Transcript 10 mos PTA

RB: A Case of
Tetraparesis
Block Y. Tagomata. Talan.
Tayag. Tolibas. Toledo. Uy.
Wi. Yu. Zaldivar. Zamora.
General Data
RB
 25/M
 From Camarines Norte
 Roman Catholic
 Married, with 1 child
 R handed
Chief Complaint
Inability to walk
History of Present Illness
10 mos PTA
(+) intermittent pain on R medial arm







“Parang binabanat ang ugat”
NPS 10/10
occurring 3x/wk
Aggravated by exertion (e.g. reaching out or lifting
an object)
Relieved by an unrecalled analgesic (0/10)
(-) numbness, (-) paresthesia, (-) skin lesions
(-) hx of trauma
History of Present Illness
10 mos PTA
 After 2 weeks, (+) similar pain on L arm and both
scapular areas
 No consult was done
History of Present Illness
9 mos PTA
 (+) weakness of R LE, (-) pain, (-)
numbness
 (+) dyspnea
 Consulted at barangay health center:
given vitamins and analgesic
History of Present Illness
9 mos PTA
 A few days later, (+) weakness of R LE
 Admitted to LH: CXR, holoabdominal UTZ,
cranial CT scan and labs done. Allegedly
normal results
 Discharged and prescribed unrecalled
medications
 Discontinued due to allergy to medications
(rashes on both thighs)
History of Present Illness
8 mos PTA
 assisted in ADLs (going to the bathroom,
going around the house)
 (+) urinary incontinence
6 mos PTA
 bedbound
 developed bowel incontinence
 (+) bedsore (approximately 1 cm, sacral)
History of Present Illness
5 mos PTA
 Consult was done at V. Luna
 A> t/c Decompression sickness
 P> recompression x 10 session
 Discontinued after 3rd session
History of Present Illness
5 mos PTA
 (+) consult at PGH OPD Ortho
 A> Pott’s disease
 P> workup and follow-up x 2 mos
History of Present Illness
3 mos PTA
 Admitted at Spine Unit
 Started on anti-TB meds
 Co-managed by Rehab
1 mo PTA
 s/p anterior decompression, debridement,
fusion(C6-T2) with fibular strut graft (7/18/12)
 With relief of pain at upper extremities and
scapular region
Day of admission, admitted at Rehab Ward for
further therapy
Review of Systems (present)
 (-)
Cough, colds, fever
 (-) headache, blurring of vision, dizziness
 (-) chest pain, difficulty of breathing
 (-) changes in appetite
 (-) heat or cold intolerance, irritability
 (-) muscle or joint pain
 (-) penile pain, discomfort, erectile
dysfunction
Past Medical History
(-) HPN, DM, BA, CA, previous hosp
(-) PTB/Primary Complex
(?) drug allergy
Family Medical History
(+) HPN, father
(+) BA, 5 siblings
(+) DM, uncle
(-) PTB
Personal and Social History
(-) smoking, alcohol intake, illicit drug use
Breadwinner of the family
Works as fisherman(diver)
Married, with 1 daughter
Finished 2nd yr HS
Functional History
Previously independent on ADL
Previously works as a fisherman (diving,
swimming)
Environmental History
