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4
Surgical Audit
TypesAudit cycleWhat to audit?
SU7.1: Describe the planning and conduct of surgical audit.
INTRODUCTION
Surgical audit can be defined as the systematic unbiased review of surgical practice with the objective of recognizing deficiencies and improving standards of care. It involves critical analysis by peers and any lapses or deficiencies detected during the course of the treatment of the patient are listed. An audit should aim at improving the standards laid down in the respective departments. It should also aim at studying morbidity and mortality. An audit is helpful in studying not only the quality of services provided by the department but is also useful to the individual surgeon to k his/her own personal outcome data. Contributing to a clinical database ensures that a surgeon’s own performance is monitored continuously. It should be compared to national data to ensure the accepted standards are achieved.
Example 1: National database of laparoscopic
cholecystectomy shows that in about 3–4% of cases, laparoscopic surgery needs to be converted to open surgery. However, if a surgeon’s own data records show more than 10% conversion rate, he needs to audit and find out the reason behind this high failure rate. Thus, an audit helps improve treatment policies, standard of care and may be more economical.
Example 2: A hospital may have set certain standards
for thyroidectomy such as “identification of the recurrent laryngeal nerve (RLN) should be done in all cases and
eep track of
What makes a good audit topic?What is not an audit?Steps of audit
that is the best method to avoid injuries to this nerve”. Audit of recurrent laryngeal nerve paralysis after total thyroidectomy would include a careful check of the operative notes to see how many surgeons identified the RLN at surgery and how many did not.
TYPES
Essentially, two types of audit may be encountered: National audits and local/hospital audits. Both are designed to improve the quality of care. National audits should be driven by needs identified during the local and hospital-based audits that are closest to the patient. Recently an audit of treatment given to COVID-19 patients was done to check whether all the guidelines given by the government were followed. Topics for hospital-based audits are often identified at the depart­mental morbidity and mortality meetings, where issues related to patient care are discussed. Tuberculosis is a notifiable disease and it is a national issue. So, hospitals can audit these types of cases. After report from the local hospitals, a national audit can be designed to be com­pleted by the local audit department and surgical teams.
Audit can also be categorised and used to study different aspects of patient care. For example, an audit of smoking behaviours of patients can be categorised into: (a) Structure of care: Refers to the resources required, e.g. the availability of a smoking cessation clinic in a locality. (b) Process of care: Refers to the actions and decisions taken by practitioners together with users, e.g. waiting times for an appointment at the smoking cessation clinic. (c) Outcome of care: or behaviour response to an intervention, e.g. the number of smokers who quit smoking for 1 year.
14
Measures the physical
Surgical Audit
15
AUDIT CYCLE
Important steps of audit cycle (audit process) are as follows:
1. Define the audit question in a multidisciplinary team.
2. Identify the evidence and current standards or guide­lines.
3. Design the audit to measure performance against agreed standards based on strong evidence. One needs to seek advice and ensure that institutions have agreed to undertake the audit.
4. Define an agreeable timeline.
5. Conduct the audit.
6. Analyse results and compare performance against agreed standards.
7. Undertake gap analysis:
a. If all standards are reached, reaudit after an agreed
interval.
b. If there is a need for improvement, identify possible
interventions such as training and agree with the involved parties.
c. Implement the changes.
8. Allow sufficient time for changes to be included in the new guidelines.
9. Reaudit, analyse and discuss whether the practice has improved.
WHAT TO AUDIT?
Surgeons can decide about the topics based on the need/ requirement. It is a good idea to find out the common surgical procedures done in the hospital and select a topic related to the procedures. Some examples are given below.
Simple questions with straightforward outcomes:
Example: Did all patients receive antibiotic prophylaxis prior to surgical incision?
Simple measurements and interventions: Are all
patients appropriately assessed for possibility of deep vein thrombosis (DVT) risks and received appropriate prophylaxis during their hospital stay? How many lymph nodes are removed after modified radical mastectomy performed for carcinoma breast or hemicolectomy for carcinoma colon.
