GC018 Health Promotion And Disease Prevention In Primary Care
Health promotion and disease prevention in primary care encompasses the systematic application of screening, immunization, counseling, and lifestyle modification strategies to maintain wellness and reduce the incidence and progression of disease at the individual and community level.
Health Promotion and Disease Prevention in Primary Care
Lecture Map
Every general-practice consultation is an opportunity to go beyond the presenting complaint and address prevention, early detection, and health promotion. This lecture, delivered by Prof William CW Wong (Department of Family Medicine & Primary Care, HKU), anchors the Family Medicine clerkship by teaching you how to think about prevention systematically — from the population level down to the individual sitting in front of you — and illustrates it with a deep-dive into Hepatitis B as a model for cross-society health promotion. [1]
- Session 1 — Preventive activities in Family Medicine: Recap the criteria and range of screening and understand what screening means for an individual person.
- Session 2 — Health promotion in primary care: Understand health promotion activities specific to primary care (using Hepatitis B as an example), recognise difficulties in delivering health promotion, and learn ways to overcome them.
- Family Medicine is one of the six whole-class sessions in the GCBC-FM curriculum. [2]
- Prevention questions are perennial in Fourth Summative SAQs and MCQs — they test your ability to classify levels of prevention, apply Wilson-Jungner screening criteria, and recognise which screenings are recommended vs. controversial vs. "recommend against." [3][4]
- The HBV case study models translational public-health thinking: from evidence (cost-effectiveness analysis) → policy → community engagement → primary care implementation — a framework applicable to any disease.
Core Concepts and Mechanisms
"~50% of all deaths in the US are attributable to modifiable behavioural causes." [1]
| Cause | Estimated Deaths | % of Total |
|---|---|---|
| Tobacco | 400,000 | 19% |
| Diet/activity patterns | 300,000 | 14% |
| Alcohol | 100,000 | 5% |
| Microbial agents | 90,000 | 4% |
| Toxic agents | 60,000 | 3% |
| Firearms | 35,000 | 2% |
| Sexual behaviour | 30,000 | 1% |
| Motor vehicles | 25,000 | 1% |
| Illicit drug use | 20,000 | < 1% |
| Total | ~1,060,000 | ~50% |
Why this matters: The top three killers are all lifestyle-related. This is the intellectual backbone of preventive medicine — if you can modify behaviour, you prevent half of all deaths. Primary care is the front line for this because it is where patients present repeatedly, often for unrelated complaints, giving you multiple "windows of opportunity."
The lecture defines four levels of prevention mapped to the disease continuum. [1]
| Level | Disease Stage | Goal | Definition | Examples |
|---|---|---|---|---|
| Primary Prevention | Normal — no problem | Prevent disease from occurring | Avoiding disease by reducing susceptibility or controlling risk factors | Immunisation, smoking cessation advice, exercise counselling, contraception |
| Secondary Prevention | Early stage, no symptoms (long pre-clinical phase) | Screening & early diagnosis → avoid irreversible damage | Avoiding irreversible damage through early detection and therapy | Cervical smear, mammography, colonoscopy for CRC, BP check, fasting glucose |
| Tertiary Prevention | Established disease with symptoms / complications | Prevent complications, disability, dependence | Avoiding complications, disability or dependence in irreversible states | Cardiac rehab post-MI, diabetic foot care, rehabilitation after stroke |
| Quaternary Prevention | Patient at risk of over-medicalisation | Protect from excessive/unnecessary medical intervention | Action to identify patients at risk of over-medicalisation, protect from new medical invasion, suggest ethically acceptable interventions | Avoiding unnecessary imaging, de-prescribing in polypharmacy, shared decision-making about cancer screening in elderly |
Quaternary Prevention — Concept Coined by Marc Jamoulle (Belgian GP)
"A set of health activities to mitigate or avoid the consequences of unnecessary or excessive intervention of the health system." This is a distinctly Family Medicine concept. It acknowledges that medicine itself can cause harm — through overdiagnosis, overtreatment, cascade effects of false positives, and medicalisation of normal life events. [1]
Exam Trap — Levels of Prevention
A colonoscopy in an asymptomatic 45-year-old with strong family history of CRC is secondary prevention (screening), NOT primary prevention. Primary prevention would be advising him to eat more fibre and exercise. The 2021 MCQ Q88 tested exactly this — the answer is B (Secondary Prevention). [3]
Similarly, monitoring blood lead levels in lead workers = secondary prevention (early detection of subclinical exposure), NOT primary prevention (which would be eliminating exposure). Tested in 2023 MCQ Q94, answer C. [4]
Every general practice consultation has four domains beyond the presenting complaint. [1]
┌─────────────────────────────────────────┐
│ GP Consultation Potential │
├───────────────────┬─────────────────────┤
│ Presenting │ Continuing care │
│ complaint │ (chronic disease │
│ (overt/covert) │ management) │
├───────────────────┼─────────────────────┤
│ Prevention, │ Modification of │
│ early detection, │ abnormal help- │
│ health promotion │ seeking behaviour │
├───────────────────┼─────────────────────┤
│ Coordination │ │
│ of care │ │
└───────────────────┴─────────────────────┘Why this model matters: A patient comes in for a sore throat. You treat the sore throat (presenting complaint). But you also notice they smoke — so you give brief smoking cessation advice (prevention). You check if their BP has been measured recently (early detection). If they've been coming in frequently for trivial complaints, you explore why (modification of health-seeking behaviour). If they have diabetes being managed by a specialist, you ensure follow-up is coordinated (coordination of care). This "opportunistic" approach is the hallmark of comprehensive primary care.
