Evidence map›Paper›PMID 24392293›Full record

ReviewBiologics in therapy2011

New Frontiers in Subcutaneous Immunoglobulin Treatment.

Stephen Jolles, Mark R Stein, Hilary J Longhurst, Michael Borte, Bruce Ritchie, Matthias H Sturzenegger, Melvin Berger

Abstract readReview
In one paragraph

Review in Biologics in therapy, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Immune Checkpoint Inhibitor-Related Myositis: From Biology to Bedside.International journal of molecular sciences · 2020
    Review
  5. Article
  6. 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.

Stephen JollesUniversity Hospital of Wales, Heath Park, Cardiff, CF14 4XW UK.
Mark R SteinAllergy Associates of the Palm Beaches, North Palm Beach, FL USA.
Hilary J LonghurstBarts and London NHS Trust London, London, UK.
Michael BorteHospital "St. Georg" GmbH Leipzig, Academic Teaching Hospital of the University of Leipzig, Leipzig, Germany.
Bruce RitchieDivision of Hematology, Faculty of Medicine, University of Alberta, Edmonton, AB Canada.
Matthias H SturzeneggerDepartment of Neurology, University Hospital and University of Berne, Berne, Switzerland.
Melvin BergerCSL Behring LLC, King of Prussia, PA USA ; Case Western Reserve University, Cleveland, OH USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Subcutaneous immunoglobulin (SCIG) treatment provides stable serum immunoglobulin G (IgG) levels, is associated with fewer systemic adverse events than intravenous immunoglobulin (IVIG) treatment, and offers the convenience of home therapy. In clinical practice, IVIG is still used preferentially for initiation of treatment in newly diagnosed patients with primary immunodeficiency (PI) and for immunomodulatory therapy, such as treatment of peripheral neuropathies, when high doses are believed to be necessary. The authors discuss recent experience in using SCIG in place of IVIG in these settings. SCIG has been successfully used for initiation of therapy in previously untreated PI patients. Seventeen of 18 PI patients achieved serum IgG levels ≥5 g/L after the loading phase. Daily treatment was well tolerated and provided opportunities for patient/parent training in self-infusion. SCIG has been used for maintenance therapy in multifocal motor neuropathy (MMN) in three recent clinical trials, with good efficacy and tolerability results. Seven of eight MMN patients maintained serum IgG levels of 14-22 g/L with a mean dose of 272 mg/kg/week, had stable muscle strength, and felt comfortable with self-administration. Four patients with polymyositis or dermatomyositis achieved improvement in serum creatine kinase levels and muscle strength with SCIG therapy. Recent experience with SCIG suggests that traditional concepts of immunoglobulin therapy may be challenged to increase available therapy options. SCIG can be used to achieve high IgG levels within several days in untreated PI patients and to maintain high serum levels, as shown in patients with MMN.

Indexed as

immunoglobulin Gimmunoglobulin therapymultifocal motor neuropathyprimary immunodeficienciesserum levelssubcutaneous administration

Identifiers

PMID24392293
PMCPMC3873072

What OpenQuestion holds

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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.