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R

R on T phenomenon.  Arises when the R wave of a ventricular ectopic beat falls on the T wave of the preceding beat. At the middle of the T wave, the myocardium is partly depolarised and partly repolarised, and thus vulnerable to establishment of re-entrant and circulatory conduction, leading to VF or VT.

R wave.  First upward deflection of the QRS complex of the ECG (see Fig. 59b; Electrocardiography). Tends to increase in size from V1 to V6, with an accompanying reduction in size of S wave across these leads. Loss of this ‘R wave progression’, with a sudden increase in R wave size in V5 or V6, may indicate old anterior MI. In V1–6, at least one normally exceeds 8 mm, but none exceeds 27 mm.

Rabeprazole sodium.  Proton pump inhibitor; actions and effects are similar to those of omeprazole.

Radford nomogram.  Diagram showing the relationship between tidal volume, patient’s weight and respiratory frequency. Used to aid appropriate selection of ventilator settings for children and adults. Now rarely used.

[Edward P Radford (1922–2001), US physiologist]

Radial artery.  Terminal branch of the brachial artery. Arises in the antecubital fossa, level with the radial neck, and runs distally on the tendons and muscles attached to the radius (biceps tendon, supinator, pronator teres, flexor digitorum superficialis, flexor pollicis longus, pronator quadratus). Lies deep to brachioradialis muscle in the upper forearm, but subcutaneous in the lower forearm and easily palpable, especially over the distal quarter of the radius. Runs deep to abductor pollicis longus and extensor pollicis brevis tendons at the radial styloid, entering the anatomical snuffbox. Then enters the palm between the first and second metacarpals, forming the deep palmar arch. Branches include a superficial palmar branch (enters the palm superficial to the flexor retinaculum), which supplies the muscles of the thenar eminence before anastomosing with the superficial palmar arch. At the wrist, it is a common site for palpation of the pulse and for arterial cannulation.

See also, Ulnar artery

Radiation.  Emission of energy in the form of waves or particles. Includes emission of electromagnetic waves (e.g. light), most of which is non-ionising (does not have sufficient energy to overcome electron binding energy). Ionising radiation may result in displacement of electrons in organic material with the potential for tissue damage, and includes:

Exposure to ionising radiation is kept to a minimum with appropriate storage and handling of radioisotopes, minimal use of X-rays and appropriate use of shielding. Formal training is required for those performing or directing radiology procedures.

See also, Environmental safety of anaesthetists

Radioisotope scanning.  Use of radioisotopes to label certain parts of the body in order to investigate organ function, either directly or attached to circulating cells. Includes the following:

The radiation contained within the body after scanning is negligible, posing no risk to staff.

Radioisotopes.  Isotopes of elements that undergo disintegration; i.e. the nucleus emits α, β or γ radiation either spontaneously or following a collision. Used clinically as labels to determine fluid compartments, blood flow, pulmonary image distribution and sites of infection. Technetium-99 m and xenon-133 are often suitable because they are easy to use and their half-lives are short. Also used to label metabolically active substances which are taken up by certain tissues, allowing imaging of the tissue concerned, e.g. fibrinogen labelled with iodine-123 accumulates in a clot and may be used to detect DVT. Therapeutic use includes radiotherapy.

See also, Radioisotope scanning

Radiology, anaesthesia for.  Most radiological procedures require neither general anaesthesia nor sedation. Anaesthesia may be required for the very young, confused or agitated patients and those with movement disorders. Procedures include CT scanning, MRI, angiography and invasive procedures, e.g. embolisation of vascular lesions in neuroradiology.

Preoperative assessment and preparation should be as for any anaesthetic procedure.

Radiotherapy.  Use of ionising radiation to treat neoplasms. May involve:

ent external radiation.

ent implantation of internal sources (brachytherapy), e.g. in gynaecological or CNS tumours.

ent administration of radioactive radioisotopes, e.g. iodine-131 in hyperthyroidism, phosphorus-32 in polycythaemia.

• General anaesthesia is rarely required, except when patients are uncooperative, i.e. mainly children and patients with movement disorders. Anaesthetic considerations:

ent general condition of the patient: features of malignancy, site and nature of the neoplasm and drug therapy. Haematological abnormalities are common.

ent repeated anaesthetics: multiple treatments are required, e.g. daily for several weeks. Considerations include fear of injections and repeated periods of starvation (especially important in children). IV cannulation may be difficult, although long-term catheters are often sited.

ent immobilisation of the head may be required, e.g. for CNS tumours; clear plastic casts that cover the whole face are often used, with risks of airway obstruction. Head-down positioning may be required.

ent treatments usually consist of short periods of radiation (e.g. a few minutes), during which the anaesthetist cannot be present. Monitoring is usually visible via remote-control cameras, but may be restricted.

Techniques used include sedation or general anaesthesia using TIVA with propofol, or intermittent boluses of ketamine (especially in children).

Patients formerly treated by radiotherapy may have inflammatory or fibrotic changes in the irradiated area. Pulmonary, cardiac, neuroendocrine, renal and hepatic involvement may be present. Tissue fibrosis around the airway may make tracheal intubation difficult.

McFadyen JG, Pelly N, Orr RJ (2011). Curr Opin Anaesthesiol; 24: 433–8

Randomisation.  Technique for allocating subjects (e.g. patients to treatment groups in clinical trials) that reduces allocation bias when samples are compared. Ensures that factors such as age, sex and weight are randomly distributed amongst the groups; i.e. any difference in these factors is due to chance alone.

• Randomisation may be:

ent simple: no restriction on allocation. Groups may be unequally sized.

ent block: allocation is performed in blocks, so that groups are equally sized within each block.

ent stratified: factors such as age and sex are randomised separately, so that they are equally distributed amongst the groups. A more sophisticated method, minimisation, involves the distribution of successive subjects to the groups by taking into account the number of subjects already allocated who have these various factors, using a scoring system. For example, if age, weight and female sex are felt to be important prognostic factors in a particular study, an obese subject may still be allocated to a group that already has several obese subjects in it, if there are fewer older subjects and females than in the other groups.

Computer-generated random numbers are usually employed. Use of coins or dice is tedious and presents the temptation to repeat an allocation if the result is not liked. Other methods have also been used, e.g. allocation of alternate patients, or according to patients’ birthdays or record numbers. However, these methods cannot always be guaranteed free of hidden bias.

Ranitidine hydrochloride.  H2 receptor antagonist; better absorbed and more potent than cimetidine, with fewer side effects. Does not inhibit hepatic enzymes or interfere with metabolism of other drugs. Oral bioavailability is about 50%. Plasma levels peak within 15 min of im injection and 2–3 h after oral administration; effect lasts about 8 h. Half-life is about 2 h. Undergoes hepatic metabolism and is excreted via urine, hence the dose is reduced in renal failure.

Ranking,  see Statistical tests

Rapacuronium bromide.  Non-depolarising neuromuscular blocking drug, introduced in the USA in 1999 and withdrawn in 2001 just before its introduction in the UK, because of reports of fatal bronchospasm. Chemically related to vecuronium, it causes rapid onset of neuromuscular blockade (tracheal intubation possible within 60 s) with fast recovery (6–30 min depending on dosage) and was thus suggested as an alternative to suxamethonium.

Rapid opioid detoxification.  Technique for treating opioid addiction by precipitating withdrawal using opioid receptor antagonists, e.g. naloxone or naltrexone, supposedly reducing relapse rates compared with conventional management. Ultra-rapid opioid detoxification refers to administration of general anaesthesia or heavy sedation for prolonged periods to reduce awareness or recall of unpleasant withdrawal symptoms whilst the opioid antagonists are given. The technique is controversial (especially the ultra-rapid form) since deaths have occurred and supportive evidence for its efficacy is poor.

Singh J, Basu D (2004). J Postgrad Med; 50: 227–32

Rapid sequence induction,  see Induction, rapid sequence

Rate–pressure product (RPP).  Product of heart rate and systolic BP, used as an indicator of myocardial workload and O2 consumption. It has been suggested that RPP should be maintained below 15 000 in patients with ischaemic heart disease during anaesthesia. Its usefulness has been questioned, since a proportional increase in rate may increase myocardial O2 demand more than the same increase in BP. A pressure–rate quotient (MAP/rate) of < 1 has been suggested as being a better predictor of myocardial ischaemia.

Reactance.  Portion of impedance to flow of an alternating current not due to resistance; e.g. due to capacitance or inductance. Given the symbol X, and measured in ohms.

