Care of the child Musculo-skeletal,Neuro,Sensory conditions Flashcards
Osteomyelitis
- inflammation of the bone
- staph aureus
- blood bone infection
s/s:
- fever
- pain
- psuedoparalysis(afraid to move)
Diagnosis
-leukocylosis
-elevated esr
+ blood culture
Treatment/Nursing care
- long term course of treatment(6-8weeks)
- bedrest
- iv antibiotics
- analgesic
- immobilization of limb
Duchenne Muscular Dystrophy(etiology)
- Hereditary sex linked recessive
- progressive neuromuscular disease, life expectancy, early 30s
- fatty infiltration of muscle cells tissue breakdown
- occur in males more
diagnosis:
- H&P
- serum enzymes
- muscle biopsy
Duchenne Muscular Dystrophy(signs n symptoms)
- incidious(comes on gradually)
- delayed walking
- decrease muscle strength
- increasing clumsiness
- lordosis(shoulders back,rounded abdomen)
- gowers sign(large muscles break down first, cant stand up straight)
- usually die from PNA, ulcer
Duchenne Muscular Dystrophy(Treatment/Nursing Care)
- poor prognosis, no cure
- life expectancy adolensence
- depititating-crutches w/ bedridden
- prevention of complication
- skin care
- PT/OT
- emotional support
COXA-PLANA Disease aka LEGG-CALVE-PERTHES Disease(Etiology)
- lack of circulation to femoral head
- 4-8 years with limp cause unknown
- trauma of synovities prior
COXA-PLANA Disease aka LEGG-CALVE-PERTHES Disease(nursing care/treatment)
- Rest, allow child to repair itself
- Bucks traction-puls in one place keeping in alignment
- hip bracing
- maintain ROM
- limit activity during treatment
- prognosis is good for hip degeneration in later years
Bone Tumors
- Benign: causes deformity and pain
- malignant-development of abnormal cells
Bone Tumors(Ewing Sarcoma)
- growth in marrow of the long bones
- metastisis tp lungs and other bones
s/s: pain,possible mass at the site,possible fx
tx:chemo and radiation, good prognosis provided caught early
Bone Tumors(Osteosarcoma)
-primary malignant tumor of long bones
-metas to the lungs
s/s:pain,limited mobility,obvious tumor mass
TX:amputation and chemo
Nursing care: post op care,potential for infection,coping family support,phantom limb pain,prosthesis-P/T
Juvenilele Rheumatoid Arthritis(Stills Disease)(Etiology)
-most common form of arthritis
-systemtic fever x10days, invovle internal organs(liver,spleen enlargement)
-polyarticular=arthritis in 5 or more joints
-pauciarticular=arthritis in 4 or more joints
S/S:swollen joints,enlarged liver and spleen,anemeia,anorexia,rash,pericarditis,myocarditis,potential for
-uueitis=inflammation of anterior chamber of the eye, check eyes every year for blindness
Dx:ANA, no cure
Juvenilele Rheumatoid Arthritis(Stills Disease)(Treatment/nursing care)
- no cure, treat symptoms
- NSAIDs, ,anti-inflammatory-hepatoxcity,effect the Gi system, ROM exerxcies
- prevent ankylosis(deformity of the joints)
- PT/OT to decrease ankylosis
- heat packs and warm showers-increase blood supply and decrease swelling
- good nutrition
- immunization delay because immunity decreased because of the use of corticorsteroids
- prognosis: subsides over a few years
Scoliosis(Etiology)
- curvture of the spine
- common in females
Functional:poor posture, no treatment
Structural:congenital,neuromuscular,diopathic(just happens we dont know)
Screening:pt. bends over feel spine
Dx: X-ray
Scoliosis(Treatment & Nursing care)
-curves under 20degrees=observation,good posture,backpack safety
-curves 20-40degrees=boston brace,milwaukee brace,daily exercise
-curves greater than 40degrees=harrington rods,spinal fusion
patient education:
-wear brace 23 hrs a day
-tee shirt under brace(skin integrity)
-body image in adolescents
-surgery:pre-op teaching,post op care, potential for constipation,log rolls,physical therapy,going to be immobile after surgery,dehersereanants after surgery because skin tight in the back, physical therapy
Hydrocephalus(etiology)
- excessive fluid in head around the brain
- increase CSF in ventricles of the brain
- increase intracranial pressure
- increase head circumference
- congenital or acquired
Hydrcephalus(Sign and symptoms)
- lethargy
- shrill cry,poor muscle tone,poor appetite
- seizures
- bulging fontanels
- increase head circumfeence
- seperated cranial sutures(increase fluid pushed them apart)
- getting sun eyes
Hydrcephalus(assessment)
- head circumference
- transillumnation
- MRI,cat scan
Hydrcephalus(treatment)
-ventriculo-peritoneal shunt
Hydrcephalus(pre-op care prior to shunt placement)
- Temp and Pulse q2h
- support head
- quiet feeding/quiet environment,prone to vomitting and seizures
- check fontanels
- monitor head circumference
Hydrcephalus(post-op care vp shunt)
- position baby on unoperative side
- initally flat then gradually increase HOB
- observe signs of malfunction
- monitor fontanels,sunken or bulging,adjust position
- observe for s/s of infection,possible menigitis/peritonitis
- skin care
- nutrition and emotional support
Hydrcephalus(parent teaching for VP shunt)
- recognize signs of increase intercranial pressure,malfunction,infection
- importance of the flu care and need for shunt revision
- safety-child may have tendency to be unbalanced
- early intervention: PT/OT/SPEECH
Spina Bifida(etiology)
- congenital embryonic neutal tube defect
- imperfect closure of spinal vertebrae
prenatal diagnosis
- alfa-fetal protein(AFP) level at 3-15weeks
- amniocentesis is indicated
- folic acid decreases incidence
Spina Bifida(2 types)
- Spina bifida Occulta
2. Spina Bifida Cystica
Spina Bifida Occulta
-minor varistion, opening in spinal column small and no protrusion of structures
s/s: -tuft of hair or small dimple
- occurs at L1 or S1 - no treatment unless symptomatic
Spina Bifida Cystica
- Meningocele: cyst containing meninges and CSF
- size varies
- usually no neuromuscular symptoms
- surgery needed
Myelomeningocele
- defect in bony canal meninges csf. and spinal cord
- S/S:
- visible sac
- B&B control poor
- leg paralysis
- hydrocephalus
Tx of Spina Bifidas
- intra-uterine surgery
- c-section and surgery within 24hrs
- repairs defect
- prevents hydrocephalus
- latex free environment
Nursing care Spina Bifida
Pre-OP
- moist saline dressing
- assesment of sack
- avoid pressure on sac
- neuro assessment
- skinn care(no diapering)
- help promotoe parent-infant relationship
Post-Op
- observe dressing
- monitor for ICP, VS,for infection,for leakage
- parent teaching/expectations
- intelligence/learning ability not effected
- independence is compromised
- long term family goals
- focus on childs accomplishments
- catherization procedures
- bowel control
- precautions of latex allergic reaction
- observe for s/s of complication of immobility
Reyes Syndrome
- viral infection
- hepatopathy: ammonia level, bleeding
- encephalopathy
- no aspirin
- neuro checks
- HIB vaccine
Meningitis(etiology)
- inflammation of the meninges
- may be viral or bacterial
- peak incidence 6 to 12 months
- droplet infection/resp infection
- HIB vaccine useful to decrease risk