Evidence map›Paper›PMID 33654519›Full record

ArticleThe Pan African medical journal2020

[A monocentric study on the management of patients with myelodysplastic syndromes in Morocco].

Hicham El Maaroufi, Mounir Ababou, Adnane Hammani, Siham Ahchouch, Salim Jennane, Mehdi Mahtat, Mohamed Mikdmae, Nezha Messaoudi, Kamal Doghmi

Open access · goldAbstract readCase Reports
In one paragraph

Article in The Pan African medical journal, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.1field-weighted citation impact, top 48% of its field
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

2 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. 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

9 authors at 1 institution in 1 country.

Hicham El MaaroufiService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Mounir AbabouService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Adnane HammaniService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Siham AhchouchService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Salim JennaneService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Mehdi MahtatService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Mohamed MikdmaeService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Nezha MessaoudiLaboratoire d´Hématologie, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Kamal DoghmiService d´Hématologie Clinique, Hôpital Militaire d´Instruction Mohammed V, Rabat, Maroc.
Mohammed V University · MA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

We conducted a retrospective descriptive analytical study in the Department of Clinical Haematology at the Mohammed V Military Training Hospital in Rabat over a period of 10 years. This study included 76 patients diagnosed with myelodysplastic syndrome (MDS) between 2008 and 2018. The average number of cases per year was 7.6. Out of 76 patients, 57% were men and 43% were women. The average age of our study population was 65.75 ± 12.55. The average age was 66.88 ± 13.10. No cases of profession exposed to disease was reported. Ninety-seven point three percent of patients had primary myelodysplastic syndrome and only 2 or 2.7% had myelodysplastic syndrome secondary to chemotherapy. The average time between the first visit and the diagnosis of myelodysplastic syndrome was, on average, 33.6 days ± 51, with a median of 19 days. The IPSS prognostic score was: low risk in 37.4% of cases, intermediate risk 1 in 46.6% of cases, intermediate risk in 12% of cases and high risk in 4% of cases. Thus, 84% of patients had low-risk MDS and 16% had high-risk MDS. Regular monitoring of patients showed many complications such as bleeding in 13% of patients, infections in 8% of cases, secondary hemochromatosis as a result of iterative transfusions in 6.6% of patients and transformation to acute myeloid leukemia in 2.7% of patients. In our study, abstention was the therapeutic choice in 42.1% of patients, transfusion was recommended in 35.5% of patients: red cells in 70% of cases, platelet concentrates in 40% of cases, iron chelators in 25% of transfused patients and EPO in 27% of patients. azacitidine was prescribed in 18% of patients, 50% had low-risk MDS and 50% had high-risk MDS. Bone marrow transplant was the only curative treatment for MDS. It was performed in a single patient with high risk MDS.

Indexed as

AdultAgedAged, 80 and overAntineoplastic AgentsAzacitidineBlood TransfusionBone Marrow TransplantationFemaleHumansLeukemia, Myeloid, AcuteMaleMiddle AgedMoroccoMyelodysplastic SyndromesRetrospective StudiesTime FactorsAntineoplastic AgentsAzacitidineMoroccoMyelodysplastic syndromestudy

Identifiers

PMID33654519
PMCPMC7881929
OpenAlexW3109688220

What OpenQuestion holds

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LicenceCC BY
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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.