This document discusses musculoskeletal impairments that can occur secondary to neurological conditions. Physically disabling neurological illnesses can lead to complications like contractures, deformities, and pain that limit function. Hemiplegic shoulder pain is one common complication after stroke and can be prevented through proper handling and positioning of the affected shoulder. Other impairments discussed include reflex sympathetic dystrophy, heterotopic ossification, and fatigue. The management of these secondary complications involves prevention through early mobility and stretching, as well as treatment through physical therapy modalities like electrical stimulation and massage.
Its about the axillary nerve which can get damage or compress which leads to loss of the sensation in shoulder area.
It also affects the range of motion of the affected side .
This can be treated conservatively.
Its about the axillary nerve which can get damage or compress which leads to loss of the sensation in shoulder area.
It also affects the range of motion of the affected side .
This can be treated conservatively.
Ataxia is a medical condition which results in the lack of muscle coordination that usually affects voluntary movements such as walking, eye movements, speech, and the patient’s ability to swallow.
Provides information concerning gravity, rotation and acceleration
Serves as a reference for the somatosensory & visual systems
Contributes to integration of arousal, conscious awareness of the body via connections with vestibular cortex, thalamus and reticular formation
Physiotherapy in MND
Dr. Quazi Ibtesaam Huma (MPT)
Dr. Suvarna Ganvir (Phd, Prof & HOD)
Dept. of Neurophysiotherapy
DVVPF’s College of Physiotherapy
Content
Introduction
Types of MND
Clinical Features of MND
Diagnostic Procedure
Management: 1) Pharmaceutical
2) Physiotherapy
Motor Neuron Disease
Motor Neuron Disease are a group of neurodegenerative disorders that affects the nerves in the spine and brain to progressively lose its function.
Motor neuron diseases (MND) include a heterogeneous spectrum of inherited and sporadic (no family history) clinical disorders of the upper motor neurons (UMNs), lower motor neurons (LMNs), or a combination of both.
Types of MND
Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease, characterized by progressive degeneration of motor neurons in the spinal cord, brain stem, and motor cortex, leading to progressive muscle atrophy and weakness.
Clinical Features
UPPER MOTOR NEURON
Loss of Dexterity
Muscle Weakness
Spasticity
Hyperreflexia
Pathological reflexes
LOWER MOTOR NEURON
Muscle Weakness
Muscle Atrophy
Hypotonicity
Hyporeflexia
Fasciculation
Muscle Cramp
Impairment related to LMN
Other clinical features
Diagnostic Criteria
Diagnostic Procedure
EMG-
It include signs of active denervation, such as fibrillation potentials and positive sharp waves;
Signs of chronic denervation, such as large motor unit potentials (increased duration, increased proportion of polyphasic potentials, increased amplitude)
Unstable motor unit potential
Nerve Conduction Velocity Studies,
Muscle And Nerve Biopsies,
Neuroimaging Studies - MRI
Management- Multidisciplinary Approach
Physical Therapy Examination
Cognition
Pain
Psychosocial Function
Joint integrity, ROM and Muscle strength.
Motor Function: Gross motor and Fine motor
Muscle tone and reflexes
Cranial nerve integrity
Sensations
Gait
Respiratory Function
Physiotherapy goals in MND treatment.
Pain reduction
Prevention for contractures
Maintenance of joint mobility
Regular review of posture
Positioning to relieve discomfort
House Modification and ergonomic advice.
Management of Sialorrhea and Pseudobulbar Affect
Management for Dysphagia
PEG procedure.
A PEG may be recommended as the disease progresses.
A PEG is a type of gastrostomy tube inserted via endoscopic surgery that creates a permanent opening into the stomach for the introduction of food.
Studies have found that PEG insertion may prolong survival. Patients with PEG were found to live 1 to 4 months longer than those individuals who refused it.
Management of Dysphagia
A palatal lift prosthesis may be prescribed for individuals with good articulation but who have a breathy voice quality or decreased loudness because of excessive air loss through the nose.
The device, a dental appliance designed to attach to the existing teeth and to elevate the soft palate, is custom-made by a prosthodontist.
Ataxia is a medical condition which results in the lack of muscle coordination that usually affects voluntary movements such as walking, eye movements, speech, and the patient’s ability to swallow.
