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••Fall 2005/Vol. 9, No. 4
A Focus on Innovation and Transfer



Letters to the EditorAbstracts from articles published in other journalsCommentary Clinical articles on the practice of Permanente medicinePoetry, Art, Musings from Permanente cliniciansArticles from a Systems perspective
Physicians in the newsBook Reviews
Kaiser Permanente in the CoOmmunity

 

 

 

 

 

 

 

 

 


Abstracts


 

Abstracts from the HMO Research Network
10th Annual HMO Research Network Conference
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With this issue we include abstracts from the 2005 11th Annual HMO Research Network Conference, held in Santa Fe, New Mexico, that focused on "Translating Research into Practice."

April 4-6, 2005 Santa Fe, NM
"Translating Research Into Practice--Scaling New Heights"

From HMO Research Network Member: Kaiser Permanente Northern California Division of Research
Chemical dependency and psychiatric services for adolescents in managed care: A research to practice integration model.
Sterling S, Chi F, Weisner C.

background: The chemical dependency (CD) field is concerned that much of what we know about effective treatment is not applied in clinical practice, particularly for adolescents. According to the literature many adolescents with CD problems have psychiatric comorbidities, and these adolescents have less successful treatment outcomes; yet research to practice studies that address integrated treatment approaches are uncommon. We examined the impact of psychiatric services on outcomes for adolescents in CD treatment and discuss them in the context of a research to practice model developed for adolescent CD treatment in a health plan.
methods: Participants were 419 adolescents, aged 12-18, seeking treatment at four CD programs of a nonprofit, group-model health system, and a parent or guardian for each adolescent. We surveyed participants at intake and six months, examined diagnostic clinical and administrative data, and CD and psychiatric utilization, and conducted qualitative interviews with health plan providers.
results: Fifty-five percent of the treatment intakes had at least one psychiatric diagnosis in addition to a substance use disorder. Thirty-one percent of the full sample had psychiatric visits in the six months after intake; among those with a psychiatric diagnosis, 54% had a psychiatric visit. Girls and those with higher psychiatric severity were more likely to have a psychiatric visit (OR = 2.27, p < .001 and OR = 1.05, p < .0001). Adolescents receiving psychiatric services were more likely to be totally abstinent than those not (OR: 1.57; CI = 0.98, 2.5), and more likely to be alcohol abstinent (OR = 1.68; CI = 1.00, 2.85). Those at co-located clinics had higher odds of abstinence from both alcohol and drugs (OR = 1.57; CI = 1.03, 2.39), drugs (OR = 1.84; CI = 1.87, 2.85), and of returning after intake to initiate CD treatment than others (OR = 2.28; CI = 1.44, 3.61, p < .001).
conclusions: Our findings on the high comorbidity of adolescents entering treatment, their need for services in addition to CD treatment, and how providing integrated psychiatric and CD services effects treatment outcomes are enabling us to help shape adolescent health services within the health plan.


From HMO Research Network Member: Scott and White Health System
Dolasetron and transdermal scopolamine vs dolasetron for prevention of postoperative nausea and vomiting in outpatients undergoing laparoscopic surgery.
Meyer T, Roberson C, McAllister R, McKinney R, Carl S, Rajab H.

introduction: Transdermal scopolamine has been reported to be effective in the prevention of postoperative nausea and vomiting (PONV) and may offer an advantage as a post-discharge antiemetic for ambulatory surgical patients with its long duration of action and antimotion sickness properties. Combining this agent with a 5HT-3 receptor antagonist may provide improved outcomes for patients undergoing day surgery. The purpose of the study was to compare the effectiveness of transdermal scopolamine 1.5 mg patch with dolasetron 12.5 mg IV vs dolasetron 12.5 mg IV alone when administered for routine prophylaxis for PONV.
methods: One hundred eighty-four consenting outpatients undergoing elective laparoscopic surgery with general anesthesia were randomly assigned to one of two antiemetic prophylaxis groups. Group 1 received transdermal scopolamine patch two hours prior to surgery and dolasetron 12.5 mg IV before the cessation of anesthesia. Group 2 received a placebo patch two hours prior to surgery and dolasetron 12.5mg IV before the cessation of anesthesia. A visual analog scale was used with a range of 0 = no nausea to 10 = worst possible nausea. Episodes of nausea and vomiting, nausea scores, time to first episode of emesis, time in PACU, total recovery time and the need for rescue antiemetics were recorded. The incidences of nausea and vomiting and nausea scores were followed during the recovery period and 24 hours after surgery.
results: There were no significant differences in the baseline characteristics. The incidence of nausea and vomiting prior to discharge was less in Group l (p = 0.02). PONV for the ride home was significantly less in Group 1 also (p = 0.02). There were no differences in side effects. Patients' satisfaction scores with their nausea and vomiting treatment were similar in both groups.
conclusions: The combination of transdermal scopolamine with dolasetron was effective and decreased the incidence of PONV prior to discharge as compared with dolasetron alone. This combination was also effective in relieving PONV for the patient's car ride home.


