The document discusses skin emergencies and defines terminology used to describe various skin conditions. It outlines clinical clues that may indicate a potential dermatologic emergency, such as fever and rash, or blistering in immunocompromised individuals. Several serious but rare conditions are then reviewed in more detail, including toxic epidermal necrolysis (TENS), Stevens-Johnson syndrome, pemphigus, pemphigoid, and necrotizing fasciitis. The document emphasizes identifying these conditions promptly and initiating appropriate treatment to prevent adverse outcomes.
hanifin and rajka criteria, entymology, definition of AD, atopy, etiopathogenesis of AD, genetics in AD, filaggrin, epidermal barrier dysfunction, atopic march, hygiene hypothesis, infantile phase of AD, childhood phase of AD, adult phase of AD, pityriasis alba, denne morgan folds, dirty neck appearence, nipple dermatitis, hanifin and rajka criteria, UK refinement of hanifin and rajka criteria, millenium criteria of AD, japanese dermatological association criteria, management of AD, wet wrap therapy,
hanifin and rajka criteria, entymology, definition of AD, atopy, etiopathogenesis of AD, genetics in AD, filaggrin, epidermal barrier dysfunction, atopic march, hygiene hypothesis, infantile phase of AD, childhood phase of AD, adult phase of AD, pityriasis alba, denne morgan folds, dirty neck appearence, nipple dermatitis, hanifin and rajka criteria, UK refinement of hanifin and rajka criteria, millenium criteria of AD, japanese dermatological association criteria, management of AD, wet wrap therapy,
Skin involvement in rheumatic diseases/ DOI 10.13140/RG.2.2.10743.32169Enida Xhaferi
Skin disorders are observed in a variety of rheumatologic conditions and constitute the primary features in lupus erythematosus, dermatomyositis and systemic sclerosis. Skin involvement is also observed in systemic vasculitides, rheumatoid arthritis, Sjögren syndrome, psoriatic arthritis, systemic-onset juvenile rheumatoid arthritis, and relapsing polychondritis. It is important for the clinician to recognize and discern the most common cutaneal lesions and patterns encountered in patients with rheumatic diseases (like makule, papule, nodul, plaque, purpura, petechia, pustul, squam, erosion, erythema, onychodystrophy, onycholysis, urticaria, butterfly rash, Gottron papules and sign etc) because they provide clues regarding the systemic involvement of the pathology, diagnosis, therapeutic approach and prognosis. Skin biopsies are usually useful in determining the precise nature of the skin disorder. Below are presented briefly the major skin manifestations observed in lupus erythematosus, dermatomiositis, scleroderma and rheumatoid arthritis
Hereditary disorder of keratinization characterized by expanding atrophic anular patch(es) surrounded by prominent keratotic ridge called the cornoid lamella
Summary of updated information about the disease of Atopic dermatitis, aetiology, immunopathogenesis, main clinical features and dianostic criteria, concepts of managemnt of Atopic dermatitis including newest treatment trends.
Dermoscopy or epiluminescence microscopy
A simple, noninvasive method to examine the subsurface features of the skin.
Structures seen
Epidermis
Dermoepidermal junction
Superficial dermis
3 types of dermoscope
1.Nonpolarized devices
2.Polarized devices
3.Hybrid devices
Dermoscopy is used in:
1.Evaluating pigmented skin lesions
2.Evaluating nonpigment skin lesions
3.Entomodermoscopy
4.Trichoscopy
5.Onychoscopy
different dermoscopic patterns are used to diagnose the dermatological diseases are
1. melanocytic patterns:
Pigmentary patterns: typical pigment pattern, atypical pigment patter, pseudonetwork
dots and globules
Blue white veil
star brust pattern
2, Non melanocytic pattern:
milia like cyst
comedo like opening
3. vascular patterns:
lacunae
arborizing vessels
comma like vessels
corkscrew vessel
red dots
glomerular vessels
linear vessels
etc
Skin involvement in rheumatic diseases/ DOI 10.13140/RG.2.2.10743.32169Enida Xhaferi
Skin disorders are observed in a variety of rheumatologic conditions and constitute the primary features in lupus erythematosus, dermatomyositis and systemic sclerosis. Skin involvement is also observed in systemic vasculitides, rheumatoid arthritis, Sjögren syndrome, psoriatic arthritis, systemic-onset juvenile rheumatoid arthritis, and relapsing polychondritis. It is important for the clinician to recognize and discern the most common cutaneal lesions and patterns encountered in patients with rheumatic diseases (like makule, papule, nodul, plaque, purpura, petechia, pustul, squam, erosion, erythema, onychodystrophy, onycholysis, urticaria, butterfly rash, Gottron papules and sign etc) because they provide clues regarding the systemic involvement of the pathology, diagnosis, therapeutic approach and prognosis. Skin biopsies are usually useful in determining the precise nature of the skin disorder. Below are presented briefly the major skin manifestations observed in lupus erythematosus, dermatomiositis, scleroderma and rheumatoid arthritis
Hereditary disorder of keratinization characterized by expanding atrophic anular patch(es) surrounded by prominent keratotic ridge called the cornoid lamella
Summary of updated information about the disease of Atopic dermatitis, aetiology, immunopathogenesis, main clinical features and dianostic criteria, concepts of managemnt of Atopic dermatitis including newest treatment trends.
