Professional Documents
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ASA
Classification
ASA I A normal healthy Healthy, non-smoking, no or
patient. minimal alcohol use
ASA II A patient with mild Mild diseases only without
systemic disease substantive functional
limitations.
Current smoker, social alcohol
drinker, pregnancy, obesity
(30<BMI<40), well-controlled
DM/HTN, mild lung disease
ASA III A patient with severe Substantive functional
systemic disease limitations; One or more
moderate to
severe diseases. Poorly
controlled DM or HTN, COPD,
morbid
obesity (BMI 240), active
hepatitis, alcohol dependence
or abuse,
implanted pacemaker, moderate
reduction of ejection fraction,
ESRD undergoing regularly
scheduled dialysis, history (3
months) of Mi, CVA, TIA, or
CAD/stents.
ASA IV A patient with severe Recent (<3 months) MI, CVA,
systemic disease that TIA or CAD/stents, ongoing
is a constant threat to cardiac
life ischemia or severe valve
dysfunction, severe reduction of
ejection fraction, shock, sepsis,
DIC, ARD or ESRD not
undergoing regularly scheduled
dialysis
ASA V A moribund patient who is not Ruptured abdominal/thoracic
expected to survive without the aneurysm, massive trauma,
operation who is not expected to
intracranial bleed with mass
effect, ischemic bowel in the
face of significant cardiac
pathology or multiple
organ/system dysfunction
ASA VI A declared brain-dead
patient whose organs.
are being removed for
donor purposes
Oesophagectomy
PreOp
Nutrition
Respiratay complications
Infection
cardiac issues
dietary hx
assess BMI
nutrional refael
dental reffrall
bruching,mouth wash
Cleaning gums
On examinatoas what to look for
Palor
Oral herine-gum
Ocelema
Hydratorm
Tx existing Rsd.
2. step stroking
Respiratay complications
3. CXR, lung function - reserve & FEV1 reduction has direct corelation with mortality
walking
stop smoking
After factors
Assess Cardiac function
DVT prophylaxis
Icu booking
Send the patient with BHT, DVT stockings + prophylactic antibiotics to the theatre
Nutrition
Clinical assessment of Micronutrient deficiencies?
BMI for Macronutrient deficiency
0 =>20.0
1 = 18.5-2.0
2=<18.5
*If height, weight or weight loss cannot be established, use documented or recalled values (if considered
reliable). When measured or recalled height cannot be obtained, use knee height as a surrogate
measure.
If neither can be calculated, obtain an overall impression of malnutrition risk (low, medium, high) using
the following:
NBM
o ● About 2nd day commence feeding via the feeding jejunostomy tube
o ● 5-7th postoperative day after intact anastomosis confirmed commence
oral feeds Start with clear fluids and then move on to semi solids and solids
o ● Small volume frequent meals (6 – 8 times per day)
o ● Confirmation of intact anastomosis by water soluble contrast study
o ● Advice on discharge and follow up
Complications and mx
Post of complications
2. No reservoir
or else NJ tube
A. tension.
Late-strictures
pyloric stenosis
To local recurrence
Pre op work up before gastrectomy
Nutritional supplement
o High protein diet, high calorie diet
o Fe, vit B12,
Anaesthetic referral
Hb level-if anaemic blood Transfusion 2 days prior to Sx to achieve 10g/dl
Pre-op Ix - FBC, BU/SE, S.creatinine, S.protein, PT/INR, ECG, CXR, 2D echo, Lung function tests
Grouping & DT 2 units of blood
Chest physiotherapy
Steam inhalation
Breathing exercise(Insentive spirometer)
If abnormality in PT/INR correct with Vit K & FFP
Overnight fasting
Graduated compression stockings or DVT prophylaxis
Icu booking
Send the patient with BHT, DVT stockings + prophylactic antibiotics to the theater
Post Op Mx
Post-op
Immediate
General immediate
Mnemonic: PROBS
P Primary hemorrhage/Pain
R Reactive hemorrhage
S Shock/Sepsis
Early
Mnemonic: ABCDE
B Breakdown of wound or anastomotic dehicence - Gastric fistula, duodenal fistula, peritonitis, intra-
abdominal abscess, seroma, heamatoma
C Confusion-acute
late
Mnemonic: RIB
R Recurrence of malignancy
I Incisional hernia
B Bowel obstruction
Postgastrectomy complications