Provides information concerning gravity, rotation and acceleration
Serves as a reference for the somatosensory & visual systems
Contributes to integration of arousal, conscious awareness of the body via connections with vestibular cortex, thalamus and reticular formation
Physiotherapy in MND
Dr. Quazi Ibtesaam Huma (MPT)
Dr. Suvarna Ganvir (Phd, Prof & HOD)
Dept. of Neurophysiotherapy
DVVPF’s College of Physiotherapy
Content
Introduction
Types of MND
Clinical Features of MND
Diagnostic Procedure
Management: 1) Pharmaceutical
2) Physiotherapy
Motor Neuron Disease
Motor Neuron Disease are a group of neurodegenerative disorders that affects the nerves in the spine and brain to progressively lose its function.
Motor neuron diseases (MND) include a heterogeneous spectrum of inherited and sporadic (no family history) clinical disorders of the upper motor neurons (UMNs), lower motor neurons (LMNs), or a combination of both.
Types of MND
Amyotrophic Lateral Sclerosis
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disease, characterized by progressive degeneration of motor neurons in the spinal cord, brain stem, and motor cortex, leading to progressive muscle atrophy and weakness.
Clinical Features
UPPER MOTOR NEURON
Loss of Dexterity
Muscle Weakness
Spasticity
Hyperreflexia
Pathological reflexes
LOWER MOTOR NEURON
Muscle Weakness
Muscle Atrophy
Hypotonicity
Hyporeflexia
Fasciculation
Muscle Cramp
Impairment related to LMN
Other clinical features
Diagnostic Criteria
Diagnostic Procedure
EMG-
It include signs of active denervation, such as fibrillation potentials and positive sharp waves;
Signs of chronic denervation, such as large motor unit potentials (increased duration, increased proportion of polyphasic potentials, increased amplitude)
Unstable motor unit potential
Nerve Conduction Velocity Studies,
Muscle And Nerve Biopsies,
Neuroimaging Studies - MRI
Management- Multidisciplinary Approach
Physical Therapy Examination
Cognition
Pain
Psychosocial Function
Joint integrity, ROM and Muscle strength.
Motor Function: Gross motor and Fine motor
Muscle tone and reflexes
Cranial nerve integrity
Sensations
Gait
Respiratory Function
Physiotherapy goals in MND treatment.
Pain reduction
Prevention for contractures
Maintenance of joint mobility
Regular review of posture
Positioning to relieve discomfort
House Modification and ergonomic advice.
Management of Sialorrhea and Pseudobulbar Affect
Management for Dysphagia
PEG procedure.
A PEG may be recommended as the disease progresses.
A PEG is a type of gastrostomy tube inserted via endoscopic surgery that creates a permanent opening into the stomach for the introduction of food.
Studies have found that PEG insertion may prolong survival. Patients with PEG were found to live 1 to 4 months longer than those individuals who refused it.
Management of Dysphagia
A palatal lift prosthesis may be prescribed for individuals with good articulation but who have a breathy voice quality or decreased loudness because of excessive air loss through the nose.
The device, a dental appliance designed to attach to the existing teeth and to elevate the soft palate, is custom-made by a prosthodontist.
Innovation in Physical Therapy - 12 Inspiring StartupsBruno Rakotozafy
Almost everyone will experience a physical injury during his life, either light or heavy. Thanks to sensors, 3D-printing or digital solutions some innovators are changing the way physical rehabilitation are performed.
Developing a Physical Therapy Marketing PlanDemandmart
The best way to start marketing your physical therapy business is to first develop a marketing plan so you know what steps you need to take to reach your goals. Marketing plans are not hard to develop but you need to know what you should include. Any small business can put together a marketing plan to work with. Take a look at our advice for what you should include in your marketing plan.
A lecture about Technology in Physical Therapy Practice. Given at the OPTA Western District Meeting on 06/30/11 by Casey Kirkes PT, DPT and Dale Boren Jr. PT, MPT, O
Holistic concept in treatment of Cerebral Palsy jitendra jain
it is very difficult to manage cerebral palsy because we cant repair brain damage but we can give good quality of independent life by combination good rehabilitation tool which include advance therapeutic technique, botulinum toxin early age child and SEMLOSSS surgical concept in others. Our aim of management is to take these person to their highest capability and decrease their physical limitation as much as possible. This ppt have brief review about latest concept in mx of cerebral aplsy
It gives an overview of the anatomy of the spine and clinical presentation, diagnostics and management options for degenerative disorders of mainly cervical and lumbar spinal cord,
Spasticity is a common motor control disorder frequently encountered in the
spectrum of the upper motor neuron (UMN) syndrome. It can result in pain,
fatigue, joint restrictions, functional impairments, and skin breakdown that may
negatively affect many domains of life by causing social avoidance and
diminished life satisfaction . Spasticity was originally defined as a velocity dependent increase in tonic stretch reflexes or muscle tone with exaggerated
tendon jerks resulting from increased excitability of the stretch reflex . This
definition has been criticized for being too narrow and inadequately depicting
the clinical sequelae. In 2005, a European Thematic Network to Develop
Standardized Measures of Spasticity (the SPASM consortium) suggested
broadening the definition to reflect a more clinical entity . They defined
spasticity as “disordered sensory-motor control, resulting from an upper motor
neuron lesion, presenting as intermittent or sustained involuntary activation of
muscles.
