Respiratory
RSV vaccine in older adults and pregnancy
— ~60,000–160,000 hospitalizations and 6,000–10,000 deaths annually in US adults ≥65
— Comparable mortality to influenza in older adults with cardiopulmonary comorbidity
— Age ≥75 years (universal recommendation)
— Age 50–74 with risk factors: COPD, asthma, CHF, CAD, CKD, diabetes with end-organ damage, chronic liver disease, immunocompromise, severe obesity (BMI ≥40), residence in nursing facility, advanced frailty
— Older adult with wheezing, new oxygen requirement, or COPD/CHF exacerbation during RSV season
— Nursing home outbreak of febrile cough illness with negative influenza/COVID testing
— Infant <6 months with apnea, poor feeding, retractions, or bronchiolitis (drives the maternal vaccine rationale)
— RSVPreF3 (Arexvy, GSK) — adjuvanted, adults ≥60 with shared decision-making for 50–59 high-risk
— RSVpreF (Abrysvo, Pfizer) — non-adjuvanted, adults ≥60 and pregnancy 32–36 weeks
— mRNA-1345 (mResvia, Moderna) — adults ≥60

— Mild upper respiratory tract infection: rhinorrhea, sore throat, low-grade fever, hoarseness
— Tracheobronchitis with prolonged post-viral cough (2–4 weeks)
— Lower respiratory tract disease: dyspnea, wheeze, hypoxemia, sometimes without fever
— Triggered exacerbations of COPD, asthma, or decompensated heart failure
— Incubation 2–8 days, viral shedding 3–8 days (longer in immunocompromised, up to 3–4 weeks)
— Older adults often present late (day 5–7) when LRTI manifests
— Maternal vaccination at 32 0/7–36 6/7 weeks transfers transplacental antibodies to protect infants from birth to ~6 months
— Counsel mothers that infant RSV LRTI in the first months of life presents with apnea, grunting, nasal flaring, poor feeding, and tachypnea — fever may be absent
— Vaccination history: prior RSV vaccine receipt (one-time dose, no annual revaccination currently recommended)
— Immunocompromise: solid organ transplant, hematologic malignancy, B-cell-depleting therapy, advanced HIV
— Pregnancy gestational age and prior nirsevimab plan for the infant
— Living situation: long-term care facility, multigenerational household with young children (RSV reservoir)

— Tachypnea (RR >22), accessory muscle use
— Diffuse expiratory wheeze — more prominent than in flu
— Coarse crackles at bases if bronchiolitis or superimposed bacterial pneumonia
— Prolonged expiratory phase
— SpO2 on room air — <92% triggers admission consideration
— Heart rate, blood pressure, mental status (qSOFA), capillary refill
— Volume status: JVP, peripheral edema — RSV frequently unmasks heart failure
— Nasal flaring, intercostal/subcostal retractions, head bobbing
— Apnea in neonates <2 months (red flag)
— Wheeze + crackles + prolonged expiration = bronchiolitis pattern
— Routine prenatal exam; document fundal height, fetal heart tones, BP screening for pre-eclampsia
— No specific RSV-related exam change post-vaccination beyond local injection-site assessment
— Injection-site pain (~60%), fatigue, headache, myalgia, arthralgia within 1–3 days
— Low-grade fever in <5%
— No expected wheeze, rash, or systemic illness — these warrant evaluation for alternative cause

— Multiplex respiratory PCR (RSV, influenza A/B, SARS-CoV-2 ± other viruses) from nasopharyngeal swab — high sensitivity in adults
— Rapid antigen tests for RSV have poor sensitivity in adults (<40%) — useful in kids, unreliable in elderly; do not exclude RSV with a negative antigen
— CBC: lymphopenia common; leukocytosis suggests bacterial superinfection
— BMP: assess AKI, hyponatremia (SIADH can accompany severe LRTI)
— CRP/procalcitonin: procalcitonin <0.25 ng/mL supports viral etiology and helps withhold antibiotics
— Lactate if sepsis physiology
— BNP/NT-proBNP if cardiac comorbidity to disentangle CHF
— Troponin if chest pain or dyspnea out of proportion — viral illness can precipitate type 2 MI
— Chest X-ray: often normal or shows peribronchial thickening, patchy interstitial opacities, or hyperinflation; focal consolidation suggests bacterial co-infection
— Chest CT reserved for diagnostic uncertainty, suspected PE, or immunocompromised host
— No labs required before RSV vaccine administration
— Pregnancy: confirm gestational age 32 0/7–36 6/7 weeks; review prenatal vaccination record

