MSK Flashcards

(84 cards)

1
Q

WHAT IS THE DEFINITION OF JIA

A

A CHRONIC INFLAMMATORY JOINT DISEASE

PERSISTENT JOINT SWELLING

IN ABSCENSE OF INFECTION OR OTHER DEFINED CAUSES

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2
Q

WHAT ARE THE SUBSTYPES OF JIA

A

OLIGOARTHRITIS

EXTENDED OLIGOATHRITIS

POLYARTHRITIS

SYSTEMIC

PSORIATIC

ENTHESITIS RELATED

UNDIFFERENTATED

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3
Q

A CHILD COMES IN WITH

  • MORNING STIFFNESS AND PAIN
  • STIFFNESS AFTER REST
  • INTERMITTENT LIMP
  • LOW MOOD
  • POOR BEHAVIOUS
  • JOINT SWELLING
  • +/- SALMON PINK RASH
A

JIA

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4
Q

WHAT ARE COMPLICATIONS OF JIA

A

CHRONIC ANTERIOR UVEITIS

FLEXION CONTRACTURES

GROWTH FAILURE

OSTEOPOROSIS

AMYLOIDOSIS

VALGUS DEFORMITY

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5
Q

HOW DO YOU MANAGE JIA

A

EDUCATION AND SUPPORT

PHYSIO

NSAID

JOINT INJECTIONS (IF OLIGOARTHRITIS)

METHOTREXATE (POLYARTHRITIS)

PULSED IV CORTICOSTERIOIDS

METHYLPREDNISOLONE FOR SYSTEMIC ARTHRITIS

BIOLOGICS

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6
Q

DESCRIBE THE ARTICULAR PATTERN OF EXTENDED OLIGOARTHRITIS

A

4< JOINT

AFTER 6M

ASSYMETRICAL JOINT DISTRIBUTION

ANA +VE

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7
Q

DESCRIBE THE ARTICULAR PATTERN + LAB RESULTS OF OLIGO ARTHRITIS

A

1-4 JOINTS

MOST COMMONLY KNEE, ANKLE, WRIST

+/-ANA +VE

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8
Q

DESCRIBE THE ARTICULAR PATTERN + LAB RESULTS POLYARTHRITS

A

SYMMETRICAL JOINTS DISTRIBUTION WITH HIGH FINGER INVOLVEMENT

1-6Y: RF -VE

10-16Y: RF +VE (POOR PROGNOSIS)

