2. Diabetes mellitus is defined as a syndrome
characterized by sustained hyperglycemia
due to insulin deficiency, impaired insulin
action or a combination of both.
3.
4. Classification of Diabetes
• Type 1 diabetes
– β-cell destruction
• Type 2 diabetes
– Progressive insulin secretory defect
• Other specific types of diabetes
– Genetic defects in β-cell function, insulin action
– Diseases of the exocrine pancreas
– Drug- or chemical-induced
• Gestational diabetes mellitus (GDM)
ADA. 2. Classification and Diagnosis. Diabetes Care 2015;38(suppl 1):S8
5. Diabetes affects 10–15% of the surgical population
patients with diabetes undergoing surgery have greater
complication rates, mortality rates and length of hospital stay.
Anaesthetists and other peri-operative care providers should
be knowledgeable and skilled in the care of patients with
diabetes.
6. high pre-operative and perioperative glucose and
glycated haemoglobin (HbA1c) levels are
associated with poor surgical outcomes.
increase in mortality
increase in the incidence of postoperative respiratory infections
a doubling of surgical site infections
increase in postoperative urinary tract infections
a doubling in the incidence of myocardial infarction
increase in acute kidney injury
Frisch et al., 2010
10. Mortality rate from heart disease is 24
times greater
A comprehensive cardiac assessment :in all
patients undergoing intermediate or major
non- cardiac surgery.
Major surgery: noninvasive myocardial function
studies (dobutamine stress echo) or coronary
angiography.
12. Early stage: abnormality of HR response during deep
breathing
Intermediate stage: abnormality of Valsalva response
Late stage: presence of postural hypotension
The test are valid marker of DAN if following factors ruled
out.
1. End organ failure
2. Concomitant illness
3. Drungs: antidepressents, antihistamines, diuretics,
vasodilators, sympathatic blockers, vagolytics.
13. Delay in gastric emptying – no gastric outlet
obstruction.
increased amount of gastric contents - the risk
of acid aspiration during the induction
fasting guidelines - preoperative prokinetic
drugs- H2 blockers.
14. Significant risk during airway management.
Affects temporomandibular, atlantooccipital, and
other cervical spine joints.
Short stature and waxy skin.
Related to chronic hyperglycemia and
nonenzymatic glycosylation of collagen and its
deposition in joints.
15. patient unable to approximate
the palmar surfaces of the
phalangeal joints while pressing
their hands together;
Represents cervical spine
immobility and the potential for
a difficult endotracheal
intubation .
17. Surgical stress response
NBM
Altered consciousness - masks the symptoms of
hypoglycaemia
Circulatory disturbances - which may alter the
absorption of s/c insulin.
18.
19. IV induction agents
Etomidate
Midazolam
Opioids
Inhalational ( in vitro)
Epidural anesthesia
20.
21.
22.
23.
24. In patients likely to miss one meal only- by
manipulating the patient’s normal medication.
Some agents (e.g. sulphonylureas and insulin)
act by lowering glucose concentrations: stop
or modify.
Others work by preventing glucose levels
from rising (e.g. metformin): continue.
25.
26.
27. VRIIIs are preferred in:
patients who will miss more than one meal
type-1 diabetes who have not received background
insulin
poorly controlled diabetes (HbA1c > 69 mol.mol1)
Most emergency surgeries.
Variable-rate intravenous insulin infusions should be
administered and monitored by appropriately
experienced and qualified staff.
28. Hazards: hypoglycaemia- hyperglycaemia -ketosis on cessation-
hyponatraemia.
written guidelines: safe use of VRIII - conversion from VRIII to
the usual diabetes treatment.
steady supply of substrate : glucose 5% in saline 0.45% with
KCL 0.15% or 0.3% as a maintenance fluid.
Delivery of the substrate solution and the VRIII must be via a single
cannula with appropriate one-way and anti-siphon valves .
hourly monitoring of the CBG (to keep the CBG at 6–10
mmol/L)
VRIII Shouldn’t be discontinued until alternative
subcutaneous insulin has been administered.
29.
30.
31. GOALS:
maintain glycaemic control (An intra-operative CBG range of 6–10
mmol/l).
prevent further deterioration of pre-existing end organ damage and
minimise the metabolic consequence of starvation and surgical stress.