The lecture lists eight domains of individual preventive activities: [1]
- Immunisation
- Birth control
- Sexually transmitted diseases
- Mental health
- Smoking
- Alcohol
- Screening
- Dental care
Each of these represents a conversation you can have during any consultation. The key is being systematic and opportunistic — you don't wait for the patient to ask; you proactively screen and counsel.
Immunisation
The lecture lists the following childhood vaccines:
| Vaccine | Disease(s) Prevented |
|---|---|
| DTaP-IPV | Diphtheria, Tetanus, Pertussis, Polio |
| Hib | Haemophilus influenzae type b |
| HBV | Hepatitis B |
| Rotavirus | Rotavirus gastroenteritis |
| MMR | Measles, Mumps, Rubella |
| BCG | Tuberculosis |
| Meningococcal | Meningococcal disease |
| Varicella/Zoster | Chickenpox / Shingles |
| Influenza | Seasonal influenza |
| COVID-19 | COVID-19 |
In Hong Kong, the Childhood Immunization Programme (HKCIP) covers most of these through MCHC visits. The ICHDP covers > 90% of newborns. [5]
| Category | Vaccines |
|---|---|
| Routine boosters | Tetanus, Diphtheria |
| Annual/seasonal | Influenza |
| Age-based | Pneumococcus |
| Pandemic | COVID-19 |
| Travel vaccines | Hepatitis A, Japanese encephalitis, Meningococcus (Hajj requirement), Typhoid, Cholera, Yellow fever |
Travel Vaccine Exam Point
2023 MCQ Q78 tested malaria prevention advice for travel to Papua New Guinea. The answer is D — Start antimalarial prophylaxis before, during and after travel. There is no malaria vaccine in routine travel use (though RTS,S exists for endemic paediatric populations). [4]
Screening
The lecture distils the 10 Wilson-Jungner criteria into 5 key points: [1]
| # | Lecture's Condensed Criterion | Full Wilson-Jungner Criterion (for reference) |
|---|---|---|
| 1 | Long pre-clinical phase & disease prevalent | Important health problem; recognisable latent stage; natural history understood |
| 2 | Treatment available to improve outcome | Accepted treatment exists; agreed policy on who to treat |
| 3 | Test sensitive | Suitable test exists |
| 4 | Test acceptable to patient | Test acceptable to population |
| 5 | Cost-effective | Costs balanced against benefits; continuing process |
Additional points from slide: RCT evidence is needed. There is huge pressure to screen. There are ethical/legal issues. [1]
Why each criterion matters from first principles:
- Long pre-clinical phase: If a disease goes from undetectable to lethal in days (e.g., pancreatic cancer), screening is futile — you can't catch it early enough. Cervical cancer takes 10-20 years to progress from dysplasia → carcinoma, making it ideal for screening.
- Treatment must improve outcome: If you can detect it early but there's no treatment that changes the natural history, you've just given the patient more years of anxiety (lead-time bias). This is the core argument against routine PSA screening.
- Sensitive test: A test that misses most cases (low sensitivity) will give false reassurance. You want high sensitivity for screening (you'll sort out false positives later with confirmatory tests).