Dermoscopy or epiluminescence microscopy
A simple, noninvasive method to examine the subsurface features of the skin.
Structures seen
Epidermis
Dermoepidermal junction
Superficial dermis
3 types of dermoscope
1.Nonpolarized devices
2.Polarized devices
3.Hybrid devices
Dermoscopy is used in:
1.Evaluating pigmented skin lesions
2.Evaluating nonpigment skin lesions
3.Entomodermoscopy
4.Trichoscopy
5.Onychoscopy
different dermoscopic patterns are used to diagnose the dermatological diseases are
1. melanocytic patterns:
Pigmentary patterns: typical pigment pattern, atypical pigment patter, pseudonetwork
dots and globules
Blue white veil
star brust pattern
2, Non melanocytic pattern:
milia like cyst
comedo like opening
3. vascular patterns:
lacunae
arborizing vessels
comma like vessels
corkscrew vessel
red dots
glomerular vessels
linear vessels
etc
basic skin diseases of the human body. it describes the basic lesions not he advanced diseases.
It is a disease affecting reticuloendothelial cells of the skin
caused by protozoan Leishmania,
transmitted by the bite of female sand fly
There is an interplay of leishmania protozoa between
Erythema multiforme, Steven-Johnson syndrome and Toxic Epidermal NecrolysisBinaya Subedi
Erythema Multiforme is a common Vesiculobullous deramtological condition with mucosal manifestations trigged by Herpes virus infection and certain sulpha containing drugs.
ABDOMINAL TRAUMA in pediatrics part one.drhasanrajab
Abdominal trauma in pediatrics refers to injuries or damage to the abdominal organs in children. It can occur due to various causes such as falls, motor vehicle accidents, sports-related injuries, and physical abuse. Children are more vulnerable to abdominal trauma due to their unique anatomical and physiological characteristics. Signs and symptoms include abdominal pain, tenderness, distension, vomiting, and signs of shock. Diagnosis involves physical examination, imaging studies, and laboratory tests. Management depends on the severity and may involve conservative treatment or surgical intervention. Prevention is crucial in reducing the incidence of abdominal trauma in children.
Title: Sense of Smell
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Basavarajeeyam is a Sreshta Sangraha grantha (Compiled book ), written by Neelkanta kotturu Basavaraja Virachita. It contains 25 Prakaranas, First 24 Chapters related to Rogas& 25th to Rasadravyas.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
Local Advanced Lung Cancer: Artificial Intelligence, Synergetics, Complex Sys...Oleg Kshivets
Overall life span (LS) was 1671.7±1721.6 days and cumulative 5YS reached 62.4%, 10 years – 50.4%, 20 years – 44.6%. 94 LCP lived more than 5 years without cancer (LS=2958.6±1723.6 days), 22 – more than 10 years (LS=5571±1841.8 days). 67 LCP died because of LC (LS=471.9±344 days). AT significantly improved 5YS (68% vs. 53.7%) (P=0.028 by log-rank test). Cox modeling displayed that 5YS of LCP significantly depended on: N0-N12, T3-4, blood cell circuit, cell ratio factors (ratio between cancer cells-CC and blood cells subpopulations), LC cell dynamics, recalcification time, heparin tolerance, prothrombin index, protein, AT, procedure type (P=0.000-0.031). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and N0-12 (rank=1), thrombocytes/CC (rank=2), segmented neutrophils/CC (3), eosinophils/CC (4), erythrocytes/CC (5), healthy cells/CC (6), lymphocytes/CC (7), stick neutrophils/CC (8), leucocytes/CC (9), monocytes/CC (10). Correct prediction of 5YS was 100% by neural networks computing (error=0.000; area under ROC curve=1.0).
