1: What is an abscess?
An abscess is a collection of pus (dead/dying neutrophils plus proteinacious material) walled off by a zone of acute inflammation.
1a) What can cause an abscess?
Acute abscess formation particularly occurs in response to pyogenic organisms that attract neutrophils but are resistant to phagocytosis and lysosomal destruction.
Main pyogenic organisms of surgical relevance are staph aureus, strep pyogenes, e.coli, coliforms and bacteroides.
Abscesses can also form in response to localised tissue necrosis and organic foreign bodies like wood splints and linen sutures.
1b) What are the symptoms and signs of an abscess?
localised inflammation- redness, heat, swelling and pain.
swinging fever- usually due to bacteraemia
fluctuant mass
lyphadenopathy
1c) If investigations show leukocytosis with more than 80% neutrophils what does this indicate?
pyogenic cause
1d) How do you treat an abscess?
Incision and drainage. If it is superficial a scalpel is used, if it is deep then US or CT guided percutaneous aspiration is conducted.
The abscess will be left open but covered with a wound dressing, so if any more pus is produced it can drain away easily. If the abscess is deep, an antiseptic dressing (gauze wick) may be placed inside the wound to keep it open and let it heal via secondary intention.
Surgery may be required if an internal abscess is too large and can’t be safely accessed.
Antibiotics is not indicated if abscess is fully formed.
If the abscess perforates then treat with IV vancomycin.
Cancer staging is the process of determining the anatomical location, size and extent of spread of the tumor or its malignant process.
The purpose is to:
Most widely used staging system is TNM. T= depth of tumor invasion (1-4) N= extent of nodal involvement (0-3) M= presence of metastatic disease (0-1) Once the TNM value is determined an overall stage is assigned.
Specific staging exists for some cancers e.g. Duke stage for colorectal cancer.
2a) What is the difference between grading and staging?
Grading is the pathological assessment of a tumor to estimate the level of malignancy based on cytological differentiation and the mitotic activity of the tumor.
It is an indicator of how quickly a tumor is likely to grow and spread. Whereas, staging refers to the actual size and spread of a tumor.
A range of investigations are used. This includes clinical exam, imaging. biochemistry and histopathology.
History and exam can be used to assess signs and symptoms of cancer and its progression. This includes the constitution symptoms like weight loss, fever, malaise, night sweats.
Furthermore, Hx and Ex can reveal evidence of organ dysfn- e.g. jaundice, SOB, changes in bowel, presence of mass.
Structural imaging can help detect the presence of tumors and extent of spread. This can include Xray (bone,lung), CT (tumor vasculature), US (breat,pelvic), MRI.
Functional imaging can detect the presence of metastatic disease in bone and soft tissue. E.g. PET Scan- only useful in metabolically active cancers.
Biochemical Ix such as tumor markers and physiological changes e.g. LFT change in liver cancer.
Histopathology allows for grading to assess the level of cellular differentiation. This includes biopsy and endoscopy.
Staging can guide management. It can help determine appropriate treatment option and approach. It can assist in identifying surgical candidate, whether there is a need for adjuvant therapy or palliative therapy is better recommended for the patient. Furthermore, it can prevent unnecessary treatment that would provide little benefit to the patient and their family. E.g. Stage IV is inoperable.
Staging can provide prognostic information via comparison to historical data to provide a 5 year relative survival rate.
Staging is used to better describe a cancer when communicating within a multidisciplinary team.
And finally, staging assists in cancer research as it proivdes information on the pattern of the cancer and can help determine eligibility for clinical trials.
Neoplasia is any new and abnormal growth of tissue.
It is a result of unchecked cell proliferation due to a combination of genetic susceptibility and environmental exposures, that results in overactive growth pathways and underactive growth suppression pathways.
The division of neoplasms as benign or malignant is based on a judgement of histological pattern and the tumors clinical behavior.
Benign neoplasia are usually slow growing, well demarcated and encapsulated. They are histologically similar to the tissue of origin and remains localised at site of origin. Examples include fibroma (fibrous tissue), lipoma, adenoma (glandular tissue).
Malignant neoplasms are fast growing, poorly differentiated with an irregular outline and non-encapsulated. Histologically they range from well differentiated to anaplastic. They can present with pleomorphic nuclei and some tumors may have stromal hyperplasia. They are locally invasive and can metastasise.
Examples include; carcinomas (tumor of epithelial tissue), sarcoma (mesenchymal tissue), melanoma (melanocytes) and teratoma (cells from more than one germ layer).
A fistula is an abnormal communication between 2 epithelial surfaces, such as two hollow organs or between a hollow organ and the exterior. The formation of a fistula generally requires inflammation and pressure.
Examples include:
6a) what are some causes of fistulas?
6b) what are some causes of a non-healing fistula?
F- foreign body R- radiation I- inflammation/infection E- epithelialisation N- neoplasia D- distal obstruction
How do you treat a fistula?
Definitive treatment requires:
A stoma is an artifical opening of an internal tube that has been brought to the surface.
They can be temporary or permanent.
Permanent stomas are necessary when there is no distal bowel segment remaining.