Lives in a 1-storey concrete house with wife,
daughter, and mother
Bathroom is approximately 10 meters from
the patient’s bedroom
Main road is approximately 15 meters from
the door of the house
Current Physical Exam
General: awake, NICRD, the patient is wearing a
Minerva orthosis
BP 110/60
HR 90
RR 18
T afebrile
HEENT: AS, pink PC, (-) CLAD/NVE (+) surgical scar on
L neck to anterior chest
Chest/Lungs: DHS, (-) murmur/thrills/heaves
ECE, clear BS (-) rales/wheeze/rhonchi
Abdomen: Flat, normoactive BS, (-)
masses/tenderness
Skin/Extremities: FEP, pink NB, (-)
edema/cyanosis/jaundice (+) sacral ulcer,
healed,
Current Physical Exam
Motor:
C5 5/5
C6 5/5
C7 5/5
C8 5/5
T1 5/5
Sensory:
ASIA Sensory:
(R)
5/5
5/5
5/5
5/5
5/5
(L)
L2
L3
L4
L5
S1
pin prick
(R)
C5-L3 2/2
L3
1/2
L4
1/2
L5-S4 S5 2/2
5/5
5/5
4/5
4/5
3/5
(L)
2/2
1/2
2/2
2/2
(R)
(L)
5/5
5/5
5/5
5/5
5/5 (Score 97)
light touch
(R)
(L)
2/2
2/2
1/2
1/2
1/2
2/2
2/2
2/2
Current Physical Exam
(-) sensory deficit
(-) Babinski/clonus, (-) Hoffman’s sign
(-) dysdiadochokinesia
Poor proprioception, bilateral LE
(+) weak sphincter tone (not lax), (+)
perianal and anal sensation
(+) bulbocavernosus reflex
P.E. on
Admission &
Course
Physical Examination on
Admission
General Survey: Awake, coherent, not in
cardiorespiratory distress
Vital signs:
BP 100/70
HR 87
RR 20
T afebrile
HEENT: Anicteric sclerae, pink palpebral
conjunctivae, no cervical lymph nodes, no
tonsillopharyngeal congestion
Physical Examination on
Admission
Chest/Respiratory: Equal chest expansion, clear
breath sounds, no thoracic spine deformity
Cardiovascular: Adynamic precordium, normal
rate regular rhythm, distinct S1 & S2, no murmurs
Gastrointestinal: Flat abdomen, normoactive
bowel sounds, no tenderness
Genitourinary: (+) weak sphincteric tone, (+)
BCR
Physical Examination on
Admission
Extremities: Full and equal pulses, no
edema,
(+) multiple pressure ulcers - sacral area,
grade 2 with undermining
(+) well healing pressure ulcer on right
posterior auricular area, right shoulder
(+) grade 1 ulcer on heel, bilateral; medial
knee, bilateral; lateral malleolus, bilateral
Physical Examination on
Admission
ASIA Motor
Right
Left
C5
5/5
5/5
C6
5/5
5/5
C7
4/5
4/5
C8
3/5
3/5
T1
3/5
3/5
L2
2/5
2/5
L3
2/5
2/5
L4
3/5
3/5
L5
3/5
3/5
S1
3/5
4/5
Physical Examination on
Admission
ASIA Sensory
Pin Prick
Light Touch
Right
Left
C5-C7
2/2
2/2
C8
2/2
T1-L2
Right
Left
C5-C7
2/2
2/2
1/2
C8
2/2
1/2
2/2
2/2
T1-L2
2/2
2/2
L3-S3
1/2
1/2
L3-S3
1/2
1/2
S4-S5
1/2
1/2
S4-S5
1/2
1/2
Physical Examination on
Admission
Tone: (+) grade 1 – 1+ spasticity on both
lower extremities
DTRs: hyporeflexia on both lower extremities,
(+) flexor spasm on both lower extremities
(+) clonus
(-) Babinski
(-) Hoffman’s
Course in the Wards