Audit anything that you are not certain about: Fluid
requirements in acute pancreatitis or non-operative management of splenic injuries, etc.
WHAT MAKES A GOOD AUDIT TOPIC?
Priorities in your hospital/department: For example:
Diabetic ulcer on the leg is common not only in our hospital but also in India and it is a relevant topic.
A topic in an area of medicine that interests you and
you may choose the topic.
Re-audits of previous projects: If there is a previous
audit that was never re-audited and the loop was not closed, then this is a good audit.
WHAT IS NOT AN AUDIT?
1. Comparison of treatment or interventions: Example: Comparing antibiotics followed by drainage versus antibiotics without drainage for breast abscess.
Outcomes of novel treatment: Example: Results of
2. endoscopic cystogastrostomy.
3. Outcomes of novel service: Example: Role of CECT scan in nutrition.
4. Pure research or service evaluation: Example: Finding a new technique for hernia repair.
5. Census work All these are considered original research work and
not an audit.
STEPS OF AUDIT
The audit process is divided into five official steps and the cycle is only considered complete if all steps are performed. The five steps of audit cycle are as follows:
Step 1: Define the standard to be reviewed—American
College or Royal College guidelines, or in sepsis— Surviving Sepsis Campaign 2021 guidelines, etc. It is important to consider local policies also.
Step 2: Decide what data to be collected? Who will
be collecting the data and is it retrospective or prospective?
Step 3: Compare standard current practice with the
actual performance data collected from the department. Evaluate how well the standards were met and if not, identify reasons for this.
Step 4: Recommend a change, if required, agree to the
changes and then implement. Example: After an audit from the hospital, it is found that when clindamycin was used, ulcers healed faster in diabetic patients.
Step 5: Close the audit cycle loop—once the suggested
change is implemented, one cycle of audit is closed.
Section I Basic Principles of Surgery
5
Principles and Steps of
Clinical Research in General Surgery
Principles of clinical researchSteps of clinical research
SU7.2: Describe the principles and steps of clinical research in
general surgery.
INTRODUCTION
The dictionary defines research as “the systematic investigation into and study of materials and sources in order to establish facts and reach new conclusions”. The keywords in this definition are: (1) ‘Systematic investigation’ meaning an orderly and methodical investigation; (2) ‘Establish facts’ meaning that you are collecting new data, ing that you are adding to the already existing knowledge.
Clinical research is research in the field of health sciences particularly clinical sciences. The National Cancer Institute defines clinical research as follows: “Research in which people, or data or samples of tissue from people, are studied to understand health and disease. Clinical research helps find new and better ways to detect, diagnose, treat, and prevent disease. Types of clinical research include clinical trials, which test new treatments for a disease, and natural history studies, which collect health information to understand how a disease develops and progresses over time”.
We live in the era of evidenced-based surgery. Society at large expects us to practice scientific surgery. As long ago as 1853, Ruskin described the concept of science as follows: “The work of science is to substitute facts for appearances and demonstrations for impressions”. Any field, including surgery, can claim to be scientific only when the body of its knowledge is backed by reliable and honest data that is collected and analysed in good research studies. Thus it is essential that practicing clinicians understand the principles that underlie
and (3) ‘Reach new conclusions’ mean-
Secondary research
scientific studies and comprehend the methodology used in research projects. Further, understanding and undertaking research projects bring with it several advantages to the practicing clinician. These include (1) gaining the respect of his/her fellow clinicians, (2) better recognition in society, and (3) getting better respect and compliance from his/her patients. Also, various organisations are making it mandatory for its members to have research publications before they can progress in their careers.
PRINCIPLES OF CLINICAL RESEARCH
Clinical research is governed by several important principles. Some of these principles are highlighted hereunder.
1. Ethical conduct: The utmost importance must be given
to ethical conduct in carrying out clinical research. The researcher must exercise total honesty and integrity. The significant qualities of an ethical researcher was laid out by Salter and has been listed in Key Box 5.1
The researcher must always have in mind the physical and emotional comfort of the subject of clinical research. The ethical principle of “do no harm” must be the primary principle while under­taking research.
