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D R M A N I S H
RAJPUT
ht t ps://dr manishr ajput .com
Bookan appointment!
IN T R O D U C T IO N
Dr
. Manish Rajput is an I
nterventional
Radiologist & Team Lead, Team I
R
Jaipur
. They are the biggest team of
I
nterventional Radiologists. They are
trained from Tata Memorial Center
,
Mumbai, I
ndia. They have worked in so
many government and corporate
hospitals across the country.
Medical school (MBBS):2005-2011: -People’s
Medical College, Bhopal(MP)
DNB (Radio diagnosis):
- Apollo hospital,
Hyderabad(Telangana)
FVIR (PDCC):- Tata Memorial Centre,
Mumbai(Maharashtra)
Senior Resident: Hinduja Hospital Mumbai, SMS
Hospital Jaipur
Past Visiting Doctor:Leelavati Hospital Mumbai,
Breach Candy Hospital Mumbai, Wockhardt
Hospital Mumbai, Hinduja Hospital Mumbai
Ex Assitant Professor:JNU Medical College, Jaipur
Currently Working as Senior Consultant
Interventional Radiologist in various corporate
hospitals of Rajasthan based in Jaipur
HIS
EDUCATION
S T R E N G T H S
Ilead the biggest I
R team in the state.
Vast portfolio for I
R services.
All the team members are from Tata
Memorial Hospital, Mumbai.
Extensive experience in performing and
interpreting basic Radio-Diagnosis.
Gained experience in performing
I
nterventional Radiologic procedures.
Ipossess oratory skill by speaking at
numerous industry events.
Ability to teach complex concepts in a basic
manner
.
Varicose Veins Prostate Artery Embolization PRG
Biopsy and
fNAC
Angioplasty & Venoplasty PCN & DJ Stenting
O
U
R
S
E
R
V
I
C
E
S
+91 7729021111
dr.manish@infinityintervention.com
O-5-A, Adinath Marg, Near Surya
Hospital, C Scheme, Ashok Nagar,
Jaipur, Rajasthan 302001
C ON TA C T
US!

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MedicoseAcademics
23 slides291 views
Good Laboratory Practices (GLP) Ensuring Quality and Compliance.pptx by Dr. Smita Kumbhar, has 53 slides with 278 views.Good Laboratory Practices (GLP): Ensuring Quality and Compliance Good Laboratory Practices (GLP) is a set of principles intended to ensure the quality, integrity, and reliability of non-clinical laboratory studies that support research and regulatory submissions. These guidelines are critical in the pharmaceutical, biotechnological, chemical, and environmental sectors, ensuring that laboratory-generated data are reproducible, credible, and internationally accepted. GLP standards primarily apply to safety studies involving pharmaceuticals, pesticides, food additives, and industrial chemicals. Regulatory agencies, including the USFDA, EMA, and OECD, enforce GLP compliance to maintain scientific rigor and public safety. USFDA GLP Regulations The U.S. Food and Drug Administration (USFDA) established Good Laboratory Practice regulations under 21 CFR Part 58. These regulations outline responsibilities for study directors, testing facilities, and personnel to maintain quality and integrity in non-clinical laboratory studies. The regulations cover various aspects, including study conduct, reporting, and archiving, ensuring consistency and accuracy in laboratory research. Controlling the GLP Inspection Process Regulatory authorities conduct inspections to verify GLP compliance. Laboratories must prepare for inspections by: • Maintaining up-to-date documentation. • Conducting internal audits. • Ensuring personnel training and awareness. • Implementing corrective actions for non-compliance. Regulatory inspections typically assess laboratory infrastructure, personnel competence, study documentation, and adherence to protocols. Laboratories must demonstrate transparency and proactive quality control measures. Documentation in GLP Accurate and comprehensive documentation is crucial in GLP compliance. Key documentation elements include: • Study protocols • Standard operating procedures (SOPs) • Raw data records • Analytical reports • Audit reports • Equipment calibration records • Archiving and retention policies Proper documentation ensures traceability, accountability, and reliability in laboratory research. Audit in GLP Compliance Auditing is a critical component of GLP, ensuring adherence to established regulations and identifying areas for improvement. Audits can be internal (self-audit) or external (regulatory or third-party audits). Goals of Laboratory Quality Audit • Ensure compliance with GLP regulations. • Identify gaps and areas for improvement. • Validate data integrity and accuracy. • Enhance operational efficiency. • Prevent regulatory penalties and study disqualification. Audit Tools in GLP Laboratories use various audit tools to assess compliance, including: • Checklists and self-assessments • Internal quality audits • Electronic data tracking systems • Third-party inspections • Root cause analysis • Corrective and preventive action (CAPA) plans Future of GLP Regulations
