Evidence map›Paper›PMID 33897426›Full record

ArticleFrontiers in pharmacology2021

A Rabbit Model for Prolonged Continuous Intravenous Infusion Via a Peripherally Inserted Central Catheter.

Eyal Dor, Tseela David, Hani Dekel Jaoui, Arieh Schwartz, Tzadok Baruchi, Amram Torgeman, Alon Ben David, Osnat Rosen, Arnon Tal, Amir Rosner and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.2field-weighted citation impact, top 56% 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

3 citing papers in PubMed, 2 citations in OpenAlex.

  1. Article
  2. Pharmacokinetic Evaluation of Topical Long-Acting Buprenorphine in New Zealand White Rabbits (Oryctolagus cuniculus).Journal of the American Association for Laboratory Animal Science : JAALAS · 2025
    Article
  3. 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

12 authors at 1 institution in 1 country.

Eyal DorDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Tseela DavidVeterinary Center for Pre-clinical Research, Israel Institute for Biological Research, Ness Ziona, Israel.
Hani Dekel JaouiVeterinary Center for Pre-clinical Research, Israel Institute for Biological Research, Ness Ziona, Israel.
Arieh SchwartzDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Tzadok BaruchiDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Amram TorgemanDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Alon Ben DavidDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Osnat RosenDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Arnon TalDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Amir RosnerVeterinary Center for Pre-clinical Research, Israel Institute for Biological Research, Ness Ziona, Israel.
Ran ZichelDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Eran DiamantDepartment of Biotechnology, Israel Institute for Biological Research, Ness Ziona, Israel.
Israel Institute for Biological Research · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Medical treatment may require the continuous intravenous (IV) infusion of drugs to sustain the therapeutic blood concentration and to minimize dosing errors. Animal disease models that ultimately mimic the intended use of new potential drugs via a continuous IV infusion in unrestrained, free roaming animals are required. While peripherally inserted central catheters (PICCs) and other central line techniques for prolonged IV infusion of drugs are prevalent in the clinic, continuous IV infusion methods in an animal model are challenging and limited. In most cases, continuous IV infusion methods require surgical knowledge as well as expensive and complicated equipment. In the current work, we established a novel rabbit model for prolonged continuous IV infusion by inserting a PICC line from the marginal ear vein to the superior vena cava and connecting it to an externally carried ambulatory infusion pump. Either saline or a clinically relevant formulation could be steadily and continuously infused at 3-6 ml/h for 11 consecutive days into freely moving rabbits while maintaining normal body temperature, weight, and respiration physiology, as determined by daily spirometry. This new model is simple to execute and can advance the ability to administer and test new drug candidates.

Indexed as

catheterinfusionintravenousmodelPICCpumprabbitspirometry

Identifiers

PMID33897426
PMCPMC8061032
OpenAlexW3153119480

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.