Early return to normal diet and usual preoperative diabetic regimen.
prevent complication.
Greater concern for aseptic precaution.
32. Timing: 1st on morning list.
Positioning: pr. Areas
Anesthetic technique: acc. To type of surgery , co-morbidities
and presence of contraindications
Induction of GA:
Careful titration
RSI
Difficult intubation
Multimodal analgesia : care with NSAIDs
Temp control : hypothermia leads to insulin R, hyperglycemia,
decreased wound healing and infection.
33. ADVANTAGES
Blunts the stress response
An awake patient –
hypoglycaemia readily
detectable.
Decreased chance of Aspiration,
PONV and Thromboembolism.
Rapid return to diet and Sc
insulin/OHA
DISADVANTAGES
If autonomic neuropathy is
present, profound hypotension
may occur.
Infections and vascular
complications may be
increased (epidural abscesses)
Medicolegal concern of risk of
nerve injuries and higher risk
of ischaemic injury due to use
of adrenaline with LA
34. If CBG exceeds 12 mmol/L, capillary blood ketone levels should be
measured (point-of-care devices are available).
If the capillary blood ketones are > 3 mmol/L or there is significant
ketonuria (> 2+ on urine sticks) the patient should be treated as
having DKA ( medical emergency).
If DKA is not present, the high blood glucose should be corrected
using SC insulin or by altering the rate of the VRIII (if in use). If two
SC insulin doses do not work, a VRIII should be started.
SC rapid-acting insulin 0.1 IU/kg (up to a maximum of 6 IU), using a
specific insulin syringe. CBG checked hourly and a second dose
considered only after 2 h. A VRIII should be considered if the patient
remains hyperglycaemic.
35. For a CBG 4.0–6.0 mmol/L :
50 ml glucose 20% (10 g) should be given
intravenously.
For hypoglycaemia < 4.0 mmol/L:
100 ml (20 g) should be given intravenously.
36. There is a limited evidence base for the
recommendation of optimal fluid management
of the adult diabetic patient undergoing
surgery.
It is now recognised that Hartmann’s solution
is safe to administer to patients with diabetes
and does not contribute to clinically significant
hyperglycaemia
37. AIM: to provide glucose as a substrate to
1. prevent proteolysis, lipolysis and ketogenesis,
2. optimise intravascular volume status
3. maintain plasma electrolytes within normal .
Avoid iatrogenic hyponatraemia from the administration of hypotonic
solutions. Glucose 5% solution should be avoided.
half strength ‘normal’ saline combined with glucose is, theoretically, a
reasonable compromise to achieve these aims.
glucose 5% in saline 0.45% pre-mixed with either KCL 0.15% (20
mmol/L) or KCL 0.3% (40 mmol/L), depending on the presence of
hypokalaemia (< 3.5 mmol/L).
Additional Hartmann’s solution or another balanced isotonic crystalloid
solution should be used to optimise intravascular volume status.
38. The postoperative blood glucose management
plan, and any alterations to existing
medications, should be clearly communicated
to ward staff.
Patients with diabetes should be involved in
planning their postoperative care.
If SC insulin is required in insulin-naive
patients, or the type of insulin or the time it is
to be given is to change, the specialist diabetes
team should be contacted for advice.
39. Choices:
1. Modification of normal medication:well pt- minor surgery
2. Use of a VRIII: default technique
3. Use of a fixed-rate IV insulin infusion :in DKA
In case of emergency surgery in patient with
DKA:
Senior multidisciplinary management
High mortality
Discussion : requirement for surgery ( -ve laparotomies??,
preoperative resuscitation ( ICU admission??)
41. Metformin :key drug in the treatment of type 2 DM.
Mechanism: insulin sensitizer, inhibits gluconeogenesis
If sole therapeutic agent, no hypoglycaemia.
To hold : no evidence
The risk of lactic acidosis in patients taking metformin is
very low, but is more likely in those with renal impairment.
Safe to coninue : except in:
1. pre-existing renal imp or significant risk of developing
AKI. (renally excreted and RF may lead to high plasma
levels - risk of lactic acidosis )
2. Use of contrast
Recommended by NHS , JBDS, AAGBI 2015
42. HA1C: optimum control- elective surgery
Sliding scale : replaced by VRIII or basal- bolus
Tight glycemic control ???