[Georg S Ohm (1787–1854), German physicist]

Rebreathing techniques,  see Carbon dioxide measurement

Receiver operating characteristic (ROC) curves.  Curves drawn to indicate the usefulness of a predictive test, originally derived from analysis of radar signals between the World Wars (i.e. did a deflection represent a real signal or just random noise; and if the former, with what degree of certainty?). For the test to be analysed (e.g. the usefulness of ASA physical status to predict mortality after anaesthesia), each cut-off level is examined in turn, and sensitivity and specificity calculated for it. Thus, for example, an ASA grade of 1 has high sensitivity (all deaths have an ASA grade of 1 or above) but low specificity (most patients with a grade of 1 or above do not die). For an ASA grade of 2, sensitivity is a little lower (some patients who die have a grade of 1, and will not be predicted by a grade of 2) whilst specificity is higher, although still poor (a grade of 2 is better at predicting death than a grade of 1, although most patients achieving 2 or above still do not die). The process continues until grade 5, which has low sensitivity (few of the deaths have a grade of 5) but high specificity (most patients who are graded 5 do, by definition, die). Sensitivity is plotted against (1 – specificity) and a curve obtained (Fig. 133); the area under the curve (AUC) represents the usefulness of the test: a perfect test includes 100% of the available area and one where prediction is no better than chance, 50%.

ROC curves may be drawn using continuous (e.g. C-reactive protein to predict infection), ordinal (e.g. ASA system) or nominal (e.g. presence of different features on the ECG to diagnose MI) scales. They may also be drawn for different tests in the same plot, allowing comparison between the tests. They also allow selection of the best cut-off to use clinically, usually the uppermost and most left-hand part of the curve, being the best compromise between sensitivity and specificity. They are increasingly used to analyse the usefulness of tests or scoring systems in anaesthesia and intensive care, including difficult tracheal intubation and other outcomes.

Galley HF (2004). Br J Anaesth; 93: 623–6

Receptor theory.  States that receptors are specific proteins or lipoproteins located on cell membranes or within cells that interact selectively with extracellular compounds (agonists) to initiate biochemical events within cells. The structures of the agonist and receptor determine the selectivity and quantitative response. Drugs that interact with the receptor and inhibit the effect of an agonist are antagonists. Degree of binding to receptors is affinity; ability to produce a response is intrinsic activity.

Initial assumptions that the degree of response is proportional to the number of receptors occupied are not universally accepted. Other suggestions include:

Interaction of drug and receptor may resemble Michaelis–Menten kinetics. Covalent, ionic and hydrogen bonding, and van der Waals forces may be involved.

• Different types of receptor:

ent ligand-gated ion channels: direct opening of membrane pores allowing passage of ions (e.g. Na+, K+, Ca2+, Cl) across the membrane, e.g. nicotinic acetylcholine receptor. Typically fast responses (< 1 ms).

ent G protein-coupled receptors: binding to the receptor causes a change in the guanine binding properties of the neighbouring G protein, which then leads to the intracellular response, e.g. adrenergic receptors. Typically of the order of many milliseconds to seconds.

ent ligand-activated tyrosine kinases: binding at the cell surface causes activation of tyrosine kinase at the inner surface of the cell, which catalyses phosphorylation of target proteins via ATP, e.g. insulin receptors. Typically minutes to hours.

ent nuclear receptors: the lipid-soluble agonist passes through the cell membrane to interact with the receptor, leading to alteration of DNA transcription, e.g. corticosteroid and thyroid hormones. Typically up to several hours.

Expression of receptors varies. Chronic stimulation (e.g. asthmatics taking β2-adrenergic receptor agonists) results in a decreased number of receptors (downregulation) whereas understimulation (e.g. following spinal cord injury) leads to an increased number of receptors (upregulation).

See also, Dose–response curves; Pharmacodynamics

Recommended International Non-proprietary Names (rINNs),  see Explanatory Notes at the beginning of this book

Record-keeping.  The first anaesthetic chart was devised by Codman and Cushing in 1894 at the Massachusetts General Hospital, for recording of respiration and pulse rate. BP charting was included in 1901 at Cushing’s insistence. FIO2 was included by McKesson in 1911.

Careful record-keeping is now recognised as essential to chart preoperative risk factors, the perioperative course of anaesthesia and postoperative events/instructions. It is particularly useful when taking over another anaesthetist’s anaesthetic, and for providing information to those administering anaesthesia subsequently. Similarly, ICU records should chart physiological data, therapy and instructions relating to the stay of any patient in an ICU. Record-keeping is also important for teaching, research and audit, and is extremely important in medicolegal aspects of anaesthesia. Although tending to include similar information, anaesthetic and intensive care charts are not standardised nationally, although this has been suggested.

Automated anaesthetic record systems are increasingly used, sometimes incorporated into anaesthetic machines or ICU monitoring systems. They provide accurate, legible and complete documents for data acquisition and subsequent scrutiny. Data from monitoring devices are incorporated with information provided by the anaesthetist/intensive care staff (e.g. drug or other interventions), although lack of familiarity with keyboards or computers may be a hindrance.

Postoperative recovery and progress may be recorded on separate charts, or on the anaesthetic chart.

[Ernest A Codman (1869–1940), US surgeon]

Recovery from anaesthesia.  Period from the end of surgery to when the patient is alert and physiologically stable. Definition is difficult because some drowsiness may persist for many hours. Recovery testing is used for more precise investigation. Time to recovery depends on the patient’s condition, drugs given, their doses, and the patient’s ability to eliminate them. For inhalational anaesthetic agents, similar considerations as for uptake are involved, plus length of operation and degree of redistribution to fat. Thus blood gas solubility is the most important factor initially, but more potent agents (e.g. isoflurane) are more extensively bound to fat after prolonged anaesthesia than less potent ones, e.g. desflurane. For iv anaesthetic agents, initial recovery is due to drug redistribution from vessel-rich to vessel-intermediate tissues; subsequent course is related to the rate of clearance from the body. Thus propofol characteristically results in rapid clear-headed emergence, whereas thiopental is more likely to produce drowsiness lasting several hours, especially after repeated dosage. Recommendations for provision of recovery care (Association of Anaesthetists):

ent designated recovery rooms or areas should be used.

ent during transfer to the recovery area O2 should be administered, and appropriate monitoring performed.

ent the anaesthetist should formally hand over the patient’s care to properly trained staff, giving details of the operation, anaesthetic technique, preoperative morbidity, perioperative problems, including blood loss, and antiemetic and analgesic drugs given.

ent all patients should be observed by at least one member of staff until there is a clear airway and cardiovascular stability, and they are able to communicate. The anaesthetist is responsible for removal of tracheal tubes.

ent O2 should be administered at least until awake.

ent level of consciousness, arterial O2 saturation, BP, heart rate, respiratory rate, pain intensity, iv infusions and drugs administered (including O2) should be recorded, along with other variables as appropriate (e.g. temperature, urine output).

ent there should be criteria for discharge, including full consciousness, clear airway, respiratory and cardiovascular stability, adequate postoperative analgesia and control of PONV, stable temperature and prescription of postoperative drugs, including O2 and iv fluids as appropriate. There should be adequate handover during discharge from the recovery area.

ent children should be recovered in a designated area.

Patients are often placed on their side, e.g. the recovery position. In the ‘tonsillar position’, the pillow is placed under the loin and the trolley tipped head-down.

• Problems during recovery:

ent respiratory, e.g. hypoventilation, hypercapnia, hypoxaemia, airway obstruction, bronchospasm, aspiration of gastric contents.

ent cardiovascular, e.g. hypotension, hypertension, arrhythmias, myocardial ischaemia.

ent confusion and agitation. Pain and bladder distension are common causes of restlessness and hypertension postoperatively. The above causes must also be excluded.

ent related to anaesthetic drugs, e.g. inadequate reversal of non-depolarising neuromuscular blockade, adverse drugs reactions, MH, dystonic reactions, emergence phenomena, central anticholinergic syndrome.

ent hypothermia, nausea and vomiting, shivering.

ent related to surgery, e.g. bleeding.

The speed and quality of recovery from anaesthesia have been proposed as a possible measure of quality of anaesthesia.

See also, Anaesthetic morbidity and mortality

Recovery position.  Position recommended for unconscious but spontaneously breathing subjects, assuming no contraindication, e.g. cervical spine injury. Encourages a clear airway and drainage of vomitus, secretions and blood away from the airway. Often used during recovery from anaesthesia.

Any recovery position is a compromise between the full prone position (better airway and drainage but more diaphragmatic splinting) and the full lateral position (less diaphragmatic splinting but less effective for the airway and less stable; also may be harmful in neck injury). Classically includes flexion of both arms with the upper hand placed under the jaw to support the airway (Fig. 134). The actual position adopted should reflect the particular circumstances of the case and the need to protect the airway, stabilise the neck and allow unhindered ventilation. It should be possible to observe the patient at all times and to turn him/her supine easily when required.

