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Study · Non-randomized trial · n = 22 · 1994

9 results

1-Deamino-8-D-arginine vasopressin (DDAVP) increases platelet membrane expression of glycoprotein Ib in patients with disorders of platelet function and after cardiopulmonary bypass.

Sloand EM, Alyono D, Klein HG, Chang P, Yu M, Lightfoot FG, Kessler C

American journal of hematology1 Jul 1994Cited by 24 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study9

9 results from studies that gave the peptide. 9 results from people.

  1. 01HumanNon-randomized trialMechanism

    In bypass patients, platelet CD42b antibody binding increased more with DDAVP than without DDAVP during 18-20 hours after surgery.

    In plain wordsAfter bypass surgery, DDAVP increased platelet CD42b antibody binding more than no DDAVP.

    Outcome
    IncreaseCD42b antibody binding after bypass
    Study

    n = 22

    Comparator
    Patients not receiving DDAVP
    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Binding of CD42b monoclonal antibody (MoAb) and anti-GPIb/IX to platelets from both groups of bypass patients increased during the 18-20 hr after surgery, but the group receiving DDAVP showed the greater increase (P = 0.032).
    2 context sentences
    Summary · context
    Platelets from 8 cardiopulmonary bypass patients, receiving DDAVP immediately after surgery, were compared to those of 14 patients not receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  2. 02HumanNon-randomized trialMechanism

    In bypass patients, platelet anti-GPIb/IX binding increased more with DDAVP than without DDAVP during 18-20 hours after surgery.

    In plain wordsAfter bypass surgery, DDAVP increased platelet anti-GPIb/IX binding more than no DDAVP.

    Outcome
    IncreaseAnti-GPIb/IX binding after bypass
    Study

    n = 22

    Comparator
    Patients not receiving DDAVP
    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Binding of CD42b monoclonal antibody (MoAb) and anti-GPIb/IX to platelets from both groups of bypass patients increased during the 18-20 hr after surgery, but the group receiving DDAVP showed the greater increase (P = 0.032).
    2 context sentences
    Summary · context
    Platelets from 8 cardiopulmonary bypass patients, receiving DDAVP immediately after surgery, were compared to those of 14 patients not receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  3. 03HumanNon-randomized trialMechanism

    In patients with von Willebrand disease, DDAVP increased platelet CD42b antibody binding.

    In plain wordsIn patients with von Willebrand disease, DDAVP increased platelet CD42b antibody binding.

    Outcome
    IncreaseCD42b antibody binding in vWD
    Study

    n = 12

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Platelets from patients receiving DDAVP for vWD or for platelet dysfunction, had increases in CD42b MoAb and anti-GPIb/IX binding (P < 0.01) that coincided with shortening of their bleeding time.
    2 context sentences
    Summary · context
    We also studied 12 patients with vWD, and 8 patients with platelet dysfunction receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  4. 04HumanNon-randomized trialMechanism

    In patients with von Willebrand disease, DDAVP increased platelet anti-GPIb/IX binding.

    In plain wordsIn patients with von Willebrand disease, DDAVP increased platelet anti-GPIb/IX binding.

    Outcome
    IncreaseAnti-GPIb/IX binding in vWD
    Study

    n = 12

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Platelets from patients receiving DDAVP for vWD or for platelet dysfunction, had increases in CD42b MoAb and anti-GPIb/IX binding (P < 0.01) that coincided with shortening of their bleeding time.
    2 context sentences
    Summary · context
    We also studied 12 patients with vWD, and 8 patients with platelet dysfunction receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  5. 05HumanNon-randomized trialEfficacy outcome

    In patients with von Willebrand disease, DDAVP shortened bleeding time alongside increased platelet antibody binding.

    In plain wordsIn patients with von Willebrand disease, DDAVP shortened bleeding time.

    Outcome
    DecreaseBleeding time in vWD
    Study

    n = 12

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Platelets from patients receiving DDAVP for vWD or for platelet dysfunction, had increases in CD42b MoAb and anti-GPIb/IX binding (P < 0.01) that coincided with shortening of their bleeding time.
    2 context sentences
    Summary · context
    We also studied 12 patients with vWD, and 8 patients with platelet dysfunction receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  6. 06HumanNon-randomized trialMechanism

    In patients with platelet dysfunction, DDAVP increased platelet CD42b antibody binding.

    In plain wordsIn patients with platelet dysfunction, DDAVP increased platelet CD42b antibody binding.

    Outcome
    IncreaseCD42b antibody binding in platelet dysfunction
    Study

    n = 8

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Platelets from patients receiving DDAVP for vWD or for platelet dysfunction, had increases in CD42b MoAb and anti-GPIb/IX binding (P < 0.01) that coincided with shortening of their bleeding time.
    2 context sentences
    Summary · context
    We also studied 12 patients with vWD, and 8 patients with platelet dysfunction receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  7. 07HumanNon-randomized trialMechanism

    In patients with platelet dysfunction, DDAVP increased platelet anti-GPIb/IX binding.

    In plain wordsIn patients with platelet dysfunction, DDAVP increased platelet anti-GPIb/IX binding.

    Outcome
    IncreaseAnti-GPIb/IX binding in platelet dysfunction
    Study

    n = 8

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Platelets from patients receiving DDAVP for vWD or for platelet dysfunction, had increases in CD42b MoAb and anti-GPIb/IX binding (P < 0.01) that coincided with shortening of their bleeding time.
    2 context sentences
    Summary · context
    We also studied 12 patients with vWD, and 8 patients with platelet dysfunction receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  8. 08HumanNon-randomized trialEfficacy outcome

    In patients with platelet dysfunction, DDAVP shortened bleeding time alongside increased platelet antibody binding.

    In plain wordsIn patients with platelet dysfunction, DDAVP shortened bleeding time.

    Outcome
    DecreaseBleeding time in platelet dysfunction
    Study

    n = 8

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    Platelets from patients receiving DDAVP for vWD or for platelet dysfunction, had increases in CD42b MoAb and anti-GPIb/IX binding (P < 0.01) that coincided with shortening of their bleeding time.
    2 context sentences
    Summary · context
    We also studied 12 patients with vWD, and 8 patients with platelet dysfunction receiving DDAVP.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.
  9. 09HumanNon-randomized trialMechanism

    In the studied patients, DDAVP did not change binding of the other platelet antibodies.

    In plain wordsIn the studied patients, DDAVP did not change binding of the other platelet antibodies.

    Outcome
    No significant changeOther platelet antibody binding
    Study

    n: not reported in source

    Outcome group
    Bleeding and clotting · Cardiovascular
    Studied dose
    0.3 microgram/kg · infusionAs given in this study (human).

    Source sentences

    Summary
    No changes were seen in binding of other antibodies.
    2 context sentences
    Summary · context
    Fixed platelets, stained with monoclonal fluorescein (FITC)-labeled antibodies directed against GPIb (CD42b antigen), GPIb/IX, GPIIb/IIIa (CD41a antigen), CD63 antigen (a platelet activation protein), and P-selectin (CD62 antigen) were studied by flow cytometry.
    Summary · context
    We studied platelet membrane glycoproteins in patients with von Willebrand disease (vWD), disorders of platelet function, and in cardiopulmonary bypass patients after infusion of 0.3 microgram/kg of DDAVP.

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Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 2Current

    28 Oct 2026, 02:03 UTC

    Study results updated

  2. Version 1

    27 Oct 2026, 16:35 UTC

    First added · source update from Europe PMC

Subjects

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