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01/06/2013
Contents:
Introduction.
Patho-physiology. Initial resuscitation.
investigations.
Management. Anaesthesia and labour analgesia. Conclusion.
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risk of developing serious complications from an infection. In UK, sepsis is leading cause for maternal deaths from CMACHE reports 2006-2008. Increased risk of community acquired haemolytic Streptococci group A infections.
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What is sepsis?
Sepsis is defined as infection together with systemic
manifestation of infection. A suspected or documented infection in the presence of two or more of the following is defined as sepsis.
Temperature more than 38 or less than 36. Heart rate more than 90/min in adult. WBC more than 12,000 or less than 4000 or more than 10%
of immature blast cells. Respiratory rate more than 20/min or PaCO2 less than 32mmHg. Blood sugar more than 140mg% in non-diabetic. Altered mental status.
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induced organ dysfunction or tissue hypo-perfusion. Sepsis induced hypotension is defined as SBP less than 90mmHg or MAP less than 65 mmHg in adult or reduction in BP less than 40% of the expected value for the age and sex after excluding the other causes of hypotension.
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syndrome where there is sepsis induced hypotension with decreased tissue perfusion and impaired oxygen delivery despite of adequate fluid resuscitation. Need for inotrope support to maintain adequate mean arterial pressure in-order to maintain tissue perfusion.
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function and patient depend on two or more organ support. Organ support could be:
Inotrope for to maintain cardiac output. Ventilation to improve lung oxygenation. Renal replacement therapy for renal impairment.
1.5.
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Common pathogens:
Aerobic bacteria: haemolytic Streptococci. Entero-coccus. Haemophilus influenza. Staphylococcus. Klebsiella. Anaerobic bacteria: Clostridium. Bacteroids. Others: Mycobacteria. Clamydia.
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Conditions predispose:
Obstetric causes: Intra-amniotic infections. Chorio-amnionitis. Septic abortions. Post partum endometritis. Non-obstetric causes: Pyelonephritis. Pelvic thrombophlebitis. Appendicular abscess. Pneumonia. Peritonitis. Wound infection.
Necrotising fasciitis.
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As a result: Vasodilatation. Increased vascular permeability. Impaired cellular integrity. Increased in gap between endothelium and cells. Therefore, high chances for intra-cellular hypoxia. Increased anaerobic metabolism. Intra-cellular lactic acidosis. Activation of coagulation cascade.
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Systemic effects:
CVS: Cardiac dysfunction. Impaired vaso-motor control. Renal: Renal hypo-perfusion. Acute renal impairment. Pulmonary: Alveolar collapse. Pulmonary shunting. Decreased compliance. Increased work of breathing. Hypoxia.
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Haematology: DIC. Low platelet count. Low fibrinogen levels. Activation of coagulation cascade. Liver: Liver dysfunction. Elevated liver enzymes. Impaired hepatic blood flow. Metabolic: Glucose- high blood glucose. Protein- high protein break down. Lipids- high lipid break down. Lactate- anaerobic metabolism and lactic acidosis.
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Age.
Nutritional status. Genetic polymorphism.
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Home deliveries. Low socio-economic status. Poor nutrition. Primi-para. Anaemia. Prolonged rupture of membrane. Prolonged labour. Multiple vaginal examinations. Caesarean section. Multiple pregnancies. Artificial reproductive techniques. Obesity related pregnancy. Obstetric manoeuvres.
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Recognition of sepsis:
Symptoms and signs: Pyrexia. Hypothermia. Persistent tachycardia. Tachypnoea. Vomiting and loose motions. Lower abdominal pain. Abnormal or absent fetal heart sounds.
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Key recommendations:
Modified Early Obstetric Warning Scores MEOWS: Mental function. Heart rate. Blood pressure- systolic and diastolic pressure. Respiratory rate. Temperature. Urine output.
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elevated serum lactate more than 4 mmol/l. Do not delay pending ICU admission. Need to give fluid either crystalloid or colloid. Need to aim to improve response.
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Resuscitation goals:
Central venous pressure more than 8mmHg. higher CVP values are recommended for patients on mechanical ventilators and those with pre-existing decreased ventricular compliance. Mean arterial pressure more than 65mmHg.
Urine output more than 0.5ml/Kg/hour. Central venous oxygen saturation more than 70% or
mixed venous oxygen saturation more than 65%. Haematocrit value more than 30%.
