MODULE 1 · GDFM PROGRAMME

M11.1: Acute Upper Respiratory Infections

📅 2026-03-01 🏛 College of Family Physicians Singapore

Learning Objectives

  • Differentiate upper respiratory tract infections (URTI) from lower respiratory tract infections (LRTI)
  • Apply clinical decision rules (McIsaac score) to guide appropriate antibiotic use in sore throat
  • Recognize and manage common viral syndromes: measles, varicella, HFMD, mononucleosis
  • Identify URTI mimics endemic to Singapore: dengue, chikungunya, zika
  • Manage COVID-19 and influenza with current MOH/CDC guidelines
  • Treat site-specific URTIs: pharyngitis, laryngitis, sinusitis, otitis media

Clinical Approach to URTI

  • URTIs are common in primary care; usually present with cough, sore throat, runny nose, fever, body aches
  • Key task: differentiate URTI from LRTI and identify need for antibiotics
  • URTI symptoms may herald serious illness (SARS 2003, COVID-19 pandemic)
  • Three clinical approaches: (1) Rule out non-infective causes, (2) Ascertain epidemiological contact, (3) Exclude LRTI

Differentiating URTI and LRTI

FeatureURTILRTI
Site affectedLarynx and proximal airwaysTrachea and distal airways
Key symptomsFever, malaise, myalgia (without localizing features)Cough, sputum, breathlessness, chest pain
Localizing signsEnlarged cervical lymph nodesCrepitations, rhonchi, tachypnoea, intercostal retractions, cyanosis
Common syndromesCoryza, ILI, rhinitis, sinusitis, pharyngitis, otitis mediaAcute/chronic bronchitis, CAP, atypical pneumonia, TB

Spectrum of Infections in URTI

  • Non-specific URTI: initial picture may evolve into unique viral syndrome or site-specific bacterial infection
  • Unique viral syndromes: pathognomonic features confirm diagnosis (e.g., rash in measles or varicella)
  • Site-specific URTI: localized infection (tonsillitis, pharyngitis, laryngitis, sinusitis, otitis media)
  • Influenza-like illness (ILI): non-specific presentation; shared by many viral pathogens

Antibiotic Use in URTI: ICE Framework

  • Generally NOT indicated: unique viral syndromes, non-specific URTI, certain viral site-specific URTIs
  • Always address patient's Ideas, Concerns, and Expectations (ICE)
  • If antibiotics unclear: use clinical judgment; consider age, comorbidities, toxicity, immunocompromise
  • If patient demands antibiotics but not indicated: explain reasoning; consider safety-net or delayed prescription
  • Communication reduces unnecessary prescribing driven by perceived patient expectations

Acute Coryza (Common Cold)

  • Mild, self-limiting: runny nose, sneezing, watery eyes, mild sore throat, minimal constitutional symptoms
  • Pathogens: Coronaviruses, Adenoviruses, Rhinoviruses, RSV, Parainfluenza, Influenza
  • Spread: respiratory droplets and contact with mucous secretions; incubation 1–3 days
  • Symptoms resolve within 1–2 weeks; cough from post-nasal drip common; fever usually <38°C
  • Muco-purulent rhinitis is NOT an indication for antibiotics without other signs of bacterial sinusitis

Cough & Cold Medicines in Children — Current HSA Guidance

Age GroupRecommendation
<2 yearsAvoid all cough/cold preparations unless prescribed by doctor after benefit-risk assessment
2–6 yearsUse only when benefits clearly outweigh risks; parental guidance essential; careful dosing
6+ yearsMay use with caution and appropriate dosing
Codeine (all ages)Contraindicated <18 years for post-operative pain (risk of fatal respiratory depression); restricted to ≥12 years for cough suppression at lowest dose, shortest duration
PromethazineContraindicated <6 months; not recommended <2 years; use caution in older children

Influenza: Pathogen & Prevention

  • Influenza A and B: historical pandemics; continue seasonal outbreaks
  • Vaccine updated biannually (Northern/Southern Hemisphere versions) to match circulating strains
  • Immunity develops ~2 weeks post-vaccination; protection lasts months to year
  • Vaccination recommended before Singapore influenza seasons: Dec–Feb and May–July

