Diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH): European Society of Gastrointestinal Endoscopy (ESGE) Guideline 2015
This document provides guidelines from the European Society of Gastrointestinal Endoscopy (ESGE) for the diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH). It recommends immediate assessment of patients' hemodynamic status and volume replacement if unstable. It also recommends early upper endoscopy within 24 hours of presentation to determine the source of bleeding and apply endoscopic hemostasis as needed. The guidelines provide recommendations on risk stratification, medication management, endoscopic diagnosis and treatment options for various bleeding lesions.
Should we routinely administer erythromycin before endoscopy in patients with...Waleed Mahrous
Erythromycin as a prokinetic treatment initiated prior to endoscopic diagnosis in upper gastrointestinal bleeding .
Should we routinely administer erythromycin before endoscopy in patients with upper GI bleeding?
Should we give a PPI IV before endoscopy in patients with upper GI bleeding?Waleed Mahrous
Proton pump inhibitor treatment initiated prior to endoscopic diagnosis in upper gastrointestinal bleeding - SIGN , BSG , NICE , ACG , AGA , ASGE Guidelines
Should we give a PPI IV before endoscopy in patients with upper GI bleeding?
Bleeding Peptic Ulcer Disease - Does Practice Meet Evidence?Jarrod Lee
Bleeding peptic ulcer is a common medical emergency. Today many good studies and evidence based guidelines have provided doctors with a strong evidence based approach to manage this condition. However, how much of daily practice actually follows the evidence? The presentation goes through common scenarios in hospital medicine, and covers the latest evidence through a case based approach.
Should we routinely administer erythromycin before endoscopy in patients with...Waleed Mahrous
Erythromycin as a prokinetic treatment initiated prior to endoscopic diagnosis in upper gastrointestinal bleeding .
Should we routinely administer erythromycin before endoscopy in patients with upper GI bleeding?
Should we give a PPI IV before endoscopy in patients with upper GI bleeding?Waleed Mahrous
Proton pump inhibitor treatment initiated prior to endoscopic diagnosis in upper gastrointestinal bleeding - SIGN , BSG , NICE , ACG , AGA , ASGE Guidelines
Should we give a PPI IV before endoscopy in patients with upper GI bleeding?
Bleeding Peptic Ulcer Disease - Does Practice Meet Evidence?Jarrod Lee
Bleeding peptic ulcer is a common medical emergency. Today many good studies and evidence based guidelines have provided doctors with a strong evidence based approach to manage this condition. However, how much of daily practice actually follows the evidence? The presentation goes through common scenarios in hospital medicine, and covers the latest evidence through a case based approach.
Peptic ulcer bleeding (PUB) carries a 10% risk of death within 30 days and accounts for 36–46% of emergency upper gastrointestinal bleedings (UGIBs). The annual incidence of hospitalization due to PUB is 19–57 per 100,000 persons. Most of these patients undergo esophago-gastro-duodenoscopy (EGD), estimated to 2000 patients in Denmark alone every year. The poor prognosis in PUB is partly due to the clinical condition itself, and partly due to the high prevalence of medical comorbidities. Hence, optimizing pre-, intra-, and post-endoscopic patient management are likely to be important in order to minimize the risk of death and improve outcome. Although duodenal ulcer (DU) and gastric ulcer (GU) seem to be identical diseases with a considerable overlap in both risk-factor profile and clinical manifestations, ulcer site could potentially affect outcome. However, the prognostic importance of ulcer site has not been extensively evaluated, and existing knowledge is ambiguous. Two systematic reviews of predictors of re-bleeding after endoscopic treatment reported that posterior DUs and ulcers on the lesser gastric curvature more often were associated with haemostatic failure. A recent cohort study reported that bleeding DU was associated with poorer outcome than bleeding GU in terms of mortality, need for surgery and readmission. However, another large cohort from Hong Kong did not find that DU site was associated with increased mortality. Limited data exist on the prognostic importance of ulcer site in patients with PPU. In a nationwide cohort study comprising more than 24,000 Danish patients with complicated PUD, a significantly higher 30- and 90-d all-cause mortality rates were found, and more re-interventions in patients with bleeding DU compared with patients with bleeding GU, suggesting that ulcer site is an important predictor for poor outcome in patients with PUB. In patients with PPU, no significant association was seen between ulcer site and mortality or re-intervention. Finally, the proportion of GU increased slightly over time. Critically ill patients in the intensive care unit (ICU) are at risk of clinically important gastrointestinal bleeding, and acid suppressants are frequently used prophylactically. However, stress ulcer prophylaxis may increase the risk of serious adverse events and, additionally, the quantity and quality of evidence supporting the use of stress ulcer prophylaxis is low. The aims of some recent trial have been to assess the benefits and harms of stress ulcer prophylaxis with a proton pump inhibitor in adult patients in the ICU. It has been hypothesized that stress ulcer prophylaxis reduces the rate of gastrointestinal bleeding, but increases rates of nosocomial infections and myocardial ischaemia. The overall effect on mortality seems to be unpredictable.
