This document discusses the challenges of managing anticoagulation in patients undergoing surgical procedures. It provides guidance on estimating thromboembolic and bleeding risk, deciding whether to interrupt anticoagulation, and timing interruptions. For patients at very high thromboembolic risk, the goal is to limit time off anticoagulation. Bleeding risk depends on procedure type and duration. Warfarin should be stopped 5 days before elective surgery to allow the INR to decrease safely.
* Fluid resuscitation is mandatory in shock from traumatic haemorrhage * Massive use of resuscitative fluids following injury is now being disputed * Adequate resuscitation is no longer judged by presence of normal vital signs * Normalcy of organ and tissue specific measured values are to be achieved * Search for a single endpoint that works for all trauma patients, is unrealistic * Resuscitate with appropriate fluid, in appropriate amount, at appropriate time
* Fluid resuscitation is mandatory in shock from traumatic haemorrhage * Massive use of resuscitative fluids following injury is now being disputed * Adequate resuscitation is no longer judged by presence of normal vital signs * Normalcy of organ and tissue specific measured values are to be achieved * Search for a single endpoint that works for all trauma patients, is unrealistic * Resuscitate with appropriate fluid, in appropriate amount, at appropriate time
Latest definition of sepsis, application of qSOFA, latest evidence on treatment of septic shock,role of fluids, role of steroids, isobalance salt solution
Updated global adult sepsis guidelines, released in October 2021 by the Surviving Sepsis Campaign (SSC), place an increased emphasis on improving the care of sepsis patients after they are discharged from the intensive care unit (ICU) and represent greater geographic and gender diversity than previous versions.
The new guidelines specifically address the challenges of treating patients experiencing the long-term effects of sepsis. Patients often experience lengthy ICU stays and then face a long, complicated road to recovery. In addition to physical rehabilitation challenges, patients and their families are often uncertain how to coordinate care that promotes recovery and matches their goals of care.
The term inotropic state is most commonly used in reference to various drugs that affect the strength of contraction of heart muscle (myocardial contractility). However, it can also refer to pathological conditions. For example, enlarged heart muscle (ventricular hypertrophy) can increase inotropic state, whereas dead heart muscle (myocardial infarction) can decrease it.
Deep vein thrombosis (DVT) and Pulmonary embolism (PE)Aminul Haque
Deep vein thrombosis (DVT) and pulmonary embolism (PE), collectively referred to as venous thromboembolism (VTE), constitute a major global burden of disease.
Latest definition of sepsis, application of qSOFA, latest evidence on treatment of septic shock,role of fluids, role of steroids, isobalance salt solution
Updated global adult sepsis guidelines, released in October 2021 by the Surviving Sepsis Campaign (SSC), place an increased emphasis on improving the care of sepsis patients after they are discharged from the intensive care unit (ICU) and represent greater geographic and gender diversity than previous versions.
The new guidelines specifically address the challenges of treating patients experiencing the long-term effects of sepsis. Patients often experience lengthy ICU stays and then face a long, complicated road to recovery. In addition to physical rehabilitation challenges, patients and their families are often uncertain how to coordinate care that promotes recovery and matches their goals of care.
The term inotropic state is most commonly used in reference to various drugs that affect the strength of contraction of heart muscle (myocardial contractility). However, it can also refer to pathological conditions. For example, enlarged heart muscle (ventricular hypertrophy) can increase inotropic state, whereas dead heart muscle (myocardial infarction) can decrease it.
Deep vein thrombosis (DVT) and Pulmonary embolism (PE)Aminul Haque
Deep vein thrombosis (DVT) and pulmonary embolism (PE), collectively referred to as venous thromboembolism (VTE), constitute a major global burden of disease.
Lecture by Dr Sujoy Dasgupta in BOGSCON 2015, the Annual Conference of Bengal Obstetric and Gynaecological Society, held at Hotel Novotel, Kolkata in January, 2015; where he had been invited as FACULTY to deliver his lecture
Physician should have a high suspicion to diagnose patient with pulmonary Embolism, this slides will give you precise Diagnosis, Investigation and guideline directed Treatment.