Upon Ward admission:
- noted (+) flexor spasm 1-3x/hr upon
movement
- able to tolerate sitting > 1 hr. during OT
- fair sitting balance unsupported but cannot
be totally challenged
- still dependent in transition with sitting and
transfer from bed
- able to eat his dinner, can sit with brace on,
independent with setup
Course in the Wards
Underwent PT exercises during the 1st month:
 Practiced transitions from supine to sitting sit
to stand
 Table tilt at 30o increasing by 15o
 Standing with || bars with PKS on (B) knees,
increasing in duration and number of reps
|| bars with one PKS || bars without PKS
 Ambulating using walker with PKSusing BAC
with 4 pt gait3 pt gait(B) Axillary crutches
Course in the Wards

8/27 – ASIA MMT:
(R)
(L)
(R)
(L)
C5 5/5
5/5
L2 2/5
2/5
C6 5/5
5/5
L3 2/5
2/5
C7 4/5
4/5
L4 3/5
3/5
C8 3/5
3/5
L5 3/5
3/5
T1 3/5
3/5
S1 3/5
4/5
- ASIA Sensory:
pin prick
light touch
(R)
(L)
(R)
(L)
C2-C7 2/2
2/2
2/2
2/2
C8
2/2
1/2
2/2
1/2
T1-L2
2/2
2/2
2/2
2/2
L3-S4 S5 1/2
1/2
1/2
1/2
DTR: hyporeflexia on (B) LE (+) flexor spasm (B) LE
pathologic reflexes: (+) clonus (-) Babinski (-) Hoffman
Course in the Wards
(R)
C5 5/5
C6 5/5
C7 4/5
C8 4/5
T1 4/5
(Score 8375)
- ASIA Sensory:

9/18 –
(L)
5/5
5/5
4/5
4/5
4/5
L2
L3
L4
L5
S1
(R)
4/5
4/5
4/5
3/5
4/5
(L)
4/5
4/5
4/5
4/5
4/5
maintained at Score of 97
Course in the Wards
Underwent PT exercises during the 2nd
month:
 Started Stepping Exercises
 Ambulating using BAC with 3 pt gait2 pt
gaitBAC/3 pt. gait on level surface
up/down stairs using BAC using quad
cane Quad cane/3 pt. gait with ramp,
stairs(B) axillary crutches Using Walker
Course in the Wards

9/26 – Fall while ambulating in bathroom (+) pain (R) lateral aspect
of foot
- maintain MMT Score of 87
- ASIA Sensory:
pin prick
light touch
(R)
(L)
(R)
(L)
C2-C7 2/2
2/2
2/2
2/2
C8
1/2
1/2
1/2
1/2
C9-L3
2/2
2/2
2/2
2/2
L4-S4 S5 1/2
1/2
1/2
1/2
A> Quadparesis and SCC secondary to Pott’s disease
ASIA D, NLC7 MLC7 SL C8
AL: C6-T1, T4 T5 T8
Sacral decubitus ulcer Gr 2
Cystitis
Course in the Wards

10/2 – increase in flexor spasm/ankle clonus ~ (R) LE
(R)
(L)
(R)
(L)
C5 5/5
5/5
L2 4/5
5/5
C6 5/5
5/5
L3 4/5
4/5
C7 5/5
5/5
L4 5/5
5/5
C8 5/5
5/5
L5 4/5
4/5
T1 4/5
4/5
S1 3/5
5/5 (Score 9187)
- ASIA Sensory:
pin prick
light touch
(R)
(L)
(R)
(L)
C2-C7 2/2
2/2
2/2
2/2
C8
2/2
1/2
2/2
1/2
C9-L3
2/2
2/2
2/2
2/2
L4-L5
1/2
1/2
1/2
1/2
S1-S4 S5 2/2
2/2
2/2
2/2 (Score 10797)
Course in the Wards

10/8 – ambulate on level surface with ramp using quad cane. Not Stairs
- increase in flexor spasm/ankle clonus ~ (R) LE
(R)
(L)
(R)
(L)
C5 5/5
5/5
L2 5/5
5/5
C6 5/5
5/5
L3 5/5
5/5
C7 5/5
5/5
L4 4/5
5/5
C8 5/5
5/5
L5 4/5
5/5
T1 5/5
5/5
S1 3/5
5/5 (Score 9791)
- ASIA Sensory:
pin prick
light touch
(R)
(L)
(R)
(L)
C5-L3 2/2
2/2
2/2
2/2
L3
1/2
1/2
1/2
1/2
L4
1/2
2/2
1/2
2/2
L5-S4 S5 2/2
2/2
2/2
2/2
Course in the Wards
 10/21
– ambulate using walker
- able to do vocational training
- (+) flexor and bladder spasm on
CMG
 10/24 – ambulate using walker
- still with weakness of (R) plantar
flexion
 10/27 – still with poor proprioception of (B)
feet
Differential Diagnoses for
Tetraparesis
 Trauma
 Tumors
 Infection
 Inflammatory
 Vascular
 Vertebral
 Others
Disease
Trauma
 Most
common cause of tetraparesis
 Ruled out because the patient has no
history of trauma
Tumors