Good Laboratory Practices (GLP) Ensuring Quality and Compliance.pptxGood Laboratory Practices (GLP) Ensuring Quality and Compliance.pptx
Good Laboratory Practices (GLP) Ensuring Quality and Compliance.pptx
Dr. Smita Kumbhar
53 slides278 views
Swasthya Samrakshana and Rog Prashamana by Ritushodhana by Ketan Mahajan, has 61 slides with 10 views.Swasthya Samrakshana and Rog Prashamana by Ritushodhana
Swasthya Samrakshana and Rog Prashamana by RitushodhanaSwasthya Samrakshana and Rog Prashamana by Ritushodhana
Swasthya Samrakshana and Rog Prashamana by Ritushodhana
Ketan Mahajan
61 slides10 views
Cardiac Amplifiers: A Deep Dive into Inotropes by Viresh Mahajani , has 71 slides with 142 views.Inotropic drugs are vital in managing acute heart failure and cardiogenic shock, directly influencing myocardial contractility. This presentation delves into their mechanisms, clinical applications, and nursing considerations. We'll explore how positive inotropes, like dobutamine and milrinone, enhance calcium influx, boosting cardiac output but also increasing myocardial oxygen demand. Conversely, we'll discuss the nuances of negative inotropes, such as beta-blockers, used in specific scenarios to reduce workload. A critical focus will be on the pharmacokinetics and pharmacodynamics of these agents, highlighting their impact on hemodynamic parameters. We'll examine the importance of meticulous monitoring, including blood pressure, heart rate, and ECG, to optimize therapy and mitigate adverse effects like arrhythmias and hypotension. Nursing implications will emphasize safe administration, patient education, and recognizing signs of drug toxicity. Case studies will illustrate the practical application of inotropic therapy in various clinical settings, reinforcing the importance of this knowledge in critical care.
Cardiac Amplifiers: A Deep Dive into InotropesCardiac Amplifiers: A Deep Dive into Inotropes
Cardiac Amplifiers: A Deep Dive into Inotropes
Viresh Mahajani
71 slides142 views
Integumentary System By Baasir Umair.pdf by Baasir Umair Khattak, has 78 slides with 109 views.The integumentary system is the largest organ system of the human body, serving as the body's first line of defense against environmental hazards. It includes the skin, hair, nails, glands, and sensory receptors. This system plays a vital role in protection, thermoregulation, sensation, excretion, and vitamin D synthesis. Understanding its structure and function is crucial for comprehending how the body interacts with its surroundings. Structure of the Integumentary System The integumentary system comprises two main components: The Skin (Cutaneous Membrane) Accessory Structures (Hair, Nails, and Glands) The Skin The skin, also called the cutaneous membrane, consists of three primary layers: 1. Epidermis The epidermis is the outermost layer of the skin, composed of stratified squamous epithelium. It lacks blood vessels and is primarily made of keratinocytes, which produce the protective protein keratin. Other important cells in the epidermis include: Melanocytes – produce melanin, which protects against UV radiation. Langerhans cells – involved in immune response. Merkel cells – associated with sensory neurons for touch perception. The epidermis has five distinct layers (from deep to superficial): Stratum basale (germinativum) – contains basal cells responsible for generating new keratinocytes. Stratum spinosum – provides structural integrity. Stratum granulosum – where keratinization begins. Stratum lucidum – found only in thick skin (palms and soles). Stratum corneum – the outermost layer made of dead keratinized cells. 2. Dermis The dermis is the thicker, connective tissue layer beneath the epidermis. It consists of collagen and elastic fibers, providing strength and flexibility. The dermis has two layers: Papillary Layer – composed of loose areolar connective tissue; contains dermal papillae, capillaries, and sensory receptors. Reticular Layer – made of dense irregular connective tissue; contains sweat glands, hair follicles, and blood vessels. 3. Hypodermis (Subcutaneous Layer) The hypodermis is a layer of adipose and connective tissue that insulates the body, stores energy, and provides cushioning. It connects the skin to underlying muscles and bones. Functions of the Integumentary System The skin performs several essential functions, including: 1. Protection The skin acts as a physical barrier against microorganisms, dehydration, UV radiation, and harmful chemicals. The acid mantle (low pH) of the skin inhibits bacterial growth. 2. Thermoregulation The skin helps maintain body temperature through: Sweating (eccrine and apocrine glands) – evaporative cooling. Vasodilation – blood vessels widen to release heat. Vasoconstriction – blood vessels narrow to retain heat. Goosebumps (arrector pili muscles) – create an insulating layer. 3. Sensation The skin contains specialized sensory receptors: Meissner’s corpuscles – detect light touch. Pacinian corpuscles – sense deep pressure and vibration. Merkel cells –