Anesthesia consideration in intestinal obstruction is gastric aspiration, rapid sequence induction, electrolyte and acid base disorder, hydration, AKI and hemodynamic status.
Hypothyroidism and hyperthyroidism have significant clinical effects. Both should be optimized. Anesthesia providers should be able to diagnose and manage.
Blood pressure optimization is important in pheochromocytoma patients before going to surgery. It is important for the anesthesia providers to diagnose, optimize and manage those patients..
Anesthetic management in Diabetic mellitusTenzin yoezer
Diabetic is a systemic disease. Preoperative assessment includes blood sugar control, involvement of systems, and types of medication. Intraoperative and postoperative management is also vital.
Describes coronary blood supply anatomy, myocardial oxygen demand and supply, and basic anesthesia consideration (history taking, special investigation, and optimization)
Scalp block is simple and easy to perform. It has the advantages of minimizing cardiovascular effects and decreasing intraoperative analgesia requirements.
New GCS, the GCS-P was adopted in 2018 by the same person who proposed GCS. It gives better prognosticate outcomes compared to GCS.
Guillain Barre’ syndrome(GBS) and Anesthesia considerationTenzin yoezer
Patients with GBS need special care when coming to the surgery. They have a high risk of aspiration, airway compromise, autonomic instability, altered response to NMBs. It is the duty of the anesthesia providers to recognize those problems and minimize the complications.
It is a rare but potentially catastrophic event that is associated with high mortality. The reported incidence of ICA varies considerably across studies.
- 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
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Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Tom Selleck Health: A Comprehensive Look at the Iconic Actor’s Wellness Journeygreendigital
Tom Selleck, an enduring figure in Hollywood. has captivated audiences for decades with his rugged charm, iconic moustache. and memorable roles in television and film. From his breakout role as Thomas Magnum in Magnum P.I. to his current portrayal of Frank Reagan in Blue Bloods. Selleck's career has spanned over 50 years. But beyond his professional achievements. fans have often been curious about Tom Selleck Health. especially as he has aged in the public eye.
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Introduction
Many have been interested in Tom Selleck health. not only because of his enduring presence on screen but also because of the challenges. and lifestyle choices he has faced and made over the years. This article delves into the various aspects of Tom Selleck health. exploring his fitness regimen, diet, mental health. and the challenges he has encountered as he ages. We'll look at how he maintains his well-being. the health issues he has faced, and his approach to ageing .
Early Life and Career
Childhood and Athletic Beginnings
Tom Selleck was born on January 29, 1945, in Detroit, Michigan, and grew up in Sherman Oaks, California. From an early age, he was involved in sports, particularly basketball. which played a significant role in his physical development. His athletic pursuits continued into college. where he attended the University of Southern California (USC) on a basketball scholarship. This early involvement in sports laid a strong foundation for his physical health and disciplined lifestyle.
Transition to Acting
Selleck's transition from an athlete to an actor came with its physical demands. His first significant role in "Magnum P.I." required him to perform various stunts and maintain a fit appearance. This role, which he played from 1980 to 1988. necessitated a rigorous fitness routine to meet the show's demands. setting the stage for his long-term commitment to health and wellness.
Fitness Regimen
Workout Routine
Tom Selleck health and fitness regimen has evolved. adapting to his changing roles and age. During his "Magnum, P.I." days. Selleck's workouts were intense and focused on building and maintaining muscle mass. His routine included weightlifting, cardiovascular exercises. and specific training for the stunts he performed on the show.
Selleck adjusted his fitness routine as he aged to suit his body's needs. Today, his workouts focus on maintaining flexibility, strength, and cardiovascular health. He incorporates low-impact exercises such as swimming, walking, and light weightlifting. This balanced approach helps him stay fit without putting undue strain on his joints and muscles.
