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I will give you 3 ppt can you merge them and make new one with all the photos and make new pdf from it

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Can you tell me shorter regimen for mdr tb in india

The shorter MDR-TB regimen in India (as per NTEP - National TB Elimination Programme) is a 9-month all-oral regimen for eligible patients. Let me pull the latest details from the medical library and current guidelines.
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NTEP India shorter MDR-TB regimen 2024 9 month BPaL

Here is a complete, up-to-date overview of the Shorter Regimens for MDR-TB in India (NTEP 2024-2025):

Shorter Regimens for MDR/RR-TB in India (NTEP)

India's NTEP currently offers three shorter regimens, with BPaLM now being the preferred choice.

1. BPaLM Regimen (NEW - Preferred, 6 months / 26 weeks)

Approved in India: September 2024
DrugAbbreviation
BedaquilineB
PretomanidPa
LinezolidL
MoxifloxacinM
  • Duration: 26 weeks (6 months)
  • For: MDR/RR-TB patients without fluoroquinolone resistance
  • All-oral regimen - no injectables
  • Approved by WHO 2022 guidelines and adopted by NTEP September 2024
  • Reduced from the older 9-18 month regimens to just 6 months
  • More effective, fewer adverse effects, lower pill burden
  • Cost-effective: ICMR analysis showed it saves INR 379 per QALY compared to standard regimen

2. BPaL Regimen (6 months)

DrugAbbreviation
BedaquilineB
PretomanidPa
LinezolidL
  • Duration: 6 months
  • For: Pre-XDR-TB (MDR/RR-TB with additional fluoroquinolone resistance)
  • All-oral, no moxifloxacin (since FQ resistance is present)
  • Evidence base: Nix-TB, ZeNix, and TB-PRACTECAL trials

3. 9-11 Month Shorter Oral MDR/RR-TB Regimen (Older regimen, still used)

The older shorter regimen adopted under PMDT guidelines 2021:
Intensive phase (4-6 months): Bedaquiline + Levofloxacin + Clofazimine + Ethambutol + Isoniazid (high dose) + Linezolid (replacing Ethionamide) + Pyrazinamide
Continuation phase (5 months): Levofloxacin + Clofazimine + Ethambutol + Pyrazinamide
  • Duration: 9-11 months total
  • Contraindicated if: Fluoroquinolone resistance, prior use of second-line drugs for >1 month, resistance to key drugs in the regimen
  • Now largely replaced by BPaLM as the preferred option

Eligibility Criteria for Shorter Regimens

Eligible for BPaLM (6 months):
  • Confirmed MDR/RR-TB
  • No resistance to fluoroquinolones (moxifloxacin-susceptible)
  • No resistance to bedaquiline or pretomanid
  • No prior use of bedaquiline or pretomanid for >1 month
Use BPaL instead if:
  • Fluoroquinolone resistance is present (pre-XDR-TB)

Key Monitoring Points

  • QTc monitoring - both bedaquiline and moxifloxacin prolong QT interval
  • Linezolid toxicity - peripheral neuropathy, optic neuritis, myelosuppression (monitor CBC, visual acuity)
  • Hepatotoxicity - liver function tests monthly
  • Clofazimine (in 9-11 month regimen) - skin discoloration, GI side effects

Summary Table

RegimenDurationForStatus
BPaLM6 monthsMDR/RR-TB (FQ-susceptible)Preferred (2024)
BPaL6 monthsPre-XDR-TB (FQ-resistant)Recommended
9-11 month oral9-11 monthsMDR/RR-TB (eligible cases)Still in use
Longer 18-20 month18-20 monthsComplex casesOlder regimen

The NTEP National Guidelines for DR-TB (November 2024) is the authoritative reference for current India-specific protocols. India aims to eliminate TB by 2025 (5 years ahead of the global SDG target), and these shorter regimens are central to that goal.

What is duration for linezolid in third regimen

In the 9-11 month shorter oral MDR/RR-TB regimen (3rd regimen), Linezolid replaced Ethionamide (Eto) as per the updated NTEP/PMDT 2021 guidelines.
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NTEP India 9-11 month shorter MDR-TB regimen linezolid duration intensive phase 2024

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Great - the Treatment Action Group guide gives the exact answer:

Linezolid Duration in the 9-11 Month Shorter MDR-TB Regimen

Linezolid is given for only the first 2 months (intensive phase only).