Integumentary System By Baasir Umair.pdfIntegumentary System By Baasir Umair.pdf
Integumentary System By Baasir Umair.pdf
Baasir Umair Khattak
78 slides109 views
1. Physiologic Model of Spatial Vision and Retinal Sampling.pptx by GauriSShrestha, has 44 slides with 17 views.rod and cones, bipolar cells, horizontal cells, amacrine cells, ganglion cells, spatial summation and resolution, retinal sampling, spatial tunning, receptive fields of retinal neural cells, retinal potentials, Ricco's law, spatial antagonism, mach band, fourier analysing of visual system
1. Physiologic Model of Spatial Vision and Retinal Sampling.pptx1. Physiologic Model of Spatial Vision and Retinal Sampling.pptx
1. Physiologic Model of Spatial Vision and Retinal Sampling.pptx
GauriSShrestha
44 slides17 views
ASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHA by KIRAN KARETHA, has 4 slides with 134 views.Asthma is defined as a chronic inflammatory disorder of the airways (specifically bronchi and bronchioles) which manifests itself as recurrent episodes of wheezing, breathlessness, chest tightness and cough.  It is characterized by bronchial hyper-responsiveness and variable airflow obstruction, that is often reversible either spontaneously or with treatment. ASTHMA ATTACK:  When breathe normally, muscles around the airways are relaxed, letting air move easily and quietly. During an asthma attack, three things can happen:  Bronchospasm: The muscles around the airways constrict (tighten). When they tighten, it makes the airways narrow. Air cannot flow freely through constricted airways.  Inflammation: The lining of the airways becomes swollen. Swollen airways don’t let as much air in or out of the lungs.  Mucus production: During the attack, body creates more mucus. This thick mucus clogs airways. CLINICAL MANIFESTATION:  Coughing  Chest tightness  Wheezing  Shortness of breath  Chronic production of cough  Dyspnea  Cyanosis  Weight loss and anorexia  Fatigue  Anxiety  Restlessness DIAGNOSTIC EVALUATION:  History collection  Physical examination  Chest X-ray  Spirometry  Blood test  Skin test: to identify allergic causes.  Sputum test  PFT DIAGNOSTIC EVALUATION:  History collection  Physical examination  Chest X-ray  Spirometry  Blood test  Skin test: to identify allergic causes.  Sputum test  PFT
ASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHAASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHA
ASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHA
KIRAN KARETHA
4 slides134 views
Renal Physiology - Regulation of Plasma Osmolarity by MedicoseAcademics, has 22 slides with 174 views.Learning Objectives: 1. Discuss free water clearance 2. Differentiate between diabetes insipidus and SIADH 3. Describe the control of extracellular fluid osmolarity and sodium concentration in terms of the osmoreceptor-ADH system and thirst mechanism 4. Describe the roles of Angiotensin II, Aldosterone, and salt appetite mechanism in the control of extracellular fluid osmolarity and sodium concentration
Renal Physiology - Regulation of Plasma OsmolarityRenal Physiology - Regulation of Plasma Osmolarity
Renal Physiology - Regulation of Plasma Osmolarity
MedicoseAcademics
22 slides174 views
Adopting Modern Management Strategies for Obesity: Treating the Patient, Not ... by PVI, PeerView Institute for Medical Education, has 49 slides with 23 views.Co-Chairs and Presenters, Professor Carel le Roux, MBChB, FRCP, FRCPath, PhD, and Donna H. Ryan, MD, FTOS, discuss obesity in this CME activity titled “Adopting Modern Management Strategies for Obesity: Treating the Patient, Not the Disease.” For the full presentation, downloadable Practice Aids, and complete CME information, and to apply for credit, please visit us at https://bit.ly/40HfQWa. CME credit will be available until March 27, 2026.
Adopting Modern Management Strategies for Obesity: Treating the Patient, Not ...Adopting Modern Management Strategies for Obesity: Treating the Patient, Not ...
Adopting Modern Management Strategies for Obesity: Treating the Patient, Not ...