Influenza Vaccine Types & Evidence

Vaccine TypeCompositionEfficacy & Recommendation
Parenteral TrivalentH1N1, H3N2, one B lineage (3 surface antigens)59% efficacy in adults 18–65 years
Parenteral QuadrivalentH1N1, H3N2, both B lineages — Victoria & Yamagata (4 antigens)Similar immunogenicity & safety; recommended for healthy adults for individual and community protection

Influenza: Clinical Presentation & Diagnosis

  • Clinical Pearl: abrupt onset of systemic symptoms (fever, malaise, arthralgia, myalgia) followed by URTI symptoms (dry cough, sore throat); lasts 3–7 days
  • Diagnosis often clinical; testing reserved for hospitalised, severe, or outbreak management
  • Rapid Influenza Diagnostic Tests (RIDTs): sensitivity 10–70%, specificity >95%; negative does NOT exclude influenza
  • RT-PCR is gold standard; point-of-care molecular tests (rapid PCR) offer near-PCR sensitivity with faster turnaround

Influenza: Antiviral Therapy — Current CDC Guidance

  • Initiate as soon as possible — ideally within 48 hours of symptom onset
  • Indicated: hospitalised patients, severe/progressive illness, high-risk complications
  • Treatment beyond 48 hours may still benefit hospitalised or high-risk patients
  • Chemoprophylaxis: consider for high-risk with close contact during infectious period; avoid in healthy individuals or contact >48 hours prior

Available Antiviral Agents (CDC 2025)

AgentRouteAge ApprovalKey Notes
Oseltamivir (Tamiflu)Oral≥2 weeks (tx); ≥1 year (ppx)First-line neuraminidase inhibitor; 5-day course
Zanamivir (Relenza)Inhaled≥7 years (tx); ≥5 years (ppx)Avoid in asthma/COPD — risk of bronchospasm
Peramivir (Rapivab)IV≥2 yearsSingle-dose option for hospitalised patients
Baloxavir (Xofluza)Oral≥5 yearsPA endonuclease inhibitor; single-dose; active vs oseltamivir-resistant; NOT in pregnancy

Infectious Mononucleosis (IM)

  • Cause: Epstein-Barr virus (HHV-4), rarely Cytomegalovirus (HHV-5)
  • Transmission: saliva ('kissing disease')
  • Clinical Pearl: IM is a SYSTEMIC infection with throat manifestations; streptococcal pharyngitis is local
  • Key differentiator: suspect IM in adolescent/young adult with severe sore throat, exudative tonsillitis, posterior cervical lymphadenopathy, fatigue, periorbital edema

Viral Exanthems: Overview & Measles

  • Exanthem: widespread rash on skin during systemic disease; key feature of measles, rubella, varicella, roseola
  • Measles (Rubeola): severe prodrome (3–5 days) with high fever, cough, coryza, conjunctivitis
  • Koplik spots on buccal mucosa appear BEFORE rash — pathognomonic
  • Morbilliform rash appears while patient is acutely ill; highly contagious; preventable by MMR
  • Complications: otitis media, pneumonia, encephalitis
Diffuse erythematous maculopapular rash on the trunk consistent with measles (morbilliform exanthem)

Diffuse erythematous maculopapular rash on the trunk consistent with measles (morbilliform exanthem)

Koplik Spots: Pathognomonic Sign of Measles

Koplik spots on buccal mucosa — pathognomonic white-centred red spots of early measles

Koplik spots on buccal mucosa — pathognomonic white-centred red spots of early measles

Varicella (Chickenpox)

Scattered papulovesicular lesions in different stages on the back, consistent with varicella (chickenpox)

Scattered papulovesicular lesions in different stages on the back, consistent with varicella (chickenpox)

Roseola Infantum (Exanthem Subitum)

Widespread blanching macular rash on the trunk of an infant following fever resolution — roseola infantum (exanthem subitum)

Widespread blanching macular rash on the trunk of an infant following fever resolution — roseola infantum (exanthem subitum)

Erythema Infectiosum ('Slapped Cheek' Disease)

Bilateral erythematous 'slapped cheek' rash with circumoral pallor — erythema infectiosum (Fifth disease, Parvovirus B19)

Bilateral erythematous 'slapped cheek' rash with circumoral pallor — erythema infectiosum (Fifth disease, Parvovirus B19)