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These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
share - Lions, tigers, AI and health misinformation, oh my!.pptxTina Purnat
• Pitfalls and pivots needed to use AI effectively in public health
• Evidence-based strategies to address health misinformation effectively
• Building trust with communities online and offline
• Equipping health professionals to address questions, concerns and health misinformation
• Assessing risk and mitigating harm from adverse health narratives in communities, health workforce and health system
DISSERTATION on NEW DRUG DISCOVERY AND DEVELOPMENT STAGES OF DRUG DISCOVERYNEHA GUPTA
The process of drug discovery and development is a complex and multi-step endeavor aimed at bringing new pharmaceutical drugs to market. It begins with identifying and validating a biological target, such as a protein, gene, or RNA, that is associated with a disease. This step involves understanding the target's role in the disease and confirming that modulating it can have therapeutic effects. The next stage, hit identification, employs high-throughput screening (HTS) and other methods to find compounds that interact with the target. Computational techniques may also be used to identify potential hits from large compound libraries.
Following hit identification, the hits are optimized to improve their efficacy, selectivity, and pharmacokinetic properties, resulting in lead compounds. These leads undergo further refinement to enhance their potency, reduce toxicity, and improve drug-like characteristics, creating drug candidates suitable for preclinical testing. In the preclinical development phase, drug candidates are tested in vitro (in cell cultures) and in vivo (in animal models) to evaluate their safety, efficacy, pharmacokinetics, and pharmacodynamics. Toxicology studies are conducted to assess potential risks.
Before clinical trials can begin, an Investigational New Drug (IND) application must be submitted to regulatory authorities. This application includes data from preclinical studies and plans for clinical trials. Clinical development involves human trials in three phases: Phase I tests the drug's safety and dosage in a small group of healthy volunteers, Phase II assesses the drug's efficacy and side effects in a larger group of patients with the target disease, and Phase III confirms the drug's efficacy and monitors adverse reactions in a large population, often compared to existing treatments.
After successful clinical trials, a New Drug Application (NDA) is submitted to regulatory authorities for approval, including all data from preclinical and clinical studies, as well as proposed labeling and manufacturing information. Regulatory authorities then review the NDA to ensure the drug is safe, effective, and of high quality, potentially requiring additional studies. Finally, after a drug is approved and marketed, it undergoes post-marketing surveillance, which includes continuous monitoring for long-term safety and effectiveness, pharmacovigilance, and reporting of any adverse effects.