Key Box 5.1
Qualities of a Good Researcher (after Salter)
Integrity Inquisitive Intelligence Innovative Ingenuity Industrious Initiative Incisive
16
Principles and Steps of Clinical Research in General Surgery
17
2. Usefulness to society: Clinical research must address
common clinical problems. It should try and answer the controversies or difficult questions that a clinician faces in everyday practice. It would be incorrect to undertake research only for the sake of research and publishing papers.
3. Propriety: The researcher must always show pro-
priety in whatever he/she does. This takes several forms including financial regularity, communication with his colleagues and his subjects, proper mainte­nance of records and transparency in sharing data with others.
4. Address biases: The researcher must be careful to
make sure that biases or prejudices do not compro­mise the conclusions that are drawn from the data. Several kinds of biases exist. The important ones are: (1) Selection bias where the subjects in each of the study groups are chosen in such a manner that the results may be skewed; (2) Observer bias where the person tabulating the end result may skew the results deliberately or even unwittingly; and (3) Confounding factor/s where an intervention or a condition other than the one being studied may influence the outcome.
This essentially means that the researcher starts by saying that the intervention proposed does not have an influence on the outcome. If the data proves otherwise, then a conclusion is drawn that the intervention is indeed helpful. Continuing the above example, the null hypothesis would be that the use of a drain would not be useful after cholecystectomy.
Step 3. Draw up a protocol. A protocol is a detailed
document that describes several aspects of the study including the aim of the study with the research question, the methods that are being used to answer this question and all the administrative issues that go with the study. The protocol is required to make sure that the researcher and his colleagues know exactly what is to be done. The steps described in the protocol are never violated. The important components of a protocol are listed below:
Title that adequately describes the study and
3a. A
does enough to arouse the curiosity of the reader.
3b. Summary of the project. This is required to be submitted for various approvals that are required before the study is undertaken.
STEPS OF CLINICAL RESEARCH
Clinical research is undertaken in a systematic manner involving several steps. These steps are summarised in Fig. 5.1.
Step 1. Recognise a clinical problem and carry out a
literature search to understand what is known thus far about the subject. Once this is determined, one can go about asking a research question. An example of a common clinical question would be whether a drain has to be used after a cholecystectomy or not.
Step 2. Asking the correct research question and putting
forth a sensible hypothesis is an important step in research. One talks of the ‘null hypothesis’ in research.
Fig. 5.1: Basic steps in clinical research
3c. Rationale of the study which describes the logic behind undertaking the study, leading up to why a particular research question had to be asked.
3d. Objectives of the study—lay down the research questions in detail and explain the outcomes that are going to be measured to get answers.
3e. Methods section of the protocol is the most important part that describes in detail what is going to be done. This has several subsections as under:
3e1. Subjects involved: Describes the characteristics of the group of patients who are going to be studied
3e2. Sample size: Explains the number of patients in the groups being studied. The sample size is important to determine the ‘power’ of the study and whether the conclusions of the study can be applied to all the patients at large, or not.
3e3. Study design: Study design is the pre-eminent component of a research project. A detailed explanation of the various kinds of studies is outside the purview of this chapter. Only the very basic principles involved will be explained. Choosing the appropriate study design for a given research question is important. The value of the research project and the conclusions drawn there­from depend on the choice of a proper study design.
Anecdotal experiences reported as case reports or
small numbers of patients (series) are of limited
Section I Basic Principles of Surgery
18
Manipal Manual of Surgery
value because the information from these studies cannot be realistically extrapolated to a population in general.
Retrospective studies collect data from patients
who have already been treated or operated on. These studies are not as valuable as prospective studies because the methodology used is not standardized, there may be several data points that may be missing, and the interventions may vary from one patient to another.
Prospective studies are a lot more reliable because
the methods employed, the interventions under­taken, the tests done and the collection of data are all well controlled. The researcher can implement further safeguards against biases in the form of randomisation and blinding. Randomisation is a process where the researcher has no role in assigning the patients to the various study groups. The allocation is generally done through computer generated numbers. This process eliminates selec­tion bias. Blinding is a process where the observer who measures the outcomes of the study is not aware of the intervention that has been undertaken in the study subject. Blinding eliminates observer bias.
