Chronic Disease Management Module supports GPs to deliver better care

Issue: BCMJ, vol. 50, No. 3, April 2008, Page 134 Family Practice Services Committee

A recent international survey[1] showed that within the year under study, only 38% of Canadians with diabetes received all four basic tests included in the recommended care guidelines.

The sizable gap between recommended care for chronic disease pa­tients and the care they actually receive—as well as the fact that such patients now account for the majority of all primary care visits—underlines the urgency of efforts by the General Practice Services Committee (GPSC) to support BC’s family physicians.

“In modern family practice, the monitoring of chronic ailments is more difficult than ever,” says GPSC co-chair Dr Bill Cavers, a Victoria physician. “Walk-in clinics are taking patients with the more easily and immediately treatable conditions, so family physicians are left to deal with ongoing and very complex care.”

Recognizing that support for family physicians has not kept pace with the changing nature of their work, the GPSC’s Practice Support Program has developed a chronic disease management (CDM) module designed to help physicians, medical office assistants, and other care pro­viders develop a more structured approach to providing evidence-based care. 

Response to the module, which is offered by practice support teams in all health authorities, has been ex­tremely positive, with 642 physicians currently enrolled and 128 registered for future sessions. 

“It’s not surprising that the CDM module is well received,” says Dr Cavers. “It provides a number of effective tools and planning elements to help GPs be proactive in terms of managing care for patients with chronic ailments.”

According to Dr Cavers, without such initiatives, care tends to be reactive and far less efficient because physicians are busy managing patients on a visit-to-visit basis. “You see a patient and order some lab work, but there’s nothing to prompt you to find out whether the lab work was done in a timely way, or to follow up with the patient about the results. It is also difficult to keep track of patients who don’t readily come in for an appointment.”

While the CDM tools and strategies facilitate such follow-up, Dr Cavers is quick to point out they do not mandate or restrict how care is provided. “There is always clinical judgment required—CDM strategies do not remove that need.”
The CDM module has three main components:

• Developing patient registries
• Using the CDM toolkit
• Implementing planned recall

A series of up to eight learning sessions, with “action” phases between them, supports the significant practice changes physicians are being asked to make in their chronic disease care. Physicians and their MOAs attend the learning sessions in their local community to learn how to develop patient registries, determine which patients require testing, manage group visits, help patients use self-management tools, and other CDM-enabling techniques.

After an initial learning session, physicians are assisted in implementing the CDM toolkit. Using the secure, web-based toolkit, doctors and MOAs fill out patient flowsheets based on clinical guidelines. They can share their de-identified results with other participants in the project and, with the patient’s permission, can share personalized information with other health care providers for better coordination of care.

“I also provide a copy of the flowsheet to patients so they are aware of their blood pressure and clinical findings, which encourages their involvement in their care,” says Dr Cavers.

The CDM toolkit also provides recall reports listing patients who are due for an office visit, or who require scheduled tests or procedures. Currently there are more than 1000 tool­kit users in BC. Physicians in Saskat­chewan, Manitoba, and Yukon are also using the toolkit. 

In addition to the obvious patient benefits of more rigorous, evidence-based care and improved outcomes, CDM practices offer significant benefits for physicians and medical staff, from better management of complex patients, to increased job satisfaction and more accurate billing.  

Other Practice Support Program modules—all based on extensive input from GPs—include advanced access (a scheduling system), group visits, and patient self-management.

The Practice Support Program is an initiative of the BCMA and the Ministry of Health via the joint GPSC. Its purpose is to provide change management strategies and support to improve physicians’ working lives and patient care. In addition, it helps physicians learn about and implement the 2006 Agreement’s financial incentives. For more information, see www.bcma.org

—Liza Kallstrom
Lead, Change Management and Practice Support

The CDM Toolkit—Frequently asked questions

What is the CDM Toolkit?
The CDM toolkit is a clinical information system that helps doctors manage their patients who have chronic conditions.

Why was it developed?
It was developed in 2003 at the request of family practitioners involved in the South Vancouver Island Health Authority’s Chronic Disease Collaborative and the province-wide CHF Collaborative.

What does the toolkit do?
It helps physicians develop a patient registry and informs a physician which patients may require intervention and follow-up.

Who funded its development?
The Ministry of Health.

Who has access to the data?
The toolkit is an extension of the physician’s medical record. No one other than the physician can authorize access to an individual patient’s information entered into the toolkit.


References

1. Schoen C, Osborn R, Doty M, et al. On the front lines of care: Primary care doctors’ office systems, experiences, and views in seven countries. Health Aff 2006;25:w555-w571.

Liza Kallstrom,. Chronic Disease Management Module supports GPs to deliver better care. BCMJ, Vol. 50, No. 3, April, 2008, Page(s) 134 - Family Practice Services Committee.



Above is the information needed to cite this article in your paper or presentation. The International Committee of Medical Journal Editors (ICMJE) recommends the following citation style, which is the now nearly universally accepted citation style for scientific papers:
Halpern SD, Ubel PA, Caplan AL, Marion DW, Palmer AM, Schiding JK, et al. Solid-organ transplantation in HIV-infected patients. N Engl J Med. 2002;347:284-7.

About the ICMJE and citation styles

The ICMJE is small group of editors of general medical journals who first met informally in Vancouver, British Columbia, in 1978 to establish guidelines for the format of manuscripts submitted to their journals. The group became known as the Vancouver Group. Its requirements for manuscripts, including formats for bibliographic references developed by the U.S. National Library of Medicine (NLM), were first published in 1979. The Vancouver Group expanded and evolved into the International Committee of Medical Journal Editors (ICMJE), which meets annually. The ICMJE created the Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly Work in Medical Journals to help authors and editors create and distribute accurate, clear, easily accessible reports of biomedical studies.

An alternate version of ICMJE style is to additionally list the month an issue number, but since most journals use continuous pagination, the shorter form provides sufficient information to locate the reference. The NLM now lists all authors.

BCMJ standard citation style is a slight modification of the ICMJE/NLM style, as follows:

  • Only the first three authors are listed, followed by "et al."
  • There is no period after the journal name.
  • Page numbers are not abbreviated.


For more information on the ICMJE Recommendations for the Conduct, Reporting, Editing, and Publication of Scholarly Work in Medical Journals, visit www.icmje.org

BCMJ Guidelines for Authors

Leave a Reply