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9
Q

WHAT DOES AMYLIODOSIS CAUSE

A

PROTEINUREA

RENAL FAILURE

HIGH MORTALITY

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10
Q

WHY DOES OSTEOPOROSIS OCCUR IN JIA

A

REDUCED WEIGHT BARING

STEROIDS

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11
Q

WHAT IS THE TREATEMENT OF JIA OSTEOPOROSIS

A

CALCIUM

VIT D

WEIGHT BARING EXCERSISES

DECREASE STERIODS

BISPHOSPHONATES

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12
Q

WHY DO FLEXION CONTRACTURES OCCUR

A

FROM HOLDING THE JOINTS IN THE MOST COMFORTABLE POSITION

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13
Q

WHAT ARE THE COMMON COMPLICATONS IN JIA FLEXION CONTRACTURES

A

JOINT DESTRUCTION REQUIRING REPLACEMENT

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14
Q

HOW DO YOU TREAT CHRONIC ANTERIOR UVEITIS

A

CORTICOSTEROID EYEDROPS

MYCROLITIC EYE DROPS

CORTICOSTEROID INJECTION

SYSTEMIC CORTICOSTEROIDS

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15
Q

WHAT IS CHRONIC ANTERIOR UVEITIS

A

INFLAMMATION OF THE ANTERIOR PART OF THE EE

VERY COMMON COMPLICATION OF IBD AND ARTHRITIS THAT CAN LEAD TO VISUAL IMPAIREMENT

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16
Q

DESCRIBE THE ARTICUALR FINDINGS OF PSORIATIC ARTHRITIS

A

ASYMMETRICAL DISTRIBUTION

DACTYLISIS

PSORIASIS

NAIL PITTING

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17
Q

WHAT IS THE PRESENTATION OF SYSTEMIC ARTHRITS

AND LAB FINDINGS

A

OLIGOARTHRITIS/POLYARTHRITIS

PAIN IN MUSCLES

ACUTE ILLNESS

SALMON PINK RASH

RAISED WCC

RAISED PLATELETS

RAISED INFLAM MARKERS

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18
Q

WHAT ARE FEATURES ONLY FOUND IN POLYARTHRITIS FROM 10-16Y

A

RHEUMATOID NODULES

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19
Q

HOW DO YOU DIAGNOSE SEPTIC ARTHRITIS

A

BLOOD CULTURES

BLOODS

JOINT ASPIRATE

US

XRAY

BRI

BONE SCAN

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20
Q

HOW DOES THE PRESENTATION OF SEPTIC ARTHRITIS DIFFER IN INFANTS

A

PEUDOPARALYSIS

CRY IF JOINT IS MOVED

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21
Q

WHAT IS THE PRESENTATION OF SEPTIC ARTHRITISIN CHILDREN

A

ERYTHETEMATOUS

ACUTELY TENDER

REDUCED ROM

ACUTELY UNWELL AND FEBRILE CHILD

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22
Q

WHAT PATHOGENS COMMONLY CAUSE SEPTIC ARTHRITIS

A

STAPH. AUREUS

HiB

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23
Q

WHAT IS TRANSIENT SYNOVITIS

A

MOST COMMON CAUSE OF HIP PAIN IN CHILDREN OFTEN ACCOMPNIED BY A VIRAL INFECTION

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24
Q

WHAT IS THE PRESENTATION OF TRANSENT SYNOVITIS

A

SUDDEN ONSET OF PAIN

LIMP

DECREASED ROM

REFFERRED KNEE PAIN

AFEBRILE/LOW GRADE FEVER

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25