Usual presentation is pain, often worse when in supine
position, which can be axial (skeletal structures
affected) or radicular (nerve roots affected)

Usually presents with constitutional symptoms (night
sweats, fever, unexplained weight loss, and anorexia)

Radiographic examination is vital

Can be metastatic (from lungs, breast, prostate and
kidney) or primary (multiple myeloma, osteogenic
sarcoma, vertebral hemangioma, chondrosarcoma,
chordoma,
ependymoma,
astrocytoma,
meningioma, schwannoma, neurofibroma)
Infection
 Bacterial

a
osteomyelitis
differential
if
the
patient
uses
IV
drugs,
immunosuppressed, or undergoing dialysis

usual etiology is Staphylococcus aureus

Check via culture and inflammatory markers
 Spinal

Usually epidural; commonly presents with fever
 HIV

abscess
infection
Can present as primary HIV myelitis, vacuolar
myelopathy, or as a result of opportunistic infection
Inflammatory

Transverse myelitis

Myelopathic process of unknown cause from inflammation of
spinal cord

May start as pain or paresthesia in localized body parts and
can progress to paresis and plegia

Multiple sclerosis

Immune-mediated demyelinating disorder which may also
initially present as pain and progress to weakness of limbs

Systemic lupus erythematosus

Autoimmune illness which usually presents with other systemic
symptoms such as pleuritis, hematologic, immunologic or
neurologic alterations, and dermatologic signs
Vascular
 Ischemia
usually
of spinal cord not very common;
associated
with
anterior
syndrome; often from:

Anterior spinal artery occlusion

Angioma

AV malformation
cord
Vertebral Disease



Vertebral disk prolapse

Usually due to a tear in the outer fibrous ring (annulus
fibrosus)

May initially present as pain of extremities and progress to
paresis depending on the level of herniation
Spondylosis

Degenerative odteoarthritis of the spine

Presents as pain, paresthesia or muscle weakness
Paget’s disease

Due to excessive breakdown and formation of bone,
followed by disorganized bone remodeling

Causes bone pain but very rarely presents as quadriparesis
Others


Hereditary spastic paraparesis

characterized by insidiously progressive bilateral lowerextremity weakness and spasticity, with family history of
similarly affected individuals

may be transmitted in an autosomal dominant, autosomal
recessive, or X-linked recessive manner
Degenerative motor neuron disease

Usually presents in the 6th-7th decades of life

heterogeneous
group
of
neurologic
diseases
characterized by progressive degeneration of upper and
lower motor neurons

Usually presents with weakness, atrophy, fasciculations,
and hypo/hyperreflexia
Others
 Decompression

syndrome
caused by intravascular or extravascular bubbles that
are formed as a result of reduction in environmental
pressure

can occur in divers, compressed air workers, aviators,
and astronauts

manifestations range from itching and minor pain to
neurological symptoms, cardiac collapse, and death

Presents acutely
Impression
Quadriplegia secondary to multiple
compression deformity secondary to
Pott’s disease (Asia D) NL: C6, AL: C6-T2,
ML: C7, SL: C7
Neurogenic bowel and bladder
Nephrolithiasis, right
Problem List
o
Medical
o
s/p ADDT
SCC sec to Pott’s Disease C7-T1
Neurogenic Bladder
Altered Body Function
Quadriparesis
Sensory impairment below C8
Grade I spasticity of bilateral LE
Poor proprioception
Goals

Short Term Goals




Long Term Goals




To improve strength of B LE
To improve ambulating using walker in level surface
and ramps
To ambulate on stairs
To ambulate using walker on level surface and ramps
To attain improvement in all aspects of ADLs
To acquire vocational training
For Discharge if:


With independent ambulation using walker on level
surface and ramps
Independent in all aspects of ADLs
Ambulatory PT
 Supine


Proper brace donning/doffing of brace
Transitional technique from supine to sitting to
standing
 Sitting


Resistance exercises of bilateral UE/LE
Transition technique from sitting to standing
 Ambulation/Standing

Ambulate using walker on level surface and ramps
Occupational Therapy

Ambulatory OT



vocational training
energy conservation techniques
Psych OT

individual counselling
Pott’s Disease




Pott disease is usually secondary to an extraspinal
source of infection.
The basic lesion is a combination of osteomyelitis
and arthritis.
The area usually affected is the anterior aspect of
the vertebral body adjacent to the subchondral
plate.
Tuberculosis may spread from that area to
adjacent intervertebral disks.