Recovery testing.  Ranges from simple clinical assessment to more sophisticated methods, e.g. used for experimental comparison between anaesthetic techniques and drugs. Routine testing is usually limited to assessment of general alertness and orientation, and ability to respond, drink, dress and walk where appropriate (e.g. day-case surgery).

• Sophisticated techniques used include tests of:

ent psychomotor function:

– assessing speed and number of errors made whilst performing set tasks:

– moving pegs from one set of holes in a board to another set.

– deleting every letter ‘p’ from a page of text.

– connecting dots on a page.

– reaction testing:

– being faced with four light sources, and pressing the correct switch (out of four choices) when one of them flashes.

– tracking moving targets with a pen or light.

ent perception:

– noting the frequency at which a flashing light appears to be continuous (critical flicker–fusion threshold).

– perception of auditory stimuli in a similar fashion, including discrimination between left and right ears.

ent memory:

– recall or recognition of objects, pictures, words or word associations shown a short time before.

– orientation in time and space.

ent cognitive function, e.g. adding/subtracting numbers, or adding values of different coins.

ent physiological function, e.g. divergence of eyes caused by reductions in extraocular muscle tone.

Problems of detailed recovery testing are related to the time taken, cumbersome equipment required, fatigue, boredom and learning if tests are repeated. Critical flicker–fusion, reaction testing, letter deletion and memory tests are most widely used and thought to be reasonably efficient, the first two especially so. General advice to patients is usually to avoid potentially dangerous activities (e.g. driving, cooking, using machinery) for 24 h following day-case anaesthesia, although subtle changes may persist beyond this period; 48 h has been suggested.

Rectal administration of anaesthetic agents.  Results in effective absorption of drugs because of a rich blood supply provided by communicating plexuses formed by the superior, middle and inferior rectal arteries and veins. Drugs undergo minimal first-pass metabolism, because the plexuses are anastomoses between portal and systemic circulations. The technique is usually restricted to children. Traditionally used more in continental Europe, e.g. France. Drugs used have included diazepam 0.4–0.5 mg/kg (widely used for treatment of convulsions in children), methohexital 15–25 mg/kg and thiopental 40–50 mg/kg as 5–10% solutions. Opioids and ketamine have also been given in this way. Diethyl ether was administered rectally by Pirogoff. Bromethol and paraldehyde were used in the 1920s to produce unconsciousness (basal narcosis).

Rectus sheath block.  Performed as part of abdominal field block or alone to reduce pain from abdominal incisions. Abdominal contents are not anaesthetised.

With the patient supine, a blunted needle is introduced 3–6 cm above and lateral to the umbilicus. A gentle ‘scratching’ motion may aid identification of the tough anterior layer of the sheath, puncture of which is accompanied by a click. The needle is advanced up to the resistance offered by the posterior layer of the sheath, and 15–20 ml local anaesthetic agent injected after negative aspiration. Deposition of solution between rectus muscle and posterior layer allows spread up and down, blocking the lower 5–6 intercostal nerves within the sheath. Spread between the muscle and anterior layer is limited by the tendinous intersections along its length. Multiple injections have been suggested between intersections, to improve spread, but the posterior layer is deficient below a point halfway between the umbilicus and pubis, and peritoneal puncture is more likely below this level.

Recurarisation.  Recurrence of non-depolarising neuromuscular blockade after apparent reversal with acetylcholinesterase inhibitors. Originally described with tubocurarine in patients with impaired renal function, where the duration of action of the neuromuscular blocking drug exceeds that of the acetylcholinesterase inhibitor. Has been described with other neuromuscular blocking drugs.

Red cell concentrates,  see Blood products

Reducing valve,  see Pressure regulators

Refeeding syndrome.  Clinical syndrome seen after reintroduction of nutrition to previously starved patients, often seen on ICU. First noted after World War II, when malnourished prisoners of war inexplicably died of cardiac failure after receiving a normal diet. Associated with any condition leading to malnutrition (e.g. anorexia nervosa, alcoholism, intra-abdominal sepsis).

• Pathophysiology:

ent restoration of carbohydrates as a dietary substrate leads to increased insulin secretion and activation of anabolic pathways. Hypophosphataemia, hypomagnesaemia, hypokalaemia and vitamin deficiency (particularly thiamine) may follow due to increased intracellular uptake on a background of whole body depletion.

ent depletion of ATP and 2,3-DPG leads to tissue hypoxia and mitochondrial dysfunction.

• Clinical features:

ent hyperglycaemia and electrolyte disturbances as above.

ent sodium and fluid retention.

ent cardiac failure, arrhythmias.

ent muscle weakness, contributing to respiratory failure and difficulty weaning from ventilators.

ent Wernicke’s encephalopathy due to thiamine deficiency.

• Prevention and treatment:

ent correction of electrolyte deficiencies before reintroducing feeding.

ent gradual introduction and escalation of caloric intake, with close monitoring of electrolytes and replacement as required.

ent vitamin supplementation.

ent close attention to fluid balance to prevent fluid overload.

Byrnes MC, Stangenes J (2011). Curr Opin Clin Nutr Metab Care; 14:186–92

Reflex arc.  Involves predictable, repetitive stereotypic responses to a particular sensory stimulus. Consists of sense organ, afferent neurone, one or more synapses, efferent neurone and effector. The afferent neurones enter the spinal cord via dorsal roots or brain via cranial nerves; the efferent neurones leave via ventral nerve roots or corresponding motor cranial nerves. Also involved in autonomic functions. The simplest reflex arc is monosynaptic, e.g. knee jerk and other stretch reflexes involving muscle spindles. Polysynaptic reflex arcs (two or more synapses) include the withdrawal reflex. Widespread effects may result from activation of a single reflex arc because of ascending, descending, excitatory and inhibitory interneurones.

Reflex sympathetic dystrophy,  see Complex regional pain syndrome

Refractometer,  see Interferometer

Refractory period.  Period during and following the action potential during which the neurone is insensitive to further stimulation. Subdivided thus:

Refrigeration anaesthesia.  Use of cold to reduce pain sensation. Used by Larrey in 1807, although the effect of cold on pain has been recognised for centuries. Up to 3 h packing in ice was recommended for operations through the thigh. The principle is still used today, e.g. ethyl chloride spray.

Regional anaesthesia.  Term originally coined by Cushing to describe techniques of abolishing pain using local anaesthetic agents as opposed to general anaesthesia. Pioneers included Halstead, Corning and Labat in the USA and Bier, Braun and Lawen in Europe.

• Techniques include:

ent topical anaesthesia.

ent infiltration anaesthesia, Vishnevisky technique and tumescent anaesthesia.

ent peripheral nerve blocks: plexus and single nerve blocks.

ent central neuraxial blockade: epidural and spinal anaesthesia.

ent IVRA and intra-arterial regional anaesthesia.

ent sympathetic nerve blocks.

ent others, e.g. interpleural analgesia.

• Advantages of regional anaesthesia:

ent conscious patient, able to assist in positioning, and warn of adverse effects (e.g. in carotid endarterectomy and TURP). There is less interruption of oral intake, especially beneficial in diabetes mellitus.

ent good postoperative analgesia.

ent reduction of certain postoperative complications, e.g. atelectasis and DVT, possibly myocardial ischaemia.

• Contraindications:

ent absolute: patient refusal, anaesthetist’s inexperience and localised infection.

ent relative: abnormal anatomy or deformity, coagulation disorders, previous failure of the technique, and neurological disease or other medicolegal considerations.

Specific contraindications may exist for specific techniques.

• Management:

ent preoperatively:

– preoperative assessment and preparation as for general anaesthesia.

– full explanation of the procedure, and consent.

– preparation of drugs and equipment for general anaesthesia and resuscitation, in addition to those required for the regional technique chosen.

ent perioperatively:

– monitoring should be applied as for general anaesthesia, i.e. before starting the procedure and continued throughout it.

– aseptic technique should be observed.

– for nerve or plexus blocks, short-bevelled needles are traditionally used to minimise nerve contact, although nerve damage may be greater should the nerve be impaled. Nerve stimulators (using 0.3–1.0 mA current lasting 1–2 ms and delivered at 1–3 Hz) increase the success of many blocks and may reduce damage further. A distant ground electrode is required. The needle (preferably sheathed) is placed near the target nerve and stimulated until paraesthesia or twitches are elicited; the output is reduced, the needle repositioned and the process repeated.

