Module 17: Genitourinary and Adolescent Health Flashcards

1
Q

UTI’S

There are different levels of UTI’s- starting from poo in bum and works its way up urinary tract to the bladder and then kidney.

Symptoms of cystitis (bladder infection)

Symptoms of Kidney infection:

What do we do?

How can we tell if its bacterial or Viral or pH?

How do we treat UTI’s in the older child?

A

Bladder infection
1. dysuria (painful urination)
2. urgency,
3. frequency,
4. suprapubic pain,
5. incontinence,
6. malodorous urine.
* Cystitis does not cause fever and does not result in renal injury.

Kidney infection of Pyelonephritis:
Clinical pyelonephritis is characterized by any or all of the following: abdominal, back, or flank pain, fever, malaise, nausea, vomiting, and, occasionally, diarrhea. Fever may be the only manifestation.

What do we do next?
We must distinguish between a pH issue, subluxation or true infection.

best way to assess this is a Urinalysis or Salivary pH
(pH should not drop below 6.5)
Compare salivary and urinary- if salivary is normal, but urinary is low its a Kidney issue.

How can we tell if its bacterial or Viral or pH?
2 tender kidneys = viral
1 tender kidney = bacterial

A Urinalysis will demonstrate Acidic pH ie <6.5
-leukocytes
-proteinuria
-haematuria (especially once in bladder and kidneys) -blood

How do we treat UTI’s in the older child?
<12 months hospital- high risk of kidney damage infancy UTI. Risk much lower after 12 months

-Adjust the spine
-First line is bicarb soda - 1/4 teaspoon every 1-2 hours in a glass of water (to decreased acidity) - being alkaline will assist in killing infection and makes spread difficult. Within 24-48 hours pH should resolve. - Get them in to retest urinary pH within 1-2 days- if not resolved within 3 days refer for further testing

Unless severe, simple UTIs and cystitis can be treated without AB.
-Arabinoguard, Ultraprobioplex
-cranberry capsules- prevent bacterial adhesion to the walls of bladder and urethra
If suspected viral issue- super mushroom powder.
Assess diet for causes of acidity- grains, dairy, meat, processed foods, soft drinks
Acidity can be cause by sever viral infections, stress or chemical exposures.

-retest UA and salivary pH to ensure resolution.
-Also VIt D!

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2
Q

Proteinuria

If this Is seen we need to determine if it is due to renal disease or due to benign process.
We need to know wether it is transient or constant- repeat tests over 2 weeks.

Transient- can be high temp, exercise, dehydration, stress, heart failure

Persistent proteinuria - Eg Orthostatic proteinuria - gravity helps them leak through membrane, so need to test in morning- if clear then it is, if not probs not.

Fixed proteinuria- seen on urine sample in morning on 3 consecutive days (indicative of renal disease)

A

yep

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3
Q

Nephrotic Syndrome

https://www.youtube.com/watch?v=ZGPa_4FN9M4

Nephrotic syndrome is a kidney disorder that causes your body to pass too much protein in your urine. Nephrotic syndrome is usually caused by damage to the clusters of small blood vessels in your kidneys that filter waste and excess water from your blood

How does it clinically present?

Whats Ddx?

Treatment?

prognosis?

A

Clinical manifestation:
Age 2-6 peak time
Usually follows minor UTI, or reaction to insect bites or stings

Mild Oedema around eyes and lower extremities, people think its an allergy but overtime it spreads to everywhere -oedema everywhere.

Ddx?
-hepatic failure
-heart failure
-protein malnutrition

Treatment:
Uncomplicated nephrotic syndrome
4-6 weeks of prednisone (corticosteroids)
low sodium diet bla bla refer GP

Prognosis: unlikely to lead to chronic kidney disease unlikely to be hereditary, etc. If it is steroid resistant - has more complications.

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4
Q

Nephritic Syndrome = blood in urine?

https://www.youtube.com/watch?v=UD47tM3iJO4

Nephritic syndrome is defined by hematuria, variable degrees of proteinuria, usually dysmorphic red blood cells (RBCs), and often RBC casts on microscopic examination of urinary sediment. Often ≥ 1 of the following elements are present: edema, hypertension, elevated serum creatinine, and oliguria.

Nephritic syndrome is characterised by?

What are the causes? Meh clogged filter = HBP

Can be from Post Streptococcal glomerulonephritis

A

The main features are hypertension and RBC casts. The proteinuria in nephritic syndrome is not usually severe, but may occasionally be significant enough to be in the range found in nephrotic syndrome.