In adults, disk disease is secondary to the spread of
infection from the vertebral body.

In children, because the disk is vascularized, it can
be a primary site.
Pott’s Disease
 Progressive
bone destruction leads to vertebral
collapse and kyphosis. The spinal canal can be
narrowed by abscesses, granulation tissue, or
direct dural invasion. This leads to spinal cord
compression and neurologic deficits.

Kyphotic deformity occurs as a consequence
of collapse in the anterior spine. Lesions in the
thoracic spine have a greater tendency for
kyphosis than those in the lumbar spine.
Pott’s Disease
 The
collapse is minimal in cervical spine
because most of the body weight is borne
through the articular processes.
 Healing
takes place by gradual fibrosis and
calcification of the granulmatous tuberculous
tissue. Eventually the fibrous tissue is ossified,
with resulting bony ankylosis of the collapsed
vertebrae.
Pott’s Disease
 Paravertebral
abscess formation occurs in
almost every case. With collapse of the
vertebral body, tuberculous granulation tissue,
caseous matter, and necrotic bone and bone
marrow are extruded through the bony cortex
and accumulate beneath the anterior
longitudinal ligament.
 These
cold abscesses gravitate along the
fascial planes and present externally at some
distance from the site of the original lesion.
Pott’s Disease
 In
the lumbar region the abscess gravitates
along the psoas fascial sheath and usually
points into the groin just below the inguinal
ligament.
 In
the thoracic region, the longitudinal
ligaments limit the abscess, which is seen in the
radiogram as a fusiform radiopaque shadow at
or just below the level of the involved vertebra.
 Thoracic
abscess may reach the anterior chest
wall in the parasternal area by tracking via the
intercostal vessels.
Lesion

The lesion could be:


Recently, two distinct
patterns of spinal TB
Florid - invasive and
can be identified, the
destructive lesion
classic form, called
Non destructive - lesion
spondylodiscitis (SPD)
suspected clinically but
identifiable by modern

Atypical form
investigations like CT
characterized by
scan or M.R.I.
spondylitis without disk

Encysted disease
involvement (SPwD)

Carries sicca

Hypertrophied
most common pattern

Periosteal lesion
of spinal TB

SPwD seems to be the
Regional Distribution
1
Cervical
12%
2
Cervicodorsal
5%
3
Dorsal
42%
4
Dorsolumbar
12%
5
Lumbar
26%
6
Lumbosacral
3%
Anatomically the lesion could be
1.
2.
3.
4.
5.
Paradiscal - destruction of
adjacent end plates and
diminution of disc space.
Appendeceal (Posterior) involvement of pedicles,
laminae, spinous process.
Central - Cystic or lytic,
concertina collapse.
Anterior –longitudinal lig,
Aneurysmal phenomenon
Synovitis in posterior facet
History
 Presentation



depends on the following:
Stage of disease
Site
Presence of complications such as neurologic deficits,
abscesses, or sinus tracts
 The
reported average duration of symptoms at the
time of diagnosis is 3-4 months.
 Back pain is the earliest and most common
symptom


Patients have usually had back pain for weeks prior to
presentation
Pain can be spinal or radicular
 Constitutional
loss
symptoms include fever and weight
History

Neurologic abnormalities occur in 50% of cases and can
include spinal cord compression with paraplegia, paresis,
impaired sensation, nerve root pain, or cauda equina
syndrome.

Cervical spine tuberculosis is a less common presentation is
characterized by pain and stiffness.

Patients with lower cervical spine disease can present
with
dysphagia or stridor.

