Evidence map›Paper›PMID 25047154›Full record

ArticleJournal of clinical immunology2014

Adequate patient's outcome achieved with short immunoglobulin replacement intervals in severe antibody deficiencies.

Cinzia Milito, Federica Pulvirenti, Anna Maria Pesce, Maria Anna Digiulio, Franco Pandolfi, Marcella Visentini, Isabella Quinti

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06089122 (Efficacy, Safety, and Pharmacokinetics of Shu Yang IVIG in Patients With Primary Immunodeficiency), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.2field-weighted citation impact, top 22% 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.

NCT06089122 phase3unknown statusnot on this mapstarted 2024, after this paper: background citation

Efficacy, Safety, and Pharmacokinetics of Shu Yang IVIG in Patients With Primary Immunodeficiency

TypeinterventionalSponsorAzidus BrasilRan2024 to 2025Enrolled50ConditionsPrimary Immunodeficiency DiseaseArmsIVIG
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
  4. X-linked Agammaglobulinemia.Indian journal of pediatrics · 2016
    Review
  5. Article
  6. Review
  7. 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 at 2 institutions in 1 country.

Cinzia MilitoDepartment of Molecular Medicine, Sapienza University of Rome, Viale dell'Università 37, Rome, Italy.
Federica Pulvirenti
Anna Maria Pesce
Maria Anna Digiulio
Franco Pandolfi
Marcella Visentini
Isabella Quinti
Sapienza University of Rome · ITUniversità Cattolica del Sacro Cuore · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe optimal immune globulin replacement dosages required over time to minimize infection risks in patients with Primary Antibody Deficiencies are not definitely established. As with many interventions, there may be specific subgroups of patients who are more likely to benefit from treatment with higher or lower dosages. The aim of the study was to verify the efficacy of a rationale for individualized immune globulin utilization and to elucidate the effects of care on patient outcome.

methodsSingle centre interventional study on 108 patients with Primary Antibody Deficiencies. The objective was to determine for each patient the best interval between immune globulins administration in order to: • Keep IgG trough levels >500 mg/dL, • Minimize of major infections (pneumonias and infections requiring hospitalization), • Minimize of adverse events (AE).

resultsNinthly eight per cent of patients achieved the objective of the study. Patients who had low switched memory B cells and low IgA serum levels and/or are affected by bronchiectasis and/or enteropathy and/or continued to experience adverse events despite pre-medications, achieved the study objective by shortening the administration intervals to 2-weeks or to 1-week without the need to increase the monthly cumulative immunoglobulin dosage and its relative cost. The adverse events were reduced by administrating low Ig dosages in a single setting. Patients without risk factors achieved the study objective with immune globulin replacement administered with the widely used interval of 3 or 4 weeks.

conclusionsThe exact timing and optimal immunoglobulin prophylaxis regimen might be tailored according to clinical and immunological markers.

Indexed as

Drug Dosage CalculationsB-LymphocytesFollow-Up StudiesHumansImmunoglobulin GImmunoglobulins, IntravenousImmunologic Deficiency SyndromesImmunologic MemoryInfection ControlInfectionsPrecision MedicineProspective StudiesTime FactorsTreatment OutcomeImmunoglobulin GImmunoglobulins, Intravenous

Identifiers

PMID25047154
PMCPMC4165867
OpenAlexW2050254523

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.