Evidence map›Paper›PMID 25654130›Full record

ReviewTheScientificWorldJournal2015

Morphine for the treatment of pain in sickle cell disease.

Mihir Gupta, Lilian Msambichaka, Samir K Ballas, Kalpna Gupta

Abstract readReview
In one paragraph

Review in TheScientificWorldJournal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing 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

28 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. A Need for Daycare Unit for Sickle Cell Disease Patients in Oman.Sultan Qaboos University medical journal · 2024
    Article
  5. Review
  6. Pain in sickle cell disease: current and potential translational therapies.Translational research : the journal of laboratory and clinical medicine · 2021
    Review
  7. Heme Causes Pain in Sickle MiceAntioxidants & redox signaling · 2021
    Article
  8. Review
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Patient-reported experience measure in sickle cell disease.Archives of disease in childhood · 2018
    Article
  16. Targeting pain at its source in sickle cell disease.American journal of physiology. Regulatory, integrative and comparative physiology · 2018
    Review
  17. Article
  18. Review
  19. Targeting novel mechanisms of pain in sickle cell disease.Hematology. American Society of Hematology. Education Program · 2017
    Review
  20. 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

4 authors.

Mihir GuptaStanford University School of Medicine, Stanford, CA 94305, USA.ORCID 0000-0003-1329-2906
Lilian MsambichakaVascular Biology Center, Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota Medical School, Mayo Mail Code 480, 420 Delaware Street SE, Minneapolis, MN 55455, USA ; Christiana Care Health System, Department of Internal Medicine & Pediatrics, Newark, DE 19713, USA.ORCID 0000-0001-5210-5339
Samir K BallasCardeza Foundation for Hematologic Research, Jefferson Medical College, Thomas Jefferson University, Philadelphia, PA 19107, USA.
Kalpna GuptaVascular Biology Center, Division of Hematology, Oncology and Transplantation, Department of Medicine, University of Minnesota Medical School, Mayo Mail Code 480, 420 Delaware Street SE, Minneapolis, MN 55455, USA.ORCID 0000-0001-9381-9979

Funding

Cannabinoid-based therapy and approaches to quantify pain in sickle cell diseaseU01HL117664 · NHLBI · UNIVERSITY OF MINNESOTA · PI GUPTA, KALPNA · 2013 to 2018
$9.6M
Opioid Activity in Endothelium in Sickle Cell Disease R01HL068802 · NHLBI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI GUPTA, KALPNA · 2002 to 2012
$2.6M
Characteristics and mechanisms of pain in sickle cell diseaseR01HL103733 · NHLBI · UNIVERSITY OF MINNESOTA · PI GUPTA, KALPNA, SIMONE, DONALD · 2010 to 2014
$1.9M
NHLBI NIH HHS HL103733-01S1NHLBI NIH HHS R01 HL068802NHLBI NIH HHS R01 HL103733NHLBI NIH HHS R01 HL103773NHLBI NIH HHS R01 HL68802NHLBI NIH HHS U01 HL117664NHLBI NIH HHS U01 HL117664-01
6 · The paper itself

Abstract

Pain is a hallmark of sickle cell disease (SCD) and its treatment remains challenging. Opioids are the major family of analgesics that are commonly used for treating severe pain. However, these are not always effective and are associated with the liabilities of their own. The pharmacology and multiorgan side effects of opioids are rapidly emerging areas of investigation, but there remains a scarcity of clinical studies. Due to opioid-induced endothelial-, mast cell-, renal mesangial-, and epithelial-cell-specific effects and proinflammatory as well as growth influencing signaling, it is likely that when used for analgesia, opioids may have organ specific pathological effects. Experimental and clinical studies, even though extremely few, suggest that opioids may exacerbate existent organ damage and also stimulate pathologies of their own. Because of the recurrent and/or chronic use of large doses of opioids in SCD, it is critical to evaluate the role and contribution of opioids in many complications of SCD. The aim of this review is to initiate inquiry to develop strategies that may prevent the inadvertent effect of opioids on organ function in SCD, should it occur, without compromising analgesia.

Indexed as

Analgesics, OpioidAnemia, Sickle CellHumansMorphinePainPain ManagementAnalgesics, OpioidMorphine

Identifiers

PMID25654130
PMCPMC4306369

What Socratic 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 Socratic graph.