— Hypoxemia refractory to low-flow O2
— Immunocompromise (transplant, hematologic malignancy, anti-CD20 therapy)
— Persistent fever or clinical worsening after 72 hours
— Chest CT: ground-glass opacities, tree-in-bud, bronchiolitis pattern; rule out PE, ARDS
— Blood and sputum cultures if bacterial superinfection suspected (S. pneumoniae, S. aureus, H. influenzae classic)
— Echocardiography if new heart failure or troponin elevation
— ABG if respiratory distress to assess hypercapnia (especially COPD overlap)
— Lower respiratory tract sampling (BAL) may be needed; upper airway PCR can miss lower tract RSV
— Quantitative RSV PCR can guide duration of isolation and infectivity in transplant units
— Do not check RSV serology before vaccination
— Do not delay vaccine for mild URI; defer only for moderate-severe acute illness or fever
— Do not co-administer with other vaccines reflexively in pregnancy without weighing reactogenicity (some experts space RSV and Tdap by ≥2 weeks to attribute reactions, though co-administration is permitted)
— Guillain-Barré syndrome (GBS) — small numerical imbalance observed post-licensure for RSVPreF3 and RSVpreF in adults ≥60; absolute risk very low (~1–9 per million doses). Disclose during shared decision-making.
— Atrial fibrillation signal in some trials — not confirmed causal
— Maternal vaccine and preterm birth: Pfizer trial showed numerical imbalance — hence the 32–36 week window, avoiding earlier administration

— Age ≥75: universal recommendation, single dose
— Age 60–74 with increased risk: recommended (no longer "shared clinical decision-making" — simplified to risk-based recommendation)
— Age 50–59 with increased risk: recommended in updated guidance (expanded eligibility)
— Pregnancy 32 0/7–36 6/7 weeks during September–January (seasonal): RSVpreF (Abrysvo) — the only RSV vaccine approved in pregnancy
— Chronic lung disease (COPD, asthma, ILD, cystic fibrosis)
— Cardiovascular: CHF, CAD, congenital heart disease
— Moderate–severe immunocompromise
— Diabetes mellitus with complications
— CKD, chronic liver disease
— Hematologic disorders, severe obesity (BMI ≥40)
— Neurologic/neuromuscular conditions compromising airway clearance
— Residence in long-term care
— Maternal RSVpreF at 32–36 weeks during RSV season, OR
— Nirsevimab (monoclonal antibody) to the infant <8 months entering first RSV season
— Use nirsevimab if mother was not vaccinated, vaccinated <14 days before delivery, has conditions reducing antibody transfer, or infant has high-risk conditions
— Administer late summer to early fall (August–October ideal) to cover winter peak
— One-time dose currently; future ACIP updates may revisit revaccination interval

— RSVPreF3 (Arexvy, GSK): adjuvanted (AS01E) prefusion F protein, single 0.5 mL IM dose, adults ≥60
— RSVpreF (Abrysvo, Pfizer): non-adjuvanted bivalent (RSV A + B) prefusion F, single 0.5 mL IM dose, adults ≥60 and pregnancy 32–36 weeks
— mRNA-1345 (mResvia, Moderna): lipid nanoparticle mRNA encoding prefusion F, single 0.5 mL IM, adults ≥60
— Deltoid IM injection, 23–25 gauge, 1–1.5 inch needle
— Store refrigerated 2–8°C; do not freeze
— Reconstitute per product (Arexvy and Abrysvo are lyophilized + diluent)
— Permitted with influenza, COVID-19, pneumococcal, Tdap, shingles vaccines — use separate anatomic sites
— In pregnancy: Tdap and RSV can be co-administered, though some clinicians space by 2 weeks to attribute local reactions
— Reactogenicity may be slightly higher with co-administration but not clinically significant
— Severe allergic reaction (anaphylaxis) to prior dose or component
— History of GBS is a precaution (not absolute contraindication) — individualize
— Moderate-to-severe acute illness with or without fever — defer until recovered
— Pregnancy <32 weeks for Abrysvo — do not administer early due to preterm birth signal
— Arexvy and mResvia are not approved in pregnancy — do not substitute
— Common: injection-site pain, fatigue, myalgia, headache (peak 24–48h, resolve in 1–3 days)
— Rare serious: GBS (~1–9/million), inflammatory neurologic events, anaphylaxis

