Format

Send to

Choose Destination
Acad Pediatr. 2015 May-Jun;15(3):289-96. doi: 10.1016/j.acap.2014.12.002.

A planned care approach and patient registry to improve adherence to clinical guidelines for the diagnosis and management of attention-deficit/hyperactivity disorder.

Author information

1
Department of Pediatrics, Cambridge Health Alliance (Cambridge, MA) and Harvard Medical School, Boston, Mass. Electronic address: pgeltman@challiance.org.
2
Institute for Community Health, Cambridge Health Alliance (Cambridge, MA) and Harvard Medical School, Boston, Mass.
3
Department of Pediatrics, Cambridge Health Alliance (Cambridge, MA) and Harvard Medical School, Boston, Mass.
4
Division of Child Psychiatry, Cambridge Health Alliance (Cambridge, MA) and Harvard Medical School, Boston, Mass.
5
Department of Pediatrics, Massachusetts General Hospital and Harvard Medical School, Boston, Mass.
6
Allegheny County Health Department and University of Pittsburgh Graduate School of Public Health, Pittsburgh, Pa.

Abstract

BACKGROUND:

Attention-deficit/hyperactivity disorder (ADHD) affects almost 2.4 million US children. Because American Academy of Pediatrics guidelines for ADHD recommend use of standardized diagnostic instruments, regular follow-up and the chronic care model, this pilot project sought to implement and assess an electronic registry of patients with ADHD combined with care coordination by a planned care team.

METHODS:

This quality improvement project was structured with 2 intervention and 2 control clinics to facilitate evaluation of the use of a planned care system for management of ADHD. Care teams included a pediatrician, nurse, medical assistant, and care coordinator and tracked patients using an electronic registry with data drawn from the EMR. Clinical work flows were pilot tested to facilitate use of the Vanderbilt scales and their incorporation into the EMR at intervention sites. Outcome measures included 2 recommended clinical follow-ups based on HEDIS measures as well as use of the Vanderbilt rating scales. Initiation phase measure was for follow-up after initiating medication, while the continuation phase measure was for subsequent follow-up during the first year of treatment. Measures were monitored during the project year and then also in the ensuing period of spread of the intervention to other sites.

RESULTS:

Although the modified HEDIS initiation phase measure for patients newly on medication remained static at approximately 50% throughout the project period, the continuation phase measure showed improvement from 35% at baseline to 45% at the end of the project assessment year, a 29% increase. Follow-up for patients stable on medications also remained unchanged during the project period, but during subsequent spreading of the intervention to nonproject sites, follow-up of these patients improved to over 90%. In adjusted analyses, patients with ADHD at intervention sites were over 2 times more likely than patients at control sites to have had a Vanderbilt score documented in their records.

CONCLUSIONS:

The project achieved modest improvements in the diagnostic and treatment process for patients with ADHD. The use of a planned care system and electronic patient registry shows promise for improving the diagnosis and treatment process for patients with ADHD.

KEYWORDS:

ADHD; planned care; primary care; quality improvement; registry

PMID:
25906699
DOI:
10.1016/j.acap.2014.12.002
[Indexed for MEDLINE]

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center