  Ultrasound imaging is increasingly used to guide needle placement. The appearance of nerves is variable but usually distinct from that of other tissues. Addition of colour Doppler imaging identifies blood vessels. Claimed advantages include more accurate placement of the needle, especially if anatomy is abnormal, reduced volume of injectate required, greater success rate and reduced complication rate.

– a single injection of local anaesthetic, repeated boluses (using repeated injections or a catheter) or continuous infusions may be used.

– the extent of the block should be assessed (e.g. by response to pinprick or cold) before allowing surgery to start.

– if sedation is used, care should be taken to ensure that respiratory and cardiovascular depression does not occur. Analgesic drugs (e.g. N2O or opioid analgesic drugs) may be used to supplement incomplete blockade. General anaesthesia may be used as a planned part of the technique, or if the technique is unsuccessful.

ent postoperatively:

– close monitoring and supervision should continue as for general anaesthesia.

– patients should be advised to protect insensate limbs e.g. using a sling for upper limb blocks.

– patients should be warned of potentially unpleasant paraesthesia as the block recedes.

– neurological complications may only become apparent once the block has worn off.

• Complications:

ent technical: direct trauma to nerves, blood vessels and pleura, breakage of needles or catheters.

ent associated with positioning of the patient, e.g. compression of an anaesthetised limb.

ent local anaesthetic toxicity: intravascular injection or systemic absorption.

ent excessive spread, e.g. total spinal block during epidural anaesthesia, or phrenic nerve block during brachial plexus block.

ent failure of the technique.

ent those of specific techniques, e.g. hypotension following spinal anaesthesia.

ent others, e.g. injection of the wrong solution through catheters.

See also, specific blocks; Nerve injury during anaesthesia

Regional tissue oxygenation.  Important because shock and hypoxaemia cause redistribution of blood flow and alter the metabolic properties of cells; global measurements thus fail to detect areas of local ischaemia. Measurement of regional tissue oxygenation may be useful in critically ill patients because deficiencies may be involved in the development and continuation of MODS. Lack of evidence of benefit and technical difficulties have hindered the more intricate techniques from becoming routine practice. Methods of assessment include:

ent blood lactate levels (> 2 mmol/l suggests insufficient oxygen delivery): a late marker.

ent mixed venous O2 saturation (image), measured using repeated blood sampling or continuous oximetry via a pulmonary artery catheter. Regional image (e.g. hepatic = image; jugular = image) can be determined using indwelling catheters.

ent intestinal regional capnography (i.e. gastric tonometry). Measures PCO2 in an air- or saline-filled tonometric balloon, placed in the GIT.

ent surface or tissue O2 electrodes: based upon the Clark electrode (see Oxygen measurement), they are formed of a noble metal (e.g. gold, silver, platinum). Change in voltage between the anode and cathode is proportional to the amount of O2 reduced at the cathode.

ent optode sensors: use the change in the optical properties (e.g. absorbance or fluorescence) of indicator substances generated by photochemical reactions to measure the concentration of a substance (e.g. O2) in tissues. Can be mounted in intravascular catheters (e.g. Paratrend monitor).

ent near infrared spectroscopy.

ent reflectance spectrophotometry. Measures the absorption of reflected visible light on a tissue surface, e.g. gut wall, fetal scalp.

ent nicotinamide adenine dinucleotide (NADH) fluorescence: during tissue hypoxia, NADH accumulates in tissues. The absorption properties of NADH, and its reduced state, NAD+, are different. Tissue catheters have been used in both animal and human models.

ent imaging using online microscopic observation of the microcirculation.

Dyson A, Singer M (2011). Curr Opin Crit Care; 17: 281–9

Regression,  see Statistical tests

Regurgitation.  Term usually describing passive passage of gastric contents into the pharynx. Silent, thus aspiration of gastric contents may occur unnoticed. Normally prevented by the lower oesophageal sphincter; however, swallowed dyes have been found to stain areas of the pharynx and larynx during/after anaesthesia in normal patients.

Relative analgesia.  Technique used in dental surgery involving nasal administration of subanaesthetic concentrations of N2O, e.g. 10% in O2, slowly increased to 30–50%. Verbal contact is maintained at all times, and the concentration of N2O reduced if excessive drowsiness occurs. Performed by the dentist, it depends partly on suggestion.

Relative risk reduction.  Indicator of treatment effect in clinical trials. For a reduction in incidence of events from a% to b%, it equals ( [ab] ÷ a)%. Gives an overestimated impression of treatment effect if events are rare, and an underestimate if events are common.

See also, Absolute risk reduction; Meta-analysis; Number needed to treat; Odds ratio

Relatives of critically ill patients.  Present particular challenges to ICU staff because of the serious nature of the patient’s condition, unfamiliarity with the ICU environment and the natural behavioural responses to extreme stress, including fear, anger and guilt. The suddenness of many severe conditions may exacerbate relatives’ distress. Relatives must be kept informed about the patient’s progress, preferably by a consistent single senior doctor accompanied by a member of the nursing staff; they should also feel included in discussions about treatment (including its withdrawal).

Honest and clear explanations, using lay language, may need repeating several times and the potential frustration felt by the medical team must not be transmitted to the relatives. Most ICUs have a separate room for interviews with patients’ families and friends, which is preferable to the open ward or corridor. In general, few restrictions are placed on visiting times, and most relatives appreciate and respect the need for staff to perform basic care and procedures during which they may be asked to leave the unit. However, some may choose to stay and participate in some aspects of their relative’s care, e.g. washing or shaving. Counselling and religious support may be required and is often best arranged via the ICU staff.

Whether relatives should witness attempts at resuscitation (e.g. in casualty departments) has attracted recent debate, with some welcoming the opportunity for relatives to see that appropriate attempts to save the patient are being made, whilst others argue that their presence may be stressful for medical and nursing staff.

Curtis JR, White DB (2008). Chest; 134: 835–43

Remifentanil.  Ultra-short-acting synthetic opioid analgesic drug, 2000 times more potent than morphine, introduced in the UK in 1997. Available as a white powder for reconstitution to a 0.1% solution which is stable for 24 h at room temperature. Further diluted for administration; in adults a 50 µg/ml solution is recommended by the manufacturer. Approximately 70% protein-bound. Rapidly metabolised by non-specific plasma and tissue esterases to remifentanil acid (very low potency) and excreted renally. Its context-sensitive half-life is about 3 min regardless of the duration of infusion; thus provides a rapid recovery when stopped.

Because it is cleared so rapidly and completely, patients very soon experience pain postoperatively unless longer-acting analgesics are given before discontinuation. In addition, it has been suggested that the hyperalgesia that can occur following remifentanil infusions may be due to upregulation of NMDA receptors. Has been used via patient-controlled analgesia during labour (see Obstetric analgesia and anaesthesia). Not recommended for epidural or spinal use since the formulation contains glycine. Postoperative respiratory depression may occur if any drug is left in the dead space of iv lines and subsequently flushed with other drugs or fluids.

Remote ischaemic preconditioning,  see Ischaemic preconditioning

Renal blood flow (RBF).  Normally 1200 ml/min (400 ml/100 g/min); i.e. 22% of cardiac output.

• Measurement:

ent direct: circumferential electromagnetic flow measurement, Doppler or thermodilution techniques.

ent indirect:

– clearance methods: a substance neither metabolised nor taken up by the kidney, and completely cleared, is required, e.g. para-amino hippuric acid (PAH). Clearance then equals renal plasma flow. RBF = plasma flow divided by (1 – haematocrit). Continuous iv infusion of PAH is required; inaccuracies may occur since clearance of PAH is only 90% in humans. Radioactive markers have been used; almost 100% cleared, they require only a single injection.

– digital subtraction angiography and radioactive inert gas washout techniques have also been used, the latter indicating regional blood flow.

• Affected by:

ent arterial BP: maintained by autoregulation at MAP between 70 and 170 mmHg in normal subjects.

ent sympathetic nervous system: stimulation causes vasoconstriction and reduction of RBF, and also increases release of renin and prostaglandins. Dopamine may increase RBF by vasodilatation via dopamine receptors.

ent renin/angiotensin system: angiotensin II decreases RBF via vasoconstriction, and increases aldosterone secretion. The latter increases fluid retention, which inhibits further renin release.

ent vasopressin: causes renal vasoconstriction, especially cortical.

ent intravascular volume: in haemorrhage, autoregulation is overridden, with vasoconstriction and intrarenal redistribution of blood away from the cortex.

ent prostaglandins: increase cortical blood flow, and reduce medullary blood flow.

ent atrial natriuretic peptide: causes vasodilatation, although effects on RBF are unclear. May alter blood flow distribution.