Importance of Flexibility and Mobility
In recent years, Selleck has emphasized the importance of flexibility and mobility in his fitness regimen. Understanding the natural decline in muscle mass and joint flexibility with age. he includes stretching and yoga in his routine. These practices help prevent injuries, improve posture, and maintain mobilit
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
Report Back from SGO 2024: What’s the Latest in Cervical Cancer?bkling
Are you curious about what’s new in cervical cancer research or unsure what the findings mean? Join Dr. Emily Ko, a gynecologic oncologist at Penn Medicine, to learn about the latest updates from the Society of Gynecologic Oncology (SGO) 2024 Annual Meeting on Women’s Cancer. Dr. Ko will discuss what the research presented at the conference means for you and answer your questions about the new developments.
MANAGEMENT OF ATRIOVENTRICULAR CONDUCTION BLOCK.pdfJim Jacob Roy
Cardiac conduction defects can occur due to various causes.
Atrioventricular conduction blocks ( AV blocks ) are classified into 3 types.
This document describes the acute management of AV block.
2. History
47 year old
G5P3A1L3 (Abortion at 2 months)
Admitted at 41 weeks for IOL
At the booking Wt = 95 kg
BMI = 45.24 Kg/m2
Not known case of HTN/ DM
Screening for HTN and DM at booking – Negative
No fetal anaomalies at regular USG scan
3. At T3
Mild pedal swelling
constipation
No SOB
No calf pain
No frontal head ache
4. All previous deliveries were SVD
No complications
PSHx – LEEP in 2003
Social hx- business
first child from second marriage
age of last child – 21years
5. After admission
CTG – reactive
Sweeping
Ordered CBC, Blood grouping and cross-matching, FBS
and PPBS
Synto 2.5 U started
Inj LMWH 80 mg SC OD (Mane)-as for prophylaxis DVT
6. During grand ward-round
Clinically SFH > POG
Urgent USG
EFW – 4.173 kg +/- 690 g
AFI – 9.4 cm
Emergency LSCS but she was on LMWH
Planned for Elective LSCS + TL
Discontinue LMWH morning dose on the day of
surgery
7. Examination
Ht- 145 cm
Wt – 105 kg (IBW = 40 kg)
BMI – 50 kg/m2
Comfortable
Afebrile
Not pale
Mild pedal oedema
8. PR – 80bpm
BP – 130/80 mmHg
NO murmur
RR – 20 bpm, VB, Grade 2 Mallampati
SFH – 47 cm
Cephalic presentation
10. Problem list
1. Morbid obesity
2. Elderly mother
3. On LMWH
4. Large baby
5. Grand Multi para
6. 1st child from 2nd husband
WHO CLASSIFICATION OF OBESITY :
Overweight – BMI of ≥25 to 29.9 kg/m2.
Obesity – BMI of ≥30 kg/m2.
Obesity class 1 – BMI of 30 to 34.9 kg/m2.
Obesity class 2 – BMI of 35 to 39.9 kg/m2.
Obesity class 3 – BMI of ≥40 kg/m2. ( severe,
extreme, or morbid obesity).
11. Intraoperative management
Confirmed the patient
Connected to 3 lead ECG, pulse oximeter, NIBP
BP- 120/80 mmHg
PR – 100 bpm
Spo2- 97 % RA
Spinal anesthesia- Sitting/ midline / L4-5
luckily was able to palpate her spine easily
22 G quince needle
injected 2 mL of 0.5% Heavy bupivacaine
immediately after lA injection- pt lie down (supine)
12. Intra Op
After 10 minutes
complained of nausea
but no chest discomfort
BP – 89/49 mmHg ( MAP - 53 mmHg)
PR – 80 bpm
Inj Ephedrine 18 mg IV bolus
Inj Odansetron 4 mg IV bolus
Thereafter uneventful surgery
13. Delivered baby boy
APGAR – 9/10
Birth weight – 4.02 kg
Blood loss – 1000 mL
Fluid – 1 L of R/L
14. Post op
Right after reaching in the ward complained of
head ache
Subsided with Diclofenac Na 75 mg IM
Baby Feeding well
LMWH 60 mg stat in the ward given and advised
to give for 5 days
However on Post Op Day 2 – stopped
Discharged on day 3
16. Introduction
The management of anticoagulation in patients undergoing
surgical procedures is challenging
Interrupting - transiently increases the risk of thromboembolism.
