Evidence map›Paper›PMID 27840337›Full record

ArticleJournal of research in health sciences2016

Economic Burden of Thalassemia Major in Iran, 2015.

Firooz Esmaeilzadeh, Azita Azarkeivan, Sara Emamgholipour, Ali Akbari Sari, Mehdi Yaseri, Batoul Ahmadi, Mohtasham Ghaffari

Abstract read
In one paragraph

Article in Journal of research in health sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed, 2 pooled it
–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

23 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. Article
  7. Global Globin Network and adopting genomic variant database requirements for thalassemia.Database : the journal of biological databases and curation · 2024
    Article
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Changing patterns in the epidemiology of β-thalassemia.European journal of haematology · 2020
    Review
  18. Cost-Utility Analysis of four Chelation Regimens for β-thalassemia Major: a Chinese Perspective.Mediterranean journal of hematology and infectious diseases · 2020
    Article
  19. Article
  20. Economic Evaluation of Chelation Regimens for β-Thalassemia Major: a Systematic Review.Mediterranean journal of hematology and infectious diseases · 2019
    Review
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

7 authors.

Firooz EsmaeilzadehPhD Candidate of Health Economics, Department of Health Economics & Management, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran. firooz.esmaeilzadeh@gmail.com.
Azita AzarkeivanPediatric Hematology Oncology, Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Department of Thalassemia Clinic, Tehran, Iran.
Sara EmamgholipourDepartment of Health Management & Economics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Ali Akbari SariDepartment of Health Management & Economics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mehdi YaseriPediatric Congenital Hematologic Disorders Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Batoul AhmadiDepartment of Health Management & Economics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Mohtasham GhaffariEnvironmental and Occupational Hazards Control Research Center, School of Public Health, Shahid Beheshti University of Medical Sciences, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMajor Thalassemia is an autosomal recessive disease with complications, mortality and serious pathology. Today, the life expectancy of patients with major thalassemia has increased along with therapeutic advances. Therefore, they need lifelong care, and caring for them would incur many costs. Being aware of the patients' costs can be effective for controlling and managing the costs and providing efficient treatments for the care of patients. Hence, this study was conducted to estimate the economic burden of the patients with major thalassemia.

methodsTotally, 198 patients with major thalassemia were randomly selected from among the patients with major thalassemia in Tehran, Iran in 2015. The economic burden of the patients was estimated from a social perspective and through a bottom-up, prevalence-based approach.

resultsThe average annual cost per patient was estimated $ 8321.8 regardless of the cost of lost welfare. Of this amount, $ 7286.8 was related to direct medical costs, $ 461.4 to direct non-medical costs, and $ 573.5 to indirect costs. In addition, the annual cost per patient was estimated $ 1360.5 due to the distress caused by the disease

conclusionsConsidering the high costs of the treatment of patients with major thalassemia, adopting new policies to reduce the costs that patients have to pay seems necessary. In addition, making new decisions regarding thalassemia screening, even with higher costs than the usual screening costs, can be useful since the costs of treatment are high.

Indexed as

Cost of IllnessHealth Care CostsHealth ExpendituresAdolescentAdultbeta-ThalassemiaChildChild, PreschoolFemaleHumansInfantInfant, NewbornIranMaleMiddle AgedYoung Adultbeta-Thalassemia MajorCost of IllnessHealth Care CostsIran

Identifiers

PMID27840337
PMCPMC7191027

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Registered trials

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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.