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Author(s): 

Issue Info: 
  • Year: 

    2021
  • Volume: 

    14
  • Issue: 

    -
  • Pages: 

    467-472
Measures: 
  • Citations: 

    1
  • Views: 

    24
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

NAJAFI ALI

Journal: 

VIRTUAL

Issue Info: 
  • Year: 

    621
  • Volume: 

    1
  • Issue: 

    1
  • Pages: 

    167-167
Measures: 
  • Citations: 

    0
  • Views: 

    87
  • Downloads: 

    0
Abstract: 

Patients with Bleeding Disorders such as hemophilia A, hemophilia B, and von Willebrand disease (VWD) are routinely treated at home, with their care managed in specialized centers. In emergency situations, these patients often present to their local emergency department, where their management can represent a challenge to the emergency physicians and staff who rarely encounter them. Delays in diagnosis and administration of replacement therapy are the factors most commonly identified as predictive of death. Patients and family members are often very well educated in the disease and its management, which can significantly reduce morbidity and mortality. Children with Bleeding Disorders confer different challenges to the emergency physician and staff: they may present with no obvious signs of trauma or they may present with bruises consistent with non-accidental injury. All possible causes of bruising/Bleeding should be investigated, although treatment should be administered promptly. The initial presentation of a Bleeding disorder in the pediatric population is often made in the emergency department. Treatment of hemophilia A and B requires rapid replacement of the deficient clotting factor, with the desired factor level and dosage dependent on the product used and the hemorrhagic situation encountered. In patients with VWD, the main treatments are desmopressin or intravenous infusion of plasma-derived concentrates containing factor VIII and von Willebrand factor.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 87

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Author(s): 

Journal: 

THROMBOSIS JOURNAL

Issue Info: 
  • Year: 

    2021
  • Volume: 

    19
  • Issue: 

    1
  • Pages: 

    54-54
Measures: 
  • Citations: 

    1
  • Views: 

    20
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 20

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Issue Info: 
  • Year: 

    2019
  • Volume: 

    4
  • Issue: 

    4
  • Pages: 

    107-111
Measures: 
  • Citations: 

    1
  • Views: 

    201
  • Downloads: 

    73
Abstract: 

Background: Congenital Bleeding Disorders (CBD) are a group of coagulopathies with different clinical and laboratory features. The prevalence of these Disorders in different parts of the world is variable. Iran as a country with a high rate of parental consanguinity has a high rate of CBDs. This study was to report the prevalence of these Disorders in Kurdistan province, west of Iran. Methods and materials: This descriptive study was conducted on patients suspected of a congenital Bleeding disorder referred to hemophilia center of this province for evaluation of underlying Bleeding diathesis. Diagnosis and classification of Disorders were made by routine and specific laboratory tests. Results: Out of 107 patients, 65. 4% affected by common Bleeding Disorders (hemophilia A and B), 23. 4% affected by rare Bleeding Disorders (RBDs) and 11. 2% had inherited platelet Disorders. Factor VII deficiency (64%) was the most common RBDs and 9 patients had von Willebrand disease. Out of three patients with inherited platelet Disorders, two had Glanzmann thrombasthenia. Conclusion: CBD pattern though has similar patterns with total pattern of the country, some of the inherited platelet Disorders are more common in Kurdish province. Determination of prevalence and distribution of these Disorders can improve health system planning and resource allocation.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 201

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Issue Info: 
  • Year: 

    2017
  • Volume: 

    9
Measures: 
  • Views: 

    115
  • Downloads: 

    74
Abstract: 

BACKGROUND AND AIM: RARE Bleeding Disorders (RBDS) ARE HETEROGENEOUS Disorders, MOSTLY INHERITED IN AN AUTOSOMAL RECESSIVE PATTERN. IRAN IS A MIDEAST COUNTRY WITH A HIGH RATE OF CONSANGUINITY THAT HAS A HIGH RATE OF RBDS. …

Yearly Impact:   مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 115

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Author(s): 

Journal: 

HEMATOLOGY

Issue Info: 
  • Year: 

    2017
  • Volume: 

    22
  • Issue: 

    4
  • Pages: 

    224-230
Measures: 
  • Citations: 

    1
  • Views: 

    87
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 87

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Issue Info: 
  • Year: 

    1394
  • Volume: 

    10
Measures: 
  • Views: 

    488
  • Downloads: 

    0
Abstract: 

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Yearly Impact:   مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Issue Info: 
  • Year: 

    2016
  • Volume: 

    24
  • Issue: 

    6
  • Pages: 

    460-467
Measures: 
  • Citations: 

    0
  • Views: 

    664
  • Downloads: 

    0
Abstract: 

Introduction: Platelets and clotting factors dysfunction lead to hereditary hemorrhagic disease. In according to the importance of these diseases, the aim of this study was the evaluation of oral health and Bleeding management of the patients with congenital Bleeding Disorders in Tehran city in 2015.Methods: In this case-control study, 68 hemophilic patients as case group were compared with 50 healthy people as control group. These samples matched in according to age and gender. DMFT/S and GI index (caries index and gingival index) was recorded and Bleeding management evaluated by the patient's medical records and interviews. Data analyzed using SPSS version 16 and the level of significant was considered p≤0.05.Results: Patients group The mean of age in hemophilic patients was 12.54±2.94 and in the control group was 12.50±3.1. DMFT, DMFS and GI index was higher in the health group. With increasing the age of the patients gingival inflammation index also increased significantly (p=0.001) so that 70% of individual with age higher than 15 had grade 3 gingival inflammation.Conclusions: Patients and parents awareness about dental hygiene and regular dental visit is very important for caries prevention and reduction of DMFT/S and GI index and regular dental visits are essential for the patients.

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

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Author(s): 

ROBATI R.

Issue Info: 
  • Year: 

    2013
  • Volume: 

    3
  • Issue: 

    4
  • Pages: 

    159-163
Measures: 
  • Citations: 

    2
  • Views: 

    155
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 155

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Journal: 

VIRTUAL

Issue Info: 
  • Year: 

    621
  • Volume: 

    1
  • Issue: 

    1
  • Pages: 

    1406-1410
Measures: 
  • Citations: 

    1
  • Views: 

    145
  • Downloads: 

    0
Keywords: 
Abstract: 

Yearly Impact: مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View 145

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