Knee osteoarthritis (OA), also known as degenerative joint disease, is typically the result of wear and tear and progressive loss of articular cartilage. It is most common in the elderly. Knee osteoarthritis can be divided into two types, primary and secondary. Primary osteoarthritis is articular degeneration without any apparent underlying reason. Secondary osteoarthritis is the consequence of either an abnormal concentration of force across the joint as with post-traumatic causes or abnormal articular cartilage, such as rheumatoid arthritis (RA).
Osteoarthritis is typically a progressive disease that may eventually lead to disability. The intensity of the clinical symptoms may vary for each individual. However, they typically become more severe, more frequent, and more debilitating over time. The rate of progression also varies for each individual. Common clinical symptoms include knee pain that is gradual in onset and worse with activity, knee stiffness and swelling, pain after prolonged sitting or resting, and pain that worsens over time. Treatment for knee osteoarthritis begins with conservative methods and progresses to surgical treatment options when conservative treatment fails. While medications can help slow the progression of RA and other inflammatory conditions, no proven disease-modifying agents for the treatment of knee osteoarthritis currently exist.
Overview of common dislocations and subluxations for undergraduate students. Includes clinical features, reduction methods and complications of commonly encountered injuries
Scoliosis – Facts and Treatment OptionsHealth Quest
The article discusses the causes, symptoms, and treatment methods for scoliosis, the sideways curvature of the spine that usually occurs during the growth spurt before puberty.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
2. Introduction
• Physically disabling neurological conditions
can result in secondary musculoskeletal
complications that limit patient’s activities
even further.
• These secondary complications can develop at
any stage after the onset of a neurological
illness, and the ability of clinicians to
recognize and treat these complications will
improve patients’ functioning.
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3. Introduction(cont…)
• The impairments caused by neurological
conditions can result in direct degenerative
complications in skeletal and soft tissues.
• Complications may also arise secondarily to
the neurological condition’s treatment.
• As trauma is a common cause of neurological
deficits, patients who have sustained trauma
often present with concomitant
musculoskeletal injuries.
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4. Common musculoskeletal impairment
in neurological condition
• Hemiplegic shoulder pain
• Reflex sympathetic dystrophy
• Contracture and deformity
• Hetrotopic ossification
• Osteoporosis
• fatigue
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5. Hemiplegic shoulder pain
• Hemiplegic shoulder pain is among the four
most common, yet preventable complication
that stroke survivor may experience
• HSP can occur in the 2nd week after stroke
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6. Hemiplegic shoulder pain(cont…)
Definition:
• HSP is a shoulder pain that is present at rest,
during passive or active movement on the
hemiplegic side after stroke with no direct
relation to trauma or injury.(kim et al 2014)
Incidence:
• rates ranging from 38 to 84% of cases.
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muscloskeletal impairment in neuroloical
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7. Causes
• In flaccid stage
– Proprioceptive impairment
– Lack of tone
– Muscle paralysis reduces the support(rotator cuff)
– Shoulder subluxatation
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8. Causes(cont…)
• In spastic stage
– Abnormal muscle tone
– Poor scapular position (depression, retraction and
downward rotation)
– Tightness in ligament, tendons and jt capsule
– Poor handling and positioning
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9. Symptoms
• Pain with or without movement of the
hemiplegic shoulder
• Sharp stabbing pain
• Early on pain can be intermittent and limited
to shoulder and later on constant severe and
more than just shoulder.
• Reduced mobility
• Tenderness
• swelling22/12/2015 9
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11. Management
• The ideal management of HSP is to prevent it
• It must be begin immediately after stroke.
• Handling and positioning
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12. Handling
• Good handling technique of the hemiplegic
upper extremity day and night is
recommended to prevent HSP because it
prevent trauma to soft tissues.
• Support is provided both proximally and
distally to the UE.