RBF and GFR are reduced by most anaesthetic agents, mainly via reduced cardiac output and BP. Volatile agents are also thought to interfere with autoregulation, although some benefit may arise from the vasodilatation they cause, maintaining blood flow. Urine output therefore often falls perioperatively.

Other factors include pre-existing renal disease or conditions predisposing to renal failure or impairment, e.g. vascular surgery, toxic drugs, trauma, jaundice, hypovolaemia.

Renal failure.  Loss of renal function causing abnormalities in electrolyte, fluid and acid–base balance with increases in plasma urea and creatinine. Divided into acute and chronic renal failure.

• Acute renal failure (see Acute kidney injury for definitions, diagnosis and management).

• Chronic renal failure (CRF):

ent irreversible, and often follows acute kidney injury.

ent glomerulonephritis is the most common cause, with others, including pyelonephritis, diabetes, polycystic disease, vascular disease and hypertension, drugs and familial causes.

ent features (may not be present until GFR falls below 15 ml/min):

– malaise, anorexia, confusion leading to convulsions and coma. Peripheral and autonomic neuropathy may occur.

– oedema, pericarditis, hypertension (in 80%; thought to result from increased renin/angiotensin system activity, sodium and water retention and secondary hyperaldosteronism), peripheral vascular disease, cardiac failure. Ischaemic heart disease is 20 times more common in CRF patients.

– nausea, vomiting, diarrhoea.

– osteomalacia, muscle weakness, bone pain, hyperparathyroidism, hyperphosphataemia.

– amenorrhoea, impotence.

– pruritus, skin pigmentation, poor healing, increased susceptibility to infection.

– normocytic normochromic anaemia: caused by reduced erythropoietin production, shortened red cell survival and bone marrow depression. Impaired platelet function may cause bruising and bleeding.

– hypernatraemia or hyponatraemia may occur. Hyperkalaemia is usual, but hypokalaemia may follow diuretic therapy. Acidosis is common.

ent management:

– reduction of dietary protein.

– control of hypertension and cardiac failure.

– erythropoietin is increasingly used for anaemia.

– dialysis.

– renal transplantation.

• Anaesthesia in renal failure:

ent preoperatively:

– features of the underlying disease must be assessed, e.g. diabetes, hypertension.

– assessment for the above features of renal failure, in particular cardiovascular complications, fluid and electrolyte and acid–base derangements. Dialysis may be required; if it has been recently performed, patients are often hypovolaemic, and therefore vulnerable to perioperative hypotension. Anaemia rarely requires transfusion because of its chronicity with compensatory mechanisms. Patients may be at risk from aspiration of gastric contents if autonomic neuropathy is present.

– drugs taken commonly include antianginal and antihypertensive drugs, insulin and corticosteroids.

– pre-existing arteriovenous fistulae or shunts should be noted.

– premedication as required.

ent perioperatively:

– iv cannulae should not be sited near arteriovenous fistulae, which should be loosely padded for protection.

– potassium-containing iv fluids should be avoided.

– drugs whose actions are not terminated by renal excretion are preferred. Thus a common technique consists of propofol followed by atracurium and isoflurane, sevoflurane or desflurane.

– drugs that accumulate in renal failure (e.g. morphine) should be used with caution. Patients are more sensitive to many iv agents, including opioids, because of smaller volumes of distribution and reduced plasma protein levels.

– suxamethonium is not contraindicated unless there is pre-existing peripheral neuropathy or hyperkalaemia.

– nephrotoxic drugs (e.g. NSAIDs) should be avoided. Enflurane has been avoided because of fluoride ion formation, although the need for this is controversial. Previous concerns regarding sevoflurane and compound A formation are not thought to be relevant in humans.

– regional techniques are often suitable, e.g. brachial plexus block for fistula formation.

ent postoperatively: close attention to fluid balance is required.

Dennen P, Douglas IS, Anderson R (2010). Crit Care Med; 38: 261–75

Renal failure index,  see Renal failure

Renal transplantation.  First performed in 1950, and now widespread but limited mainly by the supply of kidneys. Cadaveric graft survival is up to 80–90% at 2 years. Previously considered an emergency and performed on unprepared patients, but the importance of proper preoperative assessment and preparation is now generally accepted. Dialysis is usually performed within 24 h before surgery.

• Anaesthetic problems and techniques are as for chronic renal failure and transplantation. Additional points:

ent general anaesthesia is preferred, although epidural and spinal anaesthesia have been successfully used.

ent direct arterial blood pressure measurement is not necessarily required (although ischaemic heart disease and cardiac failure are common in these patients); CVP monitoring is routinely used to guide perioperative fluid therapy. Optimal hydration is vital to support graft function.

ent mannitol, furosemide, calcium channel blocking drugs and dopamine are sometimes given before the vessels to the new kidney are unclamped, in order to stimulate urine production and improve renal function.

ent transient hypertension may follow unclamping of the renal vessels.

ent there is an increased incidence of kidney rejection in patients who have received blood transfusion during transplantation; preoperative correction of anaemia with erythropoietin should be considered.

  Both live and cadaveric donors should be well hydrated to maintain urine output before harvesting.

Sarinkapoor H, Kaur R, Kaur H (2007). Acta Anaesthesiol Scand; 51: 1354–67

See also, Organ donation

Renal tubular acidosis.  Group of conditions characterised by decreased ability of each nephron to excrete hydrogen ions (cf. renal failure, where the overall number of functioning nephrons is reduced, but those that remain excrete more hydrogen ions than normal). Characterised by normal GFR, metabolic acidosis, hyperchloraemia and a normal anion gap. May be associated with distal tubule dysfunction (type 1), proximal tubule dysfunction (type 2; usually associated with other abnormalities of proximal tubule function, e.g. Fanconi’s syndrome), or aldosterone deficiency or resistance (type 4). Type 3 is now considered a combination of types 1 and 2 and not a separate entity. Acidosis may be severe, and accompanied by marked hypokalaemia (hyperkalaemia in type 4). Treatment includes alkali (e.g. oral sodium bicarbonate) in types 1 and 2, thiazides in type 2 and mineralocorticoid therapy in type 4.

[Guido Fanconi (1892–1979), Swiss paediatrician]

Reddy P (2011). Int J Clin Pract; 65: 350–60

Renin/angiotensin system.  Renin, a proteolytic enzyme (mw 37 kDa), is synthesised and secreted by the juxtacapillary apparatus of the renal tubule. Formed from two precursors, prorenin and preprorenin, its half-life is about 80 min. Secretion is increased in hypovolaemia, cardiac failure, cirrhosis and renal artery stenosis. Secretion is decreased by angiotensin II and vasopressin. Renin cleaves the circulating glycoprotein angiotensinogen with subsequent production of the peptides angiotensin I, II and III, involved in arterial BP control and fluid balance (Table 38). Angiotensin I is a precursor for angiotensin II, a powerful vasoconstrictor with a half-life of a few minutes. It causes aldosterone release from the adrenal cortex, and noradrenaline release from sympathetic nerve endings. It also stimulates thirst and release of vasopressin, and acts directly on renal tubules, resulting in sodium and water retention. Some may also be produced in the tissues. Angiotensin III also causes aldosterone release and some vasoconstriction.

Angiotensin converting enzyme inhibitors and angiotensin II receptor antagonists are used to treat hypertension. Aliskiren, a direct renin inhibitor, has recently been introduced.

Angiotensin II or its analogues have been used as vasopressor drugs when α-agonists are unable to correct severe hypotension, e.g. during surgery for hepatic tumours secreting vasodilator substances.

Reperfusion injury.  Tissue injury resulting from restoration of blood flow after a period of ischaemia. Mechanisms include intracellular calcium excess, cellular oedema and free radicals. Although any tissue may be affected, most work has focused on cardiac function following hypoxic insult or hypoperfusion. Arrhythmias and myocardial stunning (reversible impairment of cardiac function) may also follow reperfusion.

See also, Isoprostanes, No reflow phenomenon

Reptilase time,  see Coagulation studies

Reserpine.  Antihypertensive drug, rarely used now because of its unfavourable side-effect profile. Depletes postganglionic adrenergic neurones of noradrenaline by irreversibly preventing its reuptake from axoplasm into storage vesicles. Crosses the blood–brain barrier and depletes central amine stores. Effects may last 1–2 weeks.

Side effects include bradycardia and postural hypotension, depression, sedation and extrapyramidal signs. No longer available in the UK.

