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Restarting after a gap

Status: drafted · Content checked 2026-10-06

Re-titrating cautiously is usually reasonable. Changing to a medicine that has already been tried and found inadequate is a different decision, and needs reasons.

1 · Quick understanding

Two separate questions get mixed up when treatment restarts:

  1. Pace — should the dose be built up again gradually? After weeks or months off, usually yes. Tolerability, blood pressure and pulse can change, and a gap is a sensible point to reassess.
  2. Product — which medicine? A new provider may follow the standard sequence from the start. If a first-line medicine was already tried for a long time without enough benefit, repeating it is a choice that should be explained.

2 · Possible explanations

Why might a new prescriber prefer a long-acting first-line medicine? Reasonable answers include: national guidance places lisdexamfetamine and methylphenidate first; long-acting products are taken once a day; lisdexamfetamine's prodrug design is associated with lower misuse potential; and a new provider may not yet have the previous service's records.

NICE recommends offering lisdexamfetamine or methylphenidate first in adults, considering a switch after a six-week trial at an adequate dose without enough benefit, and considering dexamfetamine for adults responding to lisdexamfetamine who cannot tolerate its longer effect profile.

W1

Read carefully, that sequence also means: after an inadequate lisdexamfetamine trial, the next step NICE describes is a switch, most often to methylphenidate — not another lisdexamfetamine trial.

3 · Useful next action

Ask for the restart plan in writing, with reasons. Useful wording:

Please set out the proposed medicine, starting dose and titration steps; the reason for choosing it over the alternatives, including the medicine I responded to previously; what will be monitored; how long the trial will last; and what result would lead to a change.

4 · Treatment logic

Lisdexamfetamine is converted to the same active drug as dexamfetamine, but more gradually; the different exposure curve means tolerability and benefit can differ between them in the same person.

R10

Shared active ingredient does not prove equal safety or equal effect, in either direction. Current blood pressure, pulse, heart history, mental health and other medicines all need assessing at restart.

The dexamfetamine licence lists psychiatric and cardiovascular contraindications and cautions that a prescriber must assess for the individual.

W4

5 · Deeper explanation

A previous consultant's plan deserves weight — it records clinical reasoning made with more history than a new provider has. It does not bind every future decision. The fair test is whether the new decision engages with the old one and gives reasons.

Useful questions

Uncertainty

Evidence comparing restart strategies after a gap in adults is thin. Individual history matters more than population averages here.

Sources cited

  1. W1 NICE. Attention deficit hyperactivity disorder: diagnosis and management (NG87). 2018, updated 2019. Recommendations 1.7.11–1.7.14 (adult medication choice) and section 1.10 (review and discontinuation). link (Official text via search snippets and NHS shared-care documents quoting it; main page fetch blocked)
  2. R10 Pennick M. Absorption of lisdexamfetamine dimesylate and its enzymatic conversion to d-amphetamine. Neuropsychiatr Dis Treat 2010;6:317–27. (Abstract read (PubMed))
  3. W4 Amfexa 5 mg, 10 mg and 20 mg Tablets, Summary of Product Characteristics (Medice UK). Section 4.1: ADHD in children and adolescents aged 6–17 when response to previous methylphenidate is clinically inadequate. Section 6.1 excipients: 10 mg — isomalt, magnesium stearate, yellow iron oxide; 20 mg — isomalt, magnesium stearate, red iron oxide; 5 mg — isomalt, crospovidone, magnesium stearate. link (Sections 4.1 and 6.1 checked (emc products 5004, 7403, 7404))