  1. Haematuria with red blood cell casts
  2. Proteinuria small amounts of protein are lost in the urine,
    but this is usually trivial (<3.5 g/day)
  3. Hypertension
  4. Uraemia - due to retention of waste products
  5. Oedema – facial or body
  6. Tea or cola coloured urine

bla bla bla

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5
Q

Haematuria

The presence of at least 5 RBC per micro litre of urine

Upper Urinary tract causes and Lower Urinary tract causes;

A

Eg Inflammationm doesn’t have to be infectious
-Trauma
-heavy exercise
-Bladder tumour

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6
Q

ENURESIS
The medical name for not being able to control your pee is enuresis

It is diagnosed after 5 years of age
Affects up to 20% of children at 5 years of age.

Nocturnal (bed wetting) diagnosis isa child has not experienced a period of 30 days or more without wetting

Causes- undiagnosed UTI or other causes can be:
-Diabetes Mellitus
-Diabetes Insipidus
-Chronic renal disease

or organic cause?

A new onset of enuresis in older child is a cause for concern.

Neurological control- meh but weeing is a parasympathetic nerve activity

What ages should bladder control be developed?

What should our examination include?

What are the 3 main Retained primitive reflexes that can be retained in bed wetters?

A
  • Enlargement of the bladder capacity and maturation of the frontal and parietal lobes of the brain occur gradually between the ages of one to two years.
  • By the age of three most children have the ability to delay urination.
  • The capacity to start and stop the flow of urine usually occurs by four to five years of age.
  • The ability to initiate and stop the flow of urine at any degree of bladder fullness usually occurs by five years of age.

Examination:
1. Palpation of kidneys and
2. Palpation of bladder
3. Measuring BP
4. Urinalysis- a Chiro should be doing this with kids with enuresis. What could you see there and what could it indicate
- Glucose in urine- Diabetes mellitus
-abnormal urinary pH can affect bladder function and behaviour (normal 6.5-7)
-infections are associated with blood, leukocytes + protein

3 main primitive reflexes are: Exam Question
1. Galant
2. Perez
3. Cross adductor

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7
Q

Diabetes Insipidus

A
  • Diabetes insipidus, a disorder of vasopressin secretion from the pituitary is associated with polyuria and polydypsia and there is a daily urine output in excess of four liters per day.

> urine 4L p day

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8
Q

What is the impact of mouth breathing?

A

https://www.youtube.com/watch?v=c6Rao9TWGTU

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9
Q

unusual for paediatric back pain - unless there are obvious signs of pathology, a trial of adjustments may be carried out- No change within 2-3 adjustments warrants further evaluation.

33% post traumatic- occult fracture, spongy
33% developmental scoliosis, kyphosis
18% infection.

CASE

A

ya

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10
Q

Write down your findings

A
  • The L2 vertebra shows some loss of height of the anterior vertebral body
  • The posterior vertebral line is intact
  • A compression deformity of L2 is suspected
  • Wouldyouwantfurtherimaging?
  • If so, what?

Yes CT
*Serial cuts of L2 are shown here Write down your findings:
* There is a wedge compression deformity of L2 vertebral body with preservation of the disc spaces above and below this level
* There is minimal retropulsion of the L2 body not causing any significant compression of the thecal sac
* The superior end plate and part of the body appear fragmented as seen on image cuts 7, 8 and 9
* There is minimal prevertebral soft tissue prominence
* The bony spinal canal is normal in size and configuration
* No significant posterior bulging or herniation of the disc is present

What would you expect the treatment to be?

  • She was hospitalized under the neurosurgery service for observation and discharged home in two days with a brace
  • Would you adjust?
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11
Q

Thoraco lumbar fractures
Thoraco-lumbar fractures are a major cause of disability
* Ninety percent of all spinal fractures are in the thoraco- lumbar region
* Fractures at the thoraco-lumbar junction have an incidence of neurologic deficit of up to 40%

Several factors contribute to thoraco-lumbar vulnerability: What are they?

