01Principles and purposeThe professional or clinical skill and the decisions it supports.
Prepare the exact request, labels, specimen tubes, sterile single-use needle and holder or winged set, tourniquet, approved antiseptic, gauze, dressing, gloves, tray and sharps bin within reach. Check identity, allergies to adhesives or antiseptics, previous difficulty, fistula, lymph-node surgery, vascular devices, anticoagulation and fainting. Explain purpose and alternatives and position safely.
Use hand hygiene and clean gloves for venepuncture, adding PPE for splash risk. Select a palpable straight vein away from infection, haematoma and arterial pulsation; avoid restricted limbs according to local policy and seek help rather than repeated blind attempts. Apply the tourniquet only as long as necessary. Palpate before antisepsis, then clean and allow full drying; do not repalpate unless asepsis is restored.
Anchor the skin without contaminating the site, insert bevel up at a shallow angle until flashback, lower and advance only enough to stabilise. Attach tubes without moving the needle and follow the local laboratory order of draw and fill requirements. Release the tourniquet once flow is established and before needle removal. Ask the patient not to pump the fist because it changes analytes.
Withdraw smoothly, apply gauze pressure and activate the engineered safety feature immediately. Put the sharp directly into the nearby bin without passing, bending or resheathing. Invert additive tubes gently as manufacturer and laboratory require; do not shake. Label beside the patient with identifiers, date, time and collector, confirm against the wristband or spoken details, and send under local stability rules.
A failed attempt should not become persistent probing. Stop for electric-shock pain, paraesthesia, swelling, pallor, arterial-looking pulsatile flow, severe distress or presyncope. Remove, compress and reassess. Respect the organisation’s maximum-attempt policy and call a more experienced practitioner or vascular-access service. After fainting, lie the patient safely and assess rather than continuing upright.
Blood-culture equipment adds the correct adult or paediatric bottles, bottle-septum antisepsis and the local closed collection adapter. Verify number of sets, volume and order against current laboratory instructions because bottle systems differ. Inspect expiry, damage and fill markers. Do not cover the bottle barcode or remove detachable identifiers incorrectly.
Obtain cultures promptly when bloodstream infection is suspected, ideally before antimicrobials, without delaying urgent treatment in severe sepsis. NHS England recommends two adult sets: two aerobic and two anaerobic bottles, usually 8–10 mL in each according to the bottle instructions. Four bottles at a specified 10 mL target give 40 mL total; four at 8 mL give 32 mL. The report identifies at least 40 mL as optimal for adult detection. Paediatric volumes require a separate age/weight and bottle-specific plan.
Disinfect bottle tops and skin with the specified agent and contact time, then allow drying. Maintain non-touch technique for the venepuncture key parts. Draw separate sets from separate peripheral sites where feasible. A culture from a vascular line may answer catheter-infection questions only when paired and timed according to protocol; routine line draws increase contamination and can confuse interpretation.
Label each culture with site, date, time and collector and transport without avoidable delay; do not refrigerate unless the laboratory explicitly instructs. Document antimicrobial timing. Report difficulty, low volume or line collection because interpretation changes. Contamination can expose the patient to unnecessary antibiotics, line removal and admission, so technique is diagnostic stewardship.
Arterial sampling requires a pre-heparinised self-filling syringe, appropriate needle with safety device, antiseptic, gauze, secure cap, PPE and immediate analyser or transport arrangement. Check indication, oxygen concentration and recent change, bleeding risk, local collateral-circulation assessment, anatomy and ability to cooperate. Avoid an infected site, compromised circulation, fistula or vascular graft and seek expert help after failed attempts. Use local anaesthesia for arterial blood-gas sampling except in an emergency where it would delay necessary care.