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
2. 22
Aims
Review terminology of skin conditions
Discuss serious but rare skin disorders
Identify clinical clues to the diagnosis of
potentially life-threatening dermatologic
conditions
Discuss infectious and pharmacologic causes of
life-threatening dermatoses
3. Clues to the Presence of a Potential
Dermatologic Emergency
Fever and rash
Fever and blisters
Rash in immunocompromised
Palpable purpura
“Full body redness”
7. Petechiae
red, non blanching
spots <5mm
Purpura
red, non blanching
spots >5mm
8. Plaque = Palpable
disc shaped lesion
Wheal = Area of
dermal oedema
9. 99
History
How long
Had it before
Is it worsening / anything improving it
Distribution ie palms / plantar / face / mucosal membranes
How did it start / evolve
Itch
Social changes eg diet / work / cleaning
Meds & allergies
Cutaneous manifestations of systemic disorders eg sore joints & past medical
history
Family history
Travel
Contacts
Viral symptoms or fevers
17. 1717
VZV
Varicella / Chicken Pox – Respiratory droplets. Infectious for 2 days prior to
lesions. Ends when crusts
Rash head / trunk /
Simultaneous presence of rash at different stages. Macule / Papule / Vesicle /
Pustule / Crusts
A/w headache / malaise / anorexia / cough / coryza and sore throat / low grade
fever
Rx symptomatic. Antivirals in certain cases / Secondary infection risk
Shingles
Dermatomal distribution & enlarged draining node
Presents as pain, malaise, fever, rash in same distribution several days later
Dx Clinical but can do smears or titres or isolation of virus in blisters
Mx – antivirals / pain relief / IV antivirals if immunocompromised
Complications : Corneal ulcers / Gangrene of affected area / Phrenic Nerve palsy
/ Meningoencephalitis / Ramsay Hunt syndrome / Neuralgia / Disseminated
zoster
NB if AIDS – major CNS effects/
24. Staphylococcal Scalded Skin Syndrome
Dermatologic findings
Erythema periorificially on the face, neck, axilla,
groin. Then generalized within 48 hrs as the color
deepens
Skin tenderness
bullae w positive Nikolsky sign
Within 1-2 days, flexural areas begin to slough off
Complete re-epithelialization in 2 weeks
Nikolsky Sign
Positive when a blister occurs on normal appearing
skin after application of lateral pressure w/ a finger
Occurs in any superficial blistering process
25. Clinical presentation
Prodrome of fever, malaise, sore throat
Complication
Mortality rate is 3% in kids, > 50% in adults
and 100% in adults with underlying diseases
If in newborn nursery, needs isolation
27. Cellulitis and ErysipelasCellulitis and Erysipelas
Spreading erythema and swelling
Erysipelas when intradermal and due to GpAStrep
90% Haemolytic Strep (Group A)
10% Staphylococcus aureus
? Anaerobe involvement
Rx:
Clindamycin + Ciprofloxacin
32. Meningococcemia
Etiology
Neisseria meningitides (gram neg diplococcus) spread
by respiratory route
Often seen in young adults and children
Risk factor: immunoglobulin or terminal complement
deficiencies
Dermatologic findings
Abrupt onset of maculopapular or petechial eruption on
trunk or lower extremities -> progression to purpura in
hours
Angular edge with “gun metal gray” center
+/- mucosal involvement
45. 4545
Toxic Epidermal Necrolysis
Mostly thought to be drug related
Culprit medications: Sulfonamides, anticonvulsants,
allopurinol, NSAIDs.
Widespread rash like sunburn initially >30% TBSA with later
necrosis and sloughing. +ve Nikolsky sign
( Nikolsky’s sign -separation of skin with gentle pressure.)
Large mucous membrane involvement.
Complications:
High mortality
Ophthalmology involvement and regular eye irrigation
46. Treatment SJS/TEN:
Prompt drug withdrawal.
Admission / Burn unit, ICU
Ophthalmology, urology
IVIG
Systemic steroid is controversial
48. Angioedema
Pathophysiology
Increased intravascular permeability
Dermatologic findings
Well circumscribed acute cutaneous edema due to
increased intravascular permeability
Face, lips, extremities, genitalia
Painful, usually not pruritic
Clinical presentation
Abdominal pain
Respiratory distress
49. Etiology:
Often idiopathic
Medications
angiotensin-converting- enzyme inhibitor in 10-25%
of cases
Penicillin
NSAID
Allergens (foods, radiographic contrast media)
Physical agents (cold, vibration, etc)
C1 esterase inhibitor deficiency: hereditary vs
associated with autoimmune disorder or malignancy
50. Management
Airway management
In cases with laryngeal involvement, a definitive airway If the airway
cannot be effectively secured with an endotracheal tube, a surgical
airway is indicated, usually in the form of an emergency
cricothyrotomy
epinephrine : Used in pts who demonstrate upper airway obstruction,
respiratory failure or shock
Antihistamines
Cool compresses
Avoid triggers
For pts with C1 esterase inhibitor deficiency:
C1 esterase inhibitor concentrate,
54. 5454
Pemphigoid
More common than pemphigus
Generally benign
Also Autoimmune
Affects older age group
Affects deeper layer in skin – tense flexural areas
Treatment same as Pemphigus – steroids +/-
immunosupressants
Variants
Gestational
Mucous membrane (Cicatricial)