Surgery and invasive procedures have associated bleeding risks
If the patient bleeds from the procedure, their anticoagulant may
need to be discontinued for a longer period, resulting in a longer
period of increased thromboembolic risk.
A balance between reducing the risk of thromboembolism and
preventing excessive bleeding must be reached for each patient.
17. Other issues
vitamin K antagonist (eg, warfarin)- takes several days
until the anticoagulant effect is reduced and then
reestablished perioperatively
The risks and benefits of "bridging" with a shorter acting
agent, such as heparin, during this time are unclear.
The newer direct oral anticoagulants (eg, direct thrombin
inhibitor dabigatran, factor Xa
inhibitors rivaroxaban, apixaban, edoxaban) have shorter
half-lives, making them easier to discontinue and resume
rapidly
But the direct factor Xa inhibitors lack an approved drug-
specific antidote,
18. approach should be based on expert opinion
thrombotic and bleeding risks may vary depending on
individual circumstances,
Data from randomized trials or well-designed observational
studies are not available to guide practice in many settings.
Thus, approach should be used as clinical guidance and should
not substitute for clinician judgment in decisions about
perioperative anticoagulant management for individual
patients.
19. Decision should be on:
Estimate thromboembolic risk
Estimate bleeding risk
Determine the timing of anticoagulant interruption
Determine whether to use bridging anticoagulation
20. ESTIMATING THROMBOEMBOLIC RISK
The major factors that increase thromboembolic risk
are
1) Atrial fibrillation
2) Prosthetic heart valves
3) Recent venous or arterial thromboembolism (eg, within
the preceding three months)
21. Atrial fibrillation
Accounts for the highest percentage of patients for whom perioperative
anticoagulation questions arise.
Importantly, patients with atrial fibrillation are a heterogeneous group
Risk can be further classified according to clinical variables such as:
age
hypertension
congestive heart failure
diabetes
prior stroke
and other vascular disease
The variables are incorporated CHA2DS2-VASc score
22. CHA2DS2-VASc score
CHA2DS2-VASc risk factor Points
Congestive heart failureSigns/symptoms of heart failure or objective evidence of reduced
left-ventricular ejection fraction
+1
Hypertension-Resting blood pressure >140/90 mmHg on at least two occasions or current
antihypertensive treatment
+1
Age 75 years or older +2
Diabetes mellitusFasting glucose >125 mg/dL (7 mmol/L) or treatment with oral
hypoglycaemic agent and/or insulin
+1
Previous stroke, transient ischaemic attack, or thromboembolism +2
Vascular disease-Previous myocardial infarction, peripheral artery disease, or aortic plaque +1
Age 65-74 years +1
Sex category (female) +1
Note: use of risk scores has not been prospectively validated in the perioperative setting
23. Prosthetic heart valve
Prosthetic valve who is undergoing an invasive procedure
or surgery should take into account
the type
location
number of prosthetic heart valves
other risk factors for thromboembolism
the type of procedure
Since limited evidence is available, the recommendations
presented are based largely on expert opinion
24. Standardized protocol(2012 American College
of Chest Physicians (ACCP) guidelines)
Advance planning of perioperative anticoagulant management
(including anticoagulant discontinuation and resumption and
bridging therapy, as applicable),
Providing patients and providers with a calendar outlining the
timing of anticoagulant changes and INR testing
Providing education on injection technique for any outpatient low
molecular weight heparin (LMWH) therapy
Assessment of postoperative hemostasis.
25. The risk of major bleeding with VKA begins to rise steeply when
INR increases ≥5.
However, in patients with mechanical valves who require
interruption of VKA therapy, high-dose vitamin K should not be
routinely administered before invasive procedures
Since this will significantly delay the ability to re-anticoagulate
with VKA after the procedure
leading to subtherapeutic INRs, increases the risk of valve
thrombosis and thromboembolism.