Hematemesis- vomiting of blood , a brief studymartinshaji
There can be many causes of hematemesis, such as: bleeding ulcers. prolonged and vigorous retching that causes tears in the esophageal mucosa (known as Mallory-Weiss Syndrome) gastric or intestinal varices.Haematemesis is simply defined as “vomiting blood”. It is caused by bleeding from part of the upper portion of the gastrointestinal tract. It has a wide range of possible causes, depending on the site of blood loss and the tissue that is actively bleeding. Hence it is necessary to analyse and treat the condition perfectly , this is brief study about all the aspects hematemesis ,vomiting of blood including etiology, definition,management ,treatment by drugs etc
please comment
thank u
Upper GI Bleeding (non variceal) ASGE,ESGE, and WSES Guidelines
American Society of Gastrointestinal Endoscopy,
European Society of Gastrointestinal Endoscopy,
and, World Society of Emergency Surgery.
Peptic ulcer bleeding (PUB) carries a 10% risk of death within 30 days and accounts for 36–46% of emergency upper gastrointestinal bleedings (UGIBs). The annual incidence of hospitalization due to PUB is 19–57 per 100,000 persons. Most of these patients undergo esophago-gastro-duodenoscopy (EGD), estimated to 2000 patients in Denmark alone every year. The poor prognosis in PUB is partly due to the clinical condition itself, and partly due to the high prevalence of medical comorbidities. Hence, optimizing pre-, intra-, and post-endoscopic patient management are likely to be important in order to minimize the risk of death and improve outcome. Although duodenal ulcer (DU) and gastric ulcer (GU) seem to be identical diseases with a considerable overlap in both risk-factor profile and clinical manifestations, ulcer site could potentially affect outcome. However, the prognostic importance of ulcer site has not been extensively evaluated, and existing knowledge is ambiguous. Two systematic reviews of predictors of re-bleeding after endoscopic treatment reported that posterior DUs and ulcers on the lesser gastric curvature more often were associated with haemostatic failure. A recent cohort study reported that bleeding DU was associated with poorer outcome than bleeding GU in terms of mortality, need for surgery and readmission. However, another large cohort from Hong Kong did not find that DU site was associated with increased mortality. Limited data exist on the prognostic importance of ulcer site in patients with PPU. In a nationwide cohort study comprising more than 24,000 Danish patients with complicated PUD, a significantly higher 30- and 90-d all-cause mortality rates were found, and more re-interventions in patients with bleeding DU compared with patients with bleeding GU, suggesting that ulcer site is an important predictor for poor outcome in patients with PUB. In patients with PPU, no significant association was seen between ulcer site and mortality or re-intervention. Finally, the proportion of GU increased slightly over time. Critically ill patients in the intensive care unit (ICU) are at risk of clinically important gastrointestinal bleeding, and acid suppressants are frequently used prophylactically. However, stress ulcer prophylaxis may increase the risk of serious adverse events and, additionally, the quantity and quality of evidence supporting the use of stress ulcer prophylaxis is low. The aims of some recent trial have been to assess the benefits and harms of stress ulcer prophylaxis with a proton pump inhibitor in adult patients in the ICU. It has been hypothesized that stress ulcer prophylaxis reduces the rate of gastrointestinal bleeding, but increases rates of nosocomial infections and myocardial ischaemia. The overall effect on mortality seems to be unpredictable.