PVI, PeerView Institute for Medical Education
49 slides23 views
diabetes mcq by NAME ANKUSH GOYAL (1).pdf by Dr Ankush goyal, has 14 slides with 60 views.Diabetes Mellitus: A Comprehensive Overview Introduction Diabetes mellitus is a chronic metabolic disorder characterized by hyperglycemia due to defects in insulin secretion, insulin action, or both. It affects millions of people worldwide and is a major cause of morbidity and mortality due to its associated complications. This document provides an in-depth discussion of the types, pathophysiology, clinical features, diagnosis, management, and complications of diabetes mellitus. Types of Diabetes Mellitus 1. Type 1 Diabetes Mellitus (T1DM) Autoimmune destruction of pancreatic beta cells Absolute insulin deficiency Typically presents in childhood or adolescence Requires lifelong insulin therapy 2. Type 2 Diabetes Mellitus (T2DM) Characterized by insulin resistance and relative insulin deficiency Strong genetic predisposition Associated with obesity and sedentary lifestyle Managed with lifestyle modifications, oral hypoglycemics, and sometimes insulin 3. Gestational Diabetes Mellitus (GDM) Hyperglycemia first recognized during pregnancy Increases risk of complications for both mother and baby Usually resolves postpartum but increases the risk of T2DM later in life 4. Other Specific Types Monogenic diabetes (MODY, neonatal diabetes) Secondary diabetes (due to pancreatic diseases, endocrinopathies, drug-induced, etc.) Pathophysiology Diabetes results from impaired insulin secretion, action, or both, leading to chronic hyperglycemia. The key mechanisms include: Type 1 Diabetes: Autoimmune destruction of beta cells, leading to absolute insulin deficiency. Type 2 Diabetes: Insulin resistance in peripheral tissues and inadequate compensatory insulin secretion by beta cells. GDM: Hormonal changes in pregnancy lead to insulin resistance and beta-cell dysfunction. Clinical Features Symptoms of Hyperglycemia: Polyuria (excessive urination) Polydipsia (excessive thirst) Polyphagia (excessive hunger) Unexplained weight loss Fatigue Blurred vision Complications: Acute: Diabetic ketoacidosis (DKA), hyperosmolar hyperglycemic state (HHS) Chronic: Microvascular (retinopathy, nephropathy, neuropathy) and macrovascular (coronary artery disease, stroke, peripheral artery disease) Diagnosis The diagnosis of diabetes is based on: Fasting Plasma Glucose (FPG) ≥ 126 mg/dL Random Plasma Glucose ≥ 200 mg/dL with symptoms of hyperglycemia 2-hour Plasma Glucose ≥ 200 mg/dL during an OGTT Hemoglobin A1c ≥ 6.5% Management 1. Lifestyle Modifications Healthy diet (low glycemic index, high fiber, reduced saturated fats) Regular physical activity (at least 150 minutes per week) Weight management 2. Pharmacological Therapy Oral Hypoglycemics: Metformin (first-line), sulfonylureas, DPP-4 inhibitors, SGLT2 inhibitors, thiazolidinediones Injectable Therapy: Insulin, GLP-1 receptor agonists Insulin Therapy: Required for T1DM and some cases of T2DM 3. Monitoring and Complication Prevention Regular blood glucose
diabetes mcq by NAME ANKUSH GOYAL (1).pdfdiabetes mcq by NAME ANKUSH GOYAL (1).pdf
diabetes mcq by NAME ANKUSH GOYAL (1).pdf
Dr Ankush goyal
14 slides60 views
Plasma and Red Blood Cells - Copy - Copy_AntiCopy.pdf by MedicoseAcademics, has 30 slides with 53 views.Delve deep into the intricate world of blood physiology with “Plasma and Red Blood Cells,” a comprehensive lecture presented by Dr. Faiza, Assistant Professor of Physiology. This presentation is meticulously designed for students, educators, and healthcare professionals to enhance their understanding of hematology and the critical roles played by various blood components. In this lecture, you will: Examine Blood Composition: Learn how blood constitutes approximately 8% of total body weight, with precise volumes differing between genders. The presentation breaks down blood into its two fundamental components—plasma and blood cells—and explains their distribution and essential functions in the body. Understand Plasma Functions and Composition: Discover the key role of plasma as a transport medium for nutrients, waste products, hormones, and ions. The lecture details the high water content (~90%), the balance of inorganic (e.g., Na⁺, Cl⁻, HCO₃⁻, K⁺, Ca²⁺) and organic substances (notably plasma proteins), and how these components contribute to maintaining homeostasis, temperature regulation, and pH balance. Classify Plasma Proteins: Explore the classification of plasma proteins into albumins, globulins (alpha, beta, and gamma), and fibrinogen. Learn about their individual functions, such as maintaining colloid osmotic pressure, facilitating transport of poorly soluble substances, and contributing to immune defense and clotting processes. Analyze Hematocrit and Packed Cell Volume (PCV): Understand the significance of hematocrit or PCV as a measure of the proportion of erythrocytes in blood, including the average values observed in men and women. This metric is crucial for assessing blood viscosity and overall health. Study the Structure and Function of Erythrocytes: Gain insight into the unique characteristics of red blood cells, including their biconcave disc shape, deformability, and the absence of organelles, which all play a role in optimizing oxygen transport. Detailed discussions cover the enzymes involved in RBC metabolism and the physiological basis for their limited lifespan. Relate to Clinical and Physiological Contexts: The lecture also connects these fundamental concepts to clinical scenarios, explaining how alterations in blood composition can impact oxygen delivery, acid-base balance, and overall metabolic function. It provides a solid foundation for understanding common hematological disorders and the body’s adaptive mechanisms in various pathological conditions. Each slide is carefully structured to build a comprehensive picture of blood components and their interplay, supported by visual aids such as flow diagrams, comparative charts, and schematic representations. Dr. Faiza’s expertise is evident as she translates complex physiological processes into accessible and practical knowledge, making this presentation a valuable resource for enhancing your medical education.