The randomised controlled trial (RCT) is perhaps
the highest form of unbiased scientific study. Conclusions drawn from an RCT are rated to have the highest scientific value. However, it is not easy to conduct an RCT with sufficient numbers of patients particularly in surgical disciplines.
3e4. Interventions involve a detailed description of the tests and procedures that are going to be undertaken on the patients. These may be biochemical or radiological tests. It also includes interventions in the form of administration of the study drug or an operative procedure. In the example taken, one may consider measuring pain through regular Visual Analogue Scale (VAS) scores, get a chest X-ray to rule out atelectasis and an abdominal ultrasound to detect collections.
3e5. Outcome measurements describe the endpoints that are going to be measured in the study.
Defining the endpoints and determining the correct metrics to measure them form an impor­tant part of the protocol. In the cholecystectomy example, one can consider postoperative pain, incidence of subhepatic collections, length of stay in hospital, postoperative infection, incidence of atelectasis as possible and points of the study.
Step 4. Obtain the necessary permissions from the
regulatory authorities/bodies. Armed with the protocol, the researchers start with getting clearance from the head of the unit/the head of the department and the medical administrator. The protocol will then be scrutinized by the scientific and ethical committees of the institution. Once cleared by these committees, the study has to be registered with an authority like the Clinical Trial Registry of India.
Step 5. Conduct the study with honesty and diligence
and collect data.
Step 6. Analyse the data using the previously decided
set of statistical methods.
Step 7. Draw conclusions based on the analysis of the
data collected.
Step 8. Share the results and conclusions of the study
either in the form of a presentation read at a conference or paper published in a good journal. It is quite possible that the results of this study are so significant that one might have to change ones’ clinical practice based on the study. In the example given above, many studies have shown that using a drain after a routine cholecystectomy is actually not required at all.
SECONDARY RESEARCH
The processes described so far are considered to be primary research. There is another form of research called secondary research. Examples of secondary research include systematic reviews, meta-analysis and clinical guidelines. In secondary research, data from several studies of primary research are collated and conclusions are drawn to help clinicians carry out high quality evidence-based practice.
Section I Basic Principles of Surgery
6
Perioperative Care
Preoperative care
– Elective surgery – Emergency surgery
SU1.3: Describe basic concepts of perioperative care.
The perioperative period is a term used to describe the three distinct phases of any surgical procedure, which include the preoperative phase, the intraoperative phase, and the postoperative phase.
PREOPERATIVE CARE
Every patient presenting for surgery must be optimally prepared before surgery to ensure best possible outcome of surgery. Optimisation is done based on the urgency of surgery, nature of the disease and presence of other comorbidities.
Elective Surgery
There is sufficient time available for evaluation and preparation of patients presenting for elective surgery. Preoperative evaluation will consist of detailed history, physical examination and investigations based on the findings. There is no ‘routine’ investigation. All investiga­tions must be tailored to the patient and the surgery. A patient with no other comorbidity and minimum change in his homeostasis may require no further preparation, whereas some will require considerable preparation.
Examples:
A patient may have pre-existing conditions unrelated
to surgery such as asthma, chronic obstructive pulmonary disease, hypertension or diabetes. They must be thoroughly evaluated and their condition optimized prior to surgery. stopped at least 4 weeks before surgery. Patients with respiratory conditions and those presenting for major
Smoking should be
Intraoperative carePostoperative care
thoracic or abdominal surgery may be advised incentive spirometry and respiratory exercises to improve their breathing ability.
A patient with thyrotoxicosis must be made euthyroid
before thyroidectomy, a patient with phaeochromo­cytoma must have the hypertension well under control before surgery.
Nutrition: Nutritional support may be considered for
patients who are severely malnourished. Examples may be carcinoma esophagus, achalasia cardia or a few cases of intestinal fistulae. These patients should receive seven or more days of enteral or parenteral nutrition prior to surgery. Enteral nutrition has a number of advantages such as preservation of gut mucosa, decreased leakage of gut bacterial antigens, reduction of inflammation, maintenance of immune function and decreased hyperglycemia. Healing after surgery is improved with better nutrition.
