Analysis of Hematological Parameters of Non-Sickle Men with Priapism in Yola, Nigeria
© 2020 Emmanuel Asuquo Etim, et al, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Abstract
Background/Objective: Priapism is a penile erectile abnormality characterized by prolonged painful erection, due to disturbances in regulatory mechanism that controls penile engorgement. Despite the role of hematology in diagnosis and management of priapism in Yola, there is dearth of information regarding hematological parameters of men with priapism therefore; this study aims to evaluate some hematological parameters of men with priapism.
Material and Method: 43 subjects participated in this study comprising of 23 men of age 30±2.4years presented with priapism and 20 apparently healthy men without priapism used as control group. Men with priapism in this study presented late with very hard penis and average priapism duration of 5days. Hematological parameters of subjects were determined using Sysmex XN 550 hematological analyzer.
Result: Mean erythrocyte count of subject was 3.61±0.3 X106/μl while red cell count of control group was 4.31±0.3 X106/μl at P<0.05. Mean Cell Volume (MCV) of men with priapism was 89.2±0.8fl while MCV of the control group was 75.3±1.0fl. Furthermore, Mean Cell Hemoglobin (MCH) of control and subject groups were 25.8±0.5pg and 32.1±0.6pg respectively. Mean total leucocyte count of subjects and control group were 16.8±1.4 X103/μl and 8.9±1.6 X103/μl respectively and absolute neutrophil counts of men with priapism was 9.9±2.7 X103/μl while neutrophil count of control group was 3.5±2.9 X103/μl.
Conclusion: Men with Priapism had mild leukocytosis as well as increase neutrophil count, MCV and MCH values when compare with control group. It is believed that information provided in this study will improve the clinical care of men with priapism in this locality.
Introduction
Priapism is a penile erectile abnormality that is characterized by prolonged painful erection of the penis. It is a persistent erection that continues hours (≥4hours) after stimulation from either sexual and/or non-sexual stimulus [1]. Priapism is mostly presented as urologic emergency and prompt treatment is usually needed to prevent tissue damage that could lead to permanent inability to get or maintain an erection [2]. Priapism usually results from disturbances and imbalances in regulatory mechanism that controls penile engorgement [3]. First reported in 1845 by Tripe, priapism is now grouped into three categories: ischemic, non-ischemic, and stuttering priapism, depending on its etiology and pathophysiologic pattern [4]. Ischemic priapism, is a veno- occlusive priapism and erection in ischemic priapism is persistent and usually marked by rigidity of the corpora cavernosa with little or no cavernous arterial flow [4]. Tissue ischemia and increased pressure generated within the corporal bodies lead to pain and rigidity resulting in urologic emergency. On the other hand, Non- ischemic priapism is mostly due to trauma that creates disruption in the cavernous arterial anatomy, resulting in arteriolar-sinusoidal fistula and non-ischemic priapism can also be due to congenital arterial malformations, or iatrogenic insults [5]. Furthermore, in non-ischemic priapism, the corpora are tumescent but not rigid, and patients typically do not complain of pain with erection hence, non-ischemic priapism is not usually an emergency but may still require medical interventions [6]. While Stuttering priapism is an intermittent priapism that is characterized by recurrent episodes of ischemic priapism that can develop into major episodes of ischemic priapism so that both stuttering and ischemic priapism result in the same consequence including ischemic damage to the corporal tissue [7]. Ultimately, Ischemic priapism is the most common priapism variant and accounts for almost 95% of all diagnosed priapism episodes [3].
Priapism has been reported to have greater frequency in people with sickle cell disease when compare to the general population and Non-sickle men refers to in this study are adult male without sickle cell disease or sickle cell trait [6]. From hematological stand point, Priapism have been reported to be associated with hematological abnormalities including: glucose-6-phosphate dehydrogenase deficiency, thrombophilias, hyperviscosity states, anticoagulants and antihypertensives (α-adrenergic antagonists) medications [8]. Epidemiological studies have linked the risk of priapism to intravascular hemolysis and evaluation of hematological parameters are important in the diagnosis of all categories of priapism globally but, despite the role of hematology in diagnosis and management of priapism, in Yola like most part of Nigeria, there is dearth of information regarding hematological parameters of men with priapism therefore, this study aims to evaluate some hematological parameters of men with priapism in Yola Northeastern Nigeria so as to elucidate the status of hematological changes in this group of patients [1,3,4,5,9].