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Diagnosis:
Obtain cultures before starting antibiotics. Obtain two more blood cultures. Culture form other sites as clinically indicated. One blood culture from each vascular access sites. Perform imaging studies promptly in order to
confirm
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Antibiotic therapy:
Start antibiotics as early as possible. Always within first hour of recognising as severe sepsis
and septic shock. Start with broad spectrum antibiotics more than one agent to cover the likely pathogen with good penetration into presumed source. Reassess antibiotic regime to optimise efficacy, prevent resistance, avoid toxicity and minimise cost. Duration of therapy usually limited to 7-10 days. If response is slow should consider for un-drained focus or immune deficiency. Stop antibiotics if the cause if found non-infectious.
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established as early as possible ( within 6 hours of recognition of sepsis ). Early surgical intervention is needed like abscess drainage or wound debridement. Implement source control following successful fluid resuscitation. Choose source control measures with minimal physiological disturbances to patient. Remove IV lines if potentially infected.
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Fluid therapy:
Fluid resuscitation with colloid or crystalloid. Target CVP more than 8 ( more than 12 if mechanically
ventilated). Use a fluid challenge to check the haemodynamic response. Usual fluid challenge:
Colloids 250-500ml of either starch or gelatine
necessary for sepsis induced tissue hypo perfusion. Rate of infusion may be reduced in a patient with cardiac problems.
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Vaso-pressor support:
Main aim is to maintain mean arterial pressure more than
65mmHg. After initial fluid therapy if the response is poor can try with vasopressor support. Can try with ephedrine or phenylepherine initially. The inotrope of choice for sepsis is noradrenalin in-order to improve the after load of the myocardium. If the response is poor need to add Dobutamine in-addition to noradrenalin. Dobutamine will:
Improve myocardial dysfunction. Improve the cardiac output.
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Steroids:
Consider IV hydrocortisone. Usual dose is 50mg 6 hourly. Or 200mg given as infusion over 24 hours. Maximum recommended dose is 300mg for 24 hours. ACTH stimulation test is not recommended. Hydrocortisone is preferred to dexamethazone. Fludrocortisone could be added if the patient shows
significant lack of mineralocorticoid activity. Corticosteroids are not recommended in the absence of septic shock.
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keep Hb% above 10g% if adult to improve the tissue oxygenation. Higher Hb% is required in:
No place for erythropoietin. Use FFP if bleeding or prior to any invasive procedures. Use platelets if platelet count less than 5000 or
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Mechanical ventilation:
Can develop sepsis induced acute lung injury.
So need measures for lung protection strategies: Target tidal volume 6ml/kg. Upper limit of plateau pressure of 30cmH2O. Allow permissive hypercapnoea. PEEP should be set to avoid extensive lung collapse at the time of expiration. Try to avoid injurious levels of FiO2.
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ventilation.
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critically ill mechanically ventilated patients. Preferred as infusion with daily sedation holidays to produce awakening. Re-titrate if necessary. Avoid Neuro-muscular blockers where possible.
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Glucose control:
Use IV insulin to control high blood sugars in patients
with severe sepsis following stabilisation in ICU. Keep the blood sugar below 140mg%using a validated protocol for insulin dose adjustment. Need to monitor the blood sugar levels every 1-2 hours. Once stable 4-6 hourly. Earlier tight glycaemic control was recommended.
Keep sugar levels below 110 mg%.
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Renal replacement:
Intermittent haemodialysis or continuous veno-
venous haemo-filtration should be considered. CVVH is better in haemo-dynamically unstable patients. Early renal replacement therapy had shown improved outcome.
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Bicarbonate therapy:
Considered only when pH value less than 7.0 or
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DVT prophylaxis:
Use either unfractionated heparin or low molecular
weight heparin unless contra-indicated. Can use mechanical prophylactic device like stockings, intermittent compression device. Can use combination of mechanical and pharmacological therapy for patients with high risk for DVT. LMWH is preferred to unfractionated heparin.
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proton pump inhibitor. Improvement in cardiac output is very important to prevent stress ulcer. But potential risk of ventilator associated pneumonia with use of ulcer prophylaxis medications. Potential risk for gastro-intestinal bleeding should be weighed against the development of VAP.
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New ideas:
Statins in sepsis.
Anti-oxidants. Vitamin C and vitamin E.
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Options:
Opiods Morphine IV or sc. Pethidine IV or IM. Entonox.
Regional- epidural. Other techniques. Accupunture. Massage. Hypnotherapy.
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GA. Need RSI. Opiod based analgesia. Antibiotics. Post op ICU or HDU care. Regional. If epidural in-situ epidural top-up. Not advice to keep epidural for a long time. Single shot spinal if haemo-dynamically stable.
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