Patients with coagulopathies or bleeding disorders may
be at increased risk for bleeding. They may require peri­operative transfusion of blood products. Anti-platelet drugs should be stopped 7 days before the procedure unless they need to be continued. Low dose aspirin, however, is usually continued. Refer to Key Box 6.1.
Key Box 6.1
Elective Surgery
1. Optimise pre-existing conditions: Control of diabetes, hypertension, bronchial asthma
2. Functional status to be normal while operating on thyroid and adrenals
3. Nutritional support
4. Tailor investigations to the patient’s condition and surgery
19
20
Manipal Manual of Surgery
Emergency Surgery
These surgeries can be broadly classified further into surgeries for trauma and non-trauma.
Urgent surgery: There is usually some time available
for optimization of these patients, say a few hours, before surgery. For example, acute appendicitis, intestinal obstruction, obstructed hernia, blunt abdominal trauma. This time is utilized to treat them with intravenous fluids to optimize blood volume, correct electrolyte imbalance, administer antibiotics, bronchodilators if asthmatic and to obtain investiga­tions done such as echocardiogram. Most of abdominal emergency cases need to have a nasogastric tube inserted and urinary bladder catheterized
.
Emergency surgery: Occasionally, some surgeries are
absolutely emergent and no time should be wasted to optimize these patients. In these patients, evalua­tion, resuscitation, surgery and optimization happen simultaneously. Examples: Life-threatening conditions such as a patient with uncontrolled bleeding after polytrauma, limb-threatening conditions such as vascular injury.
Patient Preparation (Key Box 6.2)
Preoperative care also includes preparing the part for surgery, marking the site and side and obtaining informed consent (Follow WHO checklist). Consent is taken after explaining to the patient, the nature of surgery, anticipated outcome, possible complications and postoperative course, possible need of postopera­tive intensive care and even mortality (as applicable in those cases) in his own language. A witness to the process of obtaining consent must also sign on this document along with the patient and the surgeon.
In addition, the patient must be referred to the
anaesthetist (pre-anaesthesia checkup) who will once again evaluate the patient from his/her perspective, obtain additional investigations as necessary and take informed consent.
All patients are kept fasting for solids and milk for at
least 6 hours and to clear fluids for at least two hours prior to surgery. This is done to minimize the risk of
Key Box 6.2
Preparation of the Patient
1. Informed consent and signature
2. Clipping of the hair just before surgery
3. Mark the site—especially small lumps in the breast, hernias, benign lumps
4. Nil per oral 6 hours for solids, and 2 hours for liquids
5. Follow anaesthesia orders. Give drugs prescribed by
Section I Basic Principles of Surgery
anaesthetist
vomiting and pulmonary aspiration of regurgitated gastric contents during anesthesia which can lead to aspiration pneumonia.
Instructions regarding premedication, investigations
(as required on the morning of surgery) and other regular medications as prescribed by the anaesthetist must be followed (Refer to Chapter 64 on
Anaesthesia
for further details).
INTRAOPERATIVE CARE (Fig. 6.1)
The intraoperative period is the most stressful part of surgery and is the combined responsibility of the surgeon, the anesthetist, nurses and the entire surgical team.
On the day of surgery, the patient is wheeled into
the operation theatre, where his identity, surgery, site and side, availability of blood products (as necessary), fasting status and consent are once again checked before beginning anesthesia. Antibiotics are given within 30 minutes to an hour before commencement of surgery.
Once anaesthesia has been given, the anaesthetist
monitors the vitals of the patient while the surgeon concentrates on the surgery. The maintenance of depth of anaesthesia, administration of intravenous fluids, blood products, analgesics, and maintenance of physiology of the patient is the responsibility of the anaesthetist.
The surgeon undertakes the surgery with aseptic pre-
cautions, with an effort to minimize blood loss, tissue damage and in a reasonable period of time. Once surgery is done, the incision is closed after careful count of the gauzes and instruments (done by the nurse) so that nothing is left behind unintentionally inside the patient’s body.