Plasma and Red Blood Cells - Copy - Copy_AntiCopy.pdfPlasma and Red Blood Cells - Copy - Copy_AntiCopy.pdf
Plasma and Red Blood Cells - Copy - Copy_AntiCopy.pdf
MedicoseAcademics
30 slides53 views
echinocandins case presentation.dr ANKUSH GOYAL GMC PATIALA by Dr Ankush goyal, has 10 slides with 232 views.Echinocandins: A Comprehensive Overview Introduction Echinocandins are a class of antifungal agents that have gained significant prominence in the treatment of invasive fungal infections, particularly those caused by Candida and Aspergillus species. They are considered second-line or first-line treatment options in cases of azole-resistant fungal infections. This document provides an in-depth discussion of echinocandins, including their chemical structure, mechanism of action, pharmacokinetics, spectrum of activity, clinical applications, resistance mechanisms, adverse effects, and future perspectives. Historical Background Echinocandins were first discovered in the late 20th century when researchers were exploring natural antifungal compounds derived from fungi and other microorganisms. The first echinocandin, pneumocandin B0, was isolated from Glarea lozoyensis. Further modifications led to the development of caspofungin, micafungin, and anidulafungin, which are the three currently approved echinocandins for clinical use. Chemical Structure Echinocandins are cyclic lipopeptides composed of a large cyclic hexapeptide core linked to a long-chain fatty acid side group. This unique structure is crucial for their antifungal activity and their pharmacokinetic properties. The lipid tail enhances the compound's binding affinity to fungal cells, while the cyclic peptide core is responsible for inhibiting fungal cell wall synthesis. Mechanism of Action Echinocandins exert their antifungal effects by selectively inhibiting the enzyme (1→3)-β-D-glucan synthase, which is essential for the synthesis of β-glucan, a major component of the fungal cell wall. The inhibition of β-glucan synthesis results in cell wall weakening, osmotic instability, and ultimately fungal cell lysis. This mechanism makes echinocandins highly selective for fungi, as mammalian cells lack β-glucan. Pharmacokinetics Echinocandins are administered intravenously due to their poor oral bioavailability. The pharmacokinetic properties of caspofungin, micafungin, and anidulafungin vary slightly, but they share several common features: Distribution: Echinocandins exhibit extensive tissue penetration, particularly in the liver, spleen, lungs, and kidneys. However, their penetration into the cerebrospinal fluid (CSF) is limited, making them less effective for central nervous system fungal infections. Metabolism: Caspofungin undergoes hepatic metabolism through hydrolysis and N-acetylation, while micafungin is metabolized by the liver via arylsulfatase and catechol-O-methyltransferase. Anidulafungin undergoes spontaneous degradation in the plasma without significant hepatic metabolism. Elimination: The elimination of echinocandins varies; caspofungin is excreted through both hepatic and renal routes, micafungin is eliminated hepatically, and anidulafungin is primarily excreted via fecal routes due to spontaneous degradation. Half-life: Caspofungin has a half-life of approximately 9-
echinocandins case presentation.dr ANKUSH GOYAL GMC PATIALAechinocandins case presentation.dr ANKUSH GOYAL GMC PATIALA
echinocandins case presentation.dr ANKUSH GOYAL GMC PATIALA
Dr Ankush goyal
10 slides232 views
HIV TREATMENT MCQ BY DR ANKUSH GOYAL.docx by Dr Ankush goyal, has 16 slides with 162 views.