Materials and Methods
This was a prospective and descriptive study carry out at the hematology department of Federal Medical Center Yola in Adamawa State, Nigeria between March 2016 to January 2018. A total of 43 men participated in the study, comprising 23 men (age 30±2.4years) with priapism (i.e. subjects) and 20 apparently healthy men without priapism (i.e. Control group). All men with priapism in this study presented late with very hard penis and mean priapism duration of 5days and were referred to the laboratory for evaluation before commencement of therapy. Other information was retrieved from subject’s medical record while the control subjects were recruited from blood donors in the hospital’s blood bank. Hematological parameters of all subjects were determined using Sysmex XN 550 hematology analyzer. All analyses were performed according to the standard operational procedures.
Ethical Statement
Ethical approval for this study was obtain from local health research ethics committee of the hospital.
Sample Collection
3ml of blood were drawn from convenient peripheral vein of all participants into K3-EDTA vacutainer tubes. The vacuum tubes were further labeled with subject’s number and age. Hematological parameters of subject were determined within 3hours of blood collection.
Statistical Analysis
Statistical analysis was performed using SPSS computer software version 20.0 (IBM Chicago, IL, USA). Descriptive values were given as mean and standard error of mean. Categorical variables were expressed as the number of cases and the percentage value. The Student’s t-test was used to compare the means differences of the estimated parameters and all statistics were carried out at the probability level of 0.05.
Sample Analysis
Using Sysmex XN550 hematology analyzer, the procedure for hematological parameters determination was performed as follows: EDTA samples were placed in a blood mixer for three minutes and the blood cells were automatically counted through a probe fitted in the Sysmex machine. After one minute, the result of the blood cell count was printed out and displayed on the colored LCD screen of the machine.
Results
All subjects presented with ischemic priapism while Stuttering and non-ischemic priapism was not observed in Yola. Analysis of red cell indices showed that, mean red cell count of subject was 3.61±0.3 X106/μl while red cell count of control group was 4.31±0.3 X106/μl at P<0.05. In addition, red cell distribution width-coefficient of variation (RDW-CV) of men with priapism was 11.6±0.7% while the RDW-CV of control was 13.2±0.9%. Hemoglobin (HGB) level of subject and control was 11.0±0.6g/ dl and 12.3±1.2g/dl respectively. Furthermore, mean hematocrit (HCT) level of subjects was 32.2±1.1% while HCT of control group was 39.1±0.3%. On the other hand, Mean Cell Volume (MCV) of men with priapism was 89.2±0.8fl while that of control group was 75.3±1.0fl. In addition, Mean Cell Hemoglobin (MCH) of control and subject groups were 25.8±0.5pg and 32.1±0.6pg respectively. The value of Mean Cell Hemoglobin Concentration (MCHC) of men with priapism was 36.0±0.2g/dl while MCHC of control group was 33.9±0.4g/dl at P<0.05 as shown in table 1.
Table 1: Red Cell and Red Cell Indices of subject and control groupS/N | Parameters | Subject’s values | Control’s values |
---|---|---|---|
1 | RBC (X106/μl) | 3.61±0.3 | 4.31±0.8 |
2 | Hemoglobin(g/dl) | 11.0±0.6 | 12.3±1.2 |
3 | HCT (%) | 32.2±1.1 | 39.1±0.3 |
4 | MCV(fl) | 89.2±0.8 | 75.3±1.0 |
5 | MCH (pg) | 32.1±0.6 | 25.8±0.5 |
6 | MCHC(g/dl) | 36.0±0.2 | 33.9±0.4 |
7 | RDW-CV(%) | 11.6±0.7 | 13.2±0.9 |
Examination of Platelet and platelet indices reveals that mean platelet count of subject and control groups were 299±12 X103/ μl and 317 ± 19.37 X103/μl respectively and Platelet Distribution Width (PDW) of subject group was 9.7±0.4fl while PDW of control group was 11.5 ± 1.2fl. Moreover, Mean Platelet Volume (MPV) of subject and control group were 10.0±0.6fl and 9.4±1.4fl respectively. Men with priapism had Platelet Large Cell Ratio (P-LCR) of 22.7±1.0% while the control group had P-LCR of 23.4 ± 2.1% as shown in table 2.
