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Burden of Antibiotic Resistance in Gram-Negative Infections in Dutch Hospitals (GRAND-ABC)

2019年11月7日 更新者:MJM Bonten、UMC Utrecht

The Attributable Burden and Costs of Infections Caused by Antibiotic-Resistant Gram-Negative Bacteria in Dutch Hospitals

This study aims to assess how large an additional disease burden and what extra costs are generated by antibiotic resistance in patients suffering from infections caused by gram-negative bacteria, such as Escherichia coli and Pseudomonas aeruginosa, in hospitals in the Netherlands.

調査の概要

詳細な説明

This study addresses the following three aims:

  1. To provide a more accurate estimate than currently available of the incremental disease burden and attributable costs of antibiotic-resistant as compared to antibiotic-sensitive gram-negative bacteria (i.e. Enterobacteriaceae and non-fermenters). This analysis is focused on gram-negative infections for which patients are hospitalized. In a less detailed manner, the same analysis of disease burden and costs can be performed for acquiring a gram-negative infection during hospitalization.
  2. To identify determinants associated with resistance in gram-negative infections, to the extent that they are confounders of the relation between resistance and outcome.
  3. To adapt and optimize existing methodology to measure the burden of resistance, among others by calculating disability-adjusted life years (DALYs) which incorporate not merely mortality, but also morbidity.

GRAND-ABC is designed as a prospective parallel matched cohort, which will run for a year in each of the eight participating hospitals. The primary cohort is a random sample of all Gram-negative infections occurring in a participating hospital during the study period. This cohort can be divided on the basis of the primary determinant status (whether the Gram-negative pathogen is resistant or not based on Dutch guideline for multi-drug resistant organisms; Werkgroep Infectiepreventie (WIP). Bijzonder resistente micro-organismen (BRMO). December 2012. http://www.wip.nl/free_content/Richtlijnen/130424_BRMO.pdf) into two parallel subcohorts. Each patient in each of the subcohorts will be matched to one patient without a gram-negative infection. Together these will form the secondary cohort of non-infected patients: patients admitted to the hospital during the study period who are within the same risk set as the infected patients.

For all patients data collection will be performed by review of medical files, which will cover the entire admission during which they were included in the study, and all cause 30 day mortality. Data collection for the hospital stay covers confounders and effect modifiers of the associations studied, and feeds into the outcomes costs, DALYs and length of stay. For the cohort with gram-negative infections, data on infection parameters and antibiotic treatment parameters are also collected.

In addition, the subcohort with infections by multi-drug resistant organisms and a random 20% of the subcohort with infections by sensitive organisms will be selected for follow-up, consisting of sending questionnaires and renewed medical file review 30 days after the index culture date. In the case of ongoing sequelae of the gram-negative infection, this procedure is repeated 90 days after the index culture date. These questionnaires will feed into the outcomes costs, DALYs and quality-adjusted life years (QALYs).

研究の種類

観察的

入学 (実際)

3895

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究場所

      • Amersfoort、オランダ
        • Meander Medisch Centrum
      • Breda、オランダ
        • Amphia Ziekenhuis
      • Eindhoven、オランダ
        • Catharina Ziekenhuis
      • Hilversum、オランダ
        • Tergooi
      • Nieuwegein、オランダ
        • St. Antonius Ziekenhuis
      • Tilburg、オランダ
        • St. Elisabeth Ziekenhuis
      • Utrecht、オランダ
        • UMC Utrecht
      • Utrecht、オランダ
        • Diakonessenhuis

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

18年歳以上 (大人、高齢者)

健康ボランティアの受け入れ

いいえ

受講資格のある性別

全て

サンプリング方法

確率サンプル

調査対象母集団

Patients admitted to hospitals

説明

Inclusion Criteria:

  • Please refer to descriptions of two cohorts

Exclusion Criteria:

  • Patients on children's wards
  • Patients admitted to wards for long-term care or psychiatric wards, that were not subsequently admitted to acute care wards as a consequence of the infection
  • Patients admitted to wards that are excluded for logistic reasons such as the non-availability of electronic patient files, that were not subsequently admitted to included acute care wards as a consequence of the infection
  • Patients that have been included in the cohort of infected patients during the same hospitalization or within the past 30 (if not eligible for follow-up) or 90 (if eligible for follow-up) days

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

コホートと介入

グループ/コホート
Patients with gram-negative infections

Sample (5/week/hospital) of all patients in a hospital that meet all of the following:

  • meeting the criteria of at least one infection entity based on (modified) definitions of the Center for Disease Control and Infection Prevention (CDC; Am J Infect Control 2008;36:309-32) (restricted to infections that have septic potential);
  • a culture with a gram-negative isolate (Enterobacteriaceae / Pseudomonas aeruginosa / Acinetobacter spp. / Stenotrophomonas maltophilia) with minimal inhibitory concentration (MIC) results from an automated system available that can be used to identify such an infection entity according to these criteria;
  • receipt of antibiotics (oral, intravenous or intramuscular) for this infection, the choice of which is determined by the culture with the gram-negative (i.e. this isolate is seen as the causative pathogen);
  • were admitted to the hospital during (part of) the infection episode.

Date of entry into cohort: date of index culture of infection episode

Non-infected patients

Matched sample of all patients that (1) were admitted to the hospital and (2) did not have a gram-negative infection according to the 4 criteria set out in the other group on the date used for matching. Selected by matching 1:1 to patients with gram-negative infections on (1) hospital, (2) length of hospital stay on the date the index culture for the infected patient was obtained, and (3) age.

Date of cohort entry: date of index culture of matched infected patient

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
All cause mortality
時間枠:Up to 30 days
Death (whether in-hospital or after discharge) from any cause, as apparent from medical record or municipal registry.
Up to 30 days

二次結果の測定

結果測定
メジャーの説明
時間枠
Costs
時間枠:Hospital stay (all patients; expected average 1 week) and up to 90 days (follow-up patients)

Costs generated from societal perspective, including:

  • Direct costs within healthcare sector, based on relating standard Dutch reference prices to (1) restricted chart review for all patients, (2) extensive collection of cost data in two of eight participating hospitals, (3) health care use after discharge, as recorded from medical files and reported by patients in questionnaires
  • Other direct costs (own out-of-pocket expenses and time invested by caregivers), as reported by patients in questionnaires
  • Indirect productivity losses, as reported by patients in questionnaires
  • (possibly) Decision-analytic modelling of costs generated by sequelae not within 90 days of index culture date

Questionnaires are not available for the non-infected cohort, and therefore the costs for acquiring gram-negative infections can only be calculated from the hospital perspective.

Hospital stay (all patients; expected average 1 week) and up to 90 days (follow-up patients)
DALYs
時間枠:Up to 90 days

Years of Life Lost (YLL) and Years Lived with Disability (YLD) attributable to infection as apparent from an outcome tree of health outcomes related to gram-negative infections. This tree is preconceived, but modifiable according to observed sequelae in the study. A mathematical model for this outcome will be constructed that incorporates, apart from the observed sequelae in the study, factors such as (1) preexisting decreased life expectancy and quality of life due to comorbidity, (2) known transition parameters between health outcomes from literature, (3) confounding effects of comorbidity on transition parameters, (4) sequelae not observed within the time frame of data collection for the study, (5) 'baseline' change in health outcomes during hospitalization as apparent from the non-infected cohort, and (6) occupancy of several health outcome simultaneously.

This outcome will not be calculated for the non-infected cohort.

Up to 90 days
Length of stay
時間枠:Hospital stay (expected average 1 week)
Number of days until hospital discharge.
Hospital stay (expected average 1 week)

その他の成果指標

結果測定
メジャーの説明
時間枠
QALYs
時間枠:Up to 90 days

Measured by EuroQol 5 Dimensions 5 Levels (EQ-5D-5L) in questionnaires, as a confirmation of the DALY model results.

This outcome will not be calculated for the non-infected cohort.

Up to 90 days

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

捜査官

  • 主任研究者:Marc JM Bonten, MD PhD、UMC Utrecht, Utrecht, the Netherlands
  • スタディチェア:Heidi SM Ammerlaan, MD PhD、Catharina Hospital, Eindhoven, the Netherlands

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2013年6月1日

一次修了 (実際)

2016年3月1日

研究の完了 (実際)

2016年5月1日

試験登録日

最初に提出

2013年10月30日

QC基準を満たした最初の提出物

2013年12月5日

最初の投稿 (見積もり)

2013年12月10日

学習記録の更新

投稿された最後の更新 (実際)

2019年11月8日

QC基準を満たした最後の更新が送信されました

2019年11月7日

最終確認日

2019年11月1日

詳しくは

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