Symptoms can also include torticollis, hoarseness, and
neurologic deficits.

The relative proportion of individuals with Pott’s who are HIV
positive seems to be higher than HIV negative patients.
Complications of tuberculosis
1.
2.
3.
4.
5.
6.
Paraplegia
Cold abscess
Sinuses
Secondary infection
Amyloid disease
Fatality
Surgical indications
1.
No sign of neurologic recovery after trial of 3-4
weeks therapy
2.
Neurologic complication during treatment
3.
Neurologic deficit becoming worse
4.
Recurrence of neurologic complication
5.
Prevertebral cervical abscesses, neurological
signs, & difficulty in deglutition & respiration
6.
Advanced cases: sphincter involvement,
flaccid paralysis, severe flexor spasms
Other indications

Recurrent paraplegia

Painful paraplegia– d/t root compression, etc

Posterior spinal disease--involving the post
elements of vertebrae

Spinal tumor syndrome resulting in cord
compression

Rapid onset paraplegia due to thrombosis,
trauma, etc.

Severe paraplegia econdary to cervical disease
and cauda equina paralysis
1
2
3
4
5
6
Decompression
+/- fusion
Debridement+/fusion
Failed response,Too
advanced
Failed response after 3-6
months,Doubtful
diagnosis,Instability
Debridement
+/-DECOMP+/fusion
Debridement+/fusion
Anterior
transpostion
Recrudescence of disease
Laminectomy
STS,secondary stenosis,
posterior disease
Prevent severe Kyphosis
Severe Kyphosis +neural
deficit
Tuli’s recommended approach
 Cervical
 Dorsal
spine –T1  Anterior approch
spine –DL junction  Antrolateral
approch
 Lumbar
spine &Lumboscral junction
Extraperitoneal Transverse
Vertebrotomy
Problem List
Medical Problems
Spinal
cord compression
Neurogenic bowel
Neurogenic bladder
Pressure ulcers
(Possible) Medical Problems
 Cardiovascular
complications
 Hypertension
 Deep
vein thrombosis and Pulmonary
embolism
 Orthostatic hypotension
 Cardiac arrhythmia
 Pulmonary complications
 Musculoskeletal complications
 Osteoporosis
 Fractures
 Heterotrophic Ossification
Altered Body Structure and
Function
 Bilateral
LE paresis
 Bilateral
LE loss of sensation
 Neurogenic
bladder
 Neurogenic
bowel
 Pressure
 Sexual
sores
dysfunction and possible loss of
sexual desire
 Possible
MSK, cardiovascular and
pulmonary complications
Limitations in Activities of Daily
Living
 Independence
in feeding
 Dependence in self-care ADLs
 Bathing
 Grooming
 Dressing up
 Dependence in ambulation and transfers
 Poor sexual activity
Limitations in Instrumental
Activities
 Independence
 Communication
 Entertainment
 Difficulty
 Cannot
(cellphones, etc.)
(watching TV, etc.)
in child-rearing
anymore drive his motorcycle
Limitations in Participation
 Inability
to return to previous job
 Difficulty
in finding another job
 Difficulty
in community ambulation
Short-term Goals
 To
treat the underlying cause of the SCI
 Spinal
 To
TB
implement acceptable bowel and
bladder management programs
 To
address pressure ulcers and maintain
skin integrity
Long-term Goals

To maintain socially acceptable bladder and fecal
continence

To prevent possible complications of neurogenic
bladder and bowel

To prevent and treat accordingly the complications
that may arise from the thoracic-level SCI

To minimize the functional limitations and allow the
patient to complete ADLs independently or with
assistive equipment
Management of Spinal Cord Injury
and Its Various Complications
Neurogenic Bladder
 When
pathologic CNS/PNS conditions
cause disruption of the nerve control to
the urinary bladder, causing urinary
retention and/or urinary incontinence
Bladder Innervation
Pelvic Nerves
 Parasympathetic signals from S2-S3 segments to
the detrusor muscles for bladder
emptying/voiding
Hypogastric Nerves
 Sympathetic signals from T11-L2 segments for
bladder filling/storage
Pudendal Nerves
 Somatic nerve fibers from S3-4 segments to
voluntary skeletal muscles & external sphincter
Management Goals
 To
prevent urinary tract infections and
other long-term urologic sequelae
 To
maintain a socially acceptable
bladder continence
 by
developing and implementing a
bladder management program that will
allow patient to reintegrate back into
the community
Medical/Pharmacologic
Management