A
  • In the lumbar spine, there are no ribs to provide additional stability as in the thoracic region
  • The change in alignment from thoracic kyphosis to lumbar lordosis makes it an area of stress
  • Lumbar spinal segments are more mobile than thoracic segments -the coronal orientation of the facets in thoracic region is more stable then the oblique orientation of the lumbar region
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12
Q

Describe the 3 column concept

A

Lateral View of Lumbo-sacral Vertebrae:
1. The anterior column - anterior longitudinal ligament and the anterior part of the vertebral body
2. The middle column - from the middle portion of the vertebral body to the posterior aspect of the vertebral body and includes the posterior longitudinal ligament
3. The posterior column - all bony and ligamentous structures posterior to the posterior longitudinal ligament and includes the pedicles, facets, spinous processes and all associated ligaments
Stable fractures – involve only anterior column Unstable fractures – involve the middle or all 3 columns

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13
Q

Presentation:
* Thoracolumbar back ache
* 3 months duration
* Footy season started 4 months ago  Takes lots of knocks at footy
* Starting to wake him at night
* Can get worse with activity too
* Pain is usually relieved with aspirin

Exam:
* Nil neurological abnormalities
* Localised swelling and point tenderness at L2
* Mild erector spinae spasm on the right thoracolumbar region
Would you image, and what would you ask for?

A

Osteoid osteoma

  • 2:1 male predominance
  • 10-25yoa
  • Severe pain, worse at night
  • Pain dramatically relieve with aspirin – 65%
  • Painful & rigid scoliosis

 Lesion on concave side of curve  Usually lumbar – 60%
* Only 10% occur in spine
 Ivory pedicle or neural arch
* CT often required in the spine to see the nidus

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14
Q

What do you see?

A

Winking owl sign
Loss of A Pedicle

  • WinkingOwlSign:
     Loss of a pedicle outline
     All other pedicles appear normal in size and shape
     First consideration MUST be lytic metastatic disease
  • Congenital Absence of Pedicle:
     Loss of a pedicle outline
     Contralateral pedicle of the same vertebra will often be enlarged and sclerotic
     The present pedicle does this due to increased load

Unilateral Dense Pedicle
* Dense left L5 pedicle (white arrow) and an old right L5 pars fracture (pink arrow)
* Spondylolysis with stress sclerosis on the contralateral side, resulting in a dense pedicle
Other Differentials:
* Benign tumors:
 Osteoid osteoma and osteoblastoma may cause a painful rigid scoliosis, with the lesion found on the concave side of the curve. Bone island uncommonly affects the pedicles.
* Malignant tumors:
 Blastic metastases most common malignant cause of a unilateral dense pedicle
 Other malignant tumors rarely present with a unilateral dense pedicle e.g., lymphoma, multiple myeloma, Ewing sarcoma
* Iatrogenic: Laminectomy - most commonly contralateral to the dense pedicle
* Infection: Rarely affects the pedicle in isolation
* Agenetic or hypoplastic pedicle or facet: The dense pedicle in on the opposite side to the agenetic or hypoplastic pedicle or facet
* Miscellaneous:
 Tuberous sclerosis has an affinity for the posterior elements when it occurs in
the spine - multiple sclerotic pedicles
 Rarely - Paget disease, fibrous dysplasia, and sarcoidosis, may affect the pedicle in isolation

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15
Q

Adolescent Idiopathic Scoliosis

Whats the definition and curve required?

A
  • Scoliosis is defined as a lateral curvature of the spine, with a Cobb angle of more than 10 degrees.
  • Less than 10 degrees - called spinal asymmetry Juvenile Scoliosis:
  • Developing between 4-12 years of age
  • Similar presentation and progression to adolescent scoliosis

Adolescent Scoliosis:
* Develops during adolescent pubertal growth spurt
* Most research is performed in this age group
 The juvenile (detected between the ages of 4 to 10 years) scoliosis may resemble either the infantile or adolescent (detected after 10years of age) scoliosis
 As the child develops, right thoracic curves become more common and are the most common lateral curves found in adolescent children (Weinstein 2001)
* Asymmetry at a young age does not always mean the curve will progress into scoliosis

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16
Q

What are the 2 types of Scoliosis?

A

Postural scoliosis
* Long thoracolumbar curve with no compensatory curves
* Rotation of the vertebrae to the concavity
* Flexible – it disappears when the patient is prone

Functional scoliosis
* Leg length discrepancy
* Single, long thoracolumbar curve, with convexity to side of lower limb
* No compensatory curves
* Rotation of vertebrae to concavity of curve
* Curvature disappears when pelvis is levelled with a heel-lift

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17
Q

What are some of the causes of Scoliosis?
Ie Aitiology

A

Neurological:
* Abnormalities of visual, vestibular, proprioceptive and postural control
Abnormal symmetries of brain structure and function
 In cerebral hemispheres, brainstem, internal capsule and
corpus callosum

Orthopaedic:
* Increased vertebral column length in those with AIS, compared with those without it
 Not associated with longer spinal cords
 Increase in growth (ie abnormal growth) of the anterior
column of the spine,
 the adjacent intervertebral discs are wedged to a lesser degree than the vertebrae, implying that disc wedging occurs secondarily
87

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18
Q

How do you need to target your history for a scoliosis patient?