From HMO Research Network Member: Harvard Medical School and Harvard Pilgrim Health Care
Predictors of antidepressant nonadherence in a managed care population.
Baumbauer KZ, Adams AS, Soumerai SB, et al.

background: Antidepressant management scores are one component of the Health Employer Information Data Set (HEDIS) used by the National Center for Quality Assurance (NCQA) to assess quality of care in managed care organizations (MCOs). Harvard Pilgrim Health Care (HPHC), a New England MCO, was interested in what factors predicted antidepressant adherence to target interventions to improve depression treatment.
methods: We used logistic regression to examine two antidepressant medication management measures for 5107 HPHC enrollees age 18+ who initiated antidepressant treatment from May 2002--November 2002. Patients were included if they had an episode of antidepressant treatment preceded by at least 100 days without antidepressant use. Only the first such episode was included for each patient. Outcomes were based on days of antidepressant dispensed during the episode. Patients were counted as "acute phase failures" if they had gaps in coverage totaling more than 30 days during the first 84 days of treatment, approximating the HEDIS "effective acute phase treatment" measure. "Continuation phase failures" were patients with gaps totaling more than 51 days during the first 180 days of treatment, approximating the HEDIS "effective continuation phase treatment" measure. Predictors included patient age (18-65 and 65+), gender, antidepressant use in the previous six months, and total months' supply of other medications dispensed during the six months prior to the episode.
results: Thirty-five percent of patients failed to adhere to therapy during the first 84 days of treatment, and 58% during the first 180 days. History of prior antidepressant use (OR: 0.503, CI: 0.407-0.622) and other medications used (OR: 1.056, CI: 1.004-1.110) were predictors of acute phase treatment failure. Only prior antidepressant use (OR: 0.410, CI: 0.321-0.523) remained a predictor of adherence failure in the continuation phase. Gender and age were not significant predictors in either model, and other medications used was not a significant predictor of continuation phase treatment failure.
conclusions: Antidepressant adherence remains a challenging area for MCOs, as demonstrated by low adherence rates in this study. Antidepressant adherence programs should be targeted to patients without a previous history of antidepressant use and patients with comorbid illness.


From HMO Research Network Member: Kaiser Permanente Colorado Clinical Research Unit
Outcomes from a randomized control trial of an inpatient palliative care service.
Conner D, McGrady K, Richardson R, Beane J, Venohr I, Gade G.

background: Findings from previous research highlight the inadequacies of end-of-life discussions and the management of pain and other symptoms common in the hospital setting for persons who are nearing the end of life. Inpatient palliative care programs have been proposed as a strategy to improve the quality of care for hospitalized patients who are approaching the end of life.
methods: Five hundred and twelve patients from three Kaiser Permanente regions were randomized to receive care from an inpatient palliative care service (IPCS) consisting of a palliative care physician, nurse, social worker and chaplain or usual care from a hospitalist. Outcomes included: 1) changes in self-reported symptoms such as pain, nausea and sob; 2) patient satisfaction with the care they received, 3) utilization and costs for a six-month period following hospital discharge; and 4) survival, time to hospice admission, and hospice length of stay.
results: IPCS patients reported better pain management and greater satisfaction with symptom management, control over their health care choices, communication with their health care providers, and had completed significantly more advanced directives at hospital discharge. Usual care patients had significantly fewer home health visits (p = .02) and hospital outpatient visits (p = .001) than IPCS patients. IPCS patients had significantly fewer ICU stays than did controls (p = .04). IPCS patients also had significantly longer hospice lengths of stay (p = .01). IPCS patients had significantly lower costs for hospital readmissions (p = .001) and outside referrals (provider services outside of the health plan, durable medical equipment, O2 services, radiology, physician consults) (p = .03). Usual care patients had significantly lower pharmacy (p = .04) and outpatient hospital costs (p = .05). Overall there was a $65.18 per patient per day (p = .07) cost savings for IPCS patients
conclusions: IPCS patients reported decreased levels of pain, greater satisfaction with symptom management, control over their health care choices, and communication with their health care providers. Cost differences were the result of more expensive visits/admissions not more visits/admissions. The greatest cost saving was in hospital readmissions for IPCS patients. The $65.18 total per patient per day cost savings was due primarily to the IPCS savings in hospital readmission. These results were not due to differences in survival between the IPCS intervention group and usual care. IPCS teams have been operationalized as ongoing, inpatient consultative service at all three sites.

 

 

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