Viral Enanthems: HFMD & Herpangina

  • Enanthem: rash on mucous membranes (oral, genital)
  • Hand-Foot-Mouth Disease (HFMD): Coxsackievirus A, Enterovirus 71; vesicles on hands, feet, buttocks; painful oral ulcers at back of mouth
  • Herpangina: Coxsackievirus A; greyish-white papulovesicular lesions on tonsillar pillars, soft palate, uvula (posterior pharynx); sore throat and fever
  • Management: supportive care; emphasize hygiene; monitor EV71 for neurological or cardiorespiratory signs
Hand, Foot, and Mouth Disease (HFMD) — medical illustration showing blister distribution on palms, soles, and oral mucosa

Hand, Foot, and Mouth Disease (HFMD) — medical illustration showing blister distribution on palms, soles, and oral mucosa

Herpetic Gingivostomatitis

Acute haemorrhagic gingivitis with ulceration of upper anterior gingiva — primary herpetic gingivostomatitis

Acute haemorrhagic gingivitis with ulceration of upper anterior gingiva — primary herpetic gingivostomatitis

Vector-Borne URTI Mimics: Dengue Overview

  • Singapore's tropical climate and high mosquito population make dengue, chikungunya, and zika endemic URTI mimics
  • Dengue: acute onset fever, headache, backache, myalgia, rash, retro-orbital pain; three phases: febrile, critical, recovery
  • Distinguish from typical URTI: look for severe systemic symptoms, rash, warning signs (persistent vomiting, severe abdominal pain, mucosal bleeding)
  • Statutory notification required; supportive care with careful fluid management; avoid NSAIDs and contact sports during critical phase

Dengue: Clinical Course & Phases

Clinical course of dengue illness: febrile, critical, and recovery phases with temperature curve, platelet/haematocrit trends, and serology timing

Clinical course of dengue illness: febrile, critical, and recovery phases with temperature curve, platelet/haematocrit trends, and serology timing

Dengue: Severity Classification (WHO)

WHO dengue severity classification: probable dengue, dengue with warning signs, and severe dengue — criteria and management pathway

WHO dengue severity classification: probable dengue, dengue with warning signs, and severe dengue — criteria and management pathway

Dengue: Diagnostic Testing by Timing

Dengue diagnostic test timing table: NS1 antigen and PCR within 7 days of onset; IgM/IgG serology after 7 days

Dengue diagnostic test timing table: NS1 antigen and PCR within 7 days of onset; IgM/IgG serology after 7 days

Dengue Vaccine (Dengvaxia)

  • Dengvaxia: chimeric yellow fever-dengue virus vaccine; protects against dengue serotypes 1–4
  • Indicated for persons with previous dengue infection or living in high-transmission areas
  • Schedule: three doses (0, 6, 12 months) or accelerated schedule available
  • Efficacy data vary by serotype; overall ~65% efficacy in preventing symptomatic dengue
Dengue vaccine (Dengvaxia) — chimeric yellow fever-dengue virus serotypes 1–4 and summary of efficacy data

Dengue vaccine (Dengvaxia) — chimeric yellow fever-dengue virus serotypes 1–4 and summary of efficacy data

Dengue Vaccine Guidelines (Clinical & Contraindications)

  • Indicated: individuals ≥9–12 years in endemic areas with laboratory-confirmed prior dengue
  • Schedule: accelerated (0, 6-month) or standard (0, 6, 12 months) depending on urgency
  • Storage: 2–8°C; do not freeze
  • Contraindication: pregnancy (Category X) — counsel women of child-bearing age to avoid pregnancy for 3 months post-vaccination
  • Not covered by Medisave; check current MOH program eligibility
Dengue vaccine clinical guidelines table: indication, schedule, administration, storage, adverse events, contraindications, and precautions

Dengue vaccine clinical guidelines table: indication, schedule, administration, storage, adverse events, contraindications, and precautions

Chikungunya & Zika

  • 💎 Chikungunya: fever + SEVERE, debilitating polyarthralgia/polyarthritis; rash common; differentiate from typical URTI by joint involvement
  • Zika: mild URTI-like symptoms (rash, joint pain, conjunctivitis) but associated with Guillain-Barré syndrome (adults) and congenital microcephaly (maternal infection)
  • Prevention (all vector-borne): DEET-containing repellent, long clothing, eliminate stagnant water
  • Zika in pregnancy: avoid travel to affected areas; counsel on contraception if planning pregnancy