WHAT INVESTIGATIONS WOULD YOU USE TO DIFFERENTIATE TRANSIENT SYNOVITIS FROM SEPTIC ARTHRITIS
BLOOD CULTURES JOINT ASPIRATION
26
OUTLINE THE DIFFERENCES BETWEEN SEPTIC ARTHRITIS AND TRANSIENT SYNOVITIS
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27
HOW DO YOU MANAGE TRANSIENT SYNOVITIS
BED REST +/- SKIN TRACTION
28
WHAT DSEASE CAN HAVE TRANSIENT SYNOVITIS AS A PRECURSER
PERTHES
29
WHAT IS SEPTIC ARTHRITIS
A SERIOUS INFECTION OF THE JOINT SPACE WHICH CAN LEAD TO BONE DESTRUCTION
30
HOW DO YOU TREAT SEPTIC ARTHRITIS
IV ABX \> PO ABX SURGIAL LAVAGE IMMOBALIZATION OF JOINT MOBALISATION
31
WHAT ABX WOULD YOU USE IN SEPTIC ARTHRITIS FOR S. AUREUS
FLUCLOXACILLIN OR CEPHALEXIN
32
WHAT ABX WOULD YOU USE IN SEPTIC ARTHRITIS FOR HiB
CEFTRIAXONE
33
WHAT IS HIP DISPLASIA
AN ABNORMALITY OF THE HIP JOINT WHERE THE SOCKET DOESNT FULLY COVER THE BALL
34
WHAT ARE THE RISK FACTORS WHICH PREDISPOSE YOU TO HIP DYSPLASIA
FAMILY HISTORY SERTAIN SWADDLING TECHNIQUES BREECH BIRTH
35
WHAT IS THE PRESENTATION OF HIP DYSPLASIA
ASSYMPETRICAL LEG LENGTH AND SKIN FOLDS LIMP SENSATION OF INSTABILITY GROIN/HIP PAIN
36
HOW DO YOU DIAGNOSE HIP DYSPLASIA
NIPE EXAM US XR
37
WHAT IS THE TREATEMENT OF HIP DISPLASIA
CAST +/- HI TRACTION SURGERY PHYSIO MAY RESOLVE SPONTANEOUSLY
38
WHAT IS THE DEFINITION OF OSTEOMYELITIS
AN INFECTION OF THE METAPHYSIS OF LONG BONES
39
WHERE DOES OSTEOMYELITIS NORMALLY OCCUR
DISTAL FEMOUR PROXIMAL TIBIA
40
WHAT ARE COMMON PATHOGENS OF OSTEOMYELITIS
STAPH. AUREUS STREP HiB SALMONELLA -SICKLE CELL TB - IMMUNOCOMPRIMISED
41
WHAT IS THE PRESENTATION OF OSTEOMYELITIS
PAIN PSEUDOPARALYSIS SWELLING AND TENDERNESS ERYTHETEMATOUS WARM
42
HOW WOULD YOU INVESTIGATE OSTEOMYELITIS
BLOOD CULTURES BLOODS: RAISED WCC, ESR, CRP X RAYS
43
WHAT RADIOLOGICAL FINDINGS WOULD YOU HAVE IN OSTEOMYELITIS
SOFT TISSUE SWELLING SUBPERIOSTEAL NEW BONE FORMATION
44
HOW WPULD YOU TREAT OSTEOMYELITIS
PARENTERAL ABX\>IV\>PO SURGICAL DRAINIGE LIMB IN SPLINT EARLY MOBILISATION
45
WHAT IS KÖHLER DISEASE
A RARE BONE DISEASE AFFECTING CHILDREN AGED 6-9Y THERES NECROSIS OF THE NAVICULAR BONE DUE TO DECREASED BLOOD SUPPLY
46
WHAT IS THE PRESENTATION OF KOHLER DISEASE
PAIN AND SWELLING AT MIDDLE PART OF FOOT LIMP TENDERNESS AT MIDDLE FOOT
47
HOW WOULD OU INVESTIGATE KOHLER DISEASE
X RAY
48
HOW WOULD YOU TREAT KOHLER DISEASE
REST +/- CAST ANALGESIA
49
50
WHAT ARE DISCOID MENISCI
A RARE HUMAN ANATOMIC VARIENT AFFECTS LATERAL MENISCI OF THE BONE
51
DESCIBE THE WATANABE CLASSIFICTAIONS
INCOMPLETE - SLIGHTLY DEFORMED COMPLETE - FULLY ROUNDED WRISTBERG - LOCK OF POSERIOR MENISCI
52
WHAT IS THE PRESENTATION OF DISCOID MENISCI
PAIN CLICKING MECHANICAL LOCKING
53
WHEN DO DISCOID MENISCI PRESENT
ADOLESCENCE
54
HOW DO YOU DIAGNOSE DISCOID MENISCI
XRAY MRI
55
HOW WOULD YOU TREAT DISCOID MENISCI
SURGERY PHYSIO
56
WHAT IS OSGOOD SCHLATTERS