Hematemesis- vomiting of blood , a brief studymartinshaji
There can be many causes of hematemesis, such as: bleeding ulcers. prolonged and vigorous retching that causes tears in the esophageal mucosa (known as Mallory-Weiss Syndrome) gastric or intestinal varices.Haematemesis is simply defined as “vomiting blood”. It is caused by bleeding from part of the upper portion of the gastrointestinal tract. It has a wide range of possible causes, depending on the site of blood loss and the tissue that is actively bleeding. Hence it is necessary to analyse and treat the condition perfectly , this is brief study about all the aspects hematemesis ,vomiting of blood including etiology, definition,management ,treatment by drugs etc
please comment
thank u
Similar to Diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH): European Society of Gastrointestinal Endoscopy (ESGE) Guideline 2015
Upper GI Bleeding (non variceal) ASGE,ESGE, and WSES Guidelines
American Society of Gastrointestinal Endoscopy,
European Society of Gastrointestinal Endoscopy,
and, World Society of Emergency Surgery.
Some slides are taken from different textbooks of medicine like Davidson, Kumar and Clark and Oxford, and some from other presentations made by respected tutors. I'm barely responsible for compilation of various resources per my interest. These resources are free for use, and I do not claim any copyright. Hoping knowledge remains free for all, forever.
Upper GI bleeding gastroenterology .pptxKyawMyoHtet10
Upper gastroenterology bleeding
Similar to Diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH): European Society of Gastrointestinal Endoscopy (ESGE) Guideline 2015 (20)
In patients with mild symptomatic microscopic colitis, which should be considered as first-line therapy for the induction of clinical remission?
In patients with mild symptomatic microscopic colitis, budesonide should be considered as first-line therapy for the induction of clinical remission?
When a 5 asa agent no longer maintains remission in patients with ulcerative ...Waleed Mahrous
The goals of treatment for ulcerative colitis (UC) are to induce remission, maintain remission, and facilitate mucosal healing. Historically, a step-up approach has been used to accomplish these goals. Agents with the least toxicity are initially used, and agents are added or changed based on the treatment response or toxicity. The treatment of mild to moderate UC usually begins with 5-aminosalicylate acid (5-ASA), an anti-inflammatory agent. Corticosteroids may be used to reduce inflammation and to help induce disease remission when a flair of symptoms occurs. Other agents, such as thiopurine immunomodulator and biologic agents, are used to treat more severe disease, and surgery may be indicated if medical treatment fails.
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Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
New Drug Discovery and Development .....NEHA GUPTA
The "New Drug Discovery and Development" process involves the identification, design, testing, and manufacturing of novel pharmaceutical compounds with the aim of introducing new and improved treatments for various medical conditions. This comprehensive endeavor encompasses various stages, including target identification, preclinical studies, clinical trials, regulatory approval, and post-market surveillance. It involves multidisciplinary collaboration among scientists, researchers, clinicians, regulatory experts, and pharmaceutical companies to bring innovative therapies to market and address unmet medical needs.
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).
Flu Vaccine Alert in Bangalore Karnatakaaddon Scans
As flu season approaches, health officials in Bangalore, Karnataka, are urging residents to get their flu vaccinations. The seasonal flu, while common, can lead to severe health complications, particularly for vulnerable populations such as young children, the elderly, and those with underlying health conditions.
Dr. Vidisha Kumari, a leading epidemiologist in Bangalore, emphasizes the importance of getting vaccinated. "The flu vaccine is our best defense against the influenza virus. It not only protects individuals but also helps prevent the spread of the virus in our communities," he says.
This year, the flu season is expected to coincide with a potential increase in other respiratory illnesses. The Karnataka Health Department has launched an awareness campaign highlighting the significance of flu vaccinations. They have set up multiple vaccination centers across Bangalore, making it convenient for residents to receive their shots.