COVID-19: Pathogen, Transmission & Complications

  • Caused by SARS-CoV-2; asymptomatic spread and airborne transmission drive high infectivity
  • Symptoms: highly variable — non-specific URTI (sore throat, cough, headache, fatigue) to severe respiratory distress
  • Anosmia/ageusia: classic with early variants but less prominent in Omicron sub-lineages
  • Complications: acute (cardiovascular events, thrombosis, AKI) and chronic (Long COVID — fatigue, dyspnea, cognitive dysfunction)
  • Vaccination before infection appears to reduce Long COVID risk

COVID-19: Severity Classification

COVID-19 severity classification: asymptomatic, mild URTI, moderate pneumonia (SpO2 ≥94%), severe (SpO2 <94%), critical illness

COVID-19 severity classification: asymptomatic, mild URTI, moderate pneumonia (SpO2 ≥94%), severe (SpO2 <94%), critical illness

COVID-19: Diagnostic Tests Comparison (Part 1)

COVID-19 diagnostic test comparison (Part 1): PCR, antigen rapid test, and serology — scientific basis, sample type, turnaround time, performance

COVID-19 diagnostic test comparison (Part 1): PCR, antigen rapid test, and serology — scientific basis, sample type, turnaround time, performance

COVID-19: Diagnostic Tests — Limitations (Part 2)

COVID-19 diagnostic test comparison (Part 2): use cases, role in testing strategy, and limitations of PCR, ART, and serology

COVID-19 diagnostic test comparison (Part 2): use cases, role in testing strategy, and limitations of PCR, ART, and serology

COVID-19: Treatment Algorithm by Severity

COVID-19 treatment algorithm by severity: mild-moderate (oral antivirals), severe (dexamethasone ± remdesivir/baricitinib), critical (dexamethasone ± tocilizumab/baricitinib)

COVID-19 treatment algorithm by severity: mild-moderate (oral antivirals), severe (dexamethasone ± remdesivir/baricitinib), critical (dexamethasone ± tocilizumab/baricitinib)

COVID-19: Oral Antivirals & Indications

  • Indicated: mild-to-moderate disease in HIGH-RISK patients if started within 5 days of symptom onset
  • High-risk factors: not up-to-date with vaccination, age >60–70, active cancer, chronic kidney/lung/heart disease, obesity, diabetes, immunosuppression
  • Nirmatrelvir/ritonavir (Paxlovid): preferred; dose adjust for GFR 30–60; contraindicated GFR <30 or severe hepatic impairment; note CYP3A4 interactions
  • Molnupiravir/Ensitrelvir: alternatives; molnupiravir NOT in pregnancy or women unable to use contraception

COVID-19 Vaccination (MOH Singapore 2025–2026)

  • Additional dose recommended at ~1 year (minimum 5 months) from last vaccine dose
  • Recommended for: age ≥60 years, medically vulnerable ≥6 months, aged care residents
  • Immunocompromised individuals may need more frequent dosing — refer to current MOH/NCID guidance
  • Vaccines available: Pfizer-BioNTech, Moderna, Novavax, Sinovac-CoronaVac (targeting Omicron sub-lineages)
  • Vaccination reduces severe disease, hospitalization, and death; may reduce Long COVID risk

Site-Specific URTI: Acute Sore Throat (Pharyngitis)

  • Most sore throats are viral and self-limiting; challenge is identifying Group A Beta-Haemolytic Streptococcus (GABHS)
  • GABHS causes only 5–15% of adult pharyngitis but can lead to acute rheumatic fever (especially in children)
  • Use McIsaac clinical score to predict GABHS likelihood and guide testing/treatment decisions
  • Clinical Pearl: viral features (cough, coryza, conjunctivitis, diarrhea, hoarseness, oral ulcers) suggest viral; bacterial features (abrupt onset, fever, exudates, tender cervical nodes, absence of cough) suggest GABHS

McIsaac Clinical Score for Sore Throat

McIsaac CriterionPoints
Temperature >38°C+1
Absence of cough+1
Tender anterior cervical lymph nodes+1
Tonsillar swelling or exudates+1
Age 3–14 years+1
Age ≥45 years-1