Targeting the autonomic receptors

For urinary retention


Cholinergics (for detrusor contraction)

Alpha receptor antagonists (for sphincter relaxation)
For urinary incontinence

Anticholinergics ( for detrusor relaxation)

Alpha receptor agonists (for sphincter contraction)
Behavioral/Non-Pharmacologic
Management
 Catheterization
 Independent
programs
intermittent catheterization
every 4 to 6 hours, if the patient has preserved
hand function and does not have UTI
 Limitation
 Timed
voiding
 Schedule
 Use
of fluid intake
voiding
of a voiding diary
Behavioral/Non-Pharmacologic
Management
 Bladder
training programs
 Maneuvers
 Valsalva
maneuver, suprapubic application
of pressure
 Use
of appliances
 Condom,
foley, straight catheters
Surgical Management
When the mentioned medical and behavioral strategies fail…
 Augmentation
 Artificial
cystoplasty
sphincter
 Sphincterotomy
 Pudendal
neurectomy
 Bladder
outlet surgery
 Balloon
dilatation
 Interruption
of innervation
 Neurostimulation
Neurogenic Bowel
 When
pathologic CNS/PNS conditions
cause disruption of the bowel innervation,
causing stool incontinence (lax anal
sphincter) and constipation (disrupted
parasympathetic supply)
Management Goals
 To
achieve socially acceptable fecal
incontinence
 Prevention
of gastrointestinal
complications
 Fecal
impaction (most common)
Medical/Pharmacologic
Management
 Stool
softeners (e.g. docusate sodium)
 Colonic
stimulants (e.g. senna)
 Colonic
irritants (e.g. glycerin, bisacodyl)
 Prokinetic
 Rectal
 Oral
agents (e.g. metoclopramide)
suppositories
medications
Behavioral/Non-Pharmacologic
Management
 Timed/regular
 Taking
bowel movement
advantage of the gastrocolic reflex
(about 30-60 minutes after meal)
 Dietary
 High
modification
fiber diet
 Increased
 Digital
fluid intake
stimulation
 Manual
extraction
Surgical Management
 Colostomy/ileostomy
 Decreases
time required for bowel
management
 Increases
independence
Pressure Sores
 Stages
of pressure sores/ulcers (NPUAP)
 Stage
I : Nonblanchable erythema not
resolved within 30 minutes (epidermis intact)
 Stage
II : Partial thickness skin loss; blisters with
erythema, abrasion, shallow ulcer (possibly into
dermis)
 Stage
III: Full-thickness destruction of the skin;
deep crater (into subcutaneous tissue)
 Stage
IV: Full-thickness skin loss with deep-tissue
destruction (up to fascia, muscle, bone, joint)
Pressure Sores
 Management:
 Wound
cleansing with plain NSS
 Debridement
 Wound
dressing
 Topical
antibiotics (e.g. Flammazine)
 Wound
Care Modalities
 Whirlpool
therapy, UV light, ultrasound
 Surgery
 skin
grafts and skin flaps
Pressure Sores
 Prevention:
 Egg
mattress
 Proper
turning frequency (at least every
2 hours)
 Adequate
cushioning (e.g. surgical
gloves with water)
Osteoporosis
 Occurs
below the level of injury
 Cause:
reduction of bone mineral content
 Immobilization
 Lack
 Effect:
of weight-loading activities
Increased risk of lower extremity fracture
 Management:
 Ambulatory
activities
 Medications
(e.g. Vitamin D, calcitonin,
biphosphonates)
 Functional
electric stimulation
Fractures

Occurs in chronic SCI

Common causes:

