Diaphragmatic paralysis overview: Difference between revisions
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==Historical Perspective== | ==Historical Perspective== | ||
Diaphragmatic paralysis was first suggested by Steurtz, in 1911 during simple phrenicotomy for treatment of [[lung disease]]. In 1946, a case of [[poliomyelitis]]<nowiki/>with respiratory paralysis was explained in Rumania. | |||
==Classification== | ==Classification== | ||
Diaphragmatic paralysis may be classified according to involvement of leaflets into unilateral or bilateral. Bilateral diaphragmatic paralysis is a medical [[emergency]]. Unilateral diaphragmatic paralysis is often discovered incidentally on [[Chest X-ray|chest x-ray]] for other reasons. | |||
==Pathophysiology== | ==Pathophysiology== | ||
It is thought that diaphragmatic paralysis is the result of [[paralysis]] of cervical nerve roots( C3-C5 ). Diaphragmatic paralyses can be unilateral or bilateral according to involvemnet of one or two leaflets of [[diaphragm]]. In the case of unilateral diaphragm paralysis, it is compensated by other hemidiaphragm or [[accessory muscles of respiration]]. In bilateral diaphragmatic paralysis, accessory muscles do all of the work of breathing and finally it may lead to ventilatory failure. Early diaphragmatic paralysis may be one of the manifestations of genetic neuromuscular disorders such as [[spinal muscular atrophy]] ([[Werdnig-Hoffman disease|Werdnig-Hoffmann disease]]) and [[acid maltase deficiency]]. On gross and microscopic pathology, there are no characteristic findings of diaphragmatic paralysis. | |||
==Causes== | ==Causes== | ||
Common causes of unilateral diphragmatic paralysis include [[idiopathic]], [[phrenic nerve]] injury in [[cardiac surgery]] and viral infection and less common causes of it include [[cervical spondylosis]], cervical compressive tumors and blunt neck [[trauma]]. Common causes of bilateral diphragmatic paralysis include [[idiopathic]], cervical [[spinal cord]] disease and [[motor neuron disease]]. Less common causes of bilateral diphragmatic paralysis include parsonage turner syndrome and [[malnutrition]]. | |||
==Differentiating Hereditary pancreatitis from Other Diseases== | ==Differentiating Hereditary pancreatitis from Other Diseases== | ||
Unilateral diaphragmatic paralysis must be differentiated from eventration of the [[diaphragm]]. Eventration of the diaphragm is an abnormal elevation of the hemidiaphragm. [[Bilateral]] diaphragmatic paralysis must be differentiated from other diseases that cause elevation of the diaphragm such as pleural adhesions, subpulmonic effusions, [[obesity]], [[ascites]], abdominal organomegaly and [[ileus]]. Diaphragmatic paralysis must be differentiated from other disease that cause [[dyspnea]] such as [[dermatomyositis]], [[polymyositis]], [[rib fracture]], [[Pleural effusion|pleural effusions]], [[amyotrophic lateral sclerosis]]. | |||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
The [[incidence]] of diaphragmatic paralysis is unknown, but [[incidence]] of diaphragmatic paralysis after [[cardiac surgery]] is approximately 30000 to 75000 per 100,000 individuals. Prevalence of diaphragmatic paralysis after cardiac surgery is 1600 per 100,000 in children.The [[morbidity]] and [[mortality]] of the unilateral diaphragmatic paralysis is related to underlying pulmonary function and [[etiology]]. Most of the bilateral diaphragmatic paralysis are [[symptomatic]] and may develop ventilatory failure. Patients of all age groups may develop diaphragmatic paralysis. There is no racial predilection to diaphragmatic paralysis. Men are more commonly affected. | |||
==Risk Factors== | ==Risk Factors== | ||
The most potent risk factor in the development of diaphragmatic paralysis is cooling or streching in [[cardiac surgery]]. Other risk factors include [[Virus|viruses]], spinal cord transection and [[malnutrition]]. | |||
==Screening== | ==Screening== | ||
Revision as of 16:40, 28 February 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
Overview
Historical Perspective
Diaphragmatic paralysis was first suggested by Steurtz, in 1911 during simple phrenicotomy for treatment of lung disease. In 1946, a case of poliomyelitiswith respiratory paralysis was explained in Rumania.
Classification
Diaphragmatic paralysis may be classified according to involvement of leaflets into unilateral or bilateral. Bilateral diaphragmatic paralysis is a medical emergency. Unilateral diaphragmatic paralysis is often discovered incidentally on chest x-ray for other reasons.
Pathophysiology
It is thought that diaphragmatic paralysis is the result of paralysis of cervical nerve roots( C3-C5 ). Diaphragmatic paralyses can be unilateral or bilateral according to involvemnet of one or two leaflets of diaphragm. In the case of unilateral diaphragm paralysis, it is compensated by other hemidiaphragm or accessory muscles of respiration. In bilateral diaphragmatic paralysis, accessory muscles do all of the work of breathing and finally it may lead to ventilatory failure. Early diaphragmatic paralysis may be one of the manifestations of genetic neuromuscular disorders such as spinal muscular atrophy (Werdnig-Hoffmann disease) and acid maltase deficiency. On gross and microscopic pathology, there are no characteristic findings of diaphragmatic paralysis.
Causes
Common causes of unilateral diphragmatic paralysis include idiopathic, phrenic nerve injury in cardiac surgery and viral infection and less common causes of it include cervical spondylosis, cervical compressive tumors and blunt neck trauma. Common causes of bilateral diphragmatic paralysis include idiopathic, cervical spinal cord disease and motor neuron disease. Less common causes of bilateral diphragmatic paralysis include parsonage turner syndrome and malnutrition.
Differentiating Hereditary pancreatitis from Other Diseases
Unilateral diaphragmatic paralysis must be differentiated from eventration of the diaphragm. Eventration of the diaphragm is an abnormal elevation of the hemidiaphragm. Bilateral diaphragmatic paralysis must be differentiated from other diseases that cause elevation of the diaphragm such as pleural adhesions, subpulmonic effusions, obesity, ascites, abdominal organomegaly and ileus. Diaphragmatic paralysis must be differentiated from other disease that cause dyspnea such as dermatomyositis, polymyositis, rib fracture, pleural effusions, amyotrophic lateral sclerosis.
Epidemiology and Demographics
The incidence of diaphragmatic paralysis is unknown, but incidence of diaphragmatic paralysis after cardiac surgery is approximately 30000 to 75000 per 100,000 individuals. Prevalence of diaphragmatic paralysis after cardiac surgery is 1600 per 100,000 in children.The morbidity and mortality of the unilateral diaphragmatic paralysis is related to underlying pulmonary function and etiology. Most of the bilateral diaphragmatic paralysis are symptomatic and may develop ventilatory failure. Patients of all age groups may develop diaphragmatic paralysis. There is no racial predilection to diaphragmatic paralysis. Men are more commonly affected.
Risk Factors
The most potent risk factor in the development of diaphragmatic paralysis is cooling or streching in cardiac surgery. Other risk factors include viruses, spinal cord transection and malnutrition.