A 10-year-old boy presented with brown urine and puffy eyes. His history included a viral infection 2 weeks prior. Tests found elevated specific gravity in his urine, blood, and renal casts. This suggests rhabdomyolysis, which occurs when muscle breakdown releases muscle contents into blood. It can cause kidney damage. The boy's symptoms, including puffy eyes, are consistent with nephrotic syndrome, where the kidneys leak protein into urine. His elevated specific gravity and protein in urine support the diagnosis. He was given IV fluids and monitoring to prevent potential acute renal failure, a risk with rhabdomyolysis.
3. History
10 year old boy
3/7 day complaint of “brown urine”
Patient known from birth
No major illnesses or injuries
Active in a band & Cross-country Track
Denies drug use & Sexual activity
4. History (cont’d)
2/52 weeks ago, he had 2/7 day of fever &
sore throat
improved spontaneously, has been well since
R.O.S remarkable ONLY for puffy eyes
(attributed to late night studying)
11. RhabdomyolitisHow to diagnose?
Tests to determine muscle and kidney health may include determining levels of:
• Creatine kinase, which is an enzyme found in the skeletal muscles, the brain, and the heart.
• Myoglobin in blood and urine, which is a protein that’s a byproduct of muscle breakdown.
• Potassium, which is another important mineral that may leak from injured bone and muscles.
• Creatinine in blood and urine, which is a breakdown product created by muscle that’s normally
removed from the body by the kidneys.
Elevated levels of these substances are signs of muscle damage.
Learn More about Rhabdomyolitis
http://www.healthline.com/health/rhabdomyolysis#causes3
12. Urinary Tract Infection
How to diagnose?
Analyze a urine sample
Urine Culture
CT or MRI (frequent infections)
Cystoscopy
Learn more about UTI’s: http://www.mayoclinic.org/diseases-
conditions/urinary-tract-infection/basics/tests-diagnosis/con-
20037892
13. Pyelonephritis
How to diagnose?
Urinalysis
Urine Culture
Ultrasound
Computerized tomography (CT)
Dimercaptosuccinic acid (DSMA) scintigraphy
Learn more about Pyelonephritis: https://www.niddk.nih.gov/health-
information/kidney-disease/kidney-infection-pyelonephritis
14. Nephrotic Syndrome
How to diagnose?
Urinalysis
Blood Test
Biopsy
Learn more about nephrotic syndrome:
http://www.mayoclinic.org/diseases-
conditions/nephrotic-syndrome/basics/tests-
diagnosis/con-20033385
15. Nephrotic Syndrome
Nephrotic Syndrome is a kidney disorder that causes your body to excrete
too much protein in the urine. It is usually caused by damage to the small
blood vessels of the Glomeruli that filters blood. It causes oedema in the
periorbital area, ankles and feet first and can lead to Anasarca if not properly
managed. Nephrotic Syndrome can lead to serious long term health
problems and must be managed seriously.
16. Brown Urine
Hx. of URTI
Fever
UTI Pyelo
Cross
Country
Track
Rhabdo
Fever Resolved
Not ill appearing
No nitrites on dipstick
Periorbital
Oedema
Nephrotic
Syndrome
Dipstick protein <3
?Specific gravity
elevated
Normal BP
elevated specific gravity
(1.035)
Urine dipstick protein 2+
Afebrile
Active & non-toxic
Presence of Cast
18. Laboratory Test to support
Diagnosis
Elevated Creatinine Kinase >600 (usuaully
markedly elevated, can reach up to the
100,000 depending on the extent.
Myoglobin in the urine and blood
Elevated Potassium (leaked minerals bone
and muscle)(Normal 3.6 - 5.2 mmol/L)
Creatinine in blood or urine
19. Prognosis
Paediatric patients tend to have a better prognosis than
adult
Have Heme in the urine < 2+ is also associated with a
better prognosis (>2+ associated with Acute Renal Failure)
20% of person in the study with heme >2+ had acute renal
failure
30-40% of patients in another study developed renal failure,
therefore it is safe to say between 1/5 to 2/5 of patients.