A

Determine whether it is a chronic, asymptomatic scoliosis or an acute, painful scoliosis:
* Any acute, painful scoliosis needs to be investigated further for underlying pathology
* Discussed in differential diagnosis section

How long has the scoliosis been there?
* Assists with classification * Also assists with prognosis

Associated signs and symptoms
Neurological – weakness, sensation changes
Pain
Headaches
Fever
Recent infection
Weight loss
Rashes, skin lesions
Urinary incontinence
Family history of scoliosis or pathology causing scoliosis

19
Q

How do you examine a patient with Scoliosis?

A

Postural examination – gowned or shirtless
 Posterior, anterior and lateral
 Laterally -
 Shoulders posterior or anterior to sacrum  Degree of lordosis
 Thoracic kyphosis
 Position of pelvis
 Symmetry or asymmetry of the waistline
 Plumb line – from occipital protruberance to intergluteal cleft

 Identify the curve:
 Left or right – left thoracic curves are red flags for pathology  Need to rule out dextrocardia in these cases
 Thoracic, lumbar, thoracolumbar
 Double major, single major curve
 Degree of spinous process deviation
 Check position and alignment of feet, ankles, knees and hips
 Ensure equal length/size
 Measure weight-bearing and supine if concerned with ligamentous laxity
 Check for foot deformity

Skin examination
* Cafe-au-lait spots – neurofibromatosis
* Midline sacral tuft of hair, or haemangioma – spinal dysraphism * Dimples or sinus tract in sacrum – intraspinalteratoma

Adam’s test – ensure full knee extension, feet together
* Structural scoliosis – curve persists, spinous processes rotate to concavity of curve , with prominence on
convex side of curve
* Postural scoliosis – spinous processes rotate to convexity of curve, with prominence on concave side of curve

Lateral flexion – determines flexibility of curve
* If not flexible, it suggests underlying structural pathology/anomalies

Inspect the curve while prone
* Assess same landmarks as previously mentioned to note any differences * Does the curve increase or reduce
* Should reduce when functional
* Structural scoliosis will not change significantly
* Assess lateral flexion, extension (have patient lift head and shoulders)

Assess superficial abdominal reflexes
* Lack of reflex indicates syringomyelia with 89% specificity and 95% sensitivity

Hip examination
* Ober’s – hip abduction contracture * Thomas – hip flexion contracture
* Patrick Fabers
* Internal and external rotation
* Leg posture and length while supine

Overall joint assessment – rule out ligamentous laxity or hypermobility

EXAM
Muscle strength examination – particularly lower extremity Sensory examination
Muscle stretch reflexes, scapulohumeral reflex
Observe gait for abnormality or ataxia
Assess for persistent primitive reflexes such as Galants and Perez Assess for any indication of hemisphericity or vestibular imbalance
* Eyes
* Ears
* Cranial nerves
Palpate the spine
* Rule out areas of suspicion that may indicate block vertebrae or other congenital anomalies
* Find the subluxations

20
Q

What are the differential diagnosis of Scoliosis?

A

Neurological pathology
* Syringomyelia, Chiari, tethered cord, intraspinal tumours
* Scoliosis is generally acute, or quickly progressing
* May have associated pain
* Will demonstrate abnormal neurological examination findings such as change in sensation, muscle stretch reflexes or muscle strength
* Superficial abdominal reflex will be absent in one or more quadrants

Congenital anomaly
* Hemivertebrae, block vertebrae, vertebral wedging * Leg length discrepancy (structural, not functional) * Scoliosis will be more of a chronic nature
* Generally asymptomatic

Genetic syndromes
* Neurofibromatosis
* Café au lait spots
* Neurofibromas - generally systemic
* Ehlers-Danlos syndrome
* Joint hypermobility (generalised) * Skin hyperelasticity
* Excessive skin bruising

Tumour in spinal column
* Eg osteoid osteoma, osteosarcoma, aneurysmal bone cyst
* Painful, especially at night
* Acute scoliosis
* Neurological abnormalities if large enough to cause compression * May have systemic signs and symptoms is tumour is malignant
* Hepatosplenomegaly

Discitis, osteomyelitis
* Will be painful
* Recent history of infection (in most cases) * Child may appear unwell due to infection * Hepatomegaly

Subluxation
* Significant pelvic and/or sacral subluxation can change spinal curvature in sagittal and coronal planes

21
Q

How should we manage a scoliosis?

