Outpatient Cellulitis: Purulent Versus Nonpurulent Skin Infection
How the purulent versus nonpurulent split sorts skin infections, why it guides antibiotic choice, and the red flags that mean urgent care.
Health & Evidence Library
Guides to infection, antimicrobial reasoning, immune response, screening, cancer evidence, and treatment-related questions.
38 guides · Page 1 of 1
How the purulent versus nonpurulent split sorts skin infections, why it guides antibiotic choice, and the red flags that mean urgent care.
Most sinus infections are viral and clear without antibiotics. Learn the viral vs bacterial clues, the 10-day rule, and what actually relieves symptoms.
Most sore throats are viral. The Centor (McIsaac) score estimates strep odds and when a throat swab or antibiotics are actually worth it.
Tumor mutational burden counts selected mutations per megabase. It can inform immunotherapy choices, but platform and tumor context matter.
Learn how laboratories measure MIC, apply breakpoints, and report susceptible, intermediate, or resistant results, plus the limits of an antibiogram.
A vaccine correlate of protection links an immune marker with reduced risk. Learn the evidence needed, how correlates speed decisions, and their limits.
A tumor-agnostic approval targets a molecular feature across specified cancers, not every tumor. Learn how basket trials, testing, labels, and uncertainty fit.
Vaccine efficacy measures relative risk reduction in a trial; effectiveness estimates performance in practice. Learn the designs, endpoints, biases, and limits.
U=U means sustained HIV viral suppression prevents sexual transmission. Learn what the studies showed, what undetectable means, and the message's boundaries.
Trials support shorter antibiotic courses for selected infections, but the right duration depends on diagnosis, source control, response, and host risk.
A positive test can mean very different things in low-risk and high-risk groups. Learn how prevalence, pretest probability, and false positives shape PPV.
Sepsis-3 centers life-threatening organ dysfunction, not infection alone. Learn how SOFA, qSOFA, SIRS, and septic shock fit current evidence.
How antigen and molecular tests detect viruses, why results can disagree, and how timing, symptoms, specimens, and purpose change interpretation.
How two-tier Lyme serology works, why antibody tests miss early infection and stay positive after treatment, and why testing low-risk patients misleads.
FDA and CDC say a positive antibody test records prior contact with a pathogen, not immunity. Here is how it differs from a validated correlate of protection.
Herd immunity has no single threshold. The 1 minus 1/R0 formula rises with transmissibility, and its assumptions rarely hold in the real world.
Recurrent C. diff now has two FDA-approved microbiome products. Here is what Rebyota and Vowst do, and how to read their trial results honestly.
How preformed antibodies like palivizumab and nirsevimab give immediate, temporary RSV protection, and how that differs from a vaccine.
What multi-cancer early detection blood tests measure, why a randomized mortality trial is the real test, and the open overdiagnosis questions.
Why every colorectal and endometrial tumor is tested for mismatch repair loss to catch inherited Lynch syndrome, and how the specific gene guides surveillance.
A positive TB skin test or IGRA proves immune memory, not live disease. Here is why the test cannot tell latent from active, and how risk is judged.
Innate immunity reacts in hours with fixed receptors and no memory; adaptive immunity takes days but learns a specific pathogen and remembers it.
Why PrEP's roughly 99 percent figure depends on the drug being present in the body, and how trials from iPrEx to lenacapavir proved it.
Why a raw VAERS report count cannot prove a vaccine caused harm, and how controlled systems like the Vaccine Safety Datalink actually measure risk.
How USPSTF set the age and pack-year rules for low-dose CT lung screening by weighing lives saved against false positives and overdiagnosis.
Why the USPSTF lowered the colorectal screening start age to 45 and how it compares colonoscopy, FIT, and stool-DNA without naming one best test.
Why MSI-High and mismatch repair deficiency predict immunotherapy response, and how they became the first marker used to approve a drug across any solid tumor.
A plain-language guide to the three tools field epidemiologists use to read an outbreak, and the built-in blind spot in each.
How PD-1, PD-L1, and CTLA-4 blockade release the immune system's brakes, and an evidence-based look at why only some tumors respond.
How flu vaccine strains are picked months ahead, why antigenic drift causes mismatch, and how to read a low-effectiveness season.
How CAR T therapy reprograms a patient's own T cells against CD19 or BCMA, and why cytokine release syndrome and ICANS are mechanism-linked.
How the TNM system and AJCC prognostic stage groups turn tumor size, node spread, grade, and biomarkers into a survival estimate.
Why antibiotic resistance is a selection problem, how the CDC ranks the threats, and what controlled evidence says stewardship achieves.
A plain-language look at how the USPSTF turned limited trials and six simulation models into its 2024 Grade B call for mammography every two years from age 40.
BRCA testing is the end of a path, not a general screen. How a risk tool, counseling, and a result each answer a different question.
Why cancer screening trades earlier detection for overdiagnosis, and how mortality trials, not survival figures, reveal which programs truly help.
A positive C. difficile PCR can signal carriage rather than disease; smart test selection plus toxin confirmation curbs overdiagnosis.
A positive urine culture without symptoms is asymptomatic bacteriuria, not a UTI. Guidelines say leave it alone, apart from two exceptions.