Exam #2 Flashcards

1
Q

Structural GI Disorder:

  • can occur in isolation or together
  • can be bilateral or unilateral
  • requires surgical repair
  • these babies are encouraged to be breast-fed as there is more surface area & reduced additional air intake
  • baby should be fed upright (45-90 degrees) and intermittently
A

Cleft Lip & Palate

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2
Q

Structural GI Disorder:

  • knot in the groin area
  • dangerous as there are more structures nearby
  • abdominal or pelvic contents travel to the inguinal canal
  • requires reduction & possibly surgery
  • 5x more common in boys due to undescended testicles
A

Inguinal Hernia

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3
Q

Structural GI Disorder:

  • more common type seen in premature infants
  • GI issues do not typically arise
  • surgical repair is commonly done for cosmetic purposes
  • occurs due to weakening of the GI muscle
A

Umbilical Hernia

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4
Q

Treatment for Hernias

A

Push it back in
- if its affecting them structurally, or pops out every time the child cries, then surgery is considered

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5
Q

Obstructive GI Disorders:

  • __________ sphincter is not opening which occurs when the muscle thickens over time (not born w/ it)
  • cause is unknown
  • what is entering the stomach cannot exit & will come right back up
  • higher chance for boy to have it if father had it (unknown why)
  • S&S: projectile vomiting, crying, not gaining weight, olive-shaped mass in RUQ
  • seen around 3-6 weeks of life
  • Dx: ultrasound
  • Tx: pyloromyotomy - surgery to snip muscle, take thickened part out, and ensure opening remains
A

Pyloric Stenosis

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6
Q

Obstructive GI Disorders:

  • intestines telescope into itself
  • more common in males
  • occurs in kids a little older than 3-6 weeks and are intermittently fussy – when the child cries, they bear down and can pop it back out but the telescoping can happen again
  • S&S: current jelly stools, acute sudden abdominal pain, sausage-like lump in lower abdomen (typically RLQ)
  • Tx: barium or air enema (high risk of bowel perforation) OR surgery (rare)
A

Intussusception

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7
Q

Obstructive GI Disorders:

  • inflammatory disease of the intestinal tract
  • life threatening and seen often in the NICU after the first few feeds – high mortality rate
  • S&S: feeding intolerance (failure-to-thrive), lethargic, bradycardic, apneic spells, bloody diarrhea
  • Tx: surgery to remove that portion of bowel, bowel rest (TPN), antibiotics
A

Necrotizing Enterocolitis (NEC)

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8
Q

Inflammatory GI Disorders:

  • inflammation of the affected organ
  • S&S: ABD pain around belly button (RLQ), McBurney Point (rebound tenderness), poor appetite, N/V, fever (typically when perforation occurs), want to be in fetal position
  • constipation & __________ present similarly
A

Appendicitis

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9
Q

Abdominal Wall Defects:

  • birth defect due to a herniation of the ABD wall during development – born with their intestines on the outside
  • Dx: MSAFP – seen on ultrasound prior to birth
  • after C-section, intestines are exposed to air since NOT covered by peritoneal layer
  • Tx: wrapping & supporting the intestine (prevent hypothermia & fluid loss), surgical repair, SILO, TPN (bowel rest)
A

Gastroschisis

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10
Q

Abdominal Wall Defects:

  • protrusion of umbilical cord & is sealed by the peritoneal layer – typically the bowels, liver, kidneys, etc. (ALL) are developed outside the body
  • Dx: MSAFP
  • can be worse as it can take longer to put back in along w/ other complications
A

Omphalocele

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11
Q

Functional GI Conditions:

  • persistent & crying babies that are under 3 months old
  • idea for cause is that baby has a lot of gas build-up (fed a lot, not burped enough) – unknown
  • S&S: crying episodes lasting 3 hours, more than 3 days, more than 3 weeks; baby will pull legs & arms to a flexed position
  • Tx: have parents place baby in safe space after eliminating every other cause & stepping away – shaken-baby syndrome risk
A

Infantile Colic

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12
Q

Functional GI Conditions:

  • excessive loss of fluids due to vomiting & diarrhea
  • Causes: viral (most common), diet, meds, toxins
  • BRAT diet: bananas, rice, applesauce, toast
  • Tx: BRAT, rehydration, as long as dehydration not evident, can be treated at home
A

Gastroenteritis

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13
Q

Functional GI Conditions:

  • difficult or infrequent passage of hard stool
  • S&S: hard stool, poor appetite, straining when defecating
  • Tx: bowel retraining, nutrition, education (increasing fiber & water)
A

Constipation

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14
Q

Functional GI Conditions:

  • these babies spit-up a lot – need to know vomit vs. spit-up
  • they have choking episodes as well as apneic episodes (acid building up)
  • S&S: vomiting & regurgitation; fussiness; refusal to eat, choking, apnea, wheezing
  • Dx: H&P, pH study or swallow study
  • Tx: keep upright while feeding (30min-1hr) and NOT in a car seat, frequent burping, meds (Zantac)
A

Gastroesophageal Reflux Disease (GERD)

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15
Q

Functional GI Conditions:

  • congenital absence of Meissner and Auerbach autonomic plexus in the bowel wall
  • S&S: failure to pass meconium within first 48 hrs of life, failure-to-thrive, poor feeding, enterocolitis
  • Tx: surgical resection, colostomy, GI irrigation (cannot empty out, need to be flushed)
A

Hirschsprung Disease (Megacolon)

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16
Q

Hepatic Disorder:

  • liver is not working how its supposed to – blockage in bile duct
  • can be a congenital defect sometime during fetal development but commonly its an inflammation shortly after birth – idiopathic
  • S&S: jaundice, dark urine, light stools, bloated belly (round)
  • Tx: Kasai procedure (remove damaged ____ duct & reconnect SM-intestine to liver) – even w/ Tx, most kids require liver transplant; TPN/Lipids & nutritional support
A

Biliary Atresia

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17
Q

__________ system controls growth & development

A

endocrine

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18
Q
  • child will be shorter in stature & typically require growth hormone in order to grow
  • underproduction of cells
  • effects ALL of the following parts of the body: reproduction, kidney disease, heart issues, cognitive issues, etc. (every organ in the body)
  • S&S: delayed growth (3rd-5th percentile), continue to maintain baby-like facial features, skeletal growth delayed, missed milestones, delayed bodily processes
  • Dx: growth evaluation; labs; bone x-ray; brain MRI
  • some studies show children in abusive households or are abused can experience delayed growth development
  • w/o Tx, affects the entire body and leads to decompensation, and possibly death
A

HYPO-pituitary (growth hormone deficiency)

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19
Q
  • overabundance of cells (gonadotropin) – child develops at much quicker rate (reproductive organs develop much sooner)
  • early onset of menarche can be seen as child abuse
  • Boy S&S: facial hair, penile growth, masculinity
  • Girl S&S: breast development, onset of menarche
  • S&S: increase of LH, FSH, and testosterone
  • Tx: growth hormone suppressant; psychological care for both child & parent
A

Pituitary HYPER-function (Precocious puberty)

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20
Q
  • these issues are preventable by treating the issue – w/o they can experience serious delays in development
  • S&S: delayed growth, inability to tolerate cold, constipation, fatigue, poor feeding
  • Tx: now included on newborn screening, meds (Levothyroxine [Synthroid])
A

Congenital HYPO-thyroidism

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21
Q
  • underacting thyroid (autoimmune disorder) that can be caused by genetic or environmental (pollutants) factors
  • Risk factors: females, family Hx, radiation exposure, other autoimmune diseases
  • S&S: poor temperature regulation (always cold), delayed growth, fatigue, hair loss (older kids), puffy moon-face, brittle nails – goiter (palpate enlarged thyroid)
  • Dx: labs (TSH & T4)
A

Hashimoto

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22
Q
  • group of autosomal recessive inherited disorders affecting the adrenal glands
  • insufficient supply of enzymes required for production of cortisol & aldosterone
  • Cause: deficiency of 21 hydroxylase enzyme
  • Boy S&S: large genital, hyper-pigmented scrotum & start puberty at age 2 years
  • Girl S&S: in utero develops male sex characteristics, hypotension, hypoglycemia
  • S&S: electrolyte imbalance
  • Tx: meds (hydrocortisone), psychosocial care for both child & parents
A

Congenital Adrenal HYPER-plasia

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23
Q
  • damage due to autoimmune disorder – damage to gland resulting in releasing cortisol & aldosterone – hard time maintaining electrolyte balances (cannot use for energy, muscle growth, etc.)
  • S&S: constantly fatigued, always irritable, constantly losing weight, consistent muscle weakness
  • if left untreated: hypotension, kidney failure, and severe abdominal pain – will go into adrenal crisis (stress causes as well)
  • Tx: meds
A

Addison’s Disease

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24
Q
  • poorly functioning pancreas leads to excessive glucose – affects major organs (body metabolizes fats for energy)
  • autoimmune disorder
  • S&S: losing weight, constantly peeing (up at night), always thirsty, constantly eating, fruity breath
  • w/ DKA: too much ketones (acid) and presents as lethargic w/ Kussmaul respirations (NOT RESPIRATORY RELATED FOR EXAM)
  • Tx: insulin (lifelong maintenance); teach child to carb-count and check glucose levels
A