— Hydration, antipyretics (acetaminophen preferred in CKD/anticoagulated)
— Symptomatic care: saline nasal spray, honey for cough (>1 year old)
— Return precautions: dyspnea, SpO2 <94%, chest pain, confusion
— Supplemental O2 to keep SpO2 ≥92% (≥88% in COPD)
— High-flow nasal cannula (HFNC) for moderate hypoxemic respiratory failure
— Non-invasive ventilation (BiPAP) for hypercapnic COPD overlap
— Mechanical ventilation if refractory
— Bronchodilators (albuterol ± ipratropium) — empiric trial if wheezing; continue only if objective response
— Systemic corticosteroids — not routinely recommended for RSV alone; use if COPD/asthma exacerbation criteria met (prednisone 40 mg × 5 days)
— Antibiotics — only if bacterial co-infection suggested (focal consolidation, elevated procalcitonin, leukocytosis with left shift); cover S. pneumoniae and consider S. aureus post-viral
— Ribavirin — limited to select immunocompromised (stem cell transplant) — specialist-driven, not Step 3 first-line
— Palivizumab/nirsevimab — pediatric prophylaxis only, not treatment
— Supportive care, suction, hydration
— No routine bronchodilators, steroids, epinephrine, or antibiotics in typical bronchiolitis (AAP guideline)
— Hospitalize for hypoxemia, apnea, dehydration, or respiratory distress

— Highest hospitalization and mortality rates
— Single lifetime dose currently; revaccination not recommended (durability data ongoing, protection demonstrated through ≥2 seasons)
— Vaccinate even in advanced age and frailty if life expectancy >6 months and patient/surrogate consents
— Long-term care facility residents are high priority — outbreaks are devastating
— Coordinate vaccination with facility medical director and use standing orders
— No dose adjustment for RSV vaccines
— Dialysis patients are high-risk and should be vaccinated; administer on non-dialysis day to avoid attributing reactogenicity to dialysis
— Avoid IM injection into AV fistula arm
— No dose adjustment
— Chronic liver disease (cirrhosis) is itself an indication for vaccination in 50–74 group
— Patients on warfarin, DOACs, or antiplatelets can receive IM RSV vaccine
— Use 23–25 gauge needle, firm pressure ≥2 minutes post-injection
— INR within therapeutic range is acceptable; no need to hold anticoagulation
— Adjuvanted vaccine (Arexvy) may offer enhanced response in older adults, similar to high-dose flu rationale — though head-to-head data limited
— Antibody titers wane more slowly than expected; durability is a strength of prefusion F vaccines
— Use vaccination encounter to review Beers criteria meds, fall risk, advance directives