Table 2: Platelet count and Platelet Indices of subject and control groupS/N | Parameters | Subject’s values | Control’s values |
---|---|---|---|
1 | Platelet count (X10 3 /μl) | 299±12 | 317 ± 19 |
2 | PDW (fl) | 9.7±0.4 | 11.5 ± 1.2 |
3 | MPV (fl) | 10.0±0.6 | 9.4 ± 1.4 |
4 | P-LCR (%) | 22.7±1.0 | 23.4 ± 2.1 |
Evaluation of leucocyte count indicates that, mean total white cell count (tWBC) of subjects and control group were 16.8±1.4 X103/ μl and0 8.9±1.6 X103/μl respectively and neutrophil (Neut) counts of men with priapism was 9.9±2.7 X103/μl while neutrophil count of control was 3.5±2.9 X103/μl. Analysis of lymphocyte (Lymph) count shows that, subject had a mean absolute lymphocyte count of 3.7±0.9X103/μl and the control group had a lymphocyte count of 4.1±2.7X103/μl. Furthermore, monocyte (Mono) count of subject and control group were 1.1±0.3 X103/μl and 0.6±0.5 X103/μl respectively. In this study, men with priapism had eosinophil (Eosin) count of 1.9±0.1X103/μl while the eosinophil of control group was 0.5±0.3X103/μl and basophil (Baso) count of subjects and controls were 0.1±0.01 X103/μl and 0.6±0.2 X103/ μl respectively as shown in table 3.
Table 3: Total and Differential Leucocyte count of subject and control groupS/N | Parameters | Subject’s values | Control’s values |
---|---|---|---|
1 | tWBC (X10 3 /μl) | 16.8±1.4 | 8.9±1.6 |
2 | Neutrophil (X10 /μl) | 9.9±2.7 | 3.5±2.9 |
3 | Lymphocyte (X10 3 /μl) | 3.7±0.9 | 4.1±2.7 |
4 | Monocyte (X10 3 /μl) | 1.1± 0.3 | 0.6±0.5 |
5 | Eosinophil (10 /μl) | 1.9± 0.1 | 0.5±0.3 |
6 | Basophil (X10 3 /μl) | 0.1± 0.01 | 0.6±0.2 |
Discussion
Hematological parameters of men with priapism in Yola have
been analyzed, Stuttering and non-ischemic priapism was not
observed in Yola and all subject presented late with ischemic
priapism because they had prolong painful harden penis on arrival
and the reason for this late presentation is believed to be due high
patronage of folkloric medical treatment in this locality [10]. The
red blood cell count, hemoglobin and hematocrit level of subject
were slightly lower than that of the control group, this indicates
presence of unclassified mild anemia and anemia is a risk factor
for ischemia which is a consequence in priapism [11]. On the
other hand, analysis of red cell indices indicates that MCV, MCH,
and MCHC values of men with priapism were higher than that
of the control group. When the MCV is elevated, the RBCs will
be larger than normal and are termed macrocytic and MCH is
usually elevated in macrocytic anemia associated with vitamin
B 12 and folate deficiency while MCHC is elevated in condition
associated with decreased RBC survival caused by a structural
protein defect in the RBC membrane. Hence, increase values of
MCV, MCH and MCHC in this study is a pointer to the presence
of macrocytic anemia in men with priapism in Yola.
Table 2 shows that, platelet count and PDW values of subjects
were lower than that of the control group. Platelet Distribution
Width (PDW), is a measure of variability in platelet sizes and
platelet count which indicates the volume of circulating platelets
in a unit volume of blood [12]. Hence low PDW value may reflect
reduce variability in platelet size among men with priapism in this
locality. In addition, MPV and P-LCR values had no significance
difference between subject and control groups and the reason for
this results is unclear.