- Acceptable to patient: A perfect test that nobody agrees to take is useless. This is why FIT (faecal immunochemical test) has replaced guaiac FOBT — it's easier, more acceptable, and more sensitive.
- Cost-effective: Healthcare resources are finite. Screening must be compared against alternative uses of the same money.
The full 10-point Wilson-Jungner criteria are also listed in senior notes and are frequently examined. [6][7]
Chronic illnesses in four domains:
- Cardiovascular disease
- Cancers
- Degeneration
- Disability of ageing
The lecture lists the following CV risk factors to screen for:
| Risk Factor | Screening Detail |
|---|---|
| Sex | Male sex = higher risk |
| Family history | First-degree relative with premature CVD |
| Past history | Prior CV disease or diabetes |
| Diabetes | Every 3 years from age 30 or above |
| Blood pressure | Every 2 years |
| Smoking | Ask at every visit |
| Diet | Fat, Salt, K+ intake |
| Exercise | Physical activity level |
| Obesity | BMI, Waist/hip ratio, waist size |
| Alcohol | Quantity and pattern |
| Cholesterol | Lipid profile |
High Yield — Screening Intervals
Diabetes screening: every 3 years from age ≥30. Blood pressure: every 2 years. These specific intervals are directly from the lecture slides and are testable. [1]
Connection to related material: The HK Consensus 2016 on primary CVD prevention recommends non-pharmacological measures (diet, moderate-intensity exercise ≥30 min × ≥5 days/week, weight loss, smoking cessation) alongside pharmacological optimisation (BP, glucose to HbA1c < 7%, LDL targets based on risk stratification). [8]
Cancer Screening [1]
| Cancer | Screening Test | Sensitivity/Efficacy | Notes |
|---|---|---|---|
| Cervical cancer | Cervical smears | ~90% | Well-established, meets all Wilson-Jungner criteria |
| Breast cancer | Mammography, age 50-70 | ~25% reduction in mortality | Population-based programs; the slide asks "How acceptable?" |
| Colorectal cancer | Fecal occult blood (gFOBT) | ~20% | Older test, being replaced |
| FIT (Faecal Immunochemical Test) | 70-90% | Preferred stool-based test in HK; CRC screening programme uses FIT Q2 years from age 50 [9] | |
| Colonoscopy | ~99% | Gold standard but invasive; the slide asks "How affordable?" |
HK CRC Screening Programme (from senior notes, corroborating the lecture): 2-tier system — FIT every 2 years starting age 50; if FIT positive → colonoscopy. [9]
The lecture explicitly flags these as controversial:
| Condition | Test | Why Controversial |
|---|---|---|
| Breast self-examination | Clinical exam | No RCT evidence of mortality reduction; may cause anxiety and unnecessary biopsies |
| Liver cancer (HCC) | AFP, USS abdomen | AFP sensitivity only ~60-70%; USS limited in obese/cirrhotic patients [10] |
| Nasopharyngeal cancer (NPC) | EBV serology | Relevant in Southern Chinese population but no established mass screening program |
| Prostate cancer | PSA | High rate of overdiagnosis; ERSPC showed 48 men need diagnosis to prevent 1 death; PLCO showed no benefit [7] |
| Lung cancer | Low-dose CT (LDCT) | Slide says "PECT scan" — likely referring to low-dose CT; NELSON/NLST trials show mortality benefit in heavy smokers but high false-positive rate |
PSA Screening — Key Exam Points
PSA screening is controversial, not recommended against. The lecture places it in the "uncertain" category. However, the slide on "Recommend Against" does NOT include PSA — it is separated. Know the distinction: PSA has some evidence (ERSPC), but the harms of overdiagnosis/overtreatment often outweigh benefits in unselected populations. If a question asks about shared decision-making, PSA is the classic example. [1][7]
The slide says "Prob not: Mental health" and specifies:
| Condition | Approach |
|---|---|
| Depression | Awareness, not screening |
| Dementia | Awareness, not screening |
| Suicide | Awareness, not screening |
| Eating disorders | Awareness, not screening |
| Family violence | Awareness, not screening |
Why "awareness, not screening"? These conditions don't meet Wilson-Jungner criteria well — there's no single sensitive/specific test, the natural history is variable, and mass screening tools (e.g., PHQ-9 for depression) have high false-positive rates in general populations. Instead, the family doctor should be aware and ask when clinical suspicion arises (opportunistic case-finding, not population screening).