Position the wrist slightly extended without hyperextension. Palpate the radial artery with the non-dominant hand, clean and dry the site, and insert bevel up at a typical 45-degree angle for adult radial puncture, adjusted to the assessed anatomy and supervised technique while keeping fingers off key parts. Arterial pressure should fill the syringe without forceful aspiration. Take only the volume required by the analyser and withdraw at once if severe radiating pain or paraesthesia occurs.
Apply firm uninterrupted pressure immediately. WHO describes assessing haemostasis after 2–3 minutes, with 5 minutes or longer potentially needed in anticoagulation, hypertension or a bleeding disorder. Continue until bleeding stops and reassess distal circulation; elapsed time alone does not establish safety. Expel visible air without spraying, engage safety, use the approved cap and mix to distribute heparin. Analyse promptly and document oxygen device or FiO2 and other required sample conditions.
Interpret arterial blood gas systematically: pH, PaCO2, bicarbonate/base excess, oxygenation and lactate, linked to clinical context and supplemental oxygen. Air contamination can raise PaO2 and lower PaCO2; delay permits cellular metabolism to lower oxygen and pH and raise carbon dioxide. A venous sample masquerading as arterial can mislead oxygenation assessment.
After sampling, inspect haemostasis, distal colour, warmth, capillary refill, pulse, sensation and movement. Warn about bruising and delayed bleeding. Urgently review an expanding haematoma, persistent bleeding, cool painful hand or neurological change. Communicate critical results immediately and record collection site, oxygen, complications and action.
After a sharps injury, encourage bleeding without aggressive sucking, wash with soap and water, irrigate mucosa, report immediately and follow occupational-exposure protocol for risk assessment and time-critical prophylaxis. Do not conceal the event. Review device, environment and workflow to prevent recurrence.
Key points
- Perform only after training and supervised competency for the specific sampling system; arterial puncture requires additional assessment and local authorisation.
- Match two identifiers to request and labels at the bedside; never pre-label tubes for several patients.
- For routine venepuncture, choose an appropriate vein, use hand hygiene and skin antisepsis, let antiseptic dry, release the tourniquet promptly and fill tubes to local order-of-draw requirements.
- Activate the safety device immediately, discard the entire sharp directly and never resheath.
- Blood cultures need a genuine indication, antisepsis of skin and bottle septa, correct bottle set and volume, and collection before antimicrobials when possible without delaying treatment of severe sepsis.
- Do not draw cultures from an existing line unless the diagnostic question and local protocol require paired line/peripheral specimens.
- For radial arterial sampling, assess collateral circulation under the local protocol, use a heparinised gas syringe, expel air, cap, mix and analyse promptly.
- Apply firm arterial pressure longer when bleeding risk is increased; stop and escalate for distal ischaemia, expanding haematoma, severe pain, nerve symptoms or needlestick exposure.
02Situations and prioritiesThe context, relevant information and actions that matter most.
Mismatch among request, wristband, spoken identifiers or labels requires stopping before any specimen is taken.
Electric pain, paraesthesia, pulsatile flow or distal change requires immediate needle withdrawal, pressure and assessment.
Pallor, sweating, nausea or reduced response requires stopping, safe positioning and observations.
Re-palpation after antisepsis, inadequate drying, line sampling or low volume undermines diagnostic validity.
Air bubbles, clot, delay or undocumented oxygen therapy can make gas results misleading.
Pain, coolness, pallor, reduced pulse or neurological deficit requires urgent senior or vascular assessment.
03Assessment and interpretationHow to gather information, assess the situation and recognise uncertainty.
Consider the information, its meaning and its limitations before deciding what follows.
- 01
Tube and request verification - Why
- Ensure the correct specimen and additive reach the intended test.
- Interpretation and limitations
- Local laboratory order, fill and transport requirements take precedence over memorised tube colours.
- 02
Blood culture set and volume - Why
- Optimise detection of bloodstream infection.
- Interpretation and limitations
- Adequate paired adult sets and volume improve yield; low volume and contamination reduce confidence.
- 03
Arterial blood gas - Why
- Measure acid-base status, ventilation, oxygenation and lactate when indicated.