Upon completion of surgery and emergence from
anaesthesia, the patient is shifted to the postanesthetic care unit for further observation. The patient can then be shifted to the ward after fulfilling discharge criteria (hemodynamically stable with adequate oxygenation, fully conscious, is able to void if not catheterized and is pain free). The patients are shifted to high depen­dency units, if they have undergone major surgery but are stable postoperatively. If the patient needs postoperative mechanical ventilation or is hemo­dynamically unstable, then he is shifted to the intensive care unit for further management.
POSTOPERATIVE CARE (Fig. 6.2)
Upon arrival in the recovery area, the surgeon and the anaesthetist explain to the recovery nurse in charge of the patient about the surgery, intraoperative events and
instructions for postoperative care (Key Box 6.3).
give
Perioperative Care
Fig. 6.1: Intraoperative care with monitoring vitals
Fig. 6.2: Postoperative care with monitoring of vitals
Key Box 6.3
Postoperative Care
1. Vitals: Airway, breathing, circulation and disposition
2. Analgesia
3. Fluid and electrolyte balance: Intake/output chart
4. Thromboprophylaxis—mobilisation of legs
5. Nutrition
6. Antibiotics
ABCD: Monitoring and restoration to normal physio-
logy and function of organs [(A—airway, B— breathing, C—circulation and D—disposition (consciousness)]. The patients are monitored closely and appropriate management done till their vitals are normal.
21
Pain relief: Adequate analgesia is important in the
postoperative period. This may include intravenous paracetamol, opioids, nonsteroidal anti-inflammatory drugs or regional analgesia depending on the nature of the pain and severity.
Fluid and electrolyte balance: The patients are
monitored closely postoperatively to ensure their fluid and electrolyte status is normal. An intake­output chart is maintained for all patients who have undergone major surgery. Their fluid input (including blood products) is matched with output (urine, blood loss and any other excessive secretions). In the early postoperative period, one must remem­ber that antidiuretic hormone (ADH) is released which results in conserving of water. Aldosterone secretion increases leading to reabsorption of sodium and potassium secretion.
Bowel movements: Patients who undergo laparo-
tomy have paralytic ileus, so it is common not to have bowel movement for 2 to 3 days.
Once bowel sounds are heard, the patient is given sips of water followed by soft diet.
Leg movements, both passive and active are done,
to minimize thromboembolic complications. They are also prescribed thromboprophylaxis depending upon the nature of the surgery.
Nutrition: Patients who undergo gastrectomy, eso-
phageal surgeries and surgeries on intestines, may require parenteral nutrition for a few days. Enteral nutrition is resumed as early as possible.
Preventing infection: In all contaminated and dirty
cases, antibiotics have to be continued for a period of 5 to 7 days. In cases of sepsis and septic shock, they have to be continued for 14 days.
Once the patients are stable, they are discharged
home with instructions for home care and follow-up.
Section I Basic Principles of Surgery
7
Pain Management
The pain pathwayAssessment of painRoutes of administration of analgesia
SU11.5: Describe principles of providing postoperative
pain relief and management of chronic pain.
INTRODUCTION
Pain is a sensation of discomfort associated with injury. It can be acute or chronic. Acute pain (nociception) is associated with tissue damage and an inflammatory response, it is self-limiting and of short duration. Often it does not involve neural tissue. Chronic pain, however, persists long after the tissue damage is treated. Chronic pain, on the other hand, is the pain which persists even after 3 months of surgical illness. In surgical patients, it can be due to postoperative pain, malignancies or diseases such as chronic pancreatitis.
PRINCIPLES OF PROVIDING POSTOPERATIVE PAIN RELIEF
One of the main fears patients have about surgery is the postoperative pain and it is only humane that this is relieved. In addition, pain has adverse effects on various systems of the body such as tachycardia, hypertension, arrhythmias and rarely even myocardial ischaemia and infarction. The patients may not breathe properly leading to retained secretions because of inadequate cough, atelectasis, pneumonia and respira­tory failure. The hypertension can precipitate bleeding, e.g. after thyroidectomy.