Diabetes Mellitus Type I

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25
Q

behavior modification

A
  • set limits
  • do not argue, bargain, or negotiate after limits are set
  • consistent caregivers matter
  • use a low-pitched tone
  • redirect the child
  • ignore inappropriate behaviors or educate why they are inappropriate
  • praise self control & appropriate behaviors
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26
Q
  • Onset: infant or early childhood –> may notice developmental delays or loss of previous ability
  • Cause: mainly genetic –> possibly environmental (pollutants)
  • S&S: communication issues, prefer to be alone (not play w/ others), difficulty interpreting others emotions, repetitive movements or speech patterns, avoid eye contact, sensitive to loud noises, eccentric ways of moving
  • Tx: NO cure; goal is to strive for optimal functioning (provide structured environment); family support
A

autism spectrum disorder

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27
Q

Most common neurodevelopmental disorder of childhood
- Cause: genetic
- S&S: impulsive, hyperactive (cannot sit still), don’t pay a lot of attention, lack of self control (trouble keeping body calm)
- Tx: Meds [methylphenidate, dextroamphetamine; Adderall, Ritalin] & education [meds & school assistance - IEP plan]

A

attention deficit hyperactivity disorder (ADHD)

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28
Q

any injury intentionally inflicted on a child

A

physical abuse

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29
Q

sexual activity intended to provide pleasure to an adult
- can lead to inappropriate sexual behavior at a young age (child does not know its inappropriate)

A

sexual abuse

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30
Q

witnessing abuse

A

emotional abuse

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31
Q

failure to provide child w/ appropriate needs
- lack of food as punishment
- locked in a room as punishment
- has long-term effects on brain development & behavior

A

neglect

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32
Q

Long-term impact of child maltreatment –>

A
  • anxiety
  • depression
  • suicidal ideation
  • drug & alcohol use
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33
Q

parent purposely make their child sick so that they can take care of their child (caregiver has mental health issue & requires dependency from another)– don’t want to kill them, but need child to need them
- Warning signs: constant visits; caregiver is the only one talking; variations in past medical Hx (nothing makes sense); Dr. & hospital-shop/hop

A

Munchausen syndrome by proxy (medical child abuse)

34
Q

elongated, rigid cells that change shape (doesn’t allow oxygen to adhere well); stick together & start clumping so they get trapped and stuck in vasculature
- Cause: hereditary & genetic
- common in African Americans
- Assessments: pain scale (live in constant pain, 4-6)
- Tx: hydration & oxygenation (preventing VOC); pain management (NSAIDs or Tylenol or in adjunct w/ opioid); minimize risk factors (hypoxia, extreme heat/cold, infection, infarction)

A

sickle cell disease

35
Q

recycled every 120 days (4 months)

A

normal RBC lifespan

36
Q

recycled every 30 days

A

sickled cell lifespan

37
Q
  • Cause: significant blood loss; illness; high altitude; continued stress (physical or emotional); dehydration; elevated or severely decreased temperature
  • may rate pain 8/10 and be playing on their phone –> different pain tolerance, do NOT blow these kids off
A

sickle cell (Vaso occlusive) crisis

38
Q

sudden trapping of blood in the spleen –> recycles sickled cells every month (overworked) and size never decreases back to normal size
- S&S: pain; spleen overworked; spleen enlarged; pale; lethargic
- these kids CANNOT play contact sports EVER

A

splenic sequestration

39
Q

body is reacting from viral illness (commonly URI; sometimes GI bug) & is affecting vascular system –> the virus starts attacking the vascular system and starts erupting capillaries (dots = capillaries exploding); some type of inflammation occurring w/ blood leaking into small vessels
- typically affects young children under 10 & typically males
- S&S [NOT life-threatening]: purpura rash, joint pain, abdominal pain, kidney impairment (bloody urine –> kidneys extremely vascular)
- Tx: supportive care –> calm parent, give Tylenol, fluids, patience (several days to overcome)

A

Henoch-Schoenlein Purpura (HSP)

40
Q

group of X-linked recessive disorder that results in deficiency in one of the coagulation factors in the blood –> mom passes it down to son (boys only have 1-X, only need 1 from mom)
- deficiency of factor VIII (hemophilia A)
- Tx: give factor VIII (parents need to keep on them at all times); immobilize & elevate joint/affected extremity; prevent injury based on developmental age –> toddlers fall down & hit head; no contact sports when older; driving safety & avoiding piercings/tattoos in adolescents