20. Signs of Renal Failure
Peak CK level higher than 6000 IU/L
Dehydration (hematocrit >50, serum sodium level >150 mEq/L,
orthostasis, pulmonary wedge pressure < 5 mm Hg, urinary fractional
excretion of sodium < 1%)
Sepsis
Hyperkalemia or hyperphosphatemia on admission
Hypoalbuminemia
21. Follow up Care after Diagnosis
ABC’s is always first
Fluid Resuscitation ( IV fluids should be started immediately with added
bicarbonate) with strict input/output charting
Place a large bore needle
Start with >400ml/hr then titrate till urine output is aleast 200ml/hr (adults),
20ml/kg children, 1-2L/h adolescence, subsequently 2-3 times the
maintenance is also a good average
Medication (diuretics, bicarbs, underlying illness if one )
ECG if clinical cardiac symptoms/signs present (can be due to electrolyte
abnormality)
22. Follow up (cont’d)
Dialysis ( last line if Acute Renal Failure occurs or
person has impaired kidney function from before)
Monitor for Disseminated intravascular
coagulation, compartment syndrome, renal failure
& hyperkalemia
Trend bloods (CK q6-12hrly, LFT, Potassium
levels)
Associated with Low specific gravity
Normal range 1.005- 1.030
This patient had 1.035
• creatine kinase, which is an enzyme found in the skeletal muscles, the brain, and the heart
• myoglobin in blood and urine, which is a protein that’s a byproduct of muscle breakdown
• potassium, which is another important mineral that may leak from injured bone and muscles
• creatinine in blood and urine, which is a breakdown product created by muscle that’s normally removed from the body by the kidneys
Your long-term outlook depends on the degree of kidney damage. If rhabdomyolysis is caught early, you may be able to avoid major complications and return to normal health in a few weeks. Even then, however, you may still have some lingering weakness and pain in your muscles.
If major kidney damage occurs, your kidneys may be permanently damaged.
Several of the symptoms and complications of rhabdomyolysis are serious and may result in death if you don’t get treatment for them.
American Academy of Pediatrics
Rebekah Mannix, Mei Lin Tan, Robert Wright, Marc Baskin
RESULTS. Two hundred ten patients were studied. One hundred ninety-one patients met study eligibility (128 male and 63 female), with a median age of 11 years. The most common documented symptoms were muscle pain (45%), fever (40%), and symptoms of viral infection (39%). The most common causes of pediatric rhabdomyolysis were viral myositis (38%), trauma (26%), and connective tissue disease (5%). Six of 37 patients with creatinine kinase levels of ≥6000 IU/L had previously undiagnosed dermatomyositis or hereditary metabolic disease, compared with 10 of 154 patients with creatinine kinase levels of 1000 to 5999 IU/L. Nine of 191 patients developed acute renal failure. None of 99 patients with initial urinary heme dipstick results of <2+ developed acute renal failure, compared with 9 of 44 patients with urinary heme dipstick results of ≥2+. Higher initial creatinine kinase levels and higher fluid administration rates were associated with higher maximal creatinine levels.
CONCLUSIONS. The cause of acute pediatric rhabdomyolysis is different from that of adult rhabdomyolysis. The risk of acute renal failure in children is much less than the risk reported for adults.
http://pediatrics.aappublications.org/content/118/5/2119?sso=1&sso_redirect_count=1&nfstatus=401&nftoken=00000000-0000-0000-0000-000000000000&nfstatusdescription=ERROR%3A+No+local+token
Treatments options for rhabdomyolysis
If discovered early in its progression, rhabdomyolysis can be successfully treated without long-term damage to the kidneys.
Fluid recovery
Getting enough fluid into your body is the first and most important treatment. They must start IV fluids quickly. This fluid should contain bicarbonate, which helps flush the myoglobin out of your kidneys.
Medications
Your doctor may prescribe medications such as bicarbonate and certain kinds of diuretics to help keep your kidneys functioning.
They can also treat high potassium levels in the blood, or hyperkalemia, and low blood calcium levels, or hypocalcemia, with appropriate IV fluids.
Dialysis
If kidney damage and acute renal failure have already started, you may need to receive dialysis. During dialysis, blood is taken out of the body and cleaned in a special machine in order to remove waste products.
Home remedies
In mild cases of rhabdomyolysis, home treatment can help aid in the recovery process. The goals of at-home treatment include resting the body so muscles can recover and rehydration to help prevent further kidney damage.
When you’re feeling fatigued, recline in a comfortable position and try to relax. Drink plenty of water and other clear liquids, such as light broth and sports drinks.
Serial physical examinations and laboratory studies are indicated to monitor for compartment syndrome, hyperkalemia, acute oliguric or nonoliguric renal failure, and disseminated intravascular coagulation (DIC). Compartment syndrome necessitates immediate orthopedic consultation for fasciotomy. DIC should be treated with fresh frozen plasma, cryoprecipitate, and platelet transfusions. Monitor cardiac function. Monitor creatine kinase (CK) levels to show resolution of rhabdomyolysis.