The lecture explicitly recommends against screening for:
| Test | Condition | Why Not |
|---|---|---|
| Static ECG, Stress ECG | Asymptomatic CAD | High false-positive rate in low-risk populations; leads to unnecessary catheterisation |
| Urinalysis | General population | Non-specific; leads to cascade of unnecessary investigations |
| Ultrasound or CA-125 | Ovarian cancer | No mortality benefit; high false-positive rate leading to unnecessary surgery |
| Endometrial sampler | Uterine cancer | Not validated for asymptomatic screening |
| Physical exam | Testicular cancer | Self-examination not shown to reduce mortality |
| Skin examination | Skin cancer | Population screening not recommended (may be appropriate in high-risk individuals) |
Must-Know: Recommend Against List
If an exam question asks "Which of the following is NOT recommended as a screening test?", the answers above are your go-to discriminators. Ovarian cancer screening with CA-125/USS is a classic "recommend against" — this has been tested in past papers. [1]
The HBV Case Study — Health Promotion in Action
Prof Wong uses Hepatitis B as a paradigm for cross-society health promotion because:
- HBV is highly prevalent in Hong Kong and China (endemic area, ~7-8% chronic carriage rate).
- Despite neonatal vaccination since 1988, there is a huge undiagnosed pool of adults infected before universal vaccination.
- Effective treatment exists (nucleos(t)ide analogues) — meaning that finding cases saves lives.
- It illustrates the full spectrum: primary prevention (vaccination), secondary prevention (screening), tertiary prevention (treatment to prevent cirrhosis/HCC), and quaternary prevention (avoiding unnecessary invasive procedures in low-risk carriers).
In Hong Kong, only 22% of HBV-infected individuals are diagnosed, and only 17% are treated. [1]
| Country/Region | HBV Diagnosed | HBV Treated |
|---|---|---|
| Hong Kong | 22% | 17% |
| Mainland China | 19% | 11% |
| Korea | 83% | 33% |
| Japan | 72% | 32% |
| Malaysia | 9% | 5% |
| Indonesia | 3% | < 1% |
| WPRO | 19% | 10% |
| Global | 10% | 5% |
"Newborn vaccination and maternity testing alone is insufficient to eliminate HBV (requires 90% reduction in new chronic infections and 65% reduction in mortality). We need to find the missing patients!" [1]
Why this matters: Vaccination prevents new infections but does nothing for the estimated 290 million people worldwide already chronically infected. You need active case-finding (screening) + linkage to care (treatment) to reduce mortality.
The lecture highlights WHO policy guidance for targeted HBV/HCV screening:
- Dialysis patients
- Intravenous drug users
- Concomitant HIV patients
- "HBV/HCV screening should be provided in conjunction with STD screening, at intervals informed by risk assessment" [1]
Key findings (Wong WC as co-first author):
- Universal HBV screening in China is cost-effective
- Data robust in different sensitivity analyses
- Can save 3.46 million lives
- Impact decreases if screening is delayed
- Screening alone cannot reduce mortality by 65% — treatment uptake is also essential
Methodology [1]:
- Markov decision-analytic model simulating HBV natural history
- Examined 15 target groups stratified by age (18-30, 18-40, 18-50, 18-60, 18-70 years), born before HBV vaccine was integrated into the Chinese national immunisation programme (free since 2002)
- Four screening strategies compared:
- HBsAg alone
- HBsAg + HBsAb
- HBsAg + HBsAb + HBcAb
- HBsAg + HBsAb + HBeAg + HBeAb + HBcAb ("Five-test" panel)
- Three initiation years: 2021, 2026, 2031 (to show cost of delay)
Result: The five-test (HBsAg/HBsAb/HBeAg/HBeAb/HBcAb) screening in people aged 18-70 was the MOST cost-effective strategy in 2021-2031. [1]
Why five tests? Each serological marker tells you something different:
- HBsAg: Currently infected?
- HBsAb: Immune (from vaccine or resolved infection)?
- HBcAb: Ever been exposed (past or current)?
- HBeAg: Actively replicating (higher infectivity)?
- HBeAb: Seroconversion (lower replication)?
Using all five allows you to classify the patient's HBV status precisely, determine who needs treatment, who needs vaccination, and who is immune — maximising the public health impact per dollar spent.