A

hemophilia

41
Q

cancer of the bone marrow caused by an overproduction of abnormal WBCs
- Assessment: bone pain; anemia; low reticulocyte count; bleeding disorder; immunosuppression; pale, unexplained bruising, fatigued, generalized pain
- Most common cause of death: illness/infection
- Tx: ALWAYS starts w/ chemo

A

leukemia

42
Q

typically diagnosed between 2-5 yrs and affects the T&B cells
- most common Dx of leukemia in children
- Dx: bone marrow makes too many lymphocytes; low reticulocyte count
- Tx: prevent infection; chemo & radiation; bone marrow transplant (last resort)

A

acute lymphoblastic leukemia (ALL)

43
Q

hard to treat & has higher death rate than other type
- these children always have an implanted port = chemo is extremely toxic to vascular system (will kill peripheral vein)
- more common in teen & adult world
- Dx: bone marrow makes too many myeloid cells
- Tx: not as responsive to Tx

A

acute myelogenous leukemia (AML)

44
Q

most common solid tumor in children (usually 5-10yrs)
- Cause: unknown
- can take long time to Dx –> very vague symptoms, especially when they’re young (i.e., may occur in conjuncture w/ teething)
- S&S: increased ICP; headache/vomiting ONLY in the morning; new onset seizures w/o Dx; coordination issues
- Dx: CT; MRI; chemo; radiation

A

brain tumor

45
Q

tumor is small & hasn’t spread

A

Stage 1

46
Q

tumor is large but hasn’t spread

A

Stage 2

47
Q

tumor has spread to neighboring lymph nodes

A

Stage 3

48
Q

tumor has spread to other organs

A

Stage 4

49
Q

has a shape & structure that resembles healthy cells

A

well-differentiated cancer cells

50
Q

has a completely different shape and structure than healthy cells

A

poorly differentiated cancer cells

51
Q

slow-dividing of tumor cells

A

low-grade

52
Q

fast dividing of tumor cells

A

high-grade

53
Q

cancer of the bone & soft tissue – typically diagnosed in adolescence and found incidentally due to vague symptoms (dull bone pain progressing over months)
- commonly seen in long bones (femur & humerus)
- S&S: pain that never goes away (w/ Tylenol, RICE)
- cannot remove part of bone for Tx –> radiation, amputation, replaced w/ cadaver bone (at growth peak) or rods (until growth plates close; grow w/ child)

A

sarcomas

54
Q

usually in long bones proximal humerus, tibia, and femurs
- Tx: Sx to remove tumor –> chemo before & after

A

osteosarcoma

55
Q

also within the bone but is much more aggressive & metastasizes easily, usually in pelvis or femur
- Tx: radiation in addition to chemo & Sx

A

Ewing sarcoma

56
Q

renal tumor of unknown cause that grows rapidly
- typically only affects 1 kidney (not both at same time)
- Assessment: nontender mass; abdominal pain; HTN
- Do NOT continue to palpate abdomen once diagnosed –> tumor is very vascular & palpation can cause tumor seeding
- Tx: Sx to remove kidney (no way of just taking tumor); educate on protecting the single kidney (NO CONTACT SPORTS)

A

Wilms tumor

57
Q

caused by a rapid increase in temperature, typically caused by a virus
- Dx: elevated temperature & present seizure (tonic-clonic or myoclonic)
- Tx: Tylenol; ibuprofen; rectal diazepam, buccal & IM midazolam, IM lorazepam
- Education: call 911 for seizures lasting more than 5 min or multiple in same day; does NOT mean they will have lifelong seizures

A

febrile seizures

58
Q

imbalance between excitatory & inhibitory mechanism
- Tx: meds (Keppra –> reduce or control the frequency); Sx (removal of affected area OR VNS [pacemaker of the brain]; ketogenic diet (low sugar decreases excitability giving less energy); relieve anxiety

A

epilepsy

59
Q

3 categories of epilepsy

A
  • Focal: 1 hemisphere of the brain
  • Generalized: whole brain
  • Unknown: spasm
60
Q

nursing management for active seizures

A
  • maintain open airway
  • turn patient on their side
  • ensure safety
  • suction/oxygen set-up
61
Q

birth defects of the spine & brain – will be seen on US (born via C-section)
- folic acid will reduce the risk
- cause is unknown but certain factors adversely affect normal CNS development (lack of folic acid)

A

neural tube defects (spina bifida)

62
Q

overarching term for all spinal defects

A

spina bifida occulta

63
Q

spinal cord is fine but make sure that sac remains intact
- sac of spinal fluid (cords are NOT in the sac)
- prevent infection –> if you notice any leaking from sac, notify provider immediately