26. If the INR is ≥6 without bleeding, VKA should be
stopped to permit a gradual reduction in INR
small doses (1 or 2.5 mg) of oral vitamin K may be
administered to hasten the fall in INR in patients
with a high risk of bleeding.
If the INR is >10 without bleeding, VKA should be
discontinued and 1 to 2.5 mg of oral vitamin K should
be administered, with frequent INR monitoring.
27. Avoid surgery for three months after valve
surgery
The risk of thromboembolism is highest in the first
few months after mechanical or bioprosthetic
mitral replacement or mitral valve repair
28. Recent thromboembolism
Thromboembolic risk is greater in the immediate period
following a thromboembolic event and declines over time.
Individuals with a recent thromboembolic event are likely
to benefit from delaying surgery, if possible.
If emergent surgery is required (eg, acute
cholecystectomy), bridging anticoagulation may be used
to reduce the interval without an anticoagulant.
29. Venous
The perioperative risk of venous thromboembolism is
Greatest- in individuals with an event within the prior three months
eg DVT, PE
those with a history of VTE associated with a high-risk inherited
thrombophilia.
Moderate risk- Individuals with cancer
low risk - Those with an event more than one year ago have
Therefore, delaying elective surgery even if the delay is only for a few weeks will be
beneficial.
This approach is supported by data showing that the recurrence risk for individuals
with a recent VTE is highest within the initial three to four weeks and diminishes over
the following two months
Without anticoagulation, the early risk of recurrent VTE was approximately 50 percent
treatment with warfarin for one month reduced this risk to 8 to 10 percent
after three months of warfarin therapy the risk declined to 4 to 5 percent
30. Arterial
The risk of recurrent arterial embolism from any cardiac source
is approximately 0.5 percent per day in the first month after an
acute event.
The vast majority of cases are due to atrial fibrillation
Other less common cardiac sources include
paradoxical embolism
non-bacterial thrombotic endocarditis in a patient with
malignancy
dilated or poorly contractile left ventricle
left ventricular aneurysm
31. Risk stratum
Indication for anticoagulant therapy
Mechanical heart valve Atrial fibrillation VTE
Very high thrombotic risk*
Any mitral valve prosthesis
Any caged-ball or tilting disc aortic valve
prosthesis
Recent (within six months) stroke or transient
ischemic attack
CHA2DS2-VASc score of ≥6
(or CHADS2 score of 5-6)
Recent (within three months) stroke or
transient ischemic attack
Rheumatic valvular heart disease
Recent (within three months) VTE
Severe thrombophilia (eg, deficiency of
protein C, protein S, or antithrombin;
antiphospholipid antibodies; multiple
abnormalities)
High thrombotic risk
Bileaflet aortic valve prosthesis and one or
more of the of following risk factors: atrial
fibrillation, prior stroke or transient ischemic
attack, hypertension, diabetes, congestive
heart failure, age >75 years
CHA2DS2-VASc score of 4-5 or CHADS2 score of
3-4
VTE within the past 3 to 12 months
Nonsevere thrombophilia (eg, heterozygous
factor V Leiden or prothrombin gene
mutation)
Recurrent VTE
Active cancer (treated within six months or
palliative)
Moderate thrombotic risk
Bileaflet aortic valve prosthesis without atrial
fibrillation and no other risk factors for stroke
CHA2DS2-VASc score of 2-3 or CHADS2 score of
0-2 (assuming no prior stroke or transient
ischemic attack)
VTE >12 months previous and no other risk
factors
32. ESTIMATING PROCEDURAL BLEEDING RISK
As a general guideline, procedures are divided into high and low bleeding
risk (2 day risk of major bleeding 2 to 4 percent or 0 to 2 percent,
respectively)
High bleeding risk procedures include
coronary artery bypass surgery
kidney biopsy
any procedure lasting >45 minutes
low bleeding risk procedures include
cholecystectomy,
carpal tunnel repair
abdominal hysterectomy
Dental and cutaneous procedures
33. DECIDING WHETHER TO INTERRUPT
ANTICOAGULATION
Limited Data
Decisions that balance thromboembolic and bleeding risks must
be made on a case-by-case basis.