To encourage widespread vaccination, the government is also collaborating with local schools, workplaces, and community centers to facilitate vaccination drives. Special attention is being given to ensuring that the vaccine is accessible to all, including marginalized communities who may have limited access to healthcare.
Residents are reminded that the flu vaccine is safe and effective. Common side effects are mild and may include soreness at the injection site, mild fever, or muscle aches. These side effects are generally short-lived and far less severe than the flu itself.
Healthcare providers are also stressing the importance of continuing COVID-19 precautions. Wearing masks, practicing good hand hygiene, and maintaining social distancing are still crucial, especially in crowded places.
Protect yourself and your loved ones by getting vaccinated. Together, we can help keep Bangalore healthy and safe this flu season. For more information on vaccination centers and schedules, residents can visit the Karnataka Health Department’s official website or follow their social media pages.
Stay informed, stay safe, and get your flu shot today!
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.
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
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.
Muktapishti is a traditional Ayurvedic preparation made from Shoditha Mukta (Purified Pearl), is believed to help regulate thyroid function and reduce symptoms of hyperthyroidism due to its cooling and balancing properties. Clinical evidence on its efficacy remains limited, necessitating further research to validate its therapeutic benefits.
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
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
Knee anatomy and clinical tests 2024.pdfvimalpl1234
This includes all relevant anatomy and clinical tests compiled from standard textbooks, Campbell,netter etc..It is comprehensive and best suited for orthopaedicians and orthopaedic residents.
- Video recording of this lecture in English language: https://youtu.be/kqbnxVAZs-0
- Video recording of this lecture in Arabic language: https://youtu.be/SINlygW1Mpc
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
These lecture slides, by Dr Sidra Arshad, offer a quick overview of the physiological basis of a normal electrocardiogram.
Learning objectives:
1. Define an electrocardiogram (ECG) and electrocardiography
2. Describe how dipoles generated by the heart produce the waveforms of the ECG
3. Describe the components of a normal electrocardiogram of a typical bipolar lead (limb II)
4. Differentiate between intervals and segments
5. Enlist some common indications for obtaining an ECG
6. Describe the flow of current around the heart during the cardiac cycle
7. Discuss the placement and polarity of the leads of electrocardiograph
8. Describe the normal electrocardiograms recorded from the limb leads and explain the physiological basis of the different records that are obtained
9. Define mean electrical vector (axis) of the heart and give the normal range
10. Define the mean QRS vector
11. Describe the axes of leads (hexagonal reference system)
12. Comprehend the vectorial analysis of the normal ECG
13. Determine the mean electrical axis of the ventricular QRS and appreciate the mean axis deviation
14. Explain the concepts of current of injury, J point, and their significance
Study Resources:
1. Chapter 11, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 9, Human Physiology - From Cells to Systems, Lauralee Sherwood, 9th edition
3. Chapter 29, Ganong’s Review of Medical Physiology, 26th edition
4. Electrocardiogram, StatPearls - https://www.ncbi.nlm.nih.gov/books/NBK549803/
5. ECG in Medical Practice by ABM Abdullah, 4th edition
6. Chapter 3, Cardiology Explained, https://www.ncbi.nlm.nih.gov/books/NBK2214/
7. ECG Basics, http://www.nataliescasebook.com/tag/e-c-g-basics
Diagnosis and management of nonvariceal upper gastrointestinal hemorrhage (NVUGIH): European Society of Gastrointestinal Endoscopy (ESGE) Guideline 2015
1. Diagnosis and management of nonvariceal upper
gastrointestinal hemorrhage (NVUGIH): European
Society of Gastrointestinal Endoscopy (ESGE)
Guideline 2015
D R . W A L E E D K H . S . M A H R O U S
G A S T R O E N T E R O L O G Y A N D H E P A T O L O G Y
C O N S U L T A N T
محروس خالد وليدWaleed Khalid Mahrous
4. NVUGIH - MR1 - 1
ESGE recommends immediate assessment of
hemodynamic status in patients who present with
acute upper gastrointestinal hemorrhage (UGIH),
with prompt intravascular volume replacement
initially using crystalloid fluids if hemodynamic
instability exists .
