prevent addition injury.
2) immediate intubation.
3) anticoagulation therapy.
4) intravenous fluid resuscitation.
(Multiple Choice)
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Which of the following NMD can be diagnosed with genetic testing of the dystrophin gene?
1) Duchenne muscular dystrophy
2) Facioscapulohumeral dystrophy
3) Becker muscular dystrophy
4) Limb girdle muscular dystrophy
(Multiple Choice)
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The respiratory therapist can prevent increases in intracranial pressure (ICP) by:
(Multiple Choice)
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Elevation of what laboratory values suggest muscle damage?
1) Albumin
2) Aldolase
3) Immunoglobulin
4) Creatine kinase
(Multiple Choice)
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General management and care of a patient with neuromuscular disease includes:
1) nutritional assessment.
2) gastrostomy tube placement.
3) mechanical ventilation.
4) weekly nerve conduction studies.
(Multiple Choice)
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Which of the following is transmitted in X-linked, autosomal recessive, and autosomal dominant fashions in which patients typically exhibit muscle weakness and wasting in a scapulohumeroperoneal distribution?
(Multiple Choice)
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You are assisting the physician with the assessment of a patient that is thought to have ALS. What clinical cues should you be most aware of?
1) Sialorrhea
2) Muscle biopsy results
3) Tongue fasciculations
4) Nerve conduction study results
(Multiple Choice)
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Which of the following is the leading cause of death in a patient with neuromuscular disease (NMD)?
(Multiple Choice)
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Which of the following is early sign of disease seen in an infant with Duchenne muscular dystrophy?
(Multiple Choice)
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Cervical nerves _______ through _______ innervate the diaphragm.
(Multiple Choice)
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Which of the following are the two main categories of stroke?
(Multiple Choice)
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You are assessing the patient-ventilator system of a patient being treated for stroke. What parameters are you most concerned with during the assessment?
1) PEEP level of 20 cm H2O
2) Frequency of 18 breaths/min
3) MAP level of 30 mm Hg
4) Peak inspiratory pressure of 21 cm H2O
(Multiple Choice)
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You are treating a patient with a proximal distribution of weakness. Which of the following NMD is most likely?
(Multiple Choice)
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Which of the following is a progressive neurologic disorder characterized by degeneration of upper and lower motor neurons?
(Multiple Choice)
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Diagnosis of muscular dystrophy combines:
1) physical examination.
2) laboratory testing.
3) muscle biopsy findings.
4) pulmonary function testing.
(Multiple Choice)
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The use of hands and arms to "walk up" their own body from a squatting position is referred to as:
(Multiple Choice)
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