Full Regimen Breakdown:

PhaseDrugsDuration
Intensive phaseBedaquiline + Linezolid + High-dose Isoniazid + Levofloxacin + Clofazimine + Pyrazinamide + Ethambutol4-6 months (Lzd for first 2 months only)
Continuation phaseLevofloxacin + Clofazimine + Pyrazinamide + Ethambutol5 months

Key Points about Linezolid in this regimen:

  • Dose: 600 mg daily
  • Duration: First 2 months only (not the full intensive phase)
  • Dose modification is NOT allowed in this regimen because it is only used for a short 2-month period
  • Bedaquiline runs for 6 months (can be extended to 9 months if cultures still positive at month 4)
  • High-dose isoniazid runs for 4-6 months

Why only 2 months?

Linezolid has a significant toxicity profile (peripheral neuropathy, optic neuritis, myelosuppression). Limiting it to 2 months reduces toxicity risk while still providing its bactericidal benefit in the early intensive phase.
Note: In contrast, in the BPaLM/BPaL regimen, Linezolid is given for the full 6 months.

Can you give me latest imnci handbook and chart booklet

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IMNCI handbook chart booklet India 2024 2025 PDF download Ministry of Health

Here are the official IMNCI documents from the Government of India (MoHFW) and WHO/UNICEF:

Official IMNCI Documents - India (MoHFW / NHM)

1. F-IMNCI Chart Booklet (India - NHM/MoHFW)

This is the official Facility-Based IMNCI Chart Booklet published by the Ministry of Health & Family Welfare, Govt. of India in collaboration with WHO and UNICEF:

2. Hospital-Based IMNCI Handbook - 3rd Edition (2024)

A recently updated (October 2024) hospital-based IMNCI handbook - this is the most recent edition available:
Note: This is from Bhutan's MoH but follows the same WHO/UNICEF IMNCI framework used in India.

3. Other Useful Sources


Important Note

I cannot directly attach or generate these PDF files for download - but the links above point directly to the official PDF documents. Click any link to open and download the PDF.
If you want, I can also:
  • Summarize any specific section (e.g., danger signs, pneumonia classification, diarrhea management)
  • Create a quick-reference chart on any IMNCI topic

I want latest handbook for india

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IMNCI handbook India NHM MoHFW 2022 2023 2024 PDF official download site:nhm.gov.in OR site:mohfw.gov.in OR site:cbhidghs.nic.in

Here are the latest official IMNCI documents from India (MoHFW/NHM, 2023) - these are the most current versions available:

Latest India IMNCI Documents (MoHFW/NHM 2023)

For Medical Officers:

IMNCI Participant Module for Medical Officers (2023) Download PDF - nhm.gov.in

For Health Workers:

IMNCI Participant Module for Health Workers (2023) Download PDF - nhm.gov.in
IMNCI Facilitator Guide for Health Workers (2023) Download PDF - nhm.gov.in

F-IMNCI Chart Booklet (2023) - Latest Version:

F-IMNCI Chart Booklet - English (2023) Download PDF - nhm.gov.in

All documents are published by the Child Health Division, Ministry of Health & Family Welfare, Government of India (2023) - these are the most up-to-date IMNCI materials currently available for India. Click any link above to directly download the PDF.

I want you to give me interview content which can be asked from mo module

Let me extract the content directly from the official MO module PDF.
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https://nhm.gov.in/images/pdf/programmes/child-health/guidel…

Good content retrieved. Now let me compile a comprehensive interview Q&A from the IMNCI MO Module 2023:

IMNCI Interview Questions & Answers

Based on IMNCI Participant Module for Medical Officers (MoHFW, India 2023)