Reservoir bag.  Usually 2 litre capacity in most adult anaesthetic breathing systems and 0.5–1.0 litre for paediatric use; its volume must exceed tidal volume. Movement indicates ventilation, but estimation of tidal volume from the degree of movement is inaccurate. Made of rubber (increasingly, latex-free), distending when under pressure; maximal pressure is thus prevented from rising above about 60 cmH2O (Laplace’s law).

Resistance.  In electrical terms, the ratio of the potential difference across a conductor to the current flowing through it (Ohm’s law). Measured in ohms (Ω). Resistance to flow of a fluid through a circular tube is analogous to this; it equals the ratio of the pressure gradient along the tube to the flow through it.

Resistance vessels.  Term given to those blood vessels involved in regulation of SVR. 50% of resistance to blood flow is due to arterioles, which are thus the main regulators of SVR and therefore distribution of cardiac output.

Respirators,  see Ventilators

Respiratory centres,  see Breathing, control of

Respiratory depression,  see Hypoventilation

Respiratory distress syndrome (RDS; Hyaline membrane disease).  Occurs in approximately 1% of all live births, almost exclusively in premature babies. Caused by deficiency of surfactant. Surfactant is normally detectable in the fetal lung at 24 weeks’ gestation, although reversal of amniotic fluid lecithin/sphingomyelin ratio (related to fetal lung maturity) only occurs at 30 weeks. Decreased lung compliance, increased work of breathing and alveolar collapse may lead to respiratory failure, with characteristic granular appearance of the CXR.

Treatment is directed towards preventing hypoxaemia with CPAP initially, although IPPV is usually necessary, whilst trying to avoid O2 toxicity, barotrauma and retinopathy of prematurity. Exogenous surfactant given immediately after birth decreases mortality. Extracorporeal membrane oxygenation has been used.

Respiratory exchange ratio.  Estimation of respiratory quotient derived from expired CO2/inspired O2 measurements, thus dependent on ventilation.

Respiratory failure.  Defined as an arterial PO2 < 8 kPa (60 mmHg) breathing air at sea level, and at rest, without intracardiac shunting.

• Divided into:

ent type I failure: hypoxaemia with normal or low arterial PCO2. Usually due to image mismatch, with intrapulmonary right-to-left shunt if severe. Causes include chest infection, asthma, pulmonary embolus, pulmonary oedema, PE, ARDS, aspiration pneumonitis. O2 therapy improves hypoxaemia due to image mismatch but not shunt; the response to breathing 100% O2 may indicate the degree of shunt. PCO2 is often low because of hyperventilation in response to hypoxaemia.

ent type II failure (ventilatory failure): hypoxaemia accompanied by arterial PCO2 > 6.5 kPa (49 mmHg). Causes are as for hypoventilation. Acute exacerbation of COPD is a common cause.

Diagnosis is made by arterial blood gas interpretation, but may be suspected clinically by signs of hypoxaemia and hypercapnia, with tachypnoea and use of accessory respiratory muscles.

• Treatment:

ent of underlying cause.

ent sitting the patient up increases FRC and often improves oxygenation.

ent oxygen therapy: should be used cautiously in type II failure if chronic hypercapnia is suspected.

ent aminophylline may have an inotropic action on the diaphragm and may reduce respiratory muscle fatigue; it is often used in neonates.

ent carbonic anhydrase inhibitors may increase respiratory drive in COPD associated with hypercapnia.

ent respiratory stimulant drugs (e.g. doxapram) have been used to avoid IPPV, e.g. in COPD.

ent CPAP or non-invasive positive pressure ventilation may improve oxygenation and ventilation, avoiding the need for tracheal intubation.

ent IPPV may be required if PCO2 is rising or the patient is exhausted. Criteria similar to those used in weaning from ventilators have been suggested for institution of IPPV. Tracheostomy may be necessary to aid weaning from mechanical ventilation.

ent intravenous oxygenator, extracorporeal oxygenation and extracorporeal CO2 removal have been used.

Respiratory function tests,  see Lung function tests

Respiratory sounds.  Traditionally assessed with a stethoscope, more recently analysed by digital processing using microphones or accelerometers placed on the chest wall. Sounds arise from vibration of airways and movement of fluid films within them. The nature of the sounds depends on the tissue through which they pass, e.g. quiet or absent in pleural effusion and pneumothorax, increased transmission in consolidation. The pitch is related to the size of the airway involved and the density of the gas.

• Classification:

ent basic sounds: arise from:

– central airways of the lung. Normally audible throughout inspiration and the beginning of expiration, with a gap between the two.

– large airways and trachea. Typically audible throughout both inspiratory and expiratory phases, with no gap. Usually audible only over the trachea, this ‘bronchial breathing’ sound may be heard over the chest if transmitted to the stethoscope via abnormally solid tissue (e.g. consolidated lung).

 Range from under 100 Hz to over 1000–3000 Hz.

ent adventitious sounds:

– wheezing: arises from the central/lower airways with a sinusoidal frequency (polyphonic), ranging from 100 Hz to over 1000 Hz.

– rhonchi: snore-like, arise from the larger airways. Typically under 300 Hz and rapidly damped, but lasting over 100 ms. Occur in small airway collapse and secretions.

– crackles: fine; arise from the lower airways. Rapidly damped, typically lasting under 20 ms. Occur in secretions, oedema and fibrosis.

Other sounds may occur (e.g. stridor), although not from the lung itself.

Gurung A, Scrafford CG, Tielsch JM, Levine OS, Checkley W (2011). Respir Med; 105: 1396–403

Respiratory stimulant drugs,  see Analeptic drugs; Opioid receptor antagonists

Respiratory symbols.  By convention, standardised thus:

ent general variables:

  Image

P = pressure or tension

F = fractional concentration in dry gas mixture

f = respiratory frequency

C = content of a gas in blood

D = diffusing capacity

R = respiratory exchange ratio

S = saturation of haemoglobin with O2 or CO2

A dash above a symbol indicates mean value.

ent localisation (in subscript):

I = inspired gas

E = expired gas

A = alveolar gas

T = tidal gas

D = dead space gas

B = barometric

a = arterial blood

c = pulmonary capillary blood

v = venous blood

e.g. FIO2 = inspired fractional concentration of O2; PaO2 = arterial O2 tension.

SpO2 has been suggested as representing haemoglobin saturation as measured by pulse oximetry.

Respirometer.  Device for measuring expiratory gas volumes. Examples:

ent Wright’s anemometer (axial turbine flowmeter): a design commonly integrated into ventilators. Expired gas is passed into its chamber through oblique slits, creating circular gas flow that causes rotation of a double-vaned turbine within the chamber. Rotation is measured and displayed as the volume of gas passing through the device, using an indicator needle attached to the vane, and a dial. Electrical versions are also available; rotations of a disc attached to the vane interrupt passage of light between an emitter and photosensitive cell mounted astride the disc. Less prone to inertia inaccuracies than the Wright’s respirometer.

ent Wright’s respirometer: measures gas volume passing in one direction only; thus it may be placed in the two-way portion of a breathing system. It tends to underestimate at low volumes and overestimate at high volumes, due to inertia/momentum of the vane.

ent others: include flowmeters, whose signals may be integrated to indicate volume.

[B Martin Wright (1912–2001), London engineer]

See also, Spirometer

Resuscitators,  see Self-inflating bags

Reticular formation/activating system,  see Ascending reticular activating system

Retrobulbar block.  Performed to allow surgery to the globe of the eye, e.g. cataract extraction. Cranial nerves III and VI, and long and short ciliary nerves (branches of V1) are blocked within the cone formed by the extraocular muscles. Now rarely used due to its relatively high frequency of complications, including retrobulbar haemorrhage, intravascular and subarachnoid injection and globe perforation. Peribulbar block and sub-Tenon’s block are safer and equally effective alternatives.

With the patient supine and looking straight ahead, a 3.0 cm needle is inserted through the conjunctiva at the lower lateral orbital rim. It is passed backward and 10° upward until its tip has passed the mid-globe, then angled medially and upward to reach a point behind the globe at the level of the iris. After aspiration, 2–4 ml lidocaine with hyaluronidase 5 U/ml is injected.

See also, Orbital cavity

Retrolental fibroplasia,  see Retinopathy of prematurity

Retzius cave block.  Used to supplement anaesthesia for prostatectomy and bladder surgery. The cave of Retzius is the space between the bladder and pubic symphysis, containing nerves of the sacral plexus and a venous plexus. After subcutaneous infiltration 2–3 cm above the pubis, an 8 cm needle is directed to the back of the symphysis. After negative aspiration for blood, 10 ml local anaesthetic agent with adrenaline is injected in the midline, with a further injection on each side.