**HIV Treatment: A Comprehensive Overview** ## Introduction Human Immunodeficiency Virus (HIV) is a major global health challenge that affects millions of people. While there is no cure for HIV, advancements in medical research have led to effective treatment options that allow individuals with HIV to lead healthy lives. The primary treatment for HIV is antiretroviral therapy (ART), which helps to control the virus and prevent its progression to Acquired Immunodeficiency Syndrome (AIDS). This document explores the various aspects of HIV treatment, including its history, types of medications, effectiveness, side effects, challenges, and future developments. ## History of HIV Treatment The history of HIV treatment dates back to the 1980s when the first cases of AIDS were identified. Researchers quickly began searching for treatments to combat the virus. In 1987, the first antiretroviral drug, zidovudine (AZT), was approved. While it provided some benefits, AZT had significant toxicity and limited long-term efficacy. Over time, scientists developed new classes of antiretroviral drugs, leading to the combination therapy approach, which has dramatically improved patient outcomes. ## Antiretroviral Therapy (ART) ### How ART Works ART consists of a combination of drugs that target different stages of the HIV lifecycle. These medications reduce the viral load (the amount of HIV in the blood) to undetectable levels, thereby preventing the virus from weakening the immune system. ART also reduces the risk of HIV transmission to others. ### Classes of Antiretroviral Drugs There are several classes of antiretroviral drugs, each working in different ways to inhibit the replication of HIV: 1. **Nucleoside Reverse Transcriptase Inhibitors (NRTIs)** - These drugs block reverse transcriptase, an enzyme HIV uses to convert its RNA into DNA. Examples include zidovudine (AZT), lamivudine (3TC), and tenofovir (TDF). 2. **Non-Nucleoside Reverse Transcriptase Inhibitors (NNRTIs)** - NNRTIs bind directly to reverse transcriptase and inhibit its function. Examples include efavirenz and nevirapine. 3. **Protease Inhibitors (PIs)** - These drugs prevent HIV from maturing and becoming infectious by inhibiting the protease enzyme. Examples include lopinavir and atazanavir. 4. **Integrase Strand Transfer Inhibitors (INSTIs)** - These drugs prevent HIV from integrating its genetic material into human DNA. Examples include raltegravir and dolutegravir. 5. **Entry Inhibitors** - These drugs prevent HIV from entering human cells. Examples include maraviroc (CCR5 antagonist) and enfuvirtide (fusion inhibitor). 6. **Pharmacokinetic Enhancers** - These drugs improve the effectiveness of other antiretroviral medications by increasing their concentration in the bloodstream. An example is ritonavir. ## Effectiveness of HIV Treatment ### Viral Suppression When taken consistently, ART can reduce the viral load to undetectable levels. Studies have shown that individuals with u
HIV TREATMENT MCQ BY DR ANKUSH GOYAL.docxHIV TREATMENT MCQ BY DR ANKUSH GOYAL.docx
HIV TREATMENT MCQ BY DR ANKUSH GOYAL.docx
Dr Ankush goyal
16 slides162 views
antiherpes acyclovir mcq ANKUSH GOYAL GMC PATIALA.docx by Dr Ankush goyal, has 12 slides with 120 views.### **Acyclovir and Anti-Herpes Medications** **Acyclovir** is an antiviral medication used to treat infections caused by herpes viruses, including: - **Herpes simplex virus (HSV-1 & HSV-2)** – Causes cold sores and genital herpes. - **Varicella-zoster virus (VZV)** – Causes chickenpox and shingles. ### **Mechanism of Action:** Acyclovir works by inhibiting viral DNA replication. It is activated inside virus-infected cells, where it blocks viral enzymes, preventing the virus from multiplying. ### **Forms & Dosage:** - **Oral (Tablets/Capsules/Liquid)** – Used for mild to moderate infections. - **Topical (Cream/Ointment)** – For cold sores and mild skin infections. - **Intravenous (IV)** – For severe infections like herpes encephalitis. ### **Other Anti-Herpes Medications:** - **Valacyclovir (Valtrex)** – A prodrug of acyclovir with better absorption. - **Famciclovir (Famvir)** – Another antiviral with a longer duration of action. - **Penciclovir (Denavir)** – Used topically for herpes labialis (cold sores). ### **Uses:** - Treats and manages outbreaks of herpes simplex. - Reduces the severity and duration of symptoms. - Used for long-term suppression to prevent recurrent infections. - Helps in managing shingles and chickenpox. ### **Side Effects:** - Nausea, vomiting, diarrhea. - Headache, dizziness, fatigue. - Rare: Kidney issues, allergic reactions. ### **Precautions:** - Drink plenty of fluids to prevent kidney issues. - Not a cure, but helps manage symptoms. - Safe for most patients but should be used cautiously in people with kidney disease or weakened immune systems.