- Interpretation and limitations
- Interpret with oxygen delivery, timing and sample quality; a normal pH can conceal a mixed disorder.
- 04
Puncture-site neurovascular check - Why
- Detect bleeding, haematoma, nerve injury or impaired distal perfusion.
- Interpretation and limitations
- Persistent bleeding or new distal abnormality is a complication, not routine bruising.
04Worked approachesCases with ordered reasoning, an action and a check of the outcome.
01Worked case: cultures before antibioticsProtect treatment time and specimen qualityA febrile hypotensive adult needs immediate antimicrobials and cultures. Peripheral access is difficult; the available adult bottles specify 10 mL each.+
- 1Call for sepsis support and prepare two identified sets, each with one aerobic and one anaerobic bottle. Plan 4 × 10 mL = 40 mL in total while another clinician prepares urgent treatment.
- 2Reason that cultures before antibiotics improve yield but must not delay urgent antimicrobial treatment; set an attempt limit and escalate access early.
- 3If obtainable promptly, disinfect skin and bottle septa, let them dry and collect separate peripheral sets with non-touch technique, filling each to its 10 mL marker. Label site/time; urgent antimicrobials must proceed if difficult access prevents prompt completion.
- 4Verify transport, record antibiotic timing and collection limitations, communicate deterioration and review culture results and possible contamination.
02Routine venepunctureOne clean controlled passA stable patient needs venous specimens.+
- 1Verify patient, request, tubes, restrictions and equipment; position for fainting risk.
- 2Select and disinfect a vein, insert without repalpation, fill to local order and release tourniquet.
- 3Remove, compress, activate safety, label at bedside, inspect site and send correctly.
03Radial arterial samplePreserve patient and sampleAn ABG is clinically indicated and the operator is authorised.+
- 1Assess perfusion, bleeding risk, oxygen and analyser readiness; explain the procedure and provide local anaesthesia except in an emergency.
- 2For adult radial sampling use asepsis and a typical 45-degree approach, allow arterial fill and withdraw for severe radiating pain. Apply uninterrupted pressure, initially check haemostasis after 2–3 minutes and continue longer when needed, particularly with bleeding risk.
- 3Remove air, cap, mix, analyse promptly and complete distal neurovascular and result checks.
05Feedback, follow-up and evidenceReview outcomes, seek feedback and identify what to improve.
- Observe venepuncture sites until bleeding stops.
- Record failed attempts and escalate within local limits.
- Track blood cultures to preliminary and final result and assess contamination.
- Act immediately on critical blood-gas or lactate results.
- Recheck distal perfusion after arterial puncture.
- Complete occupational-exposure assessment after every needlestick.
06Special situationsVariants, exceptions and circumstances that change the usual approach.
Identity is procedural
Bedside labelling is part of sampling technique and prevents a technically perfect wrong-patient result.
Volume drives culture yield
Antisepsis prevents contamination, but underfilled bottles also reduce bloodstream-infection detection.
Drying is active
Antiseptic needs its specified contact and drying time; wiping it away removes part of the intervention.
Air changes gases
Small bubbles and transport delay can materially distort PaO2, PaCO2 and pH.
Pressure is treatment
Arterial aftercare requires uninterrupted compression and distal reassessment, especially with bleeding risk.
07Common pitfallsFrequent interpretation and management errors.
- 01
Do not pre-label specimens away from the patient.
- 02
Do not use tube colour as a universal order-of-draw standard.
- 03
Do not repalpate a disinfected culture site with an unsterile finger.
- 04
Do not delay sepsis antibiotics for prolonged culture attempts.
- 05
Do not routinely draw cultures from an existing line.
- 06
Do not forcefully aspirate an arterial syringe or leave air inside.
- 07
Do not stop arterial compression too early in anticoagulated patients.
- 08
Do not resheath, pass or carry an exposed sharp.