immune response
covered8 questions- Anaphylaxis: epinephrine first, intramuscularly, without waiting.
- Antihistamines and steroids are real treatment and far too slow to be first.
- Antihistamines and steroids make the test meaningless; beta-blockers make a reaction harder to treat.
- Epinephrine at hand, and observe afterwards.
- Screen, then confirm with a second antibody test.
- CD4+ count stages the disease and viral load monitors treatment — neither one diagnoses it.
- Type I immediate and IgE — epinephrine.
- Type II cytotoxic — transfusion reactions.
- Type III immune complexes — lupus.
- Type IV delayed cell-mediated — TB skin test and poison ivy, read at 48 to 72 hours.
- Latex allergy means avoiding every source, not just gloves.
- Banana, avocado, kiwi and chestnut cross-react.
- Powder makes it worse by aerosolizing protein.
- Early sepsis is confusion, fever, tachycardia, tachypnea, low urine output and WARM flushed skin.
- Blood pressure stays up until late — do not wait for it.
- Infection plus a falling blood pressure is sepsis.
- Cultures, fluids and antibiotics within the hour — treating the fever wastes the hour that counts.
- No spleen means encapsulated organisms can cause sepsis in hours.
- Vaccinate, and treat every fever as an emergency.
Anaphylaxis is a rapid systemic hypersensitivity reaction in which mast cell degranulation produces widespread vasodilation, increased capillary permeability and bronchoconstriction. It is recognized by involvement of more than one system — skin with urticaria, flushing and angiedema; respiratory with stridor, wheeze and a sensation of throat closing; cardiovascular with hypotension and tachycardia; and gastrointestinal with cramping and vomiting. Treatment is epinephrine given intramuscularly into the anterolateral thigh, repeated every five to fifteen minutes as needed, alongside removal of the trigger, airway support, high-flow oxygen, supine positioning with the legs raised where blood pressure allows, and rapid fluid resuscitation. Antihistamines relieve the cutaneous symptoms and corticosteroids reduce the biphasic late-phase reaction that can occur hours later, which is why clients are observed after apparent recovery. Delayed epinephrine is the factor most consistently associated with fatal outcomes.
Allergy skin testing identifies IgE-mediated sensitivity by introducing small amounts of allergen into the skin and observing for a wheal-and-flare response, read at around fifteen to twenty minutes. Percutaneous prick testing is performed first, with intradermal testing used for greater sensitivity where prick testing is negative. Preparation requires withholding medications that suppress the response: antihistamines for several days to a week depending on the agent, and topical corticosteroids at the test site, while systemic corticosteroids at usual doses generally have less effect. A positive and a negative control are applied to confirm the skin is capable of reacting and is not reacting non-specifically. The procedure carries a real risk of systemic reaction including anaphylaxis, so resuscitation equipment and epinephrine are immediately available and the client is observed for twenty to thirty minutes afterwards. Beta-blockers antagonize the response to epinephrine and complicate the treatment of anaphylaxis, so their use is identified and discussed beforehand. Sites are mapped and documented so reactions are attributed correctly, and results are interpreted alongside history rather than alone, since sensitization does not always equal clinical allergy.
HIV diagnosis requires a confirmatory antibody test after a reactive screen; CD4+ count and viral load stage and monitor established infection.
Hypersensitivity reactions are classified by immune mechanism, and the mechanism determines both the timing of onset and the effective treatment.
Latex proteins cross-react with several foods, and repeated exposure escalates reaction severity, so management requires complete avoidance.
Early sepsis causes vasodilation and compensation, so mental status, respiratory rate and urine output change before blood pressure does.
Sepsis is life-threatening organ dysfunction caused by a dysregulated host response to infection, and its recognition depends on noticing physiological deterioration in a client known or suspected to be infected. Warning features include temperature above 38 or below 36 degrees, heart rate above 90, respiratory rate above 20, altered mental status, systolic blood pressure below 100 or a substantial fall from the client's own baseline, reduced urine output, and raised lactate. Older adults and immunocompromised clients may present atypically, with confusion or hypothermia rather than fever. Management follows a time-limited bundle: obtain blood cultures and lactate, give broad-spectrum antibiotics, begin crystalloid resuscitation for hypotension or raised lactate, and reassess, with vasopressors added where fluid alone does not restore perfusion. Delay in antibiotics is consistently associated with increased mortality. Source control matters and follows stabilization, and indwelling devices such as urinary catheters are frequent sources, which is why their necessity is reviewed daily.
The spleen clears encapsulated bacteria from blood, so asplenia creates a specific and rapid sepsis risk.
How they trap you here (8)
- Both drug distractors are genuine components of anaphylaxis treatment, so the item is not asking which drugs are used but which acts fast enough to matter. That is a harder discrimination and the clinically decisive one. The positioning option catches the student reasoning from airway first, and it is actively harmful here — sitting up a profoundly hypotensive client reduces cerebral perfusion.
- The beta-blocker option is the more consequential error, because it concerns the ability to treat rather than the ability to interpret, and it is the interaction students least often encounter. The topical corticosteroid option is offered as a comfort measure, which is how it would be reached for in practice, and it invalidates the test.
- Both incorrect laboratory options are tests this client will genuinely have, which is what makes them plausible. The item turns on what each test is for rather than whether it is used in HIV care, and the source's rationale draws exactly that line.
- Option (e) is the source's own trap — it offers a delayed reaction as Type I, and the two-day delay is the only clue. Option (f) tests whether the student links treatment to mechanism rather than reaching for epinephrine at the word hypersensitivity.
- Option (e) is the source's own correction, and it reads as a protective measure. Option (f) inverts the powder issue, which is why powdered gloves were removed from most healthcare settings in the first place.
- The non-significant findings are a borderline blood pressure and a normal saturation, both of which look like the reassuring parts of a note. Because scoring is plus-minus, highlighting the whole note earns nothing — the item requires discrimination, not thoroughness.
- The antipyretic option is the designed trap and mirrors the same error tested in febrile neutropenia: fever is the visible abnormality, treating it is a reflex, and it is the least important thing happening. The catheter option is genuinely relevant, since the device is a plausible source, and it is wrong on sequence rather than on substance.
- Every option is lymphoid tissue that can be removed, so the item tests which one has a function nothing else covers.