Improving follow-up after an abnormal Pap smear: Results from a quasi-experimental intervention study

Citation
Cp. Kaplan et al., Improving follow-up after an abnormal Pap smear: Results from a quasi-experimental intervention study, J WOMEN H G, 9(7), 2000, pp. 779-790
Citations number
43
Categorie Soggetti
Public Health & Health Care Science","General & Internal Medicine
Journal title
JOURNAL OF WOMENS HEALTH & GENDER-BASED MEDICINE
ISSN journal
15246094 → ACNP
Volume
9
Issue
7
Year of publication
2000
Pages
779 - 790
Database
ISI
SICI code
1524-6094(200009)9:7<779:IFAAAP>2.0.ZU;2-P
Abstract
The success of cervical cancer control programs depends on regular screenin g with the Pap smear test and prompt and appropriate treatment of early neo plastic lesions. Recognizing the potentially grave consequences of lack of follow-up for abnormal Pap smears, numerous intervention studies have teste d the impact of a variety of strategies to increase return for follow-up. T he majority of these studies were evaluated under controlled experimental c onditions. Despite the encouraging findings of these trials, the next step in the research continuum requires that the effectiveness of these interven tions be demonstrated in real world settings before full implementation is initiated. We report the results of an evaluation study assessing the combi ned effectiveness of three intervention modalities found effective in prior randomized studies: a tracking follow-up protocol, transportation incentiv es, and financial incentives. This study used a before-after, nonequivalent control group design to assess the impact of a multifaceted intervention t hat included a computerized tracking protocol with transportation and finan cial incentives. The study was implemented at two major hospitals, two comp rehensive health centers (CHC), and nine public health centers (PHC) under the jurisdiction of the Los Angeles County Department of Health Services. O ne hospital, one CHC, and the four PHC located in the catchment area of the CHC were selected as experimental sites. The control sites-one hospital, o ne CHC, and five PHC-provided usual care. All women with an abnormal Pap sm ear at the intervention and control sites were included in the study. The s tudy consisted of a 1-year period of baseline data collection (September 19 89-August 1990), followed by a 21/2-year intervention period (September 199 0-February 1993). During the intervention period, the intervention protocol was implemented at the experimental sites, and the control sites provided usual care. Overall, we found that the rates of receipt of follow-up care w ere consistent with those found in similar studies. In contrast to results obtained in these prior randomized trials, we did not find strong and consi stent evidence for intervention effects. Significant findings emerged only at the CHC and hospital levels and only for selected years. Results undersc ore the importance of testing interventions in real world conditions before large-scale implementation is initiated. In addition, this study highlight s the challenge of detecting intervention effects in large-scale studies be cause of the greater measurement difficulties in field studies as compared with controlled experiments.