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13. Positioning
• Maintaining the upper limb in the correct
position
• The recommended position for the affected
upper limb is abduction, external rotation
with the shoulder slightly flexed.
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muscloskeletal impairment in neuroloical
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17. Strapping of the shoulder
• To prevent and reduce shoulder subluxtation
• Provide sensory stimulation
• To facilitate or inhibit musculature
surrounding the scapula.
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muscloskeletal impairment in neuroloical
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18. Slings and other devices
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muscloskeletal impairment in neuroloical
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20. Physiotherapy treatment
• Electric neuromuscular stimulation
• Positioning and handling
• Cryotherapy
• Therapeutic exercise
• Mobilization technique
• Gentle stretching
• EMG biofeedback
• Relaxation training
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21. Reflex sympathetic dystrophy
• Also known as chronic regional pain
syndrome(CPRS).
• Prolonged soft tissue injury can result in CPRS.
• This pain typically has a diffuse onset and is
characterized as aching through out the limb.
• The wrist tends to assume flexed position with
intense pain likely during wrist extension
movements.
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muscloskeletal impairment in neuroloical
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23. Stages
Stage 1
• Acute/ reversible stage
• Lasts 3weeks to 6 months
• Vasomotor changes include discoloration and
alteration in temperature.
• The skin may be hypersensitive to touch,
pressure or temperature variations.
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25. Stages (cont…)
Stage 2
• ischemic stage
• Lasts 3 to 6 months
• Characterized by subsiding pain and early
dystrophic changes
• Muscle atrophy
• Vasospasm
• hyperhydrosis
• Radiographic evidence of early osteoporosis22/12/2015 25
muscloskeletal impairment in neuroloical
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26. Stages (cont…)
Stage 3
• Atrophic stage last for months or years
• Progressive atrophy of skin, muscle and bones
• Pericapsular fibrosis and articular changes
become pronounced
• Hand typically becomes contracted in a
clawed position with MP extension and IP
flexion.
• Marked atrophy of thenar and hypothenar
muscles with flattening of the hand22/12/2015 26
muscloskeletal impairment in neuroloical
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27. Management
• Chances of reversal of signs and symptoms are
high for stage 1 and variable for stage 2, while
stage 3 changes are largely irreversible.
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28. Management (cont..,)
• Relieve pain and control edema
– TENS
– Vibration
– Ice
– Retrograde massage
– Elevation
– Elastic compression
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muscloskeletal impairment in neuroloical
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29. Management (cont..,)
• Increase mobility
– In early stage gentle active exercise
– Tendon glide exercise
– Neural mobilization
– Later on mobilization and stretching
• Improve muscle performance
– distraction(1 to 5 pounds up to 10 min)
– Isometric ex and later resisted ex
– Stress loading
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muscloskeletal impairment in neuroloical
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30. Management (cont..,)
• Improve total body circulation
– Low impact aerobic exercise
• Desensitize the area
– Work with various texture and tap or vibrate over
sensitive area
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31. Contractures and deformity
• Contracture develop secondary to prolonged
shortening of structures across or around
joint, resulting in limitation in motion.
• Contracture initially produce alteration in
muscle tissue but rapidly progress to involve
capsular and pericapsular changes.
• Once the tissue changes have occurred the
process is irreversible.
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muscloskeletal impairment in neuroloical
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32. Contractures and deformity(cont…)
• Faulty positioning, hetrotrophic ossification,
edema, and imbalance in muscle pull
contribute to the specific direction and
location of contracture development.
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33. In traumatic SCI
• Hip: flexion with adduction and IR.
• Shoulder:
– tightness in flexion or extension depending on
early positioning.
– Both patterns associated with adduction and IR.