A

Risk of progression of curve must be ascertained

  • This can be performed using Risser sign, digital skeletal age, triradiated cartilage status, and Tanner staging
  • The earlier the stage, the less mature and the more risk of progression
    Larger curves (more than 30 degrees) are also at higher risk of progression
    Premenarchal girls have a higher risk for progression than do girls 2 years after menarche with similar curves
    Single major thoracic and double major thoracic and lumbar curves are at higher risk of progression

Only 0.2-0.3% will develop progressive curves that require surgery or bracing

X-rays performed initially to measure size of curve, and rule out congenital anomalies, and assist with skeletal maturity determination

  • Cobb angle is the most common way to measure the curve
    Serial monitoring of the curve must be performed – via AP X-ray
  • Depending on risk, this can be performed every 4-6 or 12 months
    Serial height checks every 6 months to determine any periods of accelerated adolescent growth, which is a high risk period for progression

If pathology is suspected, initially an X-ray should be performed, followed by CT and/or MRI depending on suspected pathology
* CT for bony pathology
* MRI for soft tissue pathology

Bracing is sometimes used, and the newer flexible/soft braces are the better option (if necessary) as they allow spinal movement and proprioceptive activity to continue
* Used in immature patients, with curves less than 40 degrees
Exercise and transcutaneous electrical stimulation have no effect
After skeletal maturity is attained, only curves of more than 30° must be monitored for progression
Surgery is saved for those with a curve above 45-50 degrees, as they tend to continue progressing after skeletal maturity, cause loss of pulmonary function (and respiratory failure), and greater progressions of the curves are more difficult to treat with surgery

  • There have been reports of removing entire hemivertebrae to resolve postural stress due to congenitally abnormal vertebrae

Chiropractic Management:
Chiropractic adjustments can assist with correct sensorimotor integration, thus may be helpful in preventing curve progression

Early chiropractic care during life may prevent/correct cerebral hemisphericity, which has been implicated in the development of AIS

Chiropractic will not affect structural defects, but maintaining vertebral body movement may prevent progression of postural/pressure induced bony changes such as vertebral body wedging

Children with scoliosis will require more regular checks than ‘normal’ children, due to the increased postural stress on the spine, and associated underlying neurological imbalances

Chiropractic is useful for those who begin to get some postural discomfort associated with their scoliosis, depending on progression and how large the scoliosis is

22
Q

What is the

A

Syringomyelia

Syringomyelia is the development of a fluid- filled cavity or syrinx within the spinal cord
Can be due to:
* Blockage of CSF circulation
* Or may be communicating with fourth ventricle * Spinal cord injury
* Spinal disraphism
* Intramedullary tumours
* Idiopathic
Rarely occurs in adolescents – more common in 3rd and 4th decade of life

up to page 104

23
Q

Adolescent Kyphosis

Normal ranges?
Cob angle> ?
What do you need to differentiate with if you see it?

A
  • Normal range for thoracic kyphosis is 20-50 degrees of curvature between T3-T12
  • Hyperkyphosis - Cobb angle > 50 degrees
  • Must differentiate between flexible (postural) and structural kyphosis

Flexible Kyphosis
Postural hunching
 More common in insecure or shy females, and adolescents taller than their peers
 Deformity can be completely corrected voluntarily
 No abnormalities of the vertebrae on standing lateral films
 The start of degenerative changes may be noted
 Generally does not progress to a structural deformity
 Responds well to chiropractic, strengthening and stretching exercises, and conscious postural control

24
Q

What are some diagnosis of Structural Kyphosis?

