У нас вы можете посмотреть бесплатно Clinical Pharmacology, USMLE Step 1 - Full Vignette with Extended Explanations или скачать в максимальном доступном качестве, видео которое было загружено на ютуб. Для загрузки выберите вариант из формы ниже:
Если кнопки скачивания не
загрузились
НАЖМИТЕ ЗДЕСЬ или обновите страницу
Если возникают проблемы со скачиванием видео, пожалуйста напишите в поддержку по адресу внизу
страницы.
Спасибо за использование сервиса ClipSaver.ru
A pregnant woman with a history of pituitary adenoma, glomerulosclerosis, and homocystinuria seeks advice about potential antihypertensive use. She researches drug safety in pregnancy and asks about how to interpret data from a recent cohort study on possible risks to her baby. How should clinicians approach risk communication in this prenatal counseling scenario, and what detail is most important for her understanding? VIDEO INFO Category: Clinical Pharmacology, USMLE Step 1 Difficulty: Easy - Basic level - Suitable for medical students Question Type: Epidemiology Case Type: Pregnant Patient Explore more ways to learn on this and other topics by going to https://endlessmedical.academy/auth?h... QUESTION A 47-year-old woman at 11 weeks of pregnancy (in vitro fertilization) comes for counseling about whether to start an antihypertensive. She has a history of pituitary adenoma resected 6 years ago, focal segmental glomerulosclerosis in remission, and classic homocystinuria treated with pyridoxine. Medications include prenatal vitamin with folic acid, low-dose aspirin recommended by her obstetrician, and pyridoxine; she does not drink alcohol or use drugs and is celibate outside her marriage.... OPTIONS A. Use absolute risk with baseline risk and the absolute risk difference with a 95% CI, drawn from human cohort data in the FDA PLLR narrative. B. Report an odds ratio from a case-control study and interpret it as the patient s personal risk, without any baseline incidence or absolute numbers. C. Provide only a hazard ratio from a time-to-event analysis, omitting absolute risks, baseline event rates, and any confidence intervals. D. Summarize risk by the legacy FDA pregnancy letter category (for example, Category C), without narrative context or human data. CORRECT ANSWER A. Use absolute risk with baseline risk and the absolute risk difference with a 95% CI, drawn from human cohort data in the FDA PLLR narrative. EXPLANATION This patient at 11 weeks gestation asks for a number that makes sense when weighing medication risk under the FDA s Pregnancy and Lactation Labeling Rule (PLLR), which replaced the legacy A/B/C/D/X letters. For shared decision making, the clearest and most decision-useful summary is the absolute risk, presented alongside the baseline risk and the absolute risk difference with a 95% confidence interval, ideally from human cohort data. Absolute numbers answer the patient s core question, How many out of 100 like me might have a problem? This also aligns with the PLLR s narrative sections that require a human data-forward risk summary, clinical considerations, and data details. Relative measures alone can mislead in pregnancy counseling. An odds ratio from a case-control study does not equal personal risk and is best reserved for etiologic inference when incidence cannot be directly measured. A lone hazard ratio from a time-to-event analysis is likewise a relative measure lacking baseline risk and precision unless paired with absolute risks and confidence intervals. The superseded letter categories provide neither context nor quantification and are specifically discouraged by the PLLR framework.... Further reading: Links to sources are provided for optional further reading only. The questions and explanations are independently authored and do not reproduce or adapt any specific third-party text or content. --------------------------------------------------- Our cases and questions come from the https://EndlessMedical.Academy quiz engine - multi-model platform. Each question and explanation is forged by consensus between multiple top AI models (i.e. Open AI GPT, Claude, Grok, etc.), with automated web searches for the latest research and verified references. Calculations (e.g. eGFR, dosages) are checked via code execution to eliminate errors, and all references are reviewed by several AIs to minimize hallucinations. Important note: This material is entirely AI-generated and has not been verified by human experts; despite stringent consensus checks, perfect accuracy cannot be guaranteed. Exercise caution - always corroborate the content with trusted references or qualified professionals, and never apply information from this content to patient care or clinical decisions without independent verification. Clinicians already rely on AI and online tools - myself included - so treat this content as an additional focused aid, not a replacement for proper medical education. Visit https://endlessmedical.academy for more AI-supported resources and cases. This material can not be treated as medical advice. May contain errors. ---------------------------------------------------