antiherpes acyclovir mcq ANKUSH GOYAL GMC PATIALA.docxantiherpes acyclovir mcq ANKUSH GOYAL GMC PATIALA.docx
antiherpes acyclovir mcq ANKUSH GOYAL GMC PATIALA.docx
Dr Ankush goyal
12 slides120 views
Good Laboratory Practices (GLP) Ensuring Quality and Compliance.pptx by Dr. Smita Kumbhar, has 53 slides with 278 views.Good Laboratory Practices (GLP): Ensuring Quality and Compliance Good Laboratory Practices (GLP) is a set of principles intended to ensure the quality, integrity, and reliability of non-clinical laboratory studies that support research and regulatory submissions. These guidelines are critical in the pharmaceutical, biotechnological, chemical, and environmental sectors, ensuring that laboratory-generated data are reproducible, credible, and internationally accepted. GLP standards primarily apply to safety studies involving pharmaceuticals, pesticides, food additives, and industrial chemicals. Regulatory agencies, including the USFDA, EMA, and OECD, enforce GLP compliance to maintain scientific rigor and public safety. USFDA GLP Regulations The U.S. Food and Drug Administration (USFDA) established Good Laboratory Practice regulations under 21 CFR Part 58. These regulations outline responsibilities for study directors, testing facilities, and personnel to maintain quality and integrity in non-clinical laboratory studies. The regulations cover various aspects, including study conduct, reporting, and archiving, ensuring consistency and accuracy in laboratory research. Controlling the GLP Inspection Process Regulatory authorities conduct inspections to verify GLP compliance. Laboratories must prepare for inspections by: • Maintaining up-to-date documentation. • Conducting internal audits. • Ensuring personnel training and awareness. • Implementing corrective actions for non-compliance. Regulatory inspections typically assess laboratory infrastructure, personnel competence, study documentation, and adherence to protocols. Laboratories must demonstrate transparency and proactive quality control measures. Documentation in GLP Accurate and comprehensive documentation is crucial in GLP compliance. Key documentation elements include: • Study protocols • Standard operating procedures (SOPs) • Raw data records • Analytical reports • Audit reports • Equipment calibration records • Archiving and retention policies Proper documentation ensures traceability, accountability, and reliability in laboratory research. Audit in GLP Compliance Auditing is a critical component of GLP, ensuring adherence to established regulations and identifying areas for improvement. Audits can be internal (self-audit) or external (regulatory or third-party audits). Goals of Laboratory Quality Audit • Ensure compliance with GLP regulations. • Identify gaps and areas for improvement. • Validate data integrity and accuracy. • Enhance operational efficiency. • Prevent regulatory penalties and study disqualification. Audit Tools in GLP Laboratories use various audit tools to assess compliance, including: • Checklists and self-assessments • Internal quality audits • Electronic data tracking systems • Third-party inspections • Root cause analysis • Corrective and preventive action (CAPA) plans Future of GLP Regulations
Good Laboratory Practices (GLP) Ensuring Quality and Compliance.pptxGood Laboratory Practices (GLP) Ensuring Quality and Compliance.pptx
Good Laboratory Practices (GLP) Ensuring Quality and Compliance.pptx
Dr. Smita Kumbhar
53 slides278 views
Integumentary System By Baasir Umair.pdf by Baasir Umair Khattak, has 78 slides with 109 views.The integumentary system is the largest organ system of the human body, serving as the body's first line of defense against environmental hazards. It includes the skin, hair, nails, glands, and sensory receptors. This system plays a vital role in protection, thermoregulation, sensation, excretion, and vitamin D synthesis. Understanding its structure and function is crucial for comprehending how the body interacts with its surroundings. Structure of the Integumentary System The integumentary system comprises two main components: The Skin (Cutaneous Membrane) Accessory Structures (Hair, Nails, and Glands) The Skin The skin, also called the cutaneous membrane, consists of three primary layers: 1. Epidermis The epidermis is the outermost layer of the skin, composed of stratified squamous epithelium. It lacks blood vessels and is primarily made of keratinocytes, which produce the protective protein keratin. Other important cells in the epidermis include: Melanocytes – produce melanin, which protects against UV radiation. Langerhans cells – involved in immune response. Merkel cells – associated with sensory neurons for touch perception. The epidermis has five distinct layers (from deep to superficial): Stratum basale (germinativum) – contains basal cells responsible for generating new keratinocytes. Stratum spinosum – provides structural integrity. Stratum granulosum – where keratinization begins. Stratum lucidum – found only in thick skin (palms and soles). Stratum corneum – the outermost layer made of dead keratinized cells. 