A

Structural Kyphosis

Injuries – compression or burst fractures
Infections – bacterial, tubercular, fungal
Metabolic disease – osteogenesis imperfecta, osteoporosis Neoplastic conditions – leukemia
Neuromuscular diseases
Disorders of collagen – Marfans
Bone dysplasias – neurofibromatosis, achondroplasia Progressive kyphosis can be seen with radiation therapy

25
Q
A

Scheuermann’s Disease

X-ray of Scheuermann’s disease with some of the typical signs:
-narrowed disk space
-wedge shaped vertebral bodies –uneven endplates
-schmorl’s nodes

Spiral-CT sagittal reconstruction of a dorsal spine with extraordinary remnants of Scheuermann’s disease

Most common form of structural hyperkyphosis Anterior wedging of >5 degrees of 3 or more consecutive
More common in boys
Usually present during adolescent growth spurt
Most common complaint – thoracic pain
Radiographic findings –
* Irregularities in vertebral endplates
* Disc space narrowing
* Schmorls nodes
* Apex of curve towards lower thoracic spine, rather than mid thoracic
vertebral bodies at the apex of the deformity
* Measured with standing lateral films

In females it is important to rule out: *Metabolic disease
*Endocrine disease
*Osteoporosis
*Eating disorders

26
Q

Adolescent Kyphosis

Juvenile kyphosis 13yo girl
Thoracic spine lateral – midthoracic kyphosis with wedged apical vertebra, disc narrowing, end-plate irregularity, and multiple Schmorl nodes

What do we need to rule out>

A

In females it is important to rule out: *Metabolic disease
*Endocrine disease
*Osteoporosis
*Eating disorders

27
Q

Case 6:

14yo boy
 T/L pain, aches a lot
 2 months ago had antibiotics for a bacterial throat infection

 Nil radiation
* What are your Differentials?
* Main Physical Examination?
* What Imaging would you want?

X-Rays Demonstrate No Pathology
You start a trial of care
After 4 weeks and 6 adjustments, there has been no big change in the clinical picture
In fact he seems to be having an increased thoracic kyphosis & antalgic positioning
What do you do?

A

Follow-Up X-ray Findings
* Destruction T11-12 disc, and much of adjacent vertebral bodies
* Excessive sclerotic bone and paravertebral soft tissue swelling
What is your diagnosis?
What are the two key history questions?
Which part of the spine is most commonly affected?
How long doe the bony changes typically take to become apparent?

28
Q

Psychological Disorders

Anxiety disorders

Types include:
* Separation anxiety disorder (SAD),
* Childhood-onset social phobia or social anxiety disorder, generalized anxiety
disorder (GAD),
* Obsessive-compulsive disorder (OCD),
* Phobias,
* Post-traumatic stress disorder (PTSD), and * Panic disorder
* are all defined by the occurrence of either diffuse or specific anxiety, often related to predictable situations or cues
Can be diagnosed with more than one anxiety disorder at one time
Most common psychiatric disorders of childhood
* 5-18% of all children and adolescents
Anxiety and depressive disorder in adolescence predict increased risk of anxiety and depressive symptoms (including suicide attempts) in adulthood

A

Good to know I guess

29
Q

Depression:

DSM-IV-TR:
* 5 or more of the following present during a 2 week period, and represent a change from previous functioning
1.Depressed most of the day, nearly everyday
2.Markedly diminished interest or pleasure in almost all activities most of the day
3.More than 5% change in body weight in a month without dieting. Change in appetite daily
4.Insomnia or hypersomnia
5.Psychomotor agitation
6.Fatigue or loss of energy
7.Feelings of worthlessness or inappropriate guilt
8.Diminished ability to concentrate, or indecisiveness
9.Recurrent thoughts of death, suicidal ideation, plans or attempts
* Cause clinically significant distress or impairment
* Symptoms are not due to medication or drugs
* Symptoms are not accounted for by bereavement or loss * Symptoms do not fit criteria for mixed/bipolar episodes

A

4-8% of adolescents
1:2 male:female
Cumulative incidence by 18yoa – 20%
60% report thinking about suicide
30% will attempt suicide
High risk of comorbidity – anxiety disorder, disruptive behaviour, ADHD
High risk of substance abuse

30
Q

Internet Addiction:

Between 10-44% of adolescents are addicted to the internet

High comorbidity with other psychological disorders

Most likely representing a common underlying disturbance

A

Eg. Dopamine, reward pathways
Autonomic Imbalances

31
Q

Management of Psychological Disorders:

MRI doing TCMS
* Cognitive behavioural therapy (CBT) has been shown to be equally as effective as medication however it takes longer to reach the desired goal

  • Transcranial magnetic stimulation has recently been reported as more effective than medication in major depressive disorder

How can we influence Psychological disorders with Chiropractic?