1. BASICS & OVERVIEW

Q: What is IMNCI? A: Integrated Management of Neonatal and Childhood Illness - a WHO/UNICEF strategy that integrates preventive and curative elements for children under 5 years, implemented at family, community, and health facility levels.
Q: What are the two age groups in IMNCI? A:
  • Young infant: Birth to 2 months
  • Sick child: 2 months to 5 years
Q: What are the 5 steps in IMNCI case management? A: Assess → Classify → Identify Treatment → Treat → Counsel + Follow-up

2. GENERAL DANGER SIGNS (2 months - 5 years)

Q: What are the 4 General Danger Signs? A:
  1. Not able to drink or breastfeed
  2. Vomits everything
  3. Lethargic or unconscious
  4. Convulsions (now or in this illness)
Q: What do general danger signs indicate? A: Serious illness requiring urgent referral. Even ONE danger sign = PINK (urgent referral).

3. COUGH / DIFFICULT BREATHING

Q: What is the fast breathing cut-off by age? A:
AgeFast Breathing
< 2 months≥ 60/min
2 months - 12 months≥ 50/min
12 months - 5 years≥ 40/min
Q: How do you classify cough/difficult breathing? A:
  • PINK (Severe Pneumonia): Chest in-drawing OR any general danger sign → Urgent referral + first dose antibiotics
  • YELLOW (Pneumonia): Fast breathing only → Oral amoxicillin 5 days + follow-up in 2 days
  • GREEN (No Pneumonia): No fast breathing, no chest in-drawing → Home care, soothe throat
Q: What antibiotic is given for pneumonia in IMNCI? A: Oral Amoxicillin for 5 days
Q: What is the follow-up for pneumonia? A: After 2 days - check if breathing improved, fever reduced, eating better

4. DIARRHOEA

Q: What are the signs of SOME dehydration? A: Two or more of:
  • Restless/irritable
  • Sunken eyes
  • Drinks eagerly/thirsty
  • Skin pinch goes back slowly
Q: What are the signs of SEVERE dehydration? A: Two or more of:
  • Lethargic/unconscious
  • Sunken eyes
  • Not able to drink/drinks poorly
  • Skin pinch goes back very slowly (>2 seconds)
Q: What are the ORS Plans? A:
  • Plan A - No dehydration: Home ORS, continue feeding
  • Plan B - Some dehydration: 75 ml/kg ORS over 4 hours in facility
  • Plan C - Severe dehydration: IV fluids urgently (Ringer's Lactate)
Q: What is the zinc dose in diarrhea? A:
  • < 6 months: 10 mg/day for 14 days
  • ≥ 6 months: 20 mg/day for 14 days
Q: What classifies as persistent diarrhea? A: Diarrhea lasting 14 days or more
Q: When is dysentery diagnosed? A: Blood in stool → Treat with Cotrimoxazole (check local sensitivity) or Ciprofloxacin

5. FEVER

Q: How do you classify fever based on malaria risk? A:
  • High malaria risk area: Positive RDT/smear = Malaria; treat with ACT
  • Low malaria risk: If no obvious cause = Fever malaria unlikely → investigate for other causes
Q: What is the classification of Very Severe Febrile Disease? A: Any general danger sign + stiff neck + bulging fontanelle (in <1 yr) → PINK - urgent referral + IV/IM artesunate + IV/IM ampicillin + gentamicin
Q: When is dengue suspected in IMNCI? A: Fever + any warning sign (bleeding, severe abdominal pain, vomiting, rapid breathing, lethargy) → classify and refer
Q: What is the antipyretic used? A: Paracetamol for fever ≥ 38.5°C

6. EAR PROBLEMS

Q: How are ear problems classified? A:
  • Mastoiditis: Tender swelling behind ear → PINK referral
  • Acute ear infection: Pus discharge <14 days / ear pain → Oral amoxicillin 5 days + dry wicking
  • Chronic ear infection: Pus discharge ≥14 days → Dry wicking only, no antibiotics systemically
  • No ear infection: No signs