Malabsorption
Pathophysiology
o Lack of chyme stimulation + pancreatic enzyme levels → protein and carbohydrate
maldigestion → fat-soluble vitamin deficiency and weight loss
o Loss of parietal cells/absent intrinsic factor production vitamin B deficiency pernicious
anemia
o Critical reduction of the absorptive surface→↓ time for chyme absorption→↓ iron
absorption iron deficiency anemia •
Management
Diet modifications
o Increased protein intake
o Supplementation of medium-chain triglycerides
o Low carbohydrate diet
Supplementation of pancreatic enzymes and deficient nutrients (eg, vitamin B, iron, fat-soluble
vitamins)
Small intestinal bacterial overgrowth (SIBO)
• Definition: a pathologically increased growth of bacteria in the small intestine
• Etiology
Anatomic causes
o Short bowel syndrome
o Blind loop syndrome: bacterial overgrowth in the bypassed intestinal segment (blind loop)
that occurs as a result of gastrectomy
o Small bowel diverticulosis
o Inflammatory bowel disease
Motility disorders
o Irritable bowel syndrome
o Diabetes mellitus
o Scleroderma
Pathophysiology: all resulting from bacterial overgrowth Absorption of vitamin B fat-soluble
vitamins, zinc, and iron
↑ Production of folate
↑ Deconjugation of the bile acids
Clinical features
o Diarrhea, steatorrhea
o Abdominal discomfort, flatulence
o Weight loss, malabsorption
Diagnostics
o Jejunal aspirate cultures collected during endoscopy
o Positive lactulose breath test
Management
o Antibiotic therapy
o Parenteral supplementation of vitamins and proteins
o In some cases, surgical treatment
Efferent loop syndrome
•Definition: kinking or anastomotic narrowing of the efferent loop that causes emesis and/or a
feeling of fullness
• Management
o Acute abdomen requires immediate surgical treatment.
o In uncomplicated cases: watch and wait
Afferent loop syndrome
• Definition
o Biliary and pancreatic obstruction due to stenosis, kinking, or incorrect anastomosis of the
afferent loop
o Chyme enters the afferent loop instead of the efferent loop and causes loss of appetite, a
feeling of fullness, and billous vomiting with subsequent relief of nausea.
• Management surgical treatment
Dumping syndrome
Definition rapid gastric emptying as a result of defective gastric reservoir function, impaired pyloric
emptying mechanisms, or anomalous postsurgery gastric motor function
Early dumping
Pathophysiology: dysfunctional or bypassed pyloric sphincter rapid emptying of undiluted
hyperosmolar chyme into the small intestine fluid shift to the intestinal lumen small bowel
distention→ vagal stimulation increased intestinal motility
Clinical features
o Occur within 15-30 minutes after meal ingestion
o Include nausea, vomiting, diarrhea, and cramps
o Vasomotor symptoms such as sweating, flushing, and palpitations
Management
o Dietary modifications: small meals that include a combination of complex carbohydrates and
foods rich in protein and fat
o 30-60 min of rest in the supine position after meals
o Beta blockers may be helpful to ease tachycardia arising from hypovolemia
Late dumping
Pathophysiology dysfunctional pyloric sphincter rapid emptying of glucose-containing chime into the
small intestine quick reabsorption of glucose hyperglycemia excessive release of insulin hypoglycemia
and release of catecholamines
Clinical features
o Occur hours after meal ingestion
o Include signs of hypoglycemia leg, hunger, tremor, lightheadedness)
o Gl discomfort
Management
o Dietary modifications
o Second-line treatment: octreotide
o Third-line treatment surgery
Suspect late dumping syndrome in a patient with previous gastric surgery and hypoglycemia
Remnant gastric cancer 575859)
Definition: the development of carcinoma in the remnant stomach after gastrectomy,
regardless of the initial gastric condition or its duration
Pathophysiology: Studies suggest that duodenogastric reflux, chronic irritation due to billary
or pancreatic secretions, and the denervation of gastric mucosa after surgery result in
chronic inflammation of the remnant mucosa.