— RSVpreF (Abrysvo) only, single 0.5 mL IM dose at 32 0/7 to 36 6/7 weeks
— Administer during September–January (seasonal); outside this window, plan nirsevimab for the infant
— Co-administration with Tdap and influenza permitted; spacing optional
— Counsel about transient injection-site reactions; no increased risk of pre-eclampsia, gestational HTN, or fetal anomalies in trials
— Preterm birth signal led to gestational age restriction — do not administer before 32 weeks
— Maternal vaccination ≥14 days before delivery during RSV season → infant generally does not need nirsevimab
— Maternal vaccination <14 days before delivery, no vaccination, or maternal condition impairing antibody transfer → infant receives nirsevimab 50–100 mg IM (weight-based) before/during first RSV season
— High-risk infants (preterm, CHD, CLD) entering second season may receive nirsevimab again
— RSV vaccines are not approved in children
— Prevention is via maternal vaccine or nirsevimab monoclonal
— Older infants/toddlers rely on environmental measures (handwashing, avoiding sick contacts, smoke-free home)
— Vaccinate (50–74 risk group or ≥75)
— Response may be blunted in B-cell-depleted patients (rituximab, BTK inhibitors) — vaccinate when possible during a treatment gap
— Solid organ and stem cell transplant: per transplant center protocols, generally vaccinate ≥3–6 months post-transplant
— RSV vaccines compatible with breastfeeding

— Acute respiratory failure requiring HFNC, NIV, or intubation
— Bacterial superinfection — S. pneumoniae, S. aureus (including MRSA), H. influenzae
— Exacerbation of COPD, asthma, CHF — RSV is a leading trigger
— Acute cardiac events: acute MI, decompensated heart failure, new atrial fibrillation (~1 in 4 hospitalized older adults has a cardiac event)
— Acute kidney injury, often pre-renal from volume depletion
— Prolonged post-viral cough and airway hyperresponsiveness (weeks)
— Mortality in hospitalized adults ≥65: ~5–10%, higher in immunocompromised
— Apnea (especially <2 months, preterm)
— Bronchiolitis with respiratory failure
— Long-term recurrent wheezing/asthma association
— Reactogenicity: local pain (most common), fatigue, myalgia, headache — self-limited
— Guillain-Barré syndrome: rare numerical imbalance post-licensure; absolute risk ~1–9/million; counsel during consent
— Atrial fibrillation: small imbalance in some trials, not established as causal
— Anaphylaxis: very rare; observe 15 minutes post-injection if prior allergy history
— Maternal vaccine: preterm birth signal mitigated by 32-week threshold; no fetal malformations
— Hospitalization, ICU admission, prolonged disability, post-acute SNF placement
— Functional decline in elderly is often the lasting harm — not always death

— SpO2 <92% on room air (or drop from baseline)
— RR >30, accessory muscle use, inability to speak full sentences
— Altered mental status, hypotension, lactate elevation
— Inability to maintain hydration or oral intake
— Severe comorbidity decompensation (CHF, COPD exacerbation requiring NIV consideration)
— Frail elderly with poor home support
— Persistent hypoxemia despite HFNC FiO2 >50%
— Hypercapnia with pH <7.30 not responding to NIV
— Hemodynamic instability, sepsis with end-organ dysfunction
— Need for intubation or vasopressors
— Pulmonology for refractory bronchospasm, suspected superimposed ILD, or immunocompromised host
— Infectious disease for immunocompromised, transplant, or atypical course
— Cardiology for new AF, troponin elevation, or decompensated CHF
— Maternal-fetal medicine for pregnant patient with severe RSV LRTI
— Droplet + contact precautions for hospitalized RSV
— Cohort RSV-positive patients; private room preferred
— Healthcare worker masking, hand hygiene; visitor restrictions during outbreaks
— Long-term care facility outbreaks: notify public health, implement testing of symptomatic residents/staff, restrict communal activities
— Pregnant patient with RSV LRTI and hypoxemia → admit, MFM consult, continuous fetal monitoring if viable gestation, antenatal corticosteroids if delivery anticipated 24–34 weeks