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34. In stroke
• In UL:
– Elbow flexors
– Wrist and finger flexors
– Forearm pronators
• In LL:
– Planter flexion contracture
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35. In cerebral palsy
• Upper limb:
– Pronation contarcture of forearm
– Flexion deformities of the wrist and fingers
– Thumb in palm deformity
– Swan neck deformity
– Shoulder adduction and internal deformity
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36. In cerebral palsy(cont…)
• Spine:
– Scoliosis
– Kyphoscoliosis
• In hip:
– Adduction deformity
– Flexion and internal rotation deformity
– Dysplastic and subluxated hip
– Pelvic obliquity
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muscloskeletal impairment in neuroloical
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37. In cerebral palsy(cont…)
• In knee:
– Genu recuvatum
– Genu valgum
– Patella alta
– Subluxation or dislocation of patella
– Knee flexion contracture
• In foot:
– Equinus deformity
– Talipus equinovarus
– Halux valgus and claw toes22/12/2015 37
muscloskeletal impairment in neuroloical
condition
38. In poliomyelitis
• Iliotibial band contractures
• Results in 9 classical deformities
Lumbar
scoliosis Hip flex
abd
Pelvic
obliquity
ER of
femur
Flex & valgus
of knee
Post & lateral
subluxation
of tibia
ER of tibia
Equinus
foot
shortening
22/12/2015 38
muscloskeletal impairment in neuroloical
condition
39. In arthrogryposis multiplex
congenita
• foot: planovalgus and equinovarus
• Knee: flexion contracture and fixed in
extension
• Hip: extension, abduction and ER
• Shoulder: IR
• Elbow and wrist flexed
22/12/2015 39
muscloskeletal impairment in neuroloical
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40. Management
Prevention
• Early mobilization stressing out of bed upright
postures and weight bearing activities along
with the use of involved extremities.
• Consistent and concurrent program of ROM
exercise
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muscloskeletal impairment in neuroloical
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41. Management
• Use orthotic devices and splints
• Casting
• Massage therapy to relax tense muscles
• Stretching
• Prolonged stretch
• PNF technique
• Strengthening
• Electrical stimulation
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muscloskeletal impairment in neuroloical
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44. Hetrotropic ossification
• Heterotropic ossification is osteogenesis in
soft tissues below the level of lesion.
• The etiology of this abnormal bone growth is
unknown.
• However, multiple theories has been
proposed, including tissue hypoxia secondary
to circulatory stasis, abnormal calcium
metabolism, local pressure and micro trauma
related to overly aggressive ROM exercise.
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muscloskeletal impairment in neuroloical
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45. Hetrotopic ossification(cont…)
• Hetrotopic ossification is always extra-articular
and extracapsular.
• It may develop in tendons, connective tissue
between muscle, aponeurotic tissue or the
peripheral aspects of muscle.
• Typically occurs adjacent to large joints, with
the hips and knees more commonly involved.
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46. Hetrotopic ossification(cont…)
• Other joints that have demonstrated
involvement include the elbows, shoulders
and spine.
• Early symptoms are swelling, decreased ROM,
erthema and local warmth near a joint.
• Elevated serum alkaline phosphate levels
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47. Management
• Diphosphates has been used to inhibit the
formation of calcium phosphate and to
prevent ectopic bone formation.
• Combination of pharmacological therapy with
Regular exercises during the early formation
stages of ectopic development.
• Surgery is used when extreme limitations in
function impede rehabilitation.
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48. Osteoporosis
• A bone disease characterized by a
loss of bone per unit volume.
• Due to changes in calcium metabolism
• Decreased physical activity
• Changes in protein nutrition
• Hormonal and calcium deficiency
• Pt who are immobilized and restricted in
weight bearing demonstrate increase risk of
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49. Management
• High protein and
calcium reach diet
• Adequate vit D intake
and calcium intake
• Analgesics and anti
inflammatory drugs
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50. Physiotherapy Management
• Weight bearing exercise, such as walking,
jogging, stair climbing
• Resistance training
• Bicycle ergometer
• Whole body vibration as antiosteoporotic
intervention on vibration platform
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51. Fatigue
Definition:
• A subjective lack of physical and/or mental
energy that is perceived by individual or
caregiver to interfere with usual and desired
activities.
(by panel on fatigue of the MS Council for
clinical practice Guidelines)
• Fatigue is daily event, experienced by 75% to
95% of individual with the disease.
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52. Fatigue (cont…)
• Fatigue is the result of central activation
failure (central fatigue) and failure in
excitation-contraction coupling.
• Fatigue comes on abruptly, without warning
and resembles an overwhelming flu-like
exhaustion.
• Severity of disease does not seem to be
related to fatigue severity.
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53. Precipitating factors
• Physical exertion
• Exposure to heat and humidity
• Depression mood and sleep disorders
• Low-self esteem
• Medical condition and secondary complication
of disease
• Side effect of medication
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54. Evaluation
• Assess the frequency, duration and severity of
fatigue.
• Modified fatigue impact scale
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55. Management
• Aerobic exercise training
• Energy effectiveness strategies
– Activity diary (level of fatigue, value of activity,
performance of activity)
• Energy conservation
– Adoption of strategies that reduce overall energy
requirement of the task.
– By modifying the task or environment
– Broken down activity in parts.
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