Management total gastrectomy with Roux-en-Y anastomosis and radical lymph node
dissection
Colon Sx
ERAS protocol for colorectal surgery
Department of Surgery University of Kelaniya
Prehabilitation
Correction of nutrition-
o High protein diet
o Vitamns Zn, C
o Adequate Hb?/ supplementation
Structured exercise programme
Chest physiotherapy with incentive spirometer
(If Hb<79% require transfusion, If Hb>9% no transfusion, Between 7 - 99% - individual assessment)
1. Preoperative Care
2. Intraoperative Care
2.1 Surgical Site Infection Prevention
Bowel prep - gut steralisation
Shower - soap and water
Prophylactic antibiotics (metranidazol & co-amoxyclav/ cefuroxime)- 4 hourly repeat
doses
2.2 Thromboprophylaxis
Mechanical prophylaxis for all
Calf pumps during surgery (when available)
Post operative - Enoxaparin after risk assessment 40mg s/c nocte
2.3 Intraoperative Fluid Management
Intraoperative fluid management should be goal directed based on the available
parameters. These parameters include but not limited to: electrocardiogram, heart
rate, blood pressure, and urine output. In some circumstance where monitors to
measure cardiac output and stroke volume are available, fluid therapy should be
titrated to optimize cardiac performance or stroke volume
Perioperative hemodynamics should be considered relative to baseline values rather
than absolute values that need to be
maintained. Allowable changes in hemodynamics should be individualized to each
patient, but changes in heart rate and blood pressure of 20% from baseline is most
often acceptable (Level of evidence: Moderate-High)
When hypovolemia is suspected, a fluid challenge of either crystalloid or colloid (200
250 ml) should be tested. The response should be reassessed using the available
hemodynamic parameters. The fluid challenge may be repeated based on a positive
response e.g. a 10% increase in stroke volume or an increase in blood pressure.
Clinical response to fluid challenge may be monitored by change in heart rate,
measurement/estimation of the pulse pressure variation, and blood pressure before
and after receiving the fluid challenge. Fluid challenge should be repeated until
there is no further increase in stroke volume and/or improvement in the clinical
parameters (Level of evidence: Moderate-Low)
Intraoperative crystalloid administration should consist of a balanced salt solution
(either Ringer's Lactate or Plasmalyte) (Level of evidence: Moderate-Low)
The rate of intraoperative fluid for maintenance should not be more than 1-2
ml/kg/hr. If CO monitoring is available - maintainence fluid is not required; manage
with boluses. The use of an infusion pump may be considered to reduce the risk of
fluid overload (Level of evidence: Low)
The administration of fluid for purposes other than optimization of the intravascular
fluid volume should be avoided. For example, the administration of crystalloid as a
carrier for drug administration can be reduced by using an injection port as close to
the patient as possible to avoid the need to flush in drugs with large amounts of
crystalloid (Level of evidence: Moderate-Low)
For patients who have had a mechanical bowel preparation, this fluid deficit could
be replaced using crystalloid up to 500ml. Response to fluid challenge should be
considered in determining the dose of crystalloids (Level of evidence: Low)
Crystalloid can be used to replace minor blood loss. Acute blood loss during surgery
can be replaced with crystalloids or colloids. Colloids should be considered for
situations requiring a rapid replacement of intravascular volume (Level of evidence:
Moderate- Low)
Acute blood loss during the surgery can be replaced with the use of colloids on a
ratio of 1:1 (Level of evidence: Moderate-Low)
Use of normal saline should be reserved for patients who are
hyponatremic or hypochloremic (for example, those where there is drainage of large
volumes of gastric fluid or pre-existing derangements from diuretic use)
Avoidance of Prophylactic Abdominal Drains - Drains removed 24-48 hours.
The use of prophylactic abdominal drains should be avoided as much as possible
following elective colorectal surgery
Avoidance of Prophylactic Nasogastric Tubes - Prophylactic use of nasogastric tubes
for decompression should be avoided.
Postoperative Care
3.1 Mobilisation
§ Patients should ambulate every 4 to 6 hours each day while they are
§ Patients who do not have adequate oral intake should receive not more
ModerateLow)
boluses are given. Boluses should not be given because of low urine
heart rate, urine output and mental status of patients should all be
Status
evidence: ModerateLow)
day 1. Each patient should chew one stick of gum, for at least 5 minutes, ≥
coloanal anastomosis (≤6 cm the anal verge) should have their urinary
continue monitoring
monitoring purposes
PCM/ GABAPENTINE/CELECOXIB
4. Correction of coagulopathy IV Vit K 10mg/day for 3 days→ Check PT/INR after 3 days →→ If no
increase Give FFP
IV cefuroxime 750mg
IV Metronidazole 500mg
8. Anaesthetic referral
ECG
CXR
2D Echo
S. Creatinine
BU/SE
LFT
FBS
IN CASE OF DELAY OF SUGERY OR AS PALLIATION, SYMPTOMATIC RELIEF BY ERCP & STENTING HAS TO
BE DONE
10 French gauge needle (ERCP needle) & self expanding metal stent
Post-op
ICU care
Monitor PR, BP, RR. Temperature, UOP
IV fluids - N. Saline, 5% dextrose, KCL if hypokalemia develops
Pain relief - Epidural analgesia (Light bupivacaine)
Antibiotics
o Cefuroxime 750mg IV 8H
o Metronidazole 500mg 8H
Feeding
o No jejunostomy feeding till bowel sounds appear
o Then start jujunostomy feeding from the 2nd day
After 10 days do gastrographin study to exclude anatomotic leakage. If no leakage start oral sips
of fluid. Then increase gradually.