[Anders Retzius (1796–1860), Swedish anatomist]

Reuben valve,  see Non-rebreathing valves

Revised trauma score (RTS).  Trauma scale derived from the trauma score but simplified and with greater emphasis on the presence of head injury. Uses the Glasgow coma scale, systolic BP and respiratory rate, each assigned a value of 0–4 according to deviation from normal, with 0 representing the most severe. The values are added to give a total RTS, with a normal of 12. Superior to the trauma score at predicting outcome; a RTS of < 4 suggests the need for transfer to a specialist trauma unit.

Gilpin DA, Nelson PG (1991). Injury; 22: 35–7

Reye’s syndrome.  Rare condition of unknown aetiology, characterised by vomiting, depression of consciousness and hepatic failure. Jaundice is typically absent or minimal. Usually occurs in children, typically following a viral illness; aspirin has been implicated in epidemiological studies and is thus contraindicated under 16 years of age. Thought to be due to an acquired mitochondrial abnormality. Treatment is mainly supportive, with correction of metabolic disturbances, cerebral oedema and raised ICP. Thought to be improved by administering up to a third of the fluid intake as 10% dextrose.

[R Douglas Reye (1912–1977), Australian pathologist]

Rhabdomyolysis,  see Myoglobinuria

Rhesus blood groups.  System of blood group antigens first described in 1939 following work on rhesus monkeys. Includes many antigens but the terms Rhesus (Rh)-positive and -negative usually refer to the D antigen, as it is the most immunogenic. Rh-negative individuals have no D antigen, and form anti-D antibodies when injected with Rh-positive blood. 85% of Caucasians are Rh-positive, 99% of Orientals.

• Clinical importance:

ent blood transfusion reactions: administration of Rh-positive blood to Rh-negative individuals who have anti-D antibodies following previous exposure to Rh-positive blood.

ent haemolytic disease of the newborn: occurs in Rh-positive fetuses of Rh-negative mothers. Passage of fetal blood cells into the maternal circulation during pregnancy or labour causes formation of maternal anti-D antibodies. These may pass into subsequent Rh-positive fetuses, causing haemolysis, which may be fatal. Incidence of primary immunisation in primigravidae is about 15%. Uncommon now with widespread availability of anti-Rh immunoglobulin, which is administered to Rh-negative mothers at delivery, and after abortion or amniocentesis. Routine administration of anti-Rh to all Rh-negative pregnant women has been suggested as a way of reducing the problem further.

Rheumatoid arthritis (Rheumatoid disease).  Systemic inflammatory disease with many features of connective tissue diseases. Characterised by symmetrical polyarthropathy, but affects other organs too. Three times more common in females; peak incidence is at ages 30–50 years. Up to 5% of females over 60 years are affected in the UK. Aetiology is unclear but may involve an immunological process triggered by infectious agents coupled with a genetic predisposition. Recent advances in treatment, including early therapy with disease-modifying antirheumatic drugs (DMARDS), including biological agents which block tumour necrosis factor, appear to improve the course and severity of the condition.

• Anaesthetic considerations:

ent systemic effects:

– skeletal: temporomandibular joint involvement, atlantoaxial subluxation, reduced mobility of the lumbar/cervical spine.

– neuromuscular: nerve entrapment, sensory/motor neuropathy, myopathy.

– respiratory: restrictive defect due to pulmonary fibrosis and costochondral disease, pulmonary nodules, pleural effusions, cricoarytenoid arthritis.

– cardiovascular: ischaemic heart disease (often with ‘silent’ MI), pericarditis, heart block, coronary arteritis, peripheral vasculitis.

– haematological: anaemia (usually normochromic normocytic), leucopenia. Felty’s syndrome consists of rheumatoid arthritis, splenomegaly and leucopenia; thrombocytopenia, malaise and fever may occur.

– renal: amyloidosis, pyelonephritis, drug-related impairment.

– others: ophthalmic complications, including Sjögren’s syndrome, and atrophic skin and subcutaneous tissues.

ent drug therapy: may include NSAIDs, corticosteroids and immunosuppressive drugs. Gold may cause blood dyscrasias, peripheral neuritis, pulmonary fibrosis, hepatic and renal impairment. Penicillamine may cause blood dyscrasias, renal impairment, neuropathy and a myasthenia gravis-like syndrome.

ent practical considerations:

– airway maintenance difficulties: caused by involvement of the temporomandibular joint, cervical spine and larynx. Clinical evidence of laryngeal involvement should prompt a preoperative nasendoscopy to assess degree of laryngeal stenosis. The value of preoperative cervical spine X-rays is uncertain; flexion/extension radiographs may worsen atlantoaxial subluxation, are often diagnostically adequate, and may not alter anaesthetic technique (although proven cervical instability mandates minimal neck manipulation).

– venous cannulation may be difficult; skin and veins are fragile, and joints may have reduced mobility.

– discomfort lying flat; skeletal involvement may make regional techniques unsuitable. Careful positioning and padding are required. Skin is easily damaged.

– wrist and hand arthritis may preclude the use of patient-controlled analgesia.

[Augustus R Felty (1895–1963), US physician; Henrik SC Sjögren (1899–1986), Swedish ophthalmologist]

Samanta R, Shoukrey K, Griffiths R (2011). Anaesthesia; 66: 1146–59

See also, Intubation, difficult

Ribavirin (Tribavirin).  Antiviral drug; a nucleoside, it inhibits DNA synthesis and is active against many RNA and DNA viruses, although usually reserved for treatment of respiratory syncytial viral infection and Lassa fever. Also used in combination with interferon alfa for the treatment of chronic hepatitis C.

Rib fractures.  Middle ribs are most commonly affected. Fracture usually occurs at the posterior axillary line, the point of maximal stress. If the first three ribs are affected, injury to the aorta and tracheobronchial tree should be considered. If the lower ribs are involved, damage to liver, spleen and kidneys may occur. Pneumothorax and haemothorax may be present.

Rib fractures cause pain on breathing, with splinting of the chest wall, inability to cough and atelectasis. Multiple fractures may cause flail chest. The mainstay of treatment is good analgesia; this may involve systemic analgesics, epidural anaesthesia or intercostal nerve block.

General management is as for chest trauma and abdominal trauma.

Rifampicin.  Antibacterial drug, used primarily as an antituberculous drug but also in brucellosis, Legionnaires’ disease, severe staphylococcal infection, leprosy and as prophylaxis against meningococcal disease (thus may be given to ICU staff after caring for an infected patient or to household contacts). Causes hepatic enzyme induction and thus decreases the efficacy of oral contraceptives, anticoagulants and phenytoin.

Right ventricular function.  The right ventricle (RV) receives blood from systemic and coronary veins, and pumps it into the left ventricle (LV) across the pulmonary vascular bed. The pulmonary bed is of low resistance, therefore RV pressures (15–25/8–12 mmHg) are lower than systemic. The low intraventricular pressure permits right coronary blood flow to be continuous throughout the cardiac cycle. The output of the right heart is influenced by its preload, contractility and afterload.

The RV is very compliant and, when afterload increases (e.g. because of pulmonary vascular resistance secondary to lung injury), the RV dilates. The end-diastolic volume may increase to a greater extent than the preload; consequently, the RV ejection fraction will decrease markedly with increasing afterload. Changes in the geometry of the RV affect the function of the LV, and vice versa (ventricular interdependence), e.g. impaired RV function (whether acute or chronic) may hinder LV function via RV distension and deviation of the interventricular septum.

Although the RV is analogous to the LV in terms of control mechanisms, it is more difficult to assess; e.g. the relationship between RV preload, RV volume and RV filling pressures is not always constant. In addition, attempts to study RV function are hindered by the greater effect of respiratory excursions on the RV because the pressures involved are less than those on the left side of the heart.

RV function may be altered in acute respiratory failure, sepsis, chest trauma, ischaemic heart disease, and after cardiac surgery. The possibility of RV ischaemia or infarction in critically ill patients as a cause of RV dysfunction is increasingly recognised. During IPPV, decreased venous return subsequent to the increased intrathoracic pressure results in decreased RV end-diastolic volume and thus cardiac output. RV impairment may result in the classic features of right-sided cardiac failure, but may present as a general poor perfusion state.

Risk management.  Process for reducing the frequency and overall cost of adverse events, e.g. complications of anaesthesia. Consists of:

ent analysis of risks (e.g. morbidity/mortality meetings, critical incident reporting schemes). Risks are often categorised into:

– individual-based (e.g. arising from human error), e.g. wrong drug given.