2. Dermis The dermis is the thicker, connective tissue layer beneath the epidermis. It consists of collagen and elastic fibers, providing strength and flexibility. The dermis has two layers: Papillary Layer – composed of loose areolar connective tissue; contains dermal papillae, capillaries, and sensory receptors. Reticular Layer – made of dense irregular connective tissue; contains sweat glands, hair follicles, and blood vessels. 3. Hypodermis (Subcutaneous Layer) The hypodermis is a layer of adipose and connective tissue that insulates the body, stores energy, and provides cushioning. It connects the skin to underlying muscles and bones. Functions of the Integumentary System The skin performs several essential functions, including: 1. Protection The skin acts as a physical barrier against microorganisms, dehydration, UV radiation, and harmful chemicals. The acid mantle (low pH) of the skin inhibits bacterial growth. 2. Thermoregulation The skin helps maintain body temperature through: Sweating (eccrine and apocrine glands) – evaporative cooling. Vasodilation – blood vessels widen to release heat. Vasoconstriction – blood vessels narrow to retain heat. Goosebumps (arrector pili muscles) – create an insulating layer. 3. Sensation The skin contains specialized sensory receptors: Meissner’s corpuscles – detect light touch. Pacinian corpuscles – sense deep pressure and vibration. Merkel cells –
Integumentary System By Baasir Umair.pdfIntegumentary System By Baasir Umair.pdf
Integumentary System By Baasir Umair.pdf
Baasir Umair Khattak
78 slides109 views
ASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHA by KIRAN KARETHA, has 4 slides with 134 views.Asthma is defined as a chronic inflammatory disorder of the airways (specifically bronchi and bronchioles) which manifests itself as recurrent episodes of wheezing, breathlessness, chest tightness and cough.  It is characterized by bronchial hyper-responsiveness and variable airflow obstruction, that is often reversible either spontaneously or with treatment. ASTHMA ATTACK:  When breathe normally, muscles around the airways are relaxed, letting air move easily and quietly. During an asthma attack, three things can happen:  Bronchospasm: The muscles around the airways constrict (tighten). When they tighten, it makes the airways narrow. Air cannot flow freely through constricted airways.  Inflammation: The lining of the airways becomes swollen. Swollen airways don’t let as much air in or out of the lungs.  Mucus production: During the attack, body creates more mucus. This thick mucus clogs airways. CLINICAL MANIFESTATION:  Coughing  Chest tightness  Wheezing  Shortness of breath  Chronic production of cough  Dyspnea  Cyanosis  Weight loss and anorexia  Fatigue  Anxiety  Restlessness DIAGNOSTIC EVALUATION:  History collection  Physical examination  Chest X-ray  Spirometry  Blood test  Skin test: to identify allergic causes.  Sputum test  PFT DIAGNOSTIC EVALUATION:  History collection  Physical examination  Chest X-ray  Spirometry  Blood test  Skin test: to identify allergic causes.  Sputum test  PFT
ASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHAASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHA
ASTHMA.pdf FOR NURSING STUDENTS CREATED BY KIRAN KARETHA
KIRAN KARETHA
4 slides134 views

DR MANISH-2.pdf laser proctology piles and fistula

  • 1. D R M A N I S H RAJPUT ht t ps://dr manishr ajput .com Bookan appointment!
  • 2. IN T R O D U C T IO N Dr . Manish Rajput is an I nterventional Radiologist & Team Lead, Team I R Jaipur . They are the biggest team of I nterventional Radiologists. They are trained from Tata Memorial Center , Mumbai, I ndia. They have worked in so many government and corporate hospitals across the country.
  • 3. Medical school (MBBS):2005-2011: -People’s Medical College, Bhopal(MP) DNB (Radio diagnosis): - Apollo hospital, Hyderabad(Telangana) FVIR (PDCC):- Tata Memorial Centre, Mumbai(Maharashtra) Senior Resident: Hinduja Hospital Mumbai, SMS Hospital Jaipur Past Visiting Doctor:Leelavati Hospital Mumbai, Breach Candy Hospital Mumbai, Wockhardt Hospital Mumbai, Hinduja Hospital Mumbai Ex Assitant Professor:JNU Medical College, Jaipur Currently Working as Senior Consultant Interventional Radiologist in various corporate hospitals of Rajasthan based in Jaipur HIS EDUCATION
  • 4. S T R E N G T H S Ilead the biggest I R team in the state. Vast portfolio for I R services. All the team members are from Tata Memorial Hospital, Mumbai. Extensive experience in performing and interpreting basic Radio-Diagnosis. Gained experience in performing I nterventional Radiologic procedures. Ipossess oratory skill by speaking at numerous industry events. Ability to teach complex concepts in a basic manner .
  • 5. Varicose Veins Prostate Artery Embolization PRG Biopsy and fNAC Angioplasty & Venoplasty PCN & DJ Stenting O U R S E R V I C E S
  • 6. +91 7729021111 dr.manish@infinityintervention.com O-5-A, Adinath Marg, Near Surya Hospital, C Scheme, Ashok Nagar, Jaipur, Rajasthan 302001 C ON TA C T US!