GABHS Pharyngitis: Antibiotic Treatment

Antibiotic (10-day course PO)Adult DosageNotes
Penicillin V500 mg BD or 250 mg QDSFirst-line; narrow spectrum; no resistance documented
Amoxicillin50 mg/kg OD (max 1g) or 500 mg BDOften preferred for taste; broader spectrum
Cephalexin (non-anaph allergy)500 mg BD1st generation cephalosporin
Clindamycin (anaph allergy)300 mg TDSFor penicillin-allergic patients
Azithromycin500 mg OD × 5 daysIncreasing macrolide resistance; use only if susceptibility confirmed

Epiglottitis: A Medical Emergency

🚨 Emergency — Act Now
🚨
  • Acute epiglottitis is a medical emergency — airway may obstruct rapidly
  • Suspect in: severe sore throat + signs of airway obstruction (stridor, difficulty breathing, drooling, tripod position)
  • Historically Haemophilus influenzae type b; now Group A Streptococcus and other organisms due to vaccination
  • ⚠️ DO NOT examine throat with tongue depressor — risk of complete airway obstruction
  • Management: URGENT hospital referral; secure airway (intubation), IV antibiotics, corticosteroids

Acute Laryngitis

  • Typically viral; presents with hoarseness, aphonia, dry cough
  • Mainstay of treatment: voice rest and hydration
  • Antibiotics generally NOT indicated (no benefit over supportive care alone)
  • If bacterial cause strongly suspected, macrolides (e.g., erythromycin) have been suggested but evidence limited

Acute Sinusitis: Overview & Diagnosis

  • Most cases are viral; bacterial infection suspected if symptoms persist >10 days, severe from onset, or worsen after initial improvement ('double sickening')
  • Clinical predictors of ACUTE BACTERIAL SINUSITIS: maxillary toothache, purulent nasal secretion, poor response to decongestants, abnormal transillumination, coloured discharge
  • ≥4 predictors = high probability (LR 6.4); 2–3 predictors = intermediate (LR 2.6); ≤1 predictor = low probability (LR 0.5)

Acute Sinusitis: Management & Antibiotics

  • Initial therapy for uncomplicated cases: watchful waiting + symptomatic treatment (analgesics, saline irrigation) for 1 week
  • Antibiotics (5–7 day course) if indicated: amoxicillin-clavulanate (500/125 mg TDS or 875/125 mg BD) first-line
  • For penicillin allergy: doxycycline 100 mg BD or respiratory fluoroquinolone (levofloxacin 500 mg OD or moxifloxacin 400 mg OD)
  • Referral indicated: severe symptoms, failure to respond to antibiotics, suspected complications (orbital cellulitis, meningitis, cavernous sinus thrombosis)

Otitis Media: AOM vs OME

  • Acute Otitis Media (AOM): middle ear fluid + acute signs of inflammation (otalgia, fever, bulging/red TM)
  • Otitis Media with Effusion (OME): middle ear fluid WITHOUT acute signs of infection ('glue ear')
  • AOM management: analgesia (paracetamol/ibuprofen) ± observation period (48–72 hours for age ≥2 years, non-severe, unilateral)
  • OME management: watchful waiting; spontaneous resolution in ~75% within 3 months; refer to ENT if persistent >3 months with hearing loss

Acute Otitis Media: Antibiotic Treatment

Acute otitis media antibiotic treatment table: first-line amoxicillin and alternatives for initial and failed therapy, including penicillin allergy options

Acute otitis media antibiotic treatment table: first-line amoxicillin and alternatives for initial and failed therapy, including penicillin allergy options

💎 Key Summary: Approach to URTI

Key Point
Differentiate URTI from LRTI and identify serious mimics (dengue, chikungunya, COVID-19, epiglottitis)
Key Point
Use clinical decision rules (McIsaac score) to guide judicious antibiotic use — most URTIs are viral and self-limiting
Key Point
Address patient's ICE (Ideas, Concerns, Expectations); effective communication reduces inappropriate antibiotic demand
Key Point
Maintain high index of suspicion for URTI mimics endemic to Singapore, especially if severe systemic features present
Key Point
Stay updated on evolving guidelines for COVID-19 and influenza management, vaccination, and antivirals
Key Point
Treat site-specific URTIs (pharyngitis, laryngitis, sinusitis, otitis media) according to current evidence; avoid empirical antibiotics for uncomplicated viral disease

References