In general, the anticoagulant must be discontinued if the
surgical bleeding risk is high.
Those at very high or high thromboembolic risk should limit the
period without anticoagulation to the shortest possible interval
In contrast, individuals undergoing selected low bleeding risk
surgery often can continue their anticoagulant
34. Settings requiring anticoagulant
interruption
Individuals with a temporarily very high or high thromboembolic
risk in whom surgery cannot be delayed (eg, potentially curative
cancer surgery in a patient who just had an acute VTE)
For individuals with a chronically elevated thromboembolic risk
Individuals with a moderate thromboembolic risk - can interrupt
without bridging
Temporary interruption of anticoagulation for a minor procedure
such as central venous catheter placement
35. Settings in which continuing the
anticoagulant may be preferable
Dental procedures – (An exception is multiple tooth
extractions, which we consider high bleeding risk).
Cutaneous procedures - skin biopsy, tumor excision
Selected cardiac procedures
Cardiac implantable devices
Endovascular procedures and catheter ablation
36. TIMING OF ANTICOAGULANT INTERRUPTION
Warfarin
(VKA, PT/INR)
discontinue warfarin 5 days before elective surgery
(ie,last dose of warfarin is given on day minus 6)
biological half-life -36 to 42 hours
check the PT/INR on the day before surgery
If the INR is >1.5, we administer low dose oral vit K (eg, 1
to 2 mg) and recheck the following day.
when the INR is ≤1.4 - proceed with surgery
37. LMWH should be discontinued at least 24 hours
If a twice-daily LMW heparin regimen - the evening
dose the night before surgery is omitted
If a once-daily regimen - one-half of the total daily
dose is given on the morning of the day before
surgery.
Unfractionated heparin –IV infusion until four to five
hours before the procedure
If S/C, the last dose can be given the evening
before the procedure.
38. Dabigatran –
2-3 days with normal or mildly impaired renal function
(ie, creatinine clearance >50 mL/minute),
2-4 days in those with more severe renal insufficiency (eg,
creatinine clearance between 30 and 50 mL/minute)
Rivaroxaban - 2-3 days
Apixaban - 2-3 days
Edoxaban- 2-3 days
Clopidogrel 7 days
Acetylsalicylic acid(Aspirin) – can continue
39. BRIDGING ANTICOAGULATION
Involves the administration of a short-acting anticoagulant
LMW heparin or
Unfractionated heparin
Aim - to minimize the time the patient is not
anticoagulated, thereby minimizing the risk for
perioperative thromboembolism
High thromboembolic risk with prolonged interruption of
their anticoagulant [VKA])
40. Need of bridging in individuals taking warfarin for
one of the following conditions:
Embolic stroke or systemic embolic event within the previous
three months
Mechanical mitral valve
Mechanical aortic valve and additional stroke risk factors
Atrial fibrillation and very high risk of stroke (eg, CHADS2 score
of 5 or 6, stroke or systemic embolism within the previous 12
weeks)
VTE within the previous three months (preoperative and
postoperative bridging)
Recent coronary stenting (eg, within the previous 12 weeks)
Previous thromboembolism during interruption of chronic
anticoagulation
41. Postoperative timing of bridging
Postoperative resumption of unfractionated heparin and
LMW heparin is similar.
The resumption of bridging will vary depending on the
surgery type and individual patient considerations
For those undergoing major surgery or those with a high
bleeding risk procedure - should be delayed for 48 to 72
hours after hemostasis has been secured.
For most minor procedures associated with a low bleeding
- resume 24 hours after the procedure.
42. URGENT/EMERGENT INVASIVE PROCEDURE
Warfarin
If semi-urgent (eg, within one to two days),- warfarin should
be withheld and vitamin K administered (eg, 2.5 to 5.0 mg of
oral or intravenous).