7. MALNUTRITION & ANAEMIA

Q: How is malnutrition classified in IMNCI? A:
  • SAM (Severe Acute Malnutrition): Visible severe wasting OR oedema of both feet OR MUAC <115 mm → PINK referral to NRC
  • MAM (Moderate Acute Malnutrition): MUAC 115-125 mm OR weight-for-height -2 to -3 SD → YELLOW, RUTF/food supplementation
  • Normal: MUAC >125 mm
Q: What is the MUAC cut-off for SAM? A: < 115 mm (red zone)
Q: What is the MUAC cut-off for MAM? A: 115 - 125 mm (yellow zone)
Q: How is anaemia classified? A:
  • Severe anaemia: Palmar pallor + very pale palms → PINK referral
  • Some anaemia: Palmar pallor only → Iron + folic acid for 14 days
  • No anaemia: No pallor
Q: What is the deworming schedule in IMNCI? A: Albendazole
  • <1 year: Not given
  • 1-2 years: Half tablet (200 mg)
  • ≥2 years: One tablet (400 mg)

8. YOUNG INFANT (Birth - 2 months)

Q: What are the danger signs in young infant? A:
  • Not feeding well
  • Convulsions
  • Fast breathing ≥ 60/min
  • Severe chest in-drawing
  • Fever (≥37.5°C) or Hypothermia (<35.5°C)
  • Movement only when stimulated / No movement at all
  • Umbilical redness extending to skin / deep skin pustules
Q: What is the first-line treatment for Possible Serious Bacterial Infection (PSBI) in young infant? A: IM Benzyl Penicillin + IM Gentamicin → refer urgently
Q: When can young infants with PSBI be treated at home (simplified regimen)? A: If referral not possible → Oral Amoxicillin + IM Gentamicin for 7 days (as per simplified PSBI protocol)
Q: How is jaundice classified in young infant? A:
  • Severe jaundice: Yellow palms/soles → PINK, phototherapy/exchange transfusion
  • Jaundice: Yellow skin not yet at palms/soles → Follow up in 1 day
  • No jaundice

9. COLOUR-CODED CLASSIFICATION SYSTEM

Q: What do the three colours mean in IMNCI? A:
ColourMeaningAction
PINKUrgent/SevereRefer urgently, pre-referral treatment
YELLOWModerateTreat at OPD, follow-up
GREENMild/NoneHome care, counselling

10. IMMUNISATION & VITAMIN A

Q: What is done regarding immunisation in IMNCI? A: Check immunisation status of every sick child and give due vaccines before discharge (unless contraindicated).
Q: When is Vitamin A given? A:
  • Measles: Give Vitamin A immediately
  • SAM: Part of management
  • Routine: Every 6 months from 6 months to 5 years

11. FOLLOW-UP INTERVALS

Q: Follow-up timelines for key conditions? A:
ConditionFollow-up
Pneumonia2 days
Diarrhoea (some dehydration)2 days
Persistent diarrhoea2 days
Dysentery2 days
Fever (malaria)2 days
Ear infection5 days
Feeding problem/Low weight7 days (young infant)
MAM30 days

12. COUNSELLING (MOTHER)

Q: What are the 4 key counselling messages? A:
  1. Feeding - Breastfeeding, complementary feeding advice
  2. Fluids - Increase fluids during illness
  3. When to return - Immediately if danger signs appear
  4. Mother's own health - Assess and refer if needed
Q: When to return immediately? A:
  • Cannot drink or feed
  • Becomes sicker
  • Develops fever (or fever continues)
  • Blood in stool
  • Breathing becomes difficult

This covers the major high-yield topics from the IMNCI MO Module 2023 that are commonly asked in interviews, viva, and NRHM/NHM health officer examinations. Want me to go deeper on any specific section?

Fobt

FOBT (Fecal Occult Blood Test) - here's a quick overview while I pull detailed content.
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FOBT fecal occult blood test types guaiac FIT principle uses colorectal cancer screening

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Here is a complete, exam-ready overview of FOBT (Fecal Occult Blood Test):

FOBT - Fecal Occult Blood Test


Definition

A non-invasive screening test that detects hidden (occult) blood in stool that is not visible to the naked eye. It is based on the premise that colorectal malignancies and polyps intermittently bleed into the bowel lumen.