Pain relief can be given in many ways but it must be tailored to the patient since pain medications have adverse effects and hence, safety must be ensured at all times. The pain prescription must contain clear instructions regarding the name of the drug, dose, route,
Adverse effects of analgesic medicationChronic painAdjuncts
frequency, monitoring required, treatment for known side effects such as for nausea and vomiting and when to call the duty doctor.
THE PAIN PATHWAY
Postoperative pain varies with the patient’s tolerance to pain, type of surgery, anaesthetic and the site, and extent of incisions given. The pain may be somatic, visceral or both. It is important to understand how pain is transmitted and appreciated by the body to treat it effectively (Fig. 7.1).
Pain is produced in the injured tissue due to the release of prostaglandins, serotonin, substance P and acetylcholine which stimulate the peripheral nociceptors (transduction). These stimulate the peripheral nerve supplying the area and the impulses are transmitted through it to the dorsal horn of the spinal cord (transmission). These impulses then travel through the ascending tracts to the thalamus (transmission) and the sensory cortex where the pain is perceived (perception). The perception of pain can be inhibited by stimulating the descending inhibitory pathway and release of inhibitory neurotransmitters such as GABA, glycine, opioid peptides and norepinephrine (modulation). Generally, acute postsurgical pain can be controlled by addressing each component of this pain pathway and hence it is called multimodal approach to pain control.
Transduction is reduced by local anaesthetic infiltration (e.g. bupivacaine) and the use of nonsteroidal anti-inflammatory drugs (Key Box 7.1). Transmission through peripheral nerves can be blocked by nerve blocks (transverse abdominis pain block for abdominal surgery). Transmission through the spinal cord to
22
Pain Management
23
Fig. 7.1: Pain pathway, mechanisms of pain and medications that can be given to block each of these components
Key Box 7.1
Pain Mechanisms and Medications
Mechanism Medications
Transduction Local anaesthetic infiltration, NSAIDs Transmission Local anaesthetics (nerve blocks,
epidural) Perception Opioids, alpha2 agonists Modulation Opioids, alpha2 agonists, NMDA
receptor antagonists
pain and 10 represents the most severe pain they can imagine (Fig. 7.2). The patient can then be followed up using the same scale to gauge whether severity of
Fig. 7.2: Numerical rating scale
the pain has changed or whether the analgesia ascending pathways can be inhibited using epidural analgesia. Opioids (morphine, fentanyl, tramadol, nalbuphine) reduce perception. They also have a modu­lating effect on pain perception through their effects on the µ receptors in the brain as well as spinal cord.
provided is sufficient. Pain score <3 is acceptable.
NRS of 10: Very severe pain: Ureteric colic, mesenteric
ischaemia or dissecting aneurysms, etc.
NRS 4–6: Moderate pain, e.g. acute cholecystitis or
appendicitis
NRS 2–3: Dull aching pain, e.g. hepatomegaly or
ASSESSMENT OF PAIN
Pain is totally a subjective phenomenon. The patient
knows by his experience about nature of the pain and other related features. Example: Any severe pain in the abdomen results in vomiting. Thus, one can deduce that the pain is severe. Each person may respond differently to the pain. When a patient says he has pain, he probably has pain and must be believed. He can simply rate it as none, mild, moderate or severe.
Numerical rating score (NRS): In this, whenever the
patient has pain, he can be asked to rate the pain on a scale numbering from 0 to 10, where 0 means no
splenomegaly
Visual analogue scale (VAS): In this, the patient is
shown a 10 cm long scale, where one end represents no pain and the other end (10 cm) represents very severe pain (Fig. 7.3). However, unlike the NRS, the patient is not shown any number in between and the patient slides a rider across the scale to point out the level of his pain. The numbers are present on a continuous scale on the side facing the investigator and can be in fractions also.
Wong-Baker FACES scale: This scale consists of a
series of faces, where one end has a happy face representing no pain and the other end, a face
Section I Basic Principles of Surgery