— Abrupt onset, high fever, myalgia, headache prominent
— Treat with oseltamivir if within 48 hours (or any time in hospitalized/high-risk)
— Vaccine annual; antivirals available — distinguishes from RSV management
— Variable presentation; anosmia/ageusia historical clue
— Treat eligible outpatients with nirmatrelvir-ritonavir within 5 days
— Hospitalized hypoxemic: dexamethasone ± remdesivir ± baricitinib/tocilizumab
— Distinct vaccine schedule (updated annually)
— Paramyxovirus, RSV-like clinical picture in elderly and immunocompromised
— No vaccine, no specific antiviral
— Often on multiplex PCR — recognize and treat supportively
— Croup in children; LRTI in immunocompromised adults
— Supportive care
— Usually URI; can trigger COPD/asthma exacerbations
— No specific therapy
— Pharyngoconjunctival fever, occasionally severe pneumonia (military recruits, immunocompromised)
— Supportive; cidofovir in severe immunocompromised cases
— Wheeze prominence → favors RSV, hMPV
— High fever + myalgias → favors influenza
— Anosmia → favors COVID
— Conjunctivitis + pharyngitis → favors adenovirus
— Definitive: multiplex PCR

— Focal consolidation on CXR, productive purulent sputum, elevated procalcitonin
— Treat with β-lactam + macrolide or respiratory fluoroquinolone per IDSA/ATS
— Can occur after RSV as superinfection
— Increased dyspnea, sputum volume/purulence
— Treat with bronchodilators, systemic steroids, antibiotics if Anthonisen criteria met
— Always test for viral trigger — RSV/flu/COVID frequently underlie
— Orthopnea, PND, JVD, S3, BNP markedly elevated, pulmonary edema on CXR
— Diurese; viral illness can precipitate — co-existence common
— Pleuritic chest pain, tachycardia, hypoxemia without infiltrate
— D-dimer, CTPA — don't miss in elderly with sudden hypoxemia
— Younger patient, prior asthma history, peak flow reduction
— Albuterol, ipratropium, systemic steroids; viral trigger common
— Dependent lobe infiltrates, dysphagia history, stroke or dementia
— Cover anaerobes if necrotizing; mostly supportive for pneumonitis
— Smoker with persistent symptoms, weight loss, hemoptysis
— CT chest, bronchoscopy
— Acute eosinophilic pneumonia, hypersensitivity pneumonitis, drug-induced (amiodarone, methotrexate)

— Vaccinate at discharge if not previously vaccinated and eligible (one-time RSV vaccine)
— Update influenza, COVID-19, pneumococcal (PCV20 or PCV15+PPSV23), and shingles status
— Smoking cessation counseling — RSV severity correlates with smoking
— Review inhaler technique, COPD/asthma controller adequacy
— Optimize HF therapy if applicable (GDMT: ARNI/ACEi, β-blocker, MRA, SGLT2i)
— Identify RSV vaccine eligibility annually during pre-season (August–October)
— Confirm one-time dosing status — do not re-administer unless future ACIP guidance changes
— Document shared decision-making for 50–59 high-risk group
— Confirm infant RSV protection strategy: maternal vaccine effective if given ≥14 days pre-delivery in season; otherwise arrange nirsevimab
— Continue routine postpartum care; RSV vaccine does not contraindicate breastfeeding
— Hand hygiene, avoid sick contacts, mask in high-risk seasons
— Smoke-free home for infants (reduces RSV severity)
— Daycare exposure counseling
— Document in state immunization registry (IIS)
— Provide written record to patient — supports portability when seeing multiple providers
— Medicare Part D covers adult RSV vaccine with $0 cost-sharing
— Commercial insurance covers under ACA preventive services (ACIP-recommended)
— Medicaid coverage varies by state
— Pregnancy: covered under maternity benefits

— Phone or in-person check 1–2 weeks post-discharge for symptom resolution, medication reconciliation
— Pulmonary function reassessment in 4–6 weeks if persistent symptoms (COPD/asthma)
— Cardiology follow-up if new AF or troponin elevation during admission
— Pulmonary rehab referral for deconditioned COPD patients
— Expect cough to persist up to 4 weeks — reassure but evaluate if worsening
— Observe 15 minutes post-injection (30 minutes if prior anaphylaxis history)
— Counsel on injection-site reactions, expected mild systemic symptoms 1–3 days
— Advise return for: severe headache, weakness/numbness (GBS concern), persistent fever, allergic reaction
— Report adverse events to VAERS (vaers.hhs.gov)
— Routine prenatal visits continue per schedule
— Document vaccine in prenatal record and infant chart at delivery
— Pediatrician confirms maternal vaccination status at newborn visit to determine nirsevimab need
— Vaccine reduces severe LRTI and hospitalization, not all infection
— Encourage continued hygiene, masking in high-risk settings
— One-time dose currently; revaccination guidance may evolve — recheck at annual visits
— Address vaccine hesitancy with transparent risk/benefit (GBS rare; benefit substantial)
— Track RSV vaccination rates in panel; identify gaps in 75+ and high-risk 50–74
— Use EHR clinical decision support and pre-visit planning
— Standing orders empower MA/RN-driven vaccination