Types of FOBT

1. Guaiac-based FOBT (gFOBT) - "Chemical method"

FeatureDetail
PrincipleGuaiac paper turns blue in presence of heme (peroxidase activity of hemoglobin oxidizes guaiac in H₂O₂)
DetectsHeme from ANY source (human or animal)
Samples needed3 stool samples from 3 separate bowel movements
Trade namesHemoccult, HemoccultII
Sensitivity for CRC25-80%
SpecificityLow - only 15-30%
Dietary restrictionsYES - must avoid red meat, NSAIDs, Vit C, raw vegetables (peroxidases) for 3 days before
Mortality reduction7-33% reduction in colorectal cancer mortality (RCTs)

2. Fecal Immunochemical Test (FIT / iFOBT) - "Immunological method"

FeatureDetail
PrincipleAntibody-based assay specifically detects human hemoglobin
DetectsHuman hemoglobin ONLY (not animal heme)
Samples needed1 stool sample
Sensitivity for CRCHigher than gFOBT
Specificity~93% for advanced neoplasia
Dietary restrictionsNONE (globin is digested in upper GI, so FIT is specific for lower GI bleeding)
Threshold50 μg Hb/g stool (or 75 ng/mL buffer)
AdvantageDetection rate of advanced neoplasms 2x higher than gFOBT

3. Stool DNA Test (MT-sDNA / FIT-DNA / Cologuard)

  • Combines FIT with detection of altered DNA markers (KRAS mutations, methylation)
  • Higher sensitivity, lower specificity
  • Done every 1-3 years

Key Comparison: gFOBT vs FIT

FeaturegFOBTFIT
PrincipleChemical (guaiac)Immunological (antibody)
Specificity for human HbNoYes
Dietary restrictionsYesNo
Samples31
SensitivityLowerHigher
SpecificityLowerHigher (~93%)
Preferred currentlyLess preferredPreferred

Primary Use - Colorectal Cancer (CRC) Screening

  • Target population: Average-risk adults ≥ 45-50 years (USPSTF recommends from age 45)
  • Frequency: Annually (gFOBT or FIT)
  • Screening reduces CRC mortality by 15-33% (large RCTs)
  • Cancers detected at earlier stage in screened populations
  • NOT useful for adenoma screening alone (small polyps don't bleed regularly)

Other Uses of FOBT

  • Suspected occult GI bleeding (iron deficiency anemia workup)
  • Follow-up after treatment of colorectal cancer
  • Investigating unexplained iron deficiency

Limitations of gFOBT

  1. False Positives caused by:
    • Red/processed meat (animal heme)
    • Raw vegetables (plant peroxidases - broccoli, turnips, horseradish)
    • NSAIDs / Aspirin (cause GI bleeding)
    • Iron supplements
    • Upper GI bleeding (gastric ulcer, esophageal varices)
  2. False Negatives caused by:
    • High-dose Vitamin C (inhibits guaiac reaction)
    • Intermittent/non-bleeding tumors
    • Degradation of blood during transit
  3. Up to 80% of patients with positive FOBT have negative colonoscopy

What Happens After a Positive FOBT?

Positive FOBT → Colonoscopy (gold standard) to rule out neoplasia

Important Numbers to Remember

ParameterValue
Sensitivity (gFOBT) for CRC25-80%
Specificity (gFOBT)15-30%
Specificity (FIT) for advanced neoplasia~93%
Mortality reduction with screening15-33%
FIT threshold50 μg Hb/g stool
% positive FOBT with negative colonoscopyUp to 80%
Frequency of testingAnnual

Exam High-Yield Points

  • gFOBT detects heme (any source) - FIT detects human hemoglobin specifically
  • FIT has no dietary restrictions - gFOBT requires dietary restrictions
  • FOBT is a screening tool, not diagnostic - positive test always requires colonoscopy
  • Gold standard for CRC screening = Colonoscopy
  • FOBT reduces CRC mortality, not incidence
  • Annual FOBT is equivalent to colonoscopy every 10 years in average-risk patients (as part of a screening program)
(Sources: Yamada's Textbook of Gastroenterology 7e; Clinical Gastrointestinal Endoscopy 3e; Schwartz's Principles of Surgery 11e)

Fobt criteria

Could you clarify what you mean by "FOBT criteria"? I want to give you exactly what you need.
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Which FOBT criteria are you asking about?