– environment-based (e.g. arising from the interaction between anaesthetists and the operating theatre), e.g. disconnection of breathing system.

– system-based (human actions superimposed on inherent flaws in a system or process), e.g. because of alterations to the operating list caused by cancellations due to lack of beds, a patient arrives in the anaesthetic room without the diseased limb marked and has the wrong leg amputated.

ent prevention of risks associated with routine activities (e.g. proper training and supervision, provision of trained anaesthetic assistants).

ent avoidance of particularly high-risk activities (e.g. wider use of regional anaesthesia for caesarean section).

ent minimising the severity of adverse events should they occur (e.g. training in defibrillation, maintenance of emergency drugs and equipment).

ent risk financing (e.g. indemnity).

ent having a system for dealing with disasters and complaints, to reduce both psychological and legal sequelae.

Audit is an integral part of a risk management programme, the costs of which may be considerable, although the avoidance of litigation is a strong incentive. Protocols may contribute to risk management by standardising care, although they are not universally viewed with approval.

Postgraduate issue (2010). Br J Anaesth; 105: 1–101

See also, Clinical governance; Quality assurance

Ritodrine hydrochloride.  β-Adrenergic receptor agonist, used as a tocolytic drug in premature labour.

• Dosage:

ent 50–350 µg/min iv (or 10 mg 3–8-hourly, im), continued for 12–48 h after contractions have ceased.

ent 10 mg orally, 30 min before stopping iv infusion, repeated 2-hourly for 24 h then 10–20 mg 4–6-hourly.

• Side effects: nausea, vomiting, sweating, tremor, hypokalaemia, tachycardia, hypotension, pulmonary oedema, arrhythmias, increased uterine bleeding after caesarean section, blood dyscrasias and hepatic impairment on prolonged therapy. Administration of excessive volumes of iv fluids may increase the risk of pulmonary oedema.

Rivaroxaban.  Orally active direct factor Xa inhibitor, licensed in adults for DVT prophylaxis after elective hip or knee replacement surgery and, in the USA, CVA prophylaxis in non-valvular AF. More effective than enoxaparin at preventing DVT and PE, with comparable risks of haemorrhagic side effects.

Rapidly absorbed via the oral route (peak plasma concentration within 2–4 h) with 80–100% oral bioavailability. 70% undergoes hepatic metabolism (by the cytochrome P450 system) to inactive products; 30% is excreted unchanged in urine. Thus, caution is required in patients with renal failure, and those taking drugs that cause hepatic enzyme induction/inhibition.

Rocuronium bromide.  Non-depolarising neuromuscular blocking drug, introduced in 1994. Chemically related to vecuronium, with similar lack of cardiovascular effects, although tachycardia may accompany very large doses. Has been suggested as the drug of choice when suxamethonium is contraindicated. Good intubating conditions occur 60 s after an initial dose of 0.6 mg/kg; relaxation lasts for about 30–40 min (about 20 min after 0.45 mg/kg). During a rapid sequence induction, an intubating dose of 1–1.2 mg/kg is advocated by some; it produces better intubating conditions in a shorter time. Supplementary dose: 0.15 mg/kg; effects last for about 15 min. May be infused iv at 0.3–0.6 mg/kg/h after a loading dose. Primarily excreted by the liver. Cumulation is unlikely at recommended doses. Reversed by sugammadex.

Ropivacaine hydrochloride.  Amide local anaesthetic agent, introduced in 1997. Chemically related to bupivacaine (a propyl group replacing a butyl group) but less lipid-soluble and less toxic, being associated with less severe CNS and CVS adverse effects. pKa is 8.1. Presented as the (S)-enantiomer (see Isomerism). Used in 0.2–1.0% concentrations; initially reported to be approximately equipotent to bupivacaine in terms of analgesia whilst producing less motor block, e.g. for epidural anaesthesia. However, this is disputed, the reduced motor block seen with ropivacaine being related to its lower potency and thus selection of non-comparable solutions in comparative studies. In addition, comparable concentrations contain slightly less ropivacaine than bupivacaine.

Has vasoconstrictor properties; thus relatively unaffected by addition of vasoconstrictor drugs. About 94% protein-bound; undergoes hepatic metabolism with 1% excreted unchanged in the urine. Has about 40% greater clearance than bupivacaine. Maximal safe dose is estimated at 3.5 mg/kg.

Rotameter.  The trade name of a type of flowmeter commonly used on anaesthetic machines; first used in the 1930s.

• Features include:

ent constant pressure, variable orifice.

ent consists of a needle valve, below a bobbin within a tapered tube. Gas flow rates are marked along the tube’s length. Readings are taken from the top of the bobbin. Tubes are arranged in banks at the back of the anaesthetic machine, traditionally for O2, CO2 and cyclopropane (the last two on older machines only), N2O, and air, from left to right in the UK (see below).

ent accurate to within 2%.

ent bobbins are made of light metal alloy; each is individually matched to its particular tube, and specific for a certain gas.

ent the tube’s taper is narrower at the bottom to allow accurate measurement of low flow rates, and wider above to measure higher flows.

ent the space between the bobbin and walls of tube is narrow at the bottom of the tube; gas flow behaves as through a tube, i.e. is largely laminar. Thus gas viscosity is important at low flow rates. Higher up the tube, the space between the bobbin and tube is wide compared with the length of the bobbin, because of the tube’s taper. Gas flow behaves as through an orifice, i.e. is turbulent. Thus gas density is important at high flow rates.

ent inaccuracies may result from sticking of the bobbin against the sides of the tube. This is reduced by:

– keeping the tube vertical to reduce friction between bobbin and tube.

– angular notches in the bobbin, causing it to rotate when gas flows.

– regular cleaning to prevent dirt accumulating within the tube.

– reduction of static charge building up within the tube. Many are internally coated with a thin layer of gold. Alternatively, regular spraying with antistatic solution may be performed.

ent the O2 control knob is larger than the others and differently shaped to aid recognition. All are colour-coded as for cylinders.

ent on some older machines, the CO2 bobbin could be hidden at the top of the tube if the CO2 valve was accidentally left fully open.

ent with the traditional arrangement of rotameters, i.e. O2 upstream, O2 may be lost if there is a leak from a tube downstream. This may be prevented by placing the O2 inlet downstream from the others, e.g. by fitting a baffle across the top of the rotameter tubes so that N2O enters first, and O2 last.

ent in modern machines, N2O and O2 rotameters are mechanically linked such that less than 25% O2 cannot be delivered.

Rotational therapy (Kinetic therapy).  Technique in which critically ill patients are turned laterally from the horizontal to an angle of about 40°, often several times per hour on a programmable bed. Thought to reduce the incidence of nosocomial pneumonia, decubitus ulcers, DVT and PE. Also reported to shorten duration of both IPPV and ICU stay. May share mechanisms of action with prone ventilation techniques. Compared with the prone position, it has less chance of accidental displacement of tubes and catheters/cannulae, damage to eyes/face/limbs, stimulation of coughing and cardiovascular instability. Accessibility to the patient remains good.

Goldhill DR, Imhoff M, McLean B, Waldmann C (2007). Am J Crit Care; 16: 50–61

Rowbotham, Edgar Stanley (1890–1979).  English pioneer of anaesthesia. With Magill, developed tracheal intubation, including blind nasal intubation, and endotracheal anaesthesia. Also pioneered basal narcosis with rectal paraldehyde, and local and intravenous techniques. The first anaesthetist in the UK to use cyclopropane. Designed several pieces of apparatus, including a vaporiser, airway, local anaesthetic needles and other equipment. Latterly worked at Charing Cross, London. Particularly interested in anaesthesia for thyroid surgery.

Condon HA, Gilchrist E (1986). Anaesthesia; 41: 46–52

Royal College of Anaesthetists.  Arose from the granting of a Charter to the College of Anaesthetists by Queen Elizabeth II in March 1992. Regulates and promotes research, training, education and maintenance of standards in anaesthesia. Administers the FRCA examination. Has around 6500 Fellows (including overseas); together with Members (non-trainees without the Final FRCA, a membership category introduced in 2001) and registered trainees, this amounts to ~12 000 Members in total. Created the Faculty of Pain Medicine in 2007 and the Faculty of Intensive Care Medicine in 2010. The British Journal of Anaesthesia has been its official journal since 1990; it also publishes guidelines, a regular Bulletin and CEPD Reviews.

Spence AA (1992). Br J Anaesth; 68: 457–8

R–R interval.  Time between successive R waves on the ECG. Thus heart rate =

image

Normally varies by less than 0.16 s at rest (sinus arrhythmia). Useful in the diagnosis of autonomic neuropathy.