If immediate reversal - prothrombin complex concentrates
(PCCs) or plasma products (eg, Fresh Frozen Plasma [FFP],
thrombotic risk associated with these products
used only if there is life-threatening bleeding and
prolongation of the INR by a vitamin K antagonist
43. NEURAXIAL ANESTHESIA
Should not be used in anticoagulated individuals
risk of potentially catastrophic bleeding into the epidural space(both
at the time of catheter placement and the time of removal).
The timing of anticoagulant use in patients receiving neuraxial
anesthesia is illustrated by evidence-based guidelines from the
American Society of Regional Anesthesia (ASRA), which suggest the
following :
Prophylactic dose LMW heparin (eg, enoxaparin 40 mg once daily):
Before surgery, wait at least 10 to 12 hours after the last dose of
LMW heparin is administered before a spinal/epidural catheter is
placed.
After surgery, when there is adequate surgical site hemostasis,
wait at least six to eight hours after catheter removal before
resuming treatment with LMW heparins.
44. Therapeutic dose LMW heparin (eg, enoxaparin,
1 mg/kg twice daily):
Before surgery, wait at least 24 hours after the last
dose of LMW heparin is administered before
a spinal/epidural catheter is placed.
After surgery, when there is adequate surgical site
hemostasis, for twice daily dosing, wait at least 24
hours after catheter removal before resuming
therapeutic-dose LMW heparin.
For once daily dosing, wait at least six to eight hours
after catheter removal before the first dose;
45. Length of therapy
The optimal duration of anticoagulation is unknown
should be individualized on a case-by-case basis.
However, based upon extrapolated data from the general population as
well as clinical experience, the total duration of anticoagulant therapy
(pregnancy plus the postpartum period) should be at least three to six
months for women whose only risk factors for VTE were transient (eg,
pregnancy, cesarean section)
Anticoagulant therapy generally continues for at least six weeks
postpartum.
Patients with persistent risk factors for VTE may require a longer
duration of therapy.
46. American Society of Regional Anesthesia and
Pain Medicine, Number 3, April 2018
Perioperative Management of Patients on Warfarin:
Preoperative
Discontinue warfarin at least 5 days before elective procedure
Assess INR 1–2 d prior to surgery, if >1.5, consider 1–2 mg oral vitamin
K
Reversal for urgent surgery/procedure, consider 2.5–5 mg oral or IV
vitamin K; for immediate reversal, consider PCCs, fresh frozen plasma
Patients at high risk of thromboembolism
○ Bridge with therapeutic SC LMWH (preferred) or IV UFH
○ Last dose of preoperative LMWH administered 24 h before surgery,
administer half of the daily dose
○ Intravenous heparin discontinued 4–6 h before surgery
No bridging necessary for patients at low risk of thromboembolism
47. Postoperative
Patients at low risk of thromboembolism
○ Resume warfarin on POD
Patients at high risk of thromboembolism (who received
preoperative bridging therapy)
○ Minor surgical procedure—resume therapeutic LMWH
24 h postoperatively
○ Major surgical procedure—resume therapeutic LMWH
48–72 h postoperatively or administer low-dose LMWH
Assess bleeding risk and adequacy of hemostasis when
considering timing of the resumption of LMWH or UFH
therapy
48. Perioperative Management of Patients on
Antiplatelet Therapy
Patients with coronary stents
• Elective surgery postponed for the following
durations if aspirin and thienopyridine (eg,
clopidogrel or prasugrel) therapy must be
discontinued
○ Bare metal stents: 6 wk
○ Drug-eluting stents: 6 mo
• If surgery cannot be postponed, continue dual
antiplatelet therapy throughout perioperative
period
49. Patients at high risk of cardiac events (exclusive
of coronary stents)
• Continue aspirin throughout the perioperative
period
• Discontinue clopidogrel/prasugrel 5 d prior to
surgery
• Resume thienopyridine 24 h postoperatively
patients at low risk of cardiac events
• Discontinue dual antiplatelet therapy 7–10 d prior
to surgery
• Resume antiplatelet therapy 24 h postoperatively