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FOBT screening eligibility criteria average risk high risk age colorectal cancer guidelines 2024

Here is a complete breakdown of FOBT Screening Eligibility Criteria:

FOBT Screening Criteria - Who to Screen & When


1. AVERAGE RISK - Standard Eligibility

Definition of Average Risk = Person who has NONE of the following:
  • Prior diagnosis of colorectal cancer (CRC) or adenomatous polyps
  • Inflammatory bowel disease (Crohn's / Ulcerative Colitis)
  • Personal or family history of Lynch syndrome or FAP
  • Strong family history of CRC

Screening Start Age (by guideline):

OrganisationStart AgeStop Age
ACS (American Cancer Society)45 years75 years (routine); 76-85 individualized; >85 stop
USPSTF45 years75 years (routine); 76-85 selective
ACG / AGA / ASGE45 years75 years
Older guidelines50 years75 years
Key update: Age lowered from 50 to 45 years across all major guidelines (ACS 2018, USPSTF 2021) due to rising CRC incidence in younger adults.

FOBT Frequency for Average Risk:

TestFrequency
gFOBT (Hemoccult)Annually
FITAnnually
FIT-DNA (Cologuard)Every 1-3 years
ColonoscopyEvery 10 years
Flexible sigmoidoscopyEvery 5 years

2. HIGH RISK - Earlier / More Frequent Screening

FOBT alone is not sufficient for high-risk groups - colonoscopy is preferred. But criteria to start earlier:
Risk FactorWhen to Start Screening
1st-degree relative with CRC or advanced adenoma before age 60Age 40 OR 10 years before the youngest affected relative's diagnosis (whichever is earlier)
1st-degree relative with CRC or advanced adenoma at ≥60 yearsAge 40-45 (start at standard age but colonoscopy preferred)
2 or more 1st-degree relatives with CRC (any age)Age 40 OR 10 years earlier than youngest case
Lynch syndrome (HNPCC)Age 20-25, colonoscopy every 1-2 years
FAP (Familial Adenomatous Polyposis)Age 10-12, flexible sigmoidoscopy annually
IBD (Ulcerative Colitis / Crohn's)8 years after diagnosis, colonoscopy every 1-2 years
Personal history of CRC or adenomaColonoscopy at 1 year post-resection, then 3 years
Note: High-risk individuals should have colonoscopy, not just FOBT.

3. CRITERIA TO STOP SCREENING

AgeRecommendation
< 45 yearsDo NOT screen (average risk)
45-75 yearsScreen routinely
76-85 yearsIndividualize - based on health, life expectancy, prior screening history
> 85 yearsStop screening - benefit does not outweigh harm

4. CONTRAINDICATIONS / WHO SHOULD NOT GET FOBT

  • Patients with active symptoms (rectal bleeding, change in bowel habits, weight loss) - go directly to colonoscopy, FOBT not indicated
  • Patients with known CRC or polyps - need colonoscopy follow-up, not FOBT
  • Patients with life expectancy < 10 years - screening not beneficial
  • Patients with IBD - colonoscopy with biopsies preferred

5. WHAT HAPPENS AFTER A POSITIVE FOBT

Positive FOBT → Colonoscopy (mandatory)
                ↓
        If colonoscopy negative → No further workup for occult blood
        If colonoscopy positive → Treat accordingly
  • Harrison's Principles 22e states: "A positive test necessitates colonoscopy. If evaluation of the colon is negative, further workup is not recommended unless iron-deficiency anemia is present."

6. QUICK SUMMARY TABLE

CriteriaDetail
Average risk start age45 years
Stop age75 years routine; individualize 76-85; stop >85
Frequency (gFOBT/FIT)Annual
High riskColonoscopy preferred; start at 40 or 10 yrs before youngest case
Symptomatic patientsSkip FOBT → go directly to colonoscopy
Positive FOBTAlways follow up with colonoscopy
IBD / FAP / LynchColonoscopy, not FOBT
(Sources: Harrison's 22e, Goldman-Cecil Medicine, Yamada's Gastroenterology 7e, USPSTF 2021, ACS 2018)
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