Post op chest physiotherapy, steam inhalation
Sutures are removed on the 10th post-op day.
Follow up the patient at clinic with histology report.
Oncology referral
Complications
TURP
The preop evaluation generally includes a history and physical as well as baseline electrolytes,
CBC, PSA, a post-void residual determination, and urinalysis, which are reasonable preoperative
tests prior to urologic surgery. Coagulation studies are no longer considered necessary unless
there is a history of unexplained or unusual bleeding. Renal imaging studies and urodynamics
are also unnecessary in most cases.
Two weeks of finasteride therapy, a 5 alpha-reductase inhibitor, has been shown to reduce
microvascular density and intraoperative blood loss; therefore, it is recommended, especially in
larger prostates, prior to TURP.[17]
Preoperative antibiotics are recommended 1 hour before the expected start of surgery.[18]
Patients with indwelling catheters should receive extended antibiotic coverage based on urine
culture results.[19][20]
Due to the high risk of increased bleeding, venous thromboembolism prophylaxis is generally not
recommended in TURP, except for early ambulation.[21][22]
Postoperative Care
After transurethral prostate surgery, patients are typically admitted at least overnight. The
continuous bladder irrigation is titrated to a "light pink" or "pink lemonade" color. If possible, the
irrigation is stopped early the next morning to determine if it is clear enough for either a voiding
trial or discharge. If significant hematuria remains, then the irrigation needs to be continued,
and the hospital stay may need to be extended. Most patients go home with the Foley catheter
and instructions to "take it easy" for the next few days. A stool softener is often recommended to
avoid straining and Valsalva, which can increase prostatic bleeding.
Most patients will return to the clinic or office about one week after the surgery for catheter
removal and a voiding trial. Pathology results can also be reviewed with the patient at that time.
Finasteride is usually continued for an additional 2 to 4 weeks to help with hemostasis and
minimize hematuria. Anticoagulation is typically resumed 24 hours after all visual bleeding has
stopped. Some experts will recommend using 2 to 4 weeks of a low-dose antibiotic such as
trimethoprim-sulfa or nitrofurantoin as prophylaxis immediately after Foley catheter removal
based on the premise that there will be necrotic or devascularized prostatic tissue fragments
remaining in the prostatic fossa which could become infected. This appears reasonable, at least
in higher-risk patients.
There is minimal pain after surgery. Pelvic floor and Kegel exercises may help restore continence
quicker and are generally recommended. Full urinary control, continence, and hemostasis may
take 4 to 6 weeks after the procedure to fully normalize.
Vascular Surgery
Angioplasty
Preparation of pt for angioplasty
Mastectomy
● Keep the pt supine on bed with the arms by the side of the pt
● Administer adequate post op. analgesia – SC Morphine 5 mg
● Watch for bleeding & the functioning of the surgical site drain
● Monitor pulse, BP & RR
● IV fluids until oral is started
● Start oral fluids in 2hrs once the peristalsis has returned
● 2 more doses of Cefuroxime at 6hrs & 12 hrs from the time of the op.
● Steam inhalation
● Limb & chest physiotherapy
● Make the pt sit the next day
● Early ambulation
● A shower the following day
● Remove the drain when the drain is reducing & when the daily output is < 25ml
● [important properties of a surgical drain – closed drainage system, with a patent tube,
draining due to negative pressure]
● Suture removal after 7‐10 days
● Review the pt in the clinic with the histopathology report
● Refer the pt to oncologist to decide on adjuvant therapy
Complications of mastectomy and axillary clearance
1. Due to mastectomy
Immediate
● Nerve damage - long thoracic, intercostobrachial, thoracodorsal
● Bleeding
● Haematoma
Erly
● Seroma
● Wound infection & suppuration ( after 3‐4 days)
● Breast cellulitis
● Don’t mention pain
Late
● Lymphedema of the ipsilateral upper limb – high risk erysipelas & cellulitis
o o Mx – limb elevation, massaging, compression garment, prophylactic
penicillin therapy for cellulitis
● Frozen shoulder
● Axillary vein thrombosis
● Neuropraxia – resolve spontaneously in about 6/12
a) Long thoracic nerve – serratus anterior (easily damaged at
axilla during level 2 clearance)
Ask the pt press the straightened hands against the wall firmly & observe the pt from the back for any
winging of the scapula.
b) Thoracodorsal nerve – latissimus dorsi (vascular pedicle)
Ask the pt to press his hands firmly on the bed while the arms are on either side of the
body & observe from the back for the contraction of the muscles.
Patient Advise