| Literature DB >> 23350017 |
Hassan Mansouritorghabeh1, Abdollah Banihashem, Alireza Modaresi, Lida Manavifar.
Abstract
INTRODUCTION: Male circumcision practice is an invasive procedure that is using worldwide. It makes challenges to haemostatic system and its possible haemorrhagic side effects are more serious in bleeding individuals than normal subjects. In most cases, it can be complete controlled using infusion of appropriate amount of coagulation factors before and post circumcision. AIM: We aim to documentation type of coagulation therapy and post circumcision practice haemorrhagic presentation among 463 bleeder males of both common and rare bleeding disorders in north eastern part of country.Entities:
Year: 2013 PMID: 23350017 PMCID: PMC3552727 DOI: 10.4084/MJHID.2013.004
Source DB: PubMed Journal: Mediterr J Hematol Infect Dis ISSN: 2035-3006 Impact factor: 2.576
Figure 1The prevalence of male circumcision practice in various region of the world. Adapted from reference 4.
A review of total number of male individuals with various inherited bleeding disorders and numbers who experienced post circumcision bleeding in each group.
| Type of bleeding disorder | Total male Cases | Mean of age ± SD (year) | Total circumcised ones | With post circumcision bleeding | Total in group with post circumcision bleeding | Without post circumcision bleeding | Total in group without post circumcision bleeding | ||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| Without CC infusion | With RCC infusion | With Cryo, Pltb or FFP infusion | With RCC infusion | With FFP, Cryo or Pltb | Without any coagulation factor | ||||||
| 284 | 25.07 | 264 | 132 | 12 | 3 | 147 | 89 | 11 | 17 | 117 | |
| 89 | 21.90 | 81 | 43 | 6 | 1 | 50 | 29 | 1 | 1 | 31 | |
| 23 | 29.04 | 23 | 10 | - | 1 | 11 | - | 8 | 4 | 12 | |
| 19 | 34.22 | 17 | 13 | - | - | 13 | 4 | 4 | - | 4 | |
| 16 | 20.27 | 13 | 5 | - | 1 | 6 | - | 6 | 1 | 7 | |
| 12 | 32 | 12 | 6 | - | 1 | 7 | - | 2 | 3 | 5 | |
| 10 | 18.5 | 8 | 2 | 3 | - | 5 | - | - | 3 | 3 | |
| 4 | 10.5 | 1 | - | - | - | - | - | 1 | - | 1 | |
| 2 | 32.5 | 1 | - | - | - | - | - | - | 1 | 1 | |
| 2 | 11.5 | 2 | - | - | - | - | - | - | 2 | 2 | |
| 1 | 31 | 1 | 1 | - | - | - | - | - | - | - | |
SD; standard deviation, Cryo; cryoprecipitate, RCC; relevant coagulation concentrate, HA; haemophilia A, HB; haemophilia B, vWD; von Willebrand disease, CF5F8D; combined factor V and VIII deficiency, Plt; platelets disorders, FVD; factor V deficiency; FVIID; factor VII deficiency, FXIIID; factor XIII deficiency, FXD; factor X deficiency, FFP; fresh frozen plasma, Pltb; platelet bag,
age of one patient in the group;
these are 4 cases with CF5F8D who have infused both FVIIIC and FFP and has been distributed as 2 person in each groups of (with RCC infusion and with FFP or Cryo) to avoid over calculation.