Temporary stomas are necessary for:
- emergency procedures (e.g. complete bowel obstruction that is about to perforate)
- defunctioning (e.g. to protect a distal anastamosis that is at risk of leakage or breakdown)
- bowel rest (e.g. to allow a distal segment of bowel/perineum to rest from inflammatory process).
7a) What are some types of stomas?
A superficial wound infection is one that occurs in 30 days of the surgery and involves only the skin and subcutaneous tissue ad at least one of:
Risk factors can be classified into those relating to patients preoperative morbiditiy, intraoperative factors and post operative factors.
Preoperative include age, immunosuppression status, malnutrition, smoking, obesity, PVD
Intra-Op- contamination, poor aseptic technique, open procedures, duration of procedure, ABx prophylaxis adequacy, insertion of devices and blood transfusions.
Post Op- dressing and cleaning of wound, prolonged hospitalisation, glycemic control.
Inital step- perform primary survey to assess evidence for sepsis or heamodynamic compromise. If so refer to sepsis pathway.
If not, swab wound for microscopy,culture,screen and send bloods for FBC and culture before any ABx therapy.
Then open wound, irrigate and drain pus with 0.9%NaCl, apply a clean dressing and avoid topical ABx.
Relevant ABx can be provided if evidence of systemic involvement such as spreading cellulitis or sepsis.
The aim of appropriate antibiotic prophylaxis is to reduce post-operative infections without increasing antimicrobrial resistance.
It is based on three principles: indications, antibiotic selection and timeframe of administration.
Antibiotic prophylaxis should only be used if there is a significant risk of infection or if the post operative infection would have serious consequences.
Indications include:
- insertion of prosthesis or an artifical device like in hip replacements or heart valve replacement.
Antibiotic selection should be directed against most likely pathogen and should have a narrower range. The selection may need to be modified according to the patients risk factors (such as pre-exisitng infections, recent antimicrobial use, known colonisatin with multi-drug resistant organisms, prolonged hospitalisation or presence of prosthesis.)
The optimal time for preoperative IV antibiotic administration is within 60minutes before surgical incision. Vancomycin is an exception and needs to be given earlier as it can take an hour to infuse.
A repeat intraoperative dose is only required if the procedure is prolonged and the drug has a short half life.
Postoperative doses of IV ABx are only required in defined circumstances such as some cardiac and vascular surgeries and lower limb amputation.
Prophylaxis should not extend beyond 24 hours regardless of the procedure as extended prophylaxis is associated with an increased risk of adverse effects.
*First line is cephazolin 2g IV
Wound healing is achieved through four precisely and highly programmed phases: hemostasis, inflammation, proliferation, and remodeling. For a wound to heal successfully, all four phases must occur in the proper sequence and time frame. Many factors can interfere with one or more phases of this process, thus causing improper or impaired wound healing.
Surgical wound failure, or wound dehiscence, occurs when a wound fails to heal through the progressive stages of healing and possibly reopens after surgery.
Local factors that can affect wound healing include; poor oxygenation, infection, foreign body contamination, arterial or venous insufficiency, patient interference, unsuitable wound sutturing or dressing.
Systemic factors include; age, diabetes, ischemia, malnutrition, vit C or zinc deficiency, anaemia, immunosuppressive drugs or disease, lifestyle factors (like alcohol, smoking, IV drug use, neglect), autoimmune disorders like rheumatoid and collagen disorders like Marfans and cancer.
I categorise abdominal pain based on anatomical location.
If it is right hypochondrium I am thinking of hepatobiliar causes like hepatitis, cholecystitis, cholangitis.
For epigastric, i’m thinking of GIT causes like gastritis, GORD, pancreatitis and cardiovascular conditions like atypical MI and AAA.
In the left hypochondrium I’d be thinking splenic complications like infarcts, abscess or rupture.
In the Right and left lumbar regions I’d be thinking of radiating spinal nerve pain, ureteric colic or pyelonephritis.
In the periumbilical region, I’d be thinking of small bowel obstruction, IBS, IBS, mesenteric ischemia and AAA.
In the right iliac fossa- appendicitis, chrons disease, caecal volvolus, ectopic pregnancy, pelvic inflammatory disease.
suprapubic- cystitis, urinary retention, gynaecological causes in females.
left iliac fossa- diverticulitis, sigmoid volvolus, colorectal cancer, impaction.
The appendix is a vestigial structure located in the RIF, more specifically at McBurnys point which is 1/3 the distance from ASIS to the umbilicus.
Internally, it arises from the posteromedial aspect of the caecum and is approximately 2.5 cm below the ileocecal valve and the Tineae coli converge at base of appendix .
The base of the appendix is attached to the caecum but the tip is free to migrate allowing for variation in people- retrocecal, subcecal,other.
Surgical drainage and appendicectomy are the mainstays of treatment for appendicitis and antibiotic therapy remains only a bridge to surgery.
Therefore, antibiotics should be given only when the decision to operate has been made.
Empirical IV antibiotic is triple therapy which is the same as peritonitis due to perforated viscus. This includes Gentamicin, Amoxycillin and Metronidazole.
If it is uncomplicated appendicitis in surgery, then the antibiotics should be discontinued after the operation.
If the appendicitis is complicated by perforation or an abscess, then a total treatment duration of 7 days (IV + oral) is recommended.
Once susceptibility results are obtained, antibiotics should be modified appropriately.