This presentation basically talks about classification, identification, nature & composition of snake venom, snake poisoning management(treatment i.e., both ASV & supportive, don'ts in case of snake envenomation) and forensic significance.
Snake bite poisoning and its treatment by RxVichuZ!RxVichuZ
My 106th powerpoint...that deals with snake bite poisoning.
Different types of venomous snakes, their characteristics, envenomation features and treatment strategies have been explained in a summary.
Hope it is effective for the readers involved.
snake poisoning with variety of snakes and identification features, conservative treatment.Antitoxin treatment with a note on the drugs used to treat antitoxin reactions, Venom composition and venom classification, types of snakes and features. snake bite treatment at different levels of healthcare systems in India.
Snake bite poisoning and its treatment by RxVichuZ!RxVichuZ
My 106th powerpoint...that deals with snake bite poisoning.
Different types of venomous snakes, their characteristics, envenomation features and treatment strategies have been explained in a summary.
Hope it is effective for the readers involved.
snake poisoning with variety of snakes and identification features, conservative treatment.Antitoxin treatment with a note on the drugs used to treat antitoxin reactions, Venom composition and venom classification, types of snakes and features. snake bite treatment at different levels of healthcare systems in India.
Most of the world's snakes are what are referred to as clinically non-venomous. This means they do not produce a toxin that is clinically significant to people.
in this presentation i give a detailed view of the bats and the salamanders which includes the reproductive system, respiration, digestive system, circulation system, their distribution, habit and habitat, external morphology, adaptation and conservation status
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
Most of the world's snakes are what are referred to as clinically non-venomous. This means they do not produce a toxin that is clinically significant to people.
in this presentation i give a detailed view of the bats and the salamanders which includes the reproductive system, respiration, digestive system, circulation system, their distribution, habit and habitat, external morphology, adaptation and conservation status
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
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.
Integrating Ayurveda into Parkinson’s Management: A Holistic ApproachAyurveda ForAll
Explore the benefits of combining Ayurveda with conventional Parkinson's treatments. Learn how a holistic approach can manage symptoms, enhance well-being, and balance body energies. Discover the steps to safely integrate Ayurvedic practices into your Parkinson’s care plan, including expert guidance on diet, herbal remedies, and lifestyle modifications.
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.
Rasamanikya is a excellent preparation in the field of Rasashastra, it is used in various Kushtha Roga, Shwasa, Vicharchika, Bhagandara, Vatarakta, and Phiranga Roga. In this article Preparation& Comparative analytical profile for both Formulationon i.e Rasamanikya prepared by Kushmanda swarasa & Churnodhaka Shodita Haratala. The study aims to provide insights into the comparative efficacy and analytical aspects of these formulations for enhanced therapeutic outcomes.
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.
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
NVBDCP.pptx Nation vector borne disease control programSapna Thakur
NVBDCP was launched in 2003-2004 . Vector-Borne Disease: Disease that results from an infection transmitted to humans and other animals by blood-feeding arthropods, such as mosquitoes, ticks, and fleas. Examples of vector-borne diseases include Dengue fever, West Nile Virus, Lyme disease, and malaria.
1. P R ES ENT AT I ON B Y : -
M R . M A NI S H K U M A R M I S H RA
A S S T . P R O F .
P G D E PA R T MENT O F F O R ENS I C S C I ENC E,
J A I N(DEEMED T O B E ) U N I VER SI T Y,
B E NGAL URU- 2 7
Snake Envenomation-
Fundamentals
3. General Classification
Kingdom: - Animalia
Phylum: - Chordata
Subphylum: - Vertebrata
Class: - Reptilia
Order: - Squamata
Family: - Four families are there;
a) Elapidae (e.g.: - Cobra, Krait)
b) Viperidae (e.g.: - Russell’s Viper, Pit Viper)
c) Colubridae (e.g.: - Tree snake, Asian rat snake)
d) Hydrophidae ( e.g. :- Sea snakes)