Osteoporosis

Falls

Vigorous physical therapy

Common in long bones of lower extremity

Management:

Patient and family education

Training in proper transfer and ambulation
techniques

Fall prevention

Avoidance of vigorous physical therapy
Heterotopic Ossification (HO)

Development of ectopic bone within soft tissues
surrounding the joints

Often seen in the first 6 months post-injury

Incidence: 20-30%

Common areas : Hip > Knee > Shoulder > Elbow

Etiology is still unclear but may be due to metabolic,
biochemical and circulatory factors

Presentation:

Heat and swelling over the joints

Decrease in ROM

Fever
Heterotopic Ossification (HO)


Complications:

Peripheral nerve entrapment

pressure sores

Ankylosis

increased risk of DVT
Management:

ROM Exercises

Medications to limit ossification (e.g. disodium
etidronate, indomethacin)

Surgery for mature bone
Pulmonary Complications
 Depend
 C4:
on the level of the lesion
highest level with spontaneous ventilation
 Above
C8: loss of abdominal and intercostal
muscles
 T1-T12:
impairment of intercostal muscles,
reduced cough, possible paradoxical retraction
of chest wall during inspiration
 T8-T10:
 Below
impairment of abdominal muscles
T12: no impairment of respiratory function
Pulmonary Complications
 Management:
 Position
 Deep
 Use
changes/postural drainage
breathing exercises
of incentive spirometry
 Cough
assist
 Glossopharyngeal
breathing exercises.
 Pneumobelt
 Phrenic
nerve pacing
 Non-invasive
ventilatory support
CV complications: Hypertension
and Coronary Artery disease
 Inactivity
causes:
 Increased
cholesterol levels
 Increased
risk of coronary artery disease
 Management:
 Exercise/
increased activity
CV complications:
Deep Vein Thrombosis

3 important factors (Virchow’s triad)

Venous stasis

Hypercoagulability

Vessel wall damage

Highest risk period: 1st 2 weeks

Serious complication: Pulmonary embolism

Risk of death decreases over time
 210
 19.1
 8.9
times greater in the acute phase
times 2-5 years post-injury
times beyond 5 years post-injury
CV complications:
Deep Vein Thrombosis
 Management
 Pharmacologic
 Prophylactic
(e.g. heparin, coumadin)
measures
 compression
stockings, external pneumatic
compression, continuous rotation beds
 Avoid
ROM and strengthening exercises on the
affected limb
 Bed
rest until medications are given
CV Complications:
Orthostatic Hypotension

Common in higher levels of SCI

Causes:


Ineffective vasoconstriction

Pooling of blood in the lower extremities
Treatment:

Progressive elevation

Use of compression stocking and abdominal binders

Liberal salt and fluid intake

Elevated leg rests

Medications (e.g. NaCl tablets, ephedrine)
CV complications:
Cardiac Arrhythmias

Common during the acute period (14 days post injury)

Usually in cervical and complete injuries

Cause:

autonomic imbalance  sympathetic and 
parasympathetic activity


Prevention:

Use of atropine

Induced hyperventilation
Usually resolved within 6 weeks after injury
Sexual Dysfunction
 Sexual
desire is not necessarily affected but
depression, poor body image and fears of
inadequacy may alter sexual desire.
 Sexual
function, however, may be affected.
 Erection
(parasympathetic)
 Ejaculation
(sympathetic)
 Lubrication
(in women)
 Complete
SCI (no sacral reflexes): more
impairment
Sexual Dysfunction
 Addressing
concerns on body image,
maintenance of intimate relationships, etcetera
 Management
 Oral
options for erectile dysfunction:
medications (e.g. sildenafil)
 Vaccum
 Penile
devices
injection programs (papaverine)
 Surgically
implanted prosthesis
Functional Rehabilitation

Focuses on helping the patient to function at optimal
levels

Supervised PT and OT to improve strength in all active
muscle groups and ROM in all joints

Adaptive equipment

Long-handled shoehorns

Reachers

Ambulation equipment
 Low-back
wheelchairs are feasible because
patients with lower-level SCIs have better truncal
stability.
Thank You!