Evidence map›Paper›PMID 39473749›Full record

ReviewTurkish journal of medical sciences2024

Management of acute pain in adults with sickle cell disease: the experience of the Clinical Hematology Department of the University of Dakar.

Alioune Badara Diallo, Moussa Seck, Mohamed Keita, Sokhna Aissatou Toure, Elimane Seydi Bousso, Baron Ngasia, Blaise Félix Faye, Fatma Dieng, Saliou Diop

Abstract readReview
In one paragraph

Review in Turkish journal of medical sciences, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Alioune Badara DialloDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0000-0002-0620-873X
Moussa SeckDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0000-0002-0561-6707
Mohamed KeitaDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0000-0003-4100-4684
Sokhna Aissatou ToureDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0000-0003-0251-1368
Elimane Seydi BoussoDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0009-0007-3148-4289
Baron NgasiaDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0009-0007-0292-7562
Blaise Félix FayeDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0000-0001-7066-7984
Fatma DiengDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0009-0007-7717-2299
Saliou DiopDepartment of Hematology, Faculty of Medicine, Cheikh Anta Diop University, Dakar, Senegal.ORCID https://orcid.org/0000-0002-2354-3839

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background/aim: The evolution of sickle cell disease (SCD) is marked by the occurrence of painful episodes linked to the obstruction of microvessels by sickle cells, known as vaso-occlusive crisis (VOC). The aim of this work was to report the practical aspects of the management of acute pain in adults with SCD. Recommendations based on these practices are also provided. Materials and methods: This prospective, cross-sectional, descriptive, and analytical study was conducted over a four-month period of all sickle cell patients admitted to emergency departments for VOC. The parameters studied were sociodemographic, clinicobiological, therapeutic, and evolutionary. Results: There were 118 cases of VOC identified, representing a prevalence of 78.14% of sickle cell emergencies. The mean age of the patients was 28.41 years. The SS sickle cell phenotype accounted for 86.61% of the cases. Osteoarticular pain was the reason for admission for 88.39% of the patients; it was located in the lower limbs in 39.08% and in the spine in 27.1%. Pain intensity was moderate in 6.25% of the patients, intense in 31.25%, and unbearable in 55.55%. Multimodal analgesia was the most commonly used treatment method, combining those of levels one and two (74.31%) and levels one and three (8.25%). The mean dose of morphine administered was 17.14 mg when morphine alone was prescribed for titration, 13.57 mg when paracetamol and morphine were combined, and 15.83 mg when nefopam and morphine were combined. Clinical outcome was favorable in 68.87% of the cases. Conclusion: Wide variability was observed in the modalities of analgesic treatment of sickle cell VOC. These variations reflect different views on the appropriateness of opioids. This study highlights the efficacy of multimodal analgesia in the management of acute pain in patients with SCD, particularly in regard to morphine sparing. Context-specific recommendations will be needed to harmonize practices.

Indexed as

Acute PainAnemia, Sickle CellPain ManagementAdolescentAdultAnalgesics, OpioidCross-Sectional StudiesEmergency Service, HospitalFemaleHumansMaleMiddle AgedProspective StudiesSenegalYoung AdultAnalgesics, OpioidSenegalSickle cell diseasevaso-occlusive crisis

Identifiers

PMID39473749
PMCPMC11518342

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.