Furthermore, the value of total white blood cell and absolute neutrophil count was higher in men with priapism (i.e. subjects) than in men without priapism (i.e. control). This result conforms with the earlier reports by Ergene et al., in Turkey and Minckler et., in USA and there are report that leukocytosis could result in cell sludging in corpora cavernosa resulting in impairment of penile engorgement control mechanism as well as vaso-occlusion which are common episode that produces priapism [12-14]. The value of eosinophil count in subject was higher than that of the control group and the reason for this increase eosinophil result remains unclear.
Conclusion
schemic priapism was the predominant type of Priapism observed in this study, Stuttering and non-ischemic priapism was not observed in Yola. Men with Priapism had increased total white blood cell count as well as elevated neutrophil count, MCV and MCH values when compare with control group. It is believed that information provided in this study will improve the clinical care of men with priapism in this locality.
Author’s Contribution
Emmanuel Asuquo Etim assisted in sample analysis and Literature Review, while Adjekuko Ohwonigho Collins assisted in Data analysis and Drafting of the literature and Jacob Nwonoba Nweke assisted in Literature review and sample collection.
Acknowledgement
The authors are sincerely grateful to the management of Federal Medical Center Yola, for providing the environment and equipment for this research work.
References
1. Berger R, Billups K, Brock G, Broderick GA, Dhabuwala CB
(2001) Thought Leader Panel on Evaluation and Treatment
of priapism. Int J Impot Res 13: 39-43.
2. Bennett N, Mulhall J (2008) Sickle cell disease status and
outcomes of African-American men presenting with priapism.
J Sex Med 5:1244-1250.
3. Helen R Levey, Robert L Segal, Trinity J Bivalacqua (2014)
Management of Priapism: an update for clinicians. Ther Adv
Urol 6:230-244.
4. Montague DK, Jarow J, Broderick GA, Dmochowski RR,
Heaton JP, et al. (2003) Members of the Erectile Dysfunction
Guideline Update Panel American Urological Association. J
Urol 170:1318-1324.
5. Burnett AL, Sharlip ID (2013) Standard Operating Procedures
for Priapism. J Urol 10:180-194.
6. Broderick GA, Kadioglu A, Bivalacqua TJ, Ghanem H, Nehra
A, et al. (2010) Priapism: pathogenesis, epidemiology and
management. Am J Urol 7:476-500.
7. Burnett AL, Bivalacqua TJ (2007) Priapism: Current principle
and practice. Urol Clin North Am 34:631-642.
8. Kropman RF (2014) Hematoma or “partial priapism” in the
proximal part of the corpus cavernosum. J sex Med 11:2618-
2622.
9. Gregory James, Kato Gregory, James Kato (2011) Priapism
in Sickle-cell Disease: A Hematologist’s Perpective. J Sex
Med 9:70-78.
10. Etim EA, Emokpae MA, Ohwonigho AC, Yusuf AA (2018)
Association of Platelet Count and Platelet Indices with Stages
of Women Breast Cancer in Yola, Nigeria. Hematol Transfus
Int 6:00145.
11. Zeidman A, Fradin Z, Blecher A, Oster HS, Avrahami Y, et
al. (2004) Anemia as a risk factor for ischemic heart disease.
Isr Med Assoc J 6:16-18.
12. Leader A, Pereg D, Lishner M (2012) Are platelet volume indices
of clinical use? A multidisciplinary review. Ann Med 44: 805-16.
13. Ergene H, Varim C, Karacaer C, Cekdemir D (2015) Chronic
Myeloid Leukemia presented with priapism: Effective
Management with prompt leukapheresis. Niger J Clin Pract
18:828-830.
14. Micheal R Minckler, Ellie Conser, Javier J Figueroa, Aaron
J Scott, Joshua Gaither, et al. (2017) The semantics of
Priapism and the First Sign of Chronic Myeloid Leukemia.
Case Reports in Emergency Med 10:1-3.