A

Chiropractic and Psychological Disorders

Adjustments have the capacity to:
* Reduce serum cortisol
* Increase serum sIgA
* Reduce pain
* Stimulate and alter brain activity * Lead to neuroplasticity

As chiropractors we know:
* Dietary effects
* Lifestyle effects
* Nutritional support methods

All clinically significant psychological disorders must be co-managed or referred:
* GP, paediatrician * Psychologist

32
Q

Menstrual Issues:

Menstrual dysfunction occurs at some time in about 50% of adolescent females

The onset and continuation of normal menstrual cycling depend on the functional and anatomic integrity of:

A

he onset and continuation of normal menstrual cycling depend on the functional and anatomic integrity of:
* the hypothalamus together with higher centres, including possibly the pineal gland
* the anterior pituitary
* the ovary
* the uterus

Organic pathology should be considered and excluded A complete history:
* Puberty and menstrual patterns
* Family history of gynecologic problems and maternal onset of menarche
* Medical history noting hospitalizations, chronic illness, medication or substance use, and infections
* The related associations of weight change, nutrition, exercise, and sports participation can be critically important in considering a differential diagnosis

33
Q

Dysmenorrhoea

Dysmenorrhoea is the term used to describe painful periods.

How should these patients be managed?
What are some common causes?

A
  • Always requires evaluation of functional hormone balance

Common causes of imbalance:
-Poor diet, blood sugar drops
-Pituitary drive develops for the production of glucocorticoids
-Pituitary produces ACTH- affects gonads
-If Progesterone doesn’t keep pace with oestrogen, dysmenorrhea occurs

Thyroid deficiency

Cramps with period pain - calcium deficiency?
-Start high dose calcium one week prior to menstruation
-If deficient in Calcium, need to consider HCL status, Vit D and Vit E

Check Ileocaecal valve and gut dysfunction:
Pain may be secondary to gut function as pain becomes a form of detoxification

Essential Fatty acid deficiencyL
-Used to produce prostaglandins (natural anti-inflammatories)
-Used to produce Hormones
-Good source is evening primrose oil- one capsule 3 x per day

34
Q

Simple version of Chiropractic care for Period pain?

A
  1. Correct the sacrum
  2. Double check the coccyx, public symphysis
  3. Check piriformis, glut med + max, adductors
  4. Assess gait pattern
  5. Assess GIT- especially liver and ICV valve
  6. Assess Endocrine system- adrenal, thyroid, pineal and pituitary
35
Q

Amenorrhoea: Failure for menstration to begin

What are some possible causes?

A

Hypo and hyperthyroidism can cause it:
-If Thyroid dysfunction is present, check the entire HPA axis.

Hypoproteinaemnia can cause scanty menstruation.

36
Q

Chronic Fatigue syndrom:
What is the pathogenesis?

  1. The individual has had severe chronic fatigue for 6 or more consecutive months that is not due to ongoing exertion or other medical conditions associated with fatigue (these other conditions need to be ruled out by a doctor after diagnostic tests have been conducted)
  2. The fatigue significantly interferes with daily activities and work
  3. The individual concurrently has 4 or more of the following 8 symptoms:  post-exertion malaise lasting more than 24 hours
     unrefreshing sleep
     significant impairment of short-term memory or concentration
     muscle pain
     pain in the joints without swelling or redness  headaches of a new type, pattern, or severity  tender lymph nodes in the neck or armpit
     a sore throat that is frequent or recurring
A

Pathogenisis:
-Largely unknown
-Multifaceted issues
-Fatigue is a generalised complaint
-A large number have a significantly stressful event and never recover from it.

eg Viral infection- Glandula fever, Influenza
-Emotional trauma/ Stress
-Parasitic infection - gut (commonly after travel)
-After a dose of antibiotics.

37
Q

GUT
Chronic fatigue patients have been shown to have a different gut microbiome
 Fremont M, et al. Anaerobe 2013 Aug; 22:50-6
* SIBO – breath test abnormalities
 20% of controls
 77% of CFS patients
 100% of fibromyalgia patients
 The degree of somatic pain in fibromyalgia correlated significantly with they hydrogen level on the breath test
 Pimentel M, et al.
* Leaky guts drive neuroinflammation and autoimmunity

A
  • Leaky guts drive neuroinflammation and autoimmunity
38
Q

Gut Dysbiosis vs SIBO

How does each present?