INFLAMMATION OF POSTERIAL LIGAMENT AT TIBIAL TUBEROSITY
57
WHAT RF PREDISPOSE YOU TO OSGOOD
IMPACT SPORTS OVERUSE
58
WHAT IS THE PRESENTATION OF OSGOOD
PAIN IN FRONT LOWER PART OF KNEE WORSE ON USE
59
HOW WOULD YOU DIAGNOSE OSGOOD
SYMPTOMATICALLY
60
HOW DO YOU TREAT OSGOOD
PHYSIO BRACE SURGERY
61
WHAT IS SLIPPED CAPITAL FEMORAL EPIPHESIS
DISPLACEMENT OF EPIPHESIS OF FEMORAL HEAD POSTERIOINERIORLY
62
WHAT CONDITIONS ARE ASSOCIATED WITH OSGOOD
HYPOTHYROIDISM HYPOGONADISM
63
WHAT IS THE PRESENTATION OF SLIPPED CAPITAL FEMORAL EPIPHESIS
LIMP HIP PIAN REFERRED KNEE PAIN DECREASED ROM
64
WHAT INVESTIGATIONS ARE REQUIRE FOR SLIPPED CAPITAL FEMORAL EPIPHESIS
X RAY
65
HOW WOULD YOU MANAGE SLIPPED CAPITAL FEMORAL EPIPHESIS
SURGICAL PIN FIXED IN SITU
66
WHAT IS PETHES DISEASE
AVASULAR NECROSIS OF THE CAPITAL FEMORAL EPPHESIS DUE TO AN INTERUPTED BLOOD SUPPLY
67
DESCRIBE THE PHYSIOLOGICAL PATHWAY OF REVOVERY FROM PETHES DISEASE
NECROSIS REVASULARISATION REOSSIFICATION
68
WHAT IS THE PRESENTATION OF PETHES DISEASE
HIP/KNEE PAIN LIMP SIMILAR TO TRANSIENT SYNOVITIS
69
WHAT IS THE MANAGEMENT OF PERTHES
IF IDENTIFIED EARLY BED REST + TRACTION OTHERWISE SURGERY
70
WHAT IS A POSSIBLE CONSEQUENCE OF PETHES DISEASE
INCREASED RISKOF DEGENERATIVE ARTHRITIS
71
WHAT IS OSTEOGENESIS IMPERFECTA
A GROUP OF DISORDERS OF COLLAGEN METABOLISM CAUSING BONE FRAGILITY CAUSING BOWING AND FREQUENT FRACTIONS
72
WHAT ARE THE TWO TYPES OF OSTEOGENESIS IMPERFECTA
TYPE 1 - AUTOSOMAL DOMINANT TYPE 2 - SEVERE AND LIFE THREATNING
73
WHAT IS THE PRESENTATION OF T1 OSTEOGENESIS IMPERFECTA
CHILDHOOD FRACTURES BLUE SCLERA IN 50% HEARING LOSS
74
WHAT IS THE PRESENTATION OF T2 OSTEOGENESIS IMPERFECTA
LETHAL IN PERINATAL PERIOD FRACTURES PRESENT BEFORE DEATH
75
HOW DO OU DIAGNOSE OSTEOGENESIS IMPERFECTA
X RAYS DNA + COLLAGEN TESTING US - FETAL PRESENTATION OFTEN IN T2
76
WHAT IS THE THREATEMENT OF OSTEOGENESIS IMPERFECTA
PHYSIO REHAB BISPHOSPHONATES (PALANDOMIC ACID IV) SURGERY
77
WHAT IS RICKETS
A FAILURE IN MINERALISATION OF THE GROWING BONE (OSTEOID)
78
WHAT IS OPTEOMALACIA
FAILURE TO MINERALISE MATURE BONE
79
WHAT ARE THE TYPES OF RICKETS
NUTRITIONAL VIT D DEPENDANT VIT D RESISTANT
80
WHAT NUTRITIONAL DEFICIENCIES CAN CAUSE RICKETS
VIT D CALCIUM PHOSPHURUS
81
WHAT ARE THE TWO TYPES OF VITAMIN D RICKETS
TYPE 1: DECREASED VIT D HYDROXYLASE TYPE 2: DEFECTIVE VIT D RECEPTOR AND PRODUCTION OF 1,25 DIHYDROXY VIT D
82
WHAT ARE THE TWO TYPES OF VIT D RESISTENT RICKETS
X LINKED : DECREASED RENALPHOSPHUSRUS TRANSPORT /ABSORBTION = HYPOPHOPHOATREMIC HEREDIATRY : DECREASED PHOSPHATE REABSORBTION WITH RAISED LEVELS OF CALCITOL = HYPOPHOPHOATREMIC + HYPERCALCEAMIC
83
WHAT ARE CAUSES OF RICKETS
NORTHERN LATITUDES DIETARY MATERNAL VIT D DEFICIENCY COELIAC PANCREATIC INSIFFICIENCY CHOLESTATIC LIVER DISEASE CHRONIC LIVER DISEASE HEREDITARY X LINKED FANCONI SYNDROME
84