Evidence map›Paper›PMID 19618138›Full record

ArticleMedizinische Klinik (Munich, Germany : 1983)2009

[Cost analysis for ambulatory treatment of cystic fibrosis patients in Germany. Overview of the prospective study results].

Daniela Eidt, Thomas Mittendorf, Thomas O F Wagner, Andreas Reimann, J-Matthias Graf von der Schulenburg

Abstract readEnglish Abstract
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In one paragraph

Article in Medizinische Klinik (Munich, Germany : 1983), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Rare is frequent and frequent is costly: rare diseases as a challenge for health care systems.The European journal of health economics : HEPAC : health economics in prevention and care · 2015
    Article
  5. Article
  6. Article
  7. Article
  8. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Daniela EidtForschungsstelle für Gesundheitsökonomie, Leibniz Universität Hannover, Hannover. de@ivbl.uni-hannover.de
Thomas Mittendorf
Thomas O F Wagner
Andreas Reimann
J-Matthias Graf von der Schulenburg

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMain objective of this study is to assess and evaluate resource use in outpatient treatment of cystic fibrosis (CF) in Germany and to compare this with current reimbursement.

methodsOutpatient treatment was evaluated in seven different CF centers.Clinical patient data, resource use, and time consumption were recorded in 2006. A micro-costing approach was used to price resource use data.

resultsMean costs of 488 Euros per patient (n = 326) and quarter occurred. Remuneration (252 Euros per patient/quarter) covered only 52% of the total costs. Furthermore, a considerable time and financial burden for patients as well as decreasing quality of life with increasing age were found. Costs for medication came to 21,604 Euros per patient/year.

conclusionHuman resources in German CF centers today already are below the requirements set by the European consensus for standards of CF care. It will be crucial in assuring a high level of patient care to reach a cost-covering reimbursement scheme in Germany.

Indexed as

AdolescentAmbulatory CareChildChild, PreschoolCosts and Cost AnalysisCystic FibrosisDelivery of Health CareDrug CostsFemaleFinancing, PersonalGermanyHealth ResourcesHumansInfantInsurance CoverageMale

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.