A

Gut dysbiosis can present as:
 Nervousness
 Memory loss
 Forgetfulness
 Confusion
 Mind going blank
 Brain fog
 Severe fatigue
 GI symptoms may be mild to severe

SIBO symptoms:
 Diarrhoea
 Bloating
 Flatulence
 Abdominal pain  Weight loss
 Steatorrhoea
 Arthralgia
 Rosacea
 B12 &/or iron deficiency  Polyneuropathy

39
Q

What are the best screening tools for assessing the gut

A
  1. Bioscreen or SmartDNA or Nutripath
  2. Complete allergy screen blood test
    IgG and IgA – Biotek or Nutripath
  3. Gut permeability tests

Do not make the mistake of giving probiotics without knowing what is in the gut

Some may need antibiotics to clear the gut and start afresh, others may only need herbal remedies with probiotics

40
Q

Immune System:

A

Often people get multiple infections ie Candida, viral, parasitic, bacterial, mycoplasma.

Eg Candida, viral, fungal, parasitic, bacterial, mycoplasma
Chronic infections lead to central fatigue:
Increases Th1 and Th2

Leads to:
* Neuroinflammation, white matter densities, decreased gray matter volume
* Central hypometabolism & hypoperfusion
* Increased lactate
* Mitochondrial and energy disorders
* Autoimmunity
* Damage to lipids and proteins with reduced phosopholipid synthesis in the brain (esp. viral infections)

Result:
* Neuro-cognitive symptoms * Central fatigue
* Sleep disorders
* Autonomic symptoms
* Disabling muscle fatigue

41
Q

Infection vs Dysbiosis

A

ya

42
Q

Sschemia

What is ischemia? Ischemia is a condition in which the blood flow (and thus oxygen) is restricted or reduced in a part of the body. Cardiac ischemia is the name for decreased blood flow and oxygen to the heart muscle.

A

In CFS – tends to affect the brain
Brain fog, inability to concentrate, confusion
Significantly lower cerebral blood flow in CFS patients compared to controls
*Accumulation of lactate in the CSF *Low levels of glutathione
Oxidative stress at the BBB is leading to local endothelial dysfunction, reducing blood supply, promoting anaerobic metabolism in neurons

*Creates neuronal STRESS!

In fibromyalgia – tends to occur in the muscles and cause pain Tender points in FM:
* Possess even lower levels of ATP than non-painful tissues from the same patients * Therefore they are areas of extreme energy deficiency
In general the muscles have significant clinical ischaemia – detected on ultrasound
Ischaemia leads to use of anaerobic pathways
* Limits energy produced in a sustained fashion
* Inhibits utilisation of fats for energy
* Increased metabolic by-products such as lactic acid
Decreased pH triggers further oxidative stress & activates nociceptors

43
Q

Managing CFS Diet & Lifestyle (Chronic Fatigue syndrome)

Keep in mind they are so tired that every change is difficult Need to work slowly
Educate and empower them to take control of their health
What kind of diet would you recommend for CFS? What kind of exercise would you recommend? What kind of supplements would you recommend?

A

Exercise strategies:
Lack of exercise leads to decreases GABA production and increases pain

Start slow, and go slow!
* Reduce risk of exacerbating CFS post-exertion * Walk, swim, gentle body-weight exercise
* They will generally know their limit
* Worse pain/fatigue after – NO GAIN

Exercise may amplify inflammation and mitochondrial damage.
* Ensure adequate antioxidants and anti-inflammatories are taken to reduce this, especially when increasing the load

Lower exercise tolerance comes in the form of:
* Exacerbation of fatigue when pushed too hard
* Longer than ‘normal’ recovery time
* Reduced clearance of lactic acid (and generally more day-to-day lactic acid in their system)
* Increased muscle pain and weakness post-exertion

DIET:
Trial and error to find the best diet for them
* Wellness diet/anti-inflammatory diet
* FODMAP diet
* GAPS diet
* Specific carbohydrate diet
* Elimination diet
* Gluten & casein free diet
* Paleo diet – though many will have difficulty with meat and will potentially be allergic to eggs, dairy, nuts
Fasting relieves pain and enhances mood
* Ketogenic diet may be of benefit to some
* Intermittent fasting in times of stress can be of benefit
* Not great for patients with massive mitochondrial issues as their body needs a slow input of energy

SUPPLEMENTATION:
Metagenics have a great protocol to follow through different stages of CFS
Mitochondrial support:
*Glutathione
*Co-Q10
*N-acetyl cysteine (NAC)
Correct probiotics
Herbal antimicrobials
Anti-inflammatories:
*Infavanoid isointensive care
Rebalancing Th1/Th2
*Arabinoguard *Ultraprobioplex
*Super mushroom complex
Ribose for muscle recovery and pain Magnesium
EPA/DHA, phospholipid support Activated B vitamins
B12, iron
Adrenal or thyroid support where needed