The new WHO strategies recommend decentralising routine hepatitis testing and care to primary care. [1]
The lecture presents a second cost-effectiveness study comparing three scenarios:
| Scenario | Description | Result |
|---|---|---|
| 1 — Status quo | All care in specialty centres | Baseline |
| 2 — Partial shared care | HBV testing + routine follow-up in primary care; treatment initiation in specialty care | Cost US$5.79-132.43m more; gained 328-16,993 QALYs; prevented 39-1,935 deaths; not cost-effective at 1× GDP per capita WTP unless treatment initiation rate increased to 70% |
| 3 — Full shared care | HBV testing + treatment initiation + follow-up in primary care; only predetermined conditions referred to specialty | Cost-SAVING (saved US$144.59-192.93m); gained 23,814-30,476 QALYs; prevented 3,074-3,802 deaths |
"Improving HBV antiviral treatment uptake is the key to improving the shared-care models' effectiveness and cost-effectiveness." [1]
Why this is clinically important: In Hong Kong and China, most HBV patients are managed in hospital specialist clinics. This creates bottlenecks. The evidence shows that training primary care doctors to manage stable CHB (with clear referral criteria for complex cases) is not just clinically effective — it actually saves money.
The lecture outlines a multi-pronged approach:
- Policy and Guideline — e.g., HBV guideline for primary care in Mainland China (11,552 online reads)
- Evidence to do better — e.g., universal screening research
- Engaging medical professionals and industries
- Traditional and Digital Media — World Hepatitis Day promotion videos (FB views: 435,030), social media campaigns
- Community Outreach — vulnerable HCV communities, media coverage (18 outlets)
- Within and Beyond Hong Kong and China — BBC Future series, YouTube/social media channels
Why this matters for exams: Health promotion is not just about clinical knowledge — it's about communication, community engagement, policy advocacy, and using multiple channels to reach people. Family Medicine questions may ask about barriers to health promotion and how to overcome them.
| Prevention Strategy | Details |
|---|---|
| HBIG (passive immunisation) | For babies of carrier mothers, needle-stick injuries; 2 doses IM at 0 and 1 month; first dose within 24h; ~75% efficacy |
| HBV vaccine (active immunisation) | Recombinant HBsAg subunit vaccine; 3 doses IM at 0, 1, 6 months; ~95% seroconversion |
| Vertical transmission prevention | HBIG + HBV vaccine for neonate (~95% efficacy); nucleos(t)ide analogue for mother if HBV DNA > 2×10⁵ IU/mL (start last trimester, stop 3 months post-delivery) |
| Behavioural | Avoid sharing razors/toothbrushes/needles; barrier contraception; don't donate blood/organs |
| Monitoring for HCC | USG + AFP every 6 months in at-risk groups (Asian male > 40, female > 50) |
Exam Intelligence
| Year | Question | Topic | Key Point |
|---|---|---|---|
| 2016 SAQ Q11 | WHO FCTC / MPOWER | Tobacco control as primary prevention; plain packaging requirements [3] | |
| 2020 SAQ Q10 | STD screening | STD prevention = condom use; links to HBV/HCV screening at STD visits [12] | |
| 2021 MCQ Q88 | Colonoscopy for family history CRC | Secondary prevention (not primary) [3] | |
| 2023 MCQ Q94 | Lead workers: blood lead monitoring | Secondary prevention (monitoring = early detection) [4] | |
| 2023 MCQ Q78 | Malaria prevention for traveller | Antimalarial prophylaxis before/during/after travel [4] |
| Trap | Correct Thinking |
|---|---|
| Confusing primary and secondary prevention | Primary = preventing disease onset; Secondary = detecting existing subclinical disease early |
| Thinking PSA is "recommended against" | It is controversial/uncertain, not in the "recommend against" list |
| Assuming vaccination eliminates HBV burden | Vaccination only prevents new infections; the existing pool of chronically infected adults remains |
| Calling any test a "screening test" | Must meet Wilson-Jungner criteria to be valid population screening |
| Confusing awareness with screening | For mental health conditions, the lecture says awareness, not screening |
- "Name the levels of prevention": List all four (Primary, Secondary, Tertiary, Quaternary) with one-line definitions.
- "State the Wilson-Jungner criteria": List all 5 condensed points (or full 10 if asked). The 5-point version from this lecture is sufficient for FM questions.
- "What is quaternary prevention?": "Action to identify patients at risk of over-medicalisation and protect them from unnecessary medical interventions" — must include the concept of harm from medicine itself.
