Documentation for Iron Sucrose Infusion in Outpatient Daycare
Outpatient daycare notes for iron sucrose infusion must include pre-infusion assessment, administration details with vital sign monitoring, adverse event documentation, and post-infusion instructions.
Pre-Infusion Documentation
Patient Assessment and Indication
- Document the indication for IV iron therapy: intolerance to oral iron, inadequate response to oral iron, or need for rapid iron repletion 1
- Record baseline laboratory values: hemoglobin, ferritin, transferrin saturation (TSAT), and mean corpuscular volume (MCV) 2, 3
- Document iron deficiency criteria: typically TSAT <20% and ferritin <300 ng/mL in dialysis patients, or lower thresholds in other populations 3
Risk Stratification
- Assess and document high-risk features for infusion reactions: history of severe asthma, eczema, mastocytosis, multiple drug allergies, or prior reaction to IV iron 1
- Note contraindications: document absence of active infection, iron overload, or hypersensitivity to iron sucrose 4
- Record concurrent medications, particularly ACE inhibitors (which do not contraindicate use but should be noted) 3
Administration Documentation
Dosing Details
- Document the prescribed dose: maximum single dose is 200 mg for iron sucrose 1
- Record the infusion method: iron sucrose can be given as a 2-5 minute IV push (FDA-approved) or diluted in 100-150 mL normal saline over 10-30 minutes 1, 4, 5, 6
- Note that no test dose is required for iron sucrose, unlike iron dextran 7, 3
Vital Signs Monitoring
- Document baseline vital signs: blood pressure, pulse, respiratory rate, oxygen saturation, and temperature 1
- Record vital signs during the first 10 minutes of infusion, as immediate reactions typically occur within the first minute 1
- Continue monitoring throughout infusion and for at least 15-30 minutes post-infusion 1, 5
Infusion Process
- Document IV access: peripheral IV site, gauge, and any difficulties with placement 8
- Record infusion start time and rate: slower infusion rates are associated with lower reaction rates 1
- Note patient tolerance: specifically document presence or absence of metallic taste (occurs in ~18% of patients but is benign) 5
Adverse Event Documentation
Immediate Reactions
- Document any symptoms during infusion: pruritus, flushing, urticaria, chest tightness, back pain, joint pain, shortness of breath, or hypotension 1
- Classify reaction severity if present:
Management of Reactions
- Document interventions if reaction occurs: stopping infusion, switching to normal saline, administering antihistamines, corticosteroids, or epinephrine 1
- Record response to interventions and time to symptom resolution 1
- Note any rechallenge attempts: if symptoms resolved, document restart at 50% infusion rate 1
Common Minor Events
- Document transient symptoms: metallic taste (most common, 17.9% of cases), mild nausea, injection site pain, or lightheadedness 5, 6, 8
- Note that serious adverse reactions are rare (<1%) with iron sucrose 5, 2, 3
Post-Infusion Documentation
Patient Education
- Document counseling on delayed reactions: flu-like symptoms, arthralgias, myalgias, fevers that may occur hours to days after infusion 1
- Record instructions for managing delayed symptoms: use of NSAIDs for symptomatic relief 1
- Note when to seek medical attention: persistent or worsening symptoms 1
Follow-Up Plan
- Document plan for repeat dosing if needed: iron sucrose can be given up to 500 mg weekly (maximum) 1
- Record timing of follow-up laboratory monitoring: typically hemoglobin and iron studies should be rechecked 2-4 weeks after completing iron therapy 2, 3
- Note target parameters: aim for hemoglobin normalization and ferritin >100 ng/mL to replenish stores 1
Safety Considerations
Resuscitation Readiness
- Document availability of resuscitation equipment: anaphylaxis may occur with any IV iron formulation, and resuscitation facilities must be immediately available 1
- Note staff preparedness: all personnel must be trained in recognition and management of infusion reactions 1