4. Classification based on nature of Venom
S.No. Family Type of Venom COD
1 Elapidae Neurotoxic Respiratory failure
2 Viperidae Hemo/ Vasculotoxic Renal failure or
Haemorrhage
3 Hydrophidae Myotoxic Respiratory failure
5. Big four in India
1. Naja naja : - Kobra,
2. Bungarus caeruleus: - Common Krait,
3. Vipera russelli: - Russel Viper,
4. Echis carinatus: - Saw Scaled Viper
Other common venomous snakes are: -
1. Ophiophagus hannah: - King Kobra,
2. Bungarus fasciatus: - Banded Krait.
8. Fatal dose & Fatal period of few snakes
S.No. Snake Fatal dose (Dried venom) Fatal period
1 King Kobra 12 mg 30 minutes- 1 day
2 Kobra 15 mg 30 minutes- 1 day
3 Saw Scaled Viper 8 mg 2-4 days
4 Russell’s Viper 20 mg 2-4 days
9. Clinical manifestation
Any form of snake bite has two types of clinical
manifestation: -
a) Local,
b) Systemic
Note: - I ) Both manifestation can be equally potent
or otherwise is possible,
II ) 20 % of snake bites are dry bites,
III ) 3/4th of snake bites are non-venomous
and do not need any specific treatment.
10. Venom
Toxic saliva secreted by modified parotid gland of
venomous snake.
Delivered through fang.
Constituents: -
a) Agglutinin, f) Haemolysin
b) Proteolysin g) Thromboplastin
c) Fibrinolysin h) Cardio toxin
d) Neurotoxin i) Hyaluronidase
e) Cholinesterase j) Lecithinase
11. Venomous Non-venomous
Head scale- Large
(Kobra, Krait), Small
(Viper)
Belly scale- Large
(Covers entire breadth)
Caudal scales- Divided
Fang:- Short (Kobra,
Krait), Long (Viper)
Habitat- Mostly
nocturnal
Head scale- Large
Belly scale- Small
(Do not cover entire
breadth)
Caudal scales- Not
divided
Fang- None
Habitat – Diurnal or
nocturnal
Comparison between Venomous & Non-venomous
snake
14. Snake Bite Management & Treatment
Management; -
a) Identification of snake species is important,
b) Management varies based on the clinical
manifestation following the snake bite and severity
of envenomation.
Immediate care or first aid: -
a) Reassurance to relieve fear is important,
b) Immobilization of the patient especially the
affected part.
15. Say No to following
No incision or suction of wound (can lead to
secondary infection & necrosis),
No tourniquet ( inappropriate application can lead to
gangrene),
No cryotherapy ( causes ischemia & increased
possibility of tissue necrosis),
No application of herbs etc.
16. Treatement
Antisnake venom(ASV) therapy is the specific antidote
of choice for snake envenomation,
The antisnake venom(ASV) should be administered by
slow intravenous (IV) injection,
Dose: - Recommended average initial dose is 10-20 vials
for common Krait & Kobra , 10 vials for Russell’s Viper &
5 vials for Saw Scaled Viper,
Each vial of ASV is capable of neutralizing 6 mg of Kobra
& Russell’s Viper venom & 4.5 mg of Saw Scaled Viper &
Common Krait
ASV can be Monovalent of Polyvalent (Only polyvalent
ASV is used in India),
The dose of ASV is similar in children & adults.
17. Cross reactions
Indiscriminate use of ASV is discouraged because of
life threatening immune reactions like Type I
hypersensitivity (within few hours), Type III
hypersensitivity (delayed).
In case of Type I hypersensitivity ASV therapy
should be transiently discontinued and adrenaline
should be given urgently.
In case of Type III hypersensitivity antihistamines &
corticosteroids are given.
18. Supportive treatment
Clear the airways & start artificial ventilation to treat
respiratory failure,
Transfusion of fresh blood in case of Viper bites,
Treatment of hypotension & shock by Atropine
administration,
Dialysis in case of Acute Renal Failure(ARF),
Anticholinesterase [e.g. Neostigmine (IM) ] along
with atropine is administered with neurotoxic
symptoms.
19. Medico-legal importance
1. Homicide – Rare,
2. Suicide – Very rare,
3. Occupational hazard – Very common,
Autopsy :- At autopsy, skin & underlying tissues
around the alleged site of bite marks and the
control sample from another healthy site is
dissected out, and preserved in saturated saline
solution along with blood preserved in Sodium
fluoride.
20. References
1. Aggrawal,A.(2016). Textbook of Forensic Medicine &
Toxicology for MBBS, Avichal Publishing Company.
2. Bhuyan, A(2021, February 18). Despite being undercounted,
India has the most snakebite deaths in the world. Scroll.in.
https://scroll.in/article/987003/despite-being-undercounted-
india-has-the-most-snakebite-deaths-in-the-world.
3. Kanchan,T.(2018). Rapid review of TOXICOLOGY, Jaypee
Brothers Medical Publishers (P) Ltd.