Q1 (MCQ-style): A 55-year-old asymptomatic woman asks her GP about ovarian cancer screening. What should the GP advise?
- Answer: Screening with ultrasound or CA-125 is recommended against for ovarian cancer in asymptomatic women. [1]
Q2 (SAQ-style): Define the four levels of prevention and give one example of each in the context of cardiovascular disease.
- Primary: Smoking cessation advice to prevent atherosclerosis.
- Secondary: BP measurement every 2 years for early detection of hypertension.
- Tertiary: Cardiac rehabilitation post-MI to prevent further events.
- Quaternary: Avoiding stress ECG in low-risk asymptomatic individuals to prevent overdiagnosis.
Q3 (SAQ-style): List five Wilson-Jungner criteria for a valid screening programme.
- See 5-point table above.
Q4 (MCQ-style): In Hong Kong, what percentage of HBV-infected individuals have been diagnosed?
- Answer: 22% [1]
Q5 (SAQ-style): Explain why newborn HBV vaccination alone is insufficient to eliminate hepatitis B.
- Answer: Vaccination prevents new chronic infections but does not treat or identify the millions of adults already chronically infected before universal vaccination was introduced. Elimination requires both vaccination AND active screening with linkage to treatment.
High Yield Summary
Levels of Prevention: Primary (prevent disease), Secondary (screen/early detection), Tertiary (prevent complications), Quaternary (prevent over-medicalisation). Every GP consultation has preventive potential (Stott-Davis model).
Wilson-Jungner Criteria (5-point version): Long pre-clinical phase + prevalent disease; Treatment improves outcome; Test is sensitive; Test is acceptable; Cost-effective.
Recommended Screening: Cervical smear (~90%), Mammography 50-70 (~25% mortality reduction), CRC via FIT (70-90%) or colonoscopy (~99%), BP q2y, DM q3y from age 30, Cholesterol, BMI/waist.
Controversial: BSE, HCC (AFP/USS), NPC (EBV), PSA, LDCT lung.
Recommend Against: Static/stress ECG, urinalysis, ovarian CA-125/USS, endometrial sampler, testicular, skin cancer screening.
Mental Health: Awareness, NOT population screening.
HBV as Health Promotion Model: Only 22% diagnosed in HK. Universal 5-test screening is cost-effective. Shared care with primary care is cost-saving. Cross-society engagement (policy, media, community) needed.
Quaternary Prevention (Marc Jamoulle): Protect patients from harm of over-medicalisation. Distinctly FM concept.
Active Recall - Health Promotion and Disease Prevention in Primary Care
[1] Lecture slides: GC 018. Health promotion and disease prevention in primary care.pdf [2] Lecture slides: #1. GCBC_FM Introductory Seminar_2025-2026_AN23012026.pdf (p13) [3] Past papers: 2021 Fourth Summative Assessment MCQ.pdf (Q88); 2016 Fourth Summative SAQ.pdf (Q11) [4] Past papers: 2023 Fourth Summative MCQ.pdf (Q94, Q78) [5] Senior notes: Adrian Lui Pediatrics Notes.pdf (p17, ICHDP/CCDS) [6] Senior notes: MBBS Final MB (Surgery) (Felix PY Lai).pdf (p709, p848 — Wilson-Jungner criteria) [7] Senior notes: MBBS Final MB (Surgery) (Felix PY Lai).pdf (p848 — PSA screening ERSPC/PLCO) [8] Senior notes: Ryan Ho Endocrine.pdf (p127 — Primary prevention of CVD, HK Consensus 2016) [9] Senior notes: Maksim Medicine Notes.pdf (p54 — CRC screening in HK) [10] Senior notes: Maksim Medicine Notes.pdf (p143 — Management of chronic HBV, HCC surveillance) [11] Senior notes: Ryan Ho GI.pdf (p231 — Prevention of HBV infection, HBIG, vaccine, vertical transmission) [12] Past papers: 2020 Fourth Summative SAQ.pdf (Q10 — STD prevention)
GC017 Common Mental Health Problems In Primary Care
Common mental health problems in primary care are frequently encountered psychiatric conditions—principally depression, anxiety disorders, and stress-related disorders—that are initially identified and managed by general practitioners in the community setting.
GC019 The Family In Family Medicine
The family in family medicine refers to the recognition of the family as the fundamental unit of care, where family dynamics, structure, life cycle stages, and interpersonal relationships are assessed and integrated into patient management to optimize health outcomes.