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
5. ESGE recommends a restrictive red blood cell
transfusion strategy that aims for a target
hemoglobin between 7 g/dL and 9 g/dL.
A higher target hemoglobin should be
considered in patients with significant co-
morbidity (e. g., ischemic cardiovascular disease) .
(strong recommendation, moderate quality evidence).
NVUGIH – MR2 - 2
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
7. NVUGIH - 3
ESGE recommends the use of a validated risk
stratification tool to stratify patients into high
and low risk groups.
Risk stratification can aid clinical decision making
regarding timing of endoscopy and hospital
discharge.
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
محروس خالد وليدWaleed Khalid Mahrous
8. ESGE recommends the use of the Glasgow-
Blatchford Score (GBS) for pre-endoscopy risk
stratification.
Outpatients determined to be at very low risk,
based upon a GBS score of 0 – 1, do not require
early endoscopy nor hospital admission.
Discharged patients should be informed of the risk of
recurrent bleeding and be advised to maintain contact
with the discharging hospital
(strong recommendation, moderate quality evidence).
NVUGIH – MR3 - 4
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
11. NVUGIH – 5
For patients taking vitamin K antagonists (VKAs), ESGE
recommends withholding the VKA and correcting
coagulopathy while taking into account the patient's
cardiovascular risk in consultation with a cardiologist.
In patients with hemodynamic instability,
administration of vitamin K, supplemented with
intravenous prothrombin complex concentrate (PCC) or
fresh frozen plasma (FFP) if PCC is unavailable, is
recommended .
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
12. NVUGIH – 6
If the clinical situation allows, ESGE suggests an
international normalized ratio (INR) value < 2.5
before performing endoscopy with or without
endoscopic hemostasis .
(weak recommendation, moderate quality evidence).
13. NVUGIH – 7
ESGE recommends temporarily withholding new
direct oral anticoagulants (DOACs) in
patients with suspected acute NVUGIH in
coordination/consultation with the local
hematologist/cardiologist .
(strong recommendation, very low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
14. NVUGIH – 8
For patients using antiplatelet agents, ESGE
recommends the management algorithm detailed.
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
15.
16. ESGE recommends initiating high dose
intravenous proton pump inhibitors (PPI),
intravenous bolus followed by continuous infusion
(80 mg then 8 mg/hour), in patients presenting
with acute UGIH awaiting upper endoscopy.
However, PPI infusion should not delay the
performance of early endoscopy
(strong recommendation, high quality evidence).
NVUGIH - MR4 - 9
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
17. NVUGIH – 10
ESGE does not recommend the use of tranexamic
acid in patients with NVUGIH .
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
18. NVUGIH – 11
ESGE does not recommend the use of
somatostatin, or its analogue octreotide, in
patients with NVUGIH.
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
19. NVUGIH – MR5 - 12
ESGE recommends intravenous erythromycin
(single dose, 250 mg given 30 – 120 minutes prior to
upper gastrointestinal [GI] endoscopy) in patients
with clinically severe or ongoing active UGIH.
In selected patients, pre-endoscopic infusion of
erythromycin significantly improves endoscopic
visualization, reduces the need for second- look
endoscopy, decreases the number of units of
blood transfused, and reduces duration of
hospital stay.
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
20. ESGE does not recommend the routine use of
nasogastric or orogastric aspiration/lavage in
patients presenting with acute UGIH .
(strong recommendation, moderate quality evidence).
NVUGIH – MR6 - 13
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
21. NVUGIH – 14
In an effort to protect the patient's airway from
potential aspiration of gastric contents, ESGE
suggests endotracheal intubation prior to
endoscopy in patients with ongoing active
hematemesis, encephalopathy, or agitation .
(weak recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
22. NVUGIH – 15
ESGE recommends adopting the following
definitions regarding the timing of upper GI
endoscopy in acute overt UGIH relative to patient
presentation: very early < 12 hours, early ≤ 24
hours, and delayed > 24 hours.
(strong recommendation, moderate quality evidence).
23. Following hemodynamic resuscitation, ESGE
recommends early (≤24 hours) upper GI endoscopy.