Frequent intra-operative CBG monitoring
Early resumption of normal diet
Metformin: continued except in??
RL : safe
D5% should be avoided
D5 – 0.45 NS with KCL : substrate solution
43. Diabetes mellitus is likely to be the most common
comorbid factor encountered in Surgical practice.
The main peri-operative concern in diabetic
patient is optimum glycemic control.
A clear understanding of the metabolic process,
well controlled glycemic regimens and excellent
periop care will go a long way towards
decreasing the mortality and morbidity in
diabetes patients.
Editor's Notes
The classification of diabetes includes four clinical categories
Type 1 diabetes (due to β-cell destruction, usually leading to absolute insulin deficiency)
Type 2 diabetes (due to a progressive insulin secretory defect on the background of insulin resistance)
Other specific types of diabetes due to other causes; e.g., genetic defects in β-cell function, genetic defects in insulin action, diseases of the exocrine pancreas (such as cystic fibrosis), and drug- or chemical-induced diabetes (such as in the treatment of HIV/AIDS or after organ transplantation)
Gestational diabetes mellitus (GDM)(diabetes diagnosed during pregnancy that is not clearly overt diabetes)
Some patients cannot be clearly classified as having type 1 or type 2 diabetes
Clinical presentation and disease progression vary considerably in both types of diabetes
Occasionally, patients who otherwise have type 2 diabetes may present with ketoacidosis
Children with type 1 diabetes typically present with the hallmark symptoms of polyuria/polydipsia and occasionally with diabetic ketoacidosis (DKA)
However, difficulties in diagnosis may occur in children, adolescents, and adults, with the true diagnosis becoming more obvious over time
Glucose metabolism is largely a function of the liver, the pancreas, and, to a lesser degree, peripheral tissues. The liver plays a variety of roles in glucose regulation: it extracts glucose and stores it in the form of glycogen and performs gluconeogenesis as well as glycogenolysis. The pancreas secretes counterregulatory hormones: insulin from islet beta cells, which lowers blood glucose concentrations, and glucagon from islet alpha cells, which raises blood glucose concentrations. Additional contributors to glucose metabolism include the catabolic hormones: epinephrine, glucocorticoids, and growth hormone, all of which raise blood glucose concentrations. Peripheral tissues participate in glucose metabolism by extracting glucose for energy needs, thus lowering blood glucose levels. Appropriate glucose regulation preserves the availability of glucose to these tissues. For example, in the fasting state, insulin secretion decreases and catabolic hormone levels rise. In the case of absolute insulin deficiency (type 1 diabetes mellitus), unopposed catabolic action leads to hyperglycemia and, eventually, diabetic ketoacidosis. Type 2 diabetes mellitus is characterized by a peripheral resistance to insulin, and, in general, patients are less susceptible to developing ketoacidosis.
The history should assess for symptoms of cardiac, retinal, renal, neurologic, and peripheral vascular disease. Because the mortality rate from heart disease is 24 times greater in diabetic patients than nondiabetic individuals, a comprehensive cardiac history should be completed for patients undergoing intermediate or major noncardiac surgery
This slide reviews glycemic targets and treatment recommendations for non-critically ill patients with diabetes from the 2015 ADA guidelines.
Refer to source document for full recommendations, including level of evidence rating.
American Diabetes Association. Standards of medical care in diabetes—2015. Diabetes Care. 2015;38(suppl 1):S1-S93.
January 2014
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA) unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
This slide was created by Ashfield Healthcare Communications and was not associated with funding via an educational grant or a promotional/commercial interest.
This slide reviews glycemic targets and treatment recommendations for critically ill patients with diabetes from the 2015 ADA guidelines.
Refer to source document for full recommendations, including level of evidence rating.
American Diabetes Association. Standards of medical care in diabetes—2015. Diabetes Care. 2015;38(suppl 1):S1-S93.
January 2014
Any pharmacologic agents discussed are approved for use in the United States by the U.S. Food and Drug Administration (FDA) unless otherwise noted. Consult individual prescribing information for approved uses outside of the United States.
This slide was created by Ashfield Healthcare Communications and was not associated with funding via an educational grant or a promotional/commercial interest.