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Haloperidol decanoate long-acting injection (HDLAI): Results of a 1-year mirror-image study
Shubhra Mace1, Olubanke Dzahini2, Maria O'Hagan2
1Pharmacy Department, Maudsley Hospital, Denmark Hill, London SE5 8AZ, UK.
Insights
Haloperidol decanoate long-acting injection (HDLAI) showed a high discontinuation rate, but reduced hospital admissions. Patients with longer illness duration or not treated for nonadherence may benefit from HDLAI.
Area of Science:
- Psychiatry
- Pharmacology
- Clinical Medicine
Background:
- Haloperidol decanoate long-acting injection (HDLAI) is used for managing psychiatric conditions.
- Assessing the 1-year clinical outcomes of HDLAI is crucial for treatment optimization.
Purpose of the Study:
- To evaluate the clinical outcomes of haloperidol decanoate long-acting injection (HDLAI) after one year of use.
- To identify predictors of treatment discontinuation for HDLAI.
Main Methods:
- A 1-year mirror-image study involving 84 inpatients initiated on HDLAI.
- Comparison of hospital admissions and bed days in the year before and after HDLAI initiation.
- Analysis of factors influencing HDLAI treatment discontinuation.
Main Results:
- 33% of patients remained on HDLAI at 1 year; discontinuation was higher for those treated due to nonadherence.
- Patients with longer illness duration were more likely to continue HDLAI treatment.
- Significant reduction in mean hospital admissions (1.4 to 0.6 per patient/year) was observed post-HDLAI initiation.
Conclusions:
- HDLAI is associated with a high discontinuation rate but leads to reduced hospital admissions.
- Patients with longer illness duration and those not initiated for nonadherence may benefit most from HDLAI.
- No significant change in bed days was observed overall, though continuers showed reductions.
Background:
We sought to determine clinical outcomes of the prescribing of haloperidol decanoate long-acting injection (HDLAI) at 1 year.
Method:
A 1-year mirror-image study of 84 inpatients initiated on HDLAI. Admissions and bed days in the year preceding HDLAI were compared with the year after initiation. Predictors for discontinuation were evaluated.
Results:
At 1 year, 33% of patients remained on treatment. Patients starting HDLAI because of nonadherence were more likely to stop treatment [relative risk (RR) 1.72; 95% confidence interval (CI) 1.01, 2.91; p = 0.044] whilst patients with a longer duration of illness were more likely to remain on treatment (RR 0.88; 95% CI 0.78, 1.00; p = 0.050). In the bed days cohort overall, (n = 65), there was a significant reduction in mean hospital admissions (1.4/patient/year to 0.6/patient/year; p = 0.0001) but not bed days (55.6/patient to 45.0/patient; p = 0.07) in the year following HDLAI initiation compared with the year before. Continuers had a significant reduction in mean bed days (53.1 to 4.0; p = 0.0002) and hospital admissions (1.5 to 0.2; p = 0.0001). Discontinuers demonstrated a significant reduction in hospital admissions (1.5 to 0.8; p = 0.0001) but not bed days (56.7 to 64.5; p = 0.83).
Conclusion:
HDLAI was associated with a high treatment discontinuation rate. Hospital admissions fell in the year after HDLAI but there was no change in bed days. Our study suggests that patients with a longer duration of illness and patients initiated on HDLAI for reasons other than poor adherence may benefit from HDLAI initiation.
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