Very early (<12 hours) upper GI endoscopy may be
considered in patients with high risk clinical
features, namely: hemodynamic instability
(tachycardia, hypotension) that persists despite
ongoing attempts at volume resuscitation; in
hospital bloody emesis/nasogastric aspirate; or
contraindication to the interruption of
anticoagulation.
(strong recommendation, moderate quality evidence).
NVUGIH - MR7 - 16
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
24. NVUGIH - 17
ESGE recommends the availability of both an on-call
GI endoscopist proficient in endoscopic hemostasis
and on-call nursing staff with technical expertisein
the use of endoscopic devices to allow performance
of endoscopy on a 24 /7 basis .
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
26. NVUGIH - 18
ESGE recommends the Forrest (F) classification
be used in all patients with peptic ulcer
hemorrhage in order to differentiate low and high
risk endoscopic stigmata .
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
27. NVUGIH - MR8 - 19
ESGE recommends that peptic ulcers with spurting
or oozing bleeding (Forrest classification Ia
and Ib, respectively) or with a nonbleeding
visible vessel (Forrest classification IIa)
receive endoscopic hemostasis because these lesions
are at high risk for persistent bleeding or
rebleeding .
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
28. NVUGIH – MR9 - 20
ESGE recommends that peptic ulcers with an
adherent clot (Forrest classification IIb) be
considered for endoscopic clot removal.
Once the clot is removed, any identified underlying
active bleeding (Forrest classification Ia or Ib) or
nonbleeding visible vessel (Forrest classification IIa)
should receive endoscopic hemostasis.
(weak recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
29. NVUGIH – MR10 - 21
In patients with peptic ulcers having a flat
pigmented spot (Forrest classification IIc) or
clean base (Forrest classification III), ESGE
does not recommend endoscopic hemostasis as
these stigmata present a low risk of recurrent
bleeding.
In selected clinical settings, these patients may
be discharged to home on standard PPI
therapy, e. g., oral PPI once-daily .
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
30. NVUGIH – 22
ESGE does not recommend the routine use of
Doppler ultrasound or magnification
endoscopy in the evaluation of endoscopic stigmata
of peptic ulcer bleeding.
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
31. NVUGIH – MR11 – 23 - 24
For patients with actively bleeding ulcers (FIa,
FIb), ESGE recommends combining epinephrine
injection with a second hemostasis modality
(contact thermal, mechanical therapy, or injection of a
sclerosing agent).
ESGE recommends that epinephrine injection therapy
not be used as endoscopic monotherapy.
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
32. NVUGIH – 25
For patients with active NVUGIH bleeding not
controlled by standard endoscopic
hemostasis therapies, ESGE suggests the use of a
topical hemostatic spray or over-the-scope
clip as salvage endoscopic therapy.
(weak recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
34. NVUGIH – 26
For patients with acid-related causes of
NVUGIH different from peptic ulcers (e. g.,
erosive esophagitis, gastritis, duodenitis),
ESGE recommends treatment with high dose PPI.
Endoscopic hemostasis is usually not required and
selected patients may be discharged early.
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
35. NVUGIH – 27
ESGE recommends that patients with a Mallory –
Weiss lesion that is actively bleeding receive
endoscopic hemostasis.
There is currently inadequate evidence to
recommend a specific endoscopic hemostasis
modality.
Patients with a Mallory – Weiss lesion and no active
bleeding can receive high dose PPI therapy
alone.
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
36. NVUGIH – 28
ESGE recommends that a Dieulafoy lesion receive
endoscopic hemostasis using thermal, mechanical
(hemoclip or band ligation), or combination
therapy (dilute epinephrine injection combined with
contact thermal or mechanical therapy).
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
37. NVUGIH – 29
In patients bleeding from upper GI angioectasias,
ESGE recommends endoscopic hemostasis
therapy.
However, there is currently inadequate evidence to
recommend a specific endoscopic hemostasis
modality.
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
38. NVUGIH – 30
In patients bleeding from upper GI neoplasia,
ESGE recommends considering endoscopic
hemostasis in order to avert urgent surgery and
reduce blood transfusion requirements.