— Provide Vaccine Information Statement (VIS) before administration (federal NCVIA requirement for some vaccines; CDC provides VIS for RSV)
— Disclose: benefit (reduced severe LRTI/hospitalization), common reactogenicity, rare GBS signal, atrial fibrillation signal, anaphylaxis risk
— Document shared decision-making, especially in the 50–59 high-risk and 60–74 risk-based groups
— Discuss preterm birth signal context, rationale for 32–36 week window, alternative of infant nirsevimab
— Respect autonomy: patient may decline maternal vaccine and choose nirsevimab for infant
— Both options are acceptable — Step 3 tests non-coercive counseling
— Required for clinically significant adverse events
— Patients can self-report; clinicians should facilitate
— RSV vaccines are not currently covered under the National Vaccine Injury Compensation Program (VICP) for adults; Countermeasures Injury Compensation Program (CICP) may apply during emergencies — know the distinction
— Document vaccination status in discharge summary
— Communicate to PCP and (for postpartum) to pediatrician — missed maternal vaccine documentation can lead to redundant nirsevimab or unprotected infant
— Reconcile vaccine record at every transition
— Rural and minority elderly have lower RSV vaccination uptake — address access (mobile clinics, pharmacy administration)
— Pharmacist-administered vaccines under state scope-of-practice laws improve access
— Frail or cognitively impaired adults — use surrogate decision-maker if lacking capacity; document
— Long-term care: facility consent processes per state law
— Outbreaks in long-term care facilities reportable to local/state health department


— 76-year-old with COPD presents in September for annual wellness. Vaccines up to date except RSV. Answer: Administer single dose RSV vaccine (Arexvy, Abrysvo, or mResvia); no revaccination planned.
— 30-week pregnant patient in October asks about RSV vaccine. Answer: Wait until 32 weeks; administer Abrysvo at 32 0/7–36 6/7 weeks. Do not give Arexvy.
— Mother received Abrysvo at 34 weeks, delivered at 38 weeks in December. Does the newborn need nirsevimab? Answer: No — maternal antibodies sufficient.
— Mother declined RSV vaccine; baby born in November. Answer: Give nirsevimab to infant before discharge or at first well-child visit.
— 68-year-old wants flu, COVID-19, and RSV vaccines same visit. Answer: All three may be administered concurrently at separate sites.
— 72-year-old develops ascending weakness 2 weeks after RSV vaccine. Answer: Evaluate for GBS (LP, NCS/EMG, neurology consult), supportive care, IVIG or plasmapheresis if confirmed; report to VAERS.
— 80-year-old with PCR-confirmed RSV, SpO2 90%, wheezing. Answer: Droplet/contact precautions, supplemental O2, bronchodilators if responsive, no routine antibiotics, no oseltamivir, supportive care; vaccinate at discharge if not previously.
— Patient declines RSV vaccine citing GBS concern. Answer: Respect autonomy, document discussion, provide accurate risk data, re-offer at next visit.
— Multiple residents with febrile cough, RSV PCR positive. Answer: Cohort/isolate, droplet precautions, report to public health, restrict communal activities, ensure staff masking.

RSV is a vaccine-preventable cause of severe winter respiratory illness in older adults and infants, where a single-dose adult vaccine (Arexvy, Abrysvo, or mResvia) is recommended for everyone ≥75 and high-risk 50–74, and maternal Abrysvo at 32–36 weeks gestation (or infant nirsevimab) protects newborns through their first RSV season.