A

meningocele (spina bifida cystica) - mild

64
Q

most severe type and child does not have a lot of sensory or motor function below the defect
- cords are WITHIN the sac of the spinal fluid
- diagnosed in utero w/ spinal cord involvement

A

myelomeningocele (spina bifida cystica) - severe

65
Q

missing parts or all brain hemispheres, skull, and scalp
- Dx: visualized on US
- Prognosis: usually stillborn or pass within a few hours after birth; brainstem intact allowing infant to breath and have some reflexes
- Management: provide comfort measures; family support; grief support; place infant cap on child immediately

A

anencephaly

66
Q

defect of brain & meninges protruding through the skull – collection of fluid at the base of the skull
- Prognosis: Dx in utero (delivered via C-section); Sx needed to correct
- Management: pre- & post-Sx care; monitor for increased ICP (herniation of brainstem) & head circumference; side-lying position; prevent ruptures of sac & infection

A

encephalocele

67
Q

displaced cerebellar structure – usually found accidentally when children have head trauma & require imaging
- S&S: maybe walk differently but go on w/ life; headache; neck pain; coughing & laughing make pain worse
- Management: routine imaging & follow-up; S&S of increased ICP and any CNS injuries (new onset seizure, headache, vomiting, etc.); pre- & post-op care

A

Chiari malformation

68
Q

results from brain disorder that cause an imbalance in production & absorption of CSF – increased fluid in ventricles = increase in head circumference
- S&S: seizures, macrocephaly, bulging fontanels, increased head circumference, vomiting, headache, lethargy, delayed development
- Tx: VP shunt
- Management: support & educate family; shunt malfunction; assess for complications; children at risk for peritonitis (where shunt drains)

A

hydrocephalus

69
Q

rare congenital disorder – large, intertwining bundles of blood vessels in the brain
- S&S: intracranial hemorrhage; seizure; headache; progressive neurologic defects (vision changes, loss of speech, memory, problems)
- Tx: Sx to excise bundles & embolize around area; may need short-term shunt to Tx hydrocephalus
- Management: support; monitor for neurological changes, seizure activity, S&S of ICP or intracranial hemorrhage (stroke)

A

intracranial arteriovenous malformation (AVM)

70
Q

premature closure of the cranial sutures (most common is sagittal)
- Cause: unknown
- Tx: Sx if 2 or more close
- Management: measure head circumference, palpate suture lines, helmet
- Education: blood loss, infection risk, swelling (eyes may swell shut post-op), encourage parents to hold child (bond)

A

craniosynostosis

71
Q

asymmetry of head shape; torticollis can contribute to severity (twisting of neck to look at something)
- Tx: increase tummy time; helmet; repositioning
- often seen in children who are not held enough AND children in the NICU

A

positional plagiocephaly

72
Q

most commonly seen in children ages 2-6yrs
- kids are not good at wiping –> require education about front-to-back wiping
- Cause: E. coli (most common)
- Tx: antibiotics
- S&S: hurts to pee, frequency, itching

A

urinary tract infections (UTIs)

73
Q

Most common abnormality for urinary system in children
condition in which urine flows back up the ureters; increased pressure placed upon the kidney can cause renal scarring and lead to HTN later in life and, if severe, renal insufficiency or failure
- Tx: antibiotic prophylaxis; hygiene & voiding practices; serial urine cultures
- grade III, IV, and V usually warrant Sx

A

vesicoureteral reflux (VUR)

74
Q

urine backflow is only in the ureters

A

grade I VUR

75
Q

urine backflow beings to enter the kidneys

A

grade II VUR

76
Q

urine backflow is a lot in the kidneys

A

grade III VUR

77
Q

urine backflow covers most of the kidney

A

grade IV VUR

78
Q

urine backflow covers all of the kidney

A

grade V VUR

79
Q

inflammation of the glomeruli after an illness – often after Strep – immune mechanism causes inflammation which alters glomerular structure
- S&S: painless hematuria; edema; HTN
- Tx: nothing specific – goal is to maintain fluid volume & managing HTN; antihypertensives (Nifedipine), antibiotics (if Strep present), furosemide (Lasix)

A

acute postinfectious glomerulonephritis

80
Q

etiology is currently unknown –> kids can get bacteria from undercooked food (i.e., ground beef) OR petting zoos
- Triad of S&S: bloody diarrhea, decreased UOP, pallor, HTN
- Tx: fluids & antibiotics (can lead to nephrotoxicity); blood transfusion

A

hemolytic uremic syndrome (HUS)