1) The splanchnic circulation supplies blood to the gastrointestinal tract and accounts for 30% of total cardiac output. It is regulated by intrinsic, humoral, and extrinsic factors. Disorders include ischemic reperfusion injury and sepsis.
2) Abdominal compartment syndrome occurs when intra-abdominal pressure exceeds 20 mmHg and leads to organ dysfunction. It can be caused by diminished abdominal wall compliance, increased abdominal contents, or fluid resuscitation.
3) Abdominal compartment syndrome causes cardiovascular, respiratory, renal, and central nervous system effects by increasing intra-abdominal and intrathoracic pressures. Management includes lowering intra-abdominal pressure non-surgically or with
2. ⢠Briefly describe the splanchnic circulation.
⢠What is abdominal compartment syndrome
⢠What are the pathophysiological effects of abdominal compartment
syndrome
⢠Out line the management of abdominal compartment syndrome.
⢠Splanchnic circulation in Anaesthesia and critical care.
Objectives
8. ⢠Inferior mesenteric L3
1. Left colic
2. Sigmoid branches
3. Superior rectal
SBF about 25-30% of COP
30ml/min/100g ( <10ml/min/100g-250ml/min/100g)
Highly adaptive and act as a reservoir of blood
9. Physiological regulation of SBF
Intrinsic
control
Humoral control
Extrinsic
control
Metabolic
H+, K+ , adenosine , CO2
, hypoxia
Myogenic
Mechano sensitive Na+
Channels,
Depolarization,
Ca2+ channels
Sympathetic NS
Noradrenaline mediated
- adrenergic
vasoconstriction
Parasympathetic NS
Vagal and pelvic nerves
M1 mediated NO release
Vasodialators
Bradykinin, gastrin,
secretin, cholecystokinin,
substance P, dopamine,
Vasoconstrictors
Vasopressin, Angiotensin
ii,
Neuropeptide Y,
10. Disorders of Splanchnic Blood flow
1. Ischemic reperfusion injury
2. Sepsis /gut origin hypothesis
3. Portal hypertention
What is abdominal compartment syndrome 5%
11. ⢠Intra Abdominal Hypertention.
Normal IA pressure is 5-7mmHg, if it increases more than 12mmHg
⢠Intra Abdominal Compartment syndrome
When IA pressure exceeds 20mmHg .
⢠Grade 1 - 12â15 mm Hg;
⢠Grade 2 - 16â20 mm Hg;
⢠Grade 3 - 21â25 mm Hg;
⢠Grade 4 - >25mm Hg.
Definitions
What is abdominal compartment syndrome 5%
12. 1. Diminished abdominal wall compliance
ďAcute respiratory failure, especially with elevated Intra thoracic
pressure
ďAbdominal surgery with subjectively tight primary closure
ďMajor trauma/burns
ďProne positioning, head of bed elevated >30°
ďHigh BMI, central obesity
Causes for IA compartment syndrome
14. 4. Capillary leak/fluid resuscitation
ď Acidosis (pH <7.2)
ď Hypotension
ď Hypothermia (core temperature <33°C)
ď Polytransfusion (>10 units of blood/24 h)
ď Coagulopathy (platelets ,55 000 mm-3, prothrombin time >15 s,
partial thromboplastin time 2 times normal, or international
standardized ratio >1.5)
19. What are the pathophysiological effects of
Abdominal Compartment Syndrome 15%
20. Cardiovascular System
⢠Increase IAP Direct pressure over abdominal vasculature
Compression of IVC Compression of Aorta
Reduce preload Increase afterload
Increase intra
thoracic
pressure
Reduce compliance and
contractility Reduce COP
Catastrophic intra abdominal ischaemia
21. ⢠basal collapse/atelectasis,
⢠increasing V/Q mismatch
⢠decreased pulmonary and chest wall compliance
⢠increasing hypoxia and hypercarbia
⢠increased inspiratory pressures and PEEP in ventilated pts can
further compromise VR and COP
Respiratory system
25. FG = ( MAP - IAP ) - IAP
= MAP - 2IAP
If PTP = IAP, then
26. Hormonal effects from activation of the renin/angiotensin
system and increased ADH have a further adverse effect.
27. Central nervous system
Increased IAP Increased intra thoracic pressure
Reduced venous return
Increased ICP
hypercarbia
Cerebral
vasodilatation
28. ⢠The decrease in gut perfusion
⢠increased venous obstruction leading to bowel wall oedema.
leading to bowel ischaemia
⢠loss of cellular integrity, and translocation of bacteria into the systemic
circulation
Gastrointestinal system
29. Hepatic blood flow within the hepatic artery, vein, and
portal system is also adversely affected, leading to
mitochondrial dysfunction and eventually liver
dysfunction and failure.
30. Out line the management of abdominal
compartment syndrome.
Non-surgical
management
surgical
management
Lowering intra abdominal pressure
Organ support
open abdomen
31. ⢠supine positioning ?? Aspiration
⢠passing a nasogastric tube
⢠Enemas, flatus tubes, aperients, and pro-kinetic agents
⢠endoscopic or percutaneous decompression of the
gastrointestinal tract
⢠Avoid Coughing, straining, and ventilator dyssynchrony
Lowering intra abdominal pressure
32. ď optimize cardiac output
ď targetâ abdominal perfusion pressure of 60 mm Hg
ď Initial fluid resuscitation should be aimed at restoring normovolaemia.
ď inotrope or vasopressor
ď Renal replacement therapy may be necessary
ď Lung protective strategies
Organ support
34. Group 1 Group 2
Class 1 82 95
Class 2 76 88
Class 3 84 90
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Editor's Notes
What is splanchnic circulation- the term SC describes blood flow to abdominal GI organs.
<10ml/min/100g in low COP states
250ml/min/100g after a meal
Causes for non occlusive ischemia
Low COP ( septic shock, hypovolemic shock, cardiogenic shock)
Abdominaal compartment Xd
When pressure inside a fixed myofascial compartment is increased to a certain level sufficient to compromise perfusion, it is called compartment Xd.
In direct method we introduce needle/line connected to pressure transducer into peritonium
The pressure is transmitted to the glomeruli aswell
The FG is the pressure difference between the abdominal perfusion
pressure and the proximal tubular pressure (PTP)
Healing of bowel anastamosis and abdominal
wounds is impaired leading to anastomotic and wound breakdown
failure of clotting factor and protein synthesis,
increased susceptibility to infection, and encephalopathy. Lactic
acid clearance is compromised, making it less useful as a marker
of resuscitation and drug metabolism may also be affected, so
careful consideration to drug pharmacokinetics and dynamics is
needed.
for this reason, adequate sedation is
essential and a period of muscular paralysis may be beneficial
There is no
clear evidence as to which inotrope or vasopressor should be started as
first line, but therapy should be tailored to the individual patient.
RRT may be necessary in all patients with clinical and biochemical signs of
renal dysfunction.