However, no currently available endoscopic
treatment appears to have long-term efficacy.
(weak recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
39. NVUGIH – 30
Transcatheter angiographic embolization
(TAE) or surgery should be considered if
endoscopic treatment fails or is not technically
feasible .
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
41. NVUGIH – MR12 -31
ESGE recommends PPI therapy for patients who
receive endoscopic hemostasis and for
patients with adherent clot not receiving
endoscopic hemostasis. PPI therapy should
be high dose and administered as an
intravenous bolus followed by continuous
infusion (80 mg then 8 mg/hour) for 72 hours post
endoscopy
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
42. NVUGIH – 32
ESGE suggests considering PPI therapy as
intermittent intravenous bolus dosing (at least
twice-daily) for 72 hours post endoscopy for
patients who receive endoscopic hemostasis
and for patients with adherent clot not
receiving endoscopic hemostasis.
If the patient’s condition permits, high dose oral
PPI may also be an option in those able to tolerate
oral medications.
(weak recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
43. NVUGIH – MR13 – 33- 34
ESGE does not recommend routine second-look
endoscopy as part of the management of nonvariceal
upper gastrointestinal hemorrhage (NVUGIH).
However, in patients with clinical evidence of
rebleeding following successful initial endoscopic
hemostasis, ESGE recommends repeat upper
endoscopy with hemostasis if indicated.
In the case of failure of this second attempt at
hemostasis, transcatheter angiographic
embolization (TAE) or surgery should be
considered .
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
44. NVUGIH – MR14 - 35
In patients with NVUGIH secondary to peptic ulcer,
ESGE recommends investigating for the presence of
Helicobacter pylori in the acute setting with initiation
of appropriate antibiotic therapy when H. pylori is
detected.
Retesting for H. pylori should be performed in those
patients with a negative test in the acute setting.
Documentation of successful H. pylori
eradication is recommended .
(strong recommendation, high quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
45. NVUGIH – 36
ESGE recommends restarting anticoagulant therapy
following NVUGIH in patients with an indication for
long-term anticoagulation.
The timing for resumption of anticoagulation should be
assessed on a patient by patient basis.
Resuming warfarin between 7 and 15 days
following the bleeding event appears safe and effective in
preventing thromboembolic complications for most
patients.
Earlier resumption, within the first 7 days, may
be indicated for patients at high thrombotic risk.
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
46. NVUGIH – 37
In patients receiving low dose aspirin for primary
cardiovascular prophylaxis who develop peptic
ulcer bleeding, ESGE recommends withholding
aspirin, revaluating the risks/benefits of ongoing
aspirin use in consultation with a cardiologist, and
resuming low dose aspirin following ulcer healing or
earlier if clinically indicated.
(strong recommendation, low quality evidence).
محروس خالد وليدWaleed Khalid Mahrous
47. NVUGIH – MR15 - 38
In patients receiving low dose aspirin for secondary
cardiovascular prophylaxis who develop peptic ulcer
bleeding, ESGE recommends aspirin be resumed
immediately following index endoscopy if the
risk of rebleeding is low (e. g., FIIc, FIII).
In patients with high risk peptic ulcer (FIa, FIb, FIIa,
FIIb), early reintroduction of aspirin by day 3 after
index endoscopy is recommended, provided that
adequate hemostasis has been established .
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
48. Algorithm for the
management of
patients with acute
upper gastrointestinal
hemorrhage who are
using antiplatelet
agent(s)
49. NVUGIH – MR39
In patients receiving dual antiplatelet therapy
(DAPT) who develop peptic ulcer bleeding, ESGE
recommends continuing low dose aspirin
therapy.
Early cardiology consultation should be obtained
regarding the timing of resuming the second
antiplatelet agent.
(strong recommendation, low quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous
50. NVUGIH – MR40
In patients requiring dual antiplatelet therapy
(DAPT) and who have had NVUGIH, ESGE
recommends the use of a PPI as co-therapy.
(strong recommendation, moderate quality evidence).
Nonvariceal upper gastrointestinal hemorrhage: ESGE Guideline 2015
محروس خالد وليدWaleed Khalid Mahrous