ABSTRACT

Objective:

Every day, many patients visit hospital due to hematuria. Ultrasonography and/or cystoscopy are performed in the initial evaluation and management. In this study, we compared ultrasonography and cystoscopy in the evaluation of microscopic or macroscopic hematuria.

Materials and Methods:

A total of 55 patients, who presented to our clinic with the complaint of hematuria between July 2016 and October 2017, were enrolled in this study. After obtaining informed consent, the patients were directed to urinary ultrasonography and cystoscopy for the evaluation of hematuria.

Results:

Ultrasonography showed 45 (81.8%) normal bladder and 10 (18.2%) masses, and cystoscopy detected 39 (70.9%) normal bladder and 16 (29.1%) masses in the bladder (p=0.001). Ultrasonography was able to report only 8 (50%) of 16 masses detected via cystoscopy. Two (20%) of 10 masses reported by ultrasonography were not confirmed through cystoscopy. The sensitivity and specificity of ultrasonography in detecting and excluding masses in the bladder were calculated to be 50% and 94.9%, respectively. Ultrasonography failed to detect lesions at the posterior, dome and right side and bladder neck. The cut-off value for blood cell count in urine to refer the patient to a cystoscopy procedure was detected to be 15 with 60% sensitivity and 50% specificity.

Conclusion:

With low sensitivity, ultrasonography could not offer enough knowledge about the bladder masses as sufficient as cystoscopy.

Keywords:

Cystoscopy, Hematuria, Ultrasonography

What’s known on the subject? and What does the study add?

Hematuria is a prevalent symptom and it may be an occult sign of genitourinary abnormality. It is necessary to find the underlying cause of hematuria. In some of patients, malignancy can be detected during the evaluation of hematuria. In this study, we compared the results of ultrasonography and cystoscopy in the evaluation of hematuria. When the literature is examined, there is no study that examines the relationship between the number of red blood cells in urinalysis and the requirement of cystoscopy procedure.

Introduction

Hematuria is a common clinical finding and it can be a sign or symptom of an important disease in the practice of urology. The prevalence of hematuria is variable but estimated at 2.5% to 20% in the adult patients (1). Hematuria is described as the presence of an abnormal number of red blood cells (RBCs) in a urine sample and it can be classified as microscopic or macroscopic (gross) hematuria (2). According to the latest American Urological Association guidelines, microscopic hematuria can be defined as more than 3 RBCs per high-power field (hpf) in a properly collected urine sample (3). In most cases of microscopic hematuria, there is no etiology or pathology and this condition is called as asymptomatic microscopic hematuria with a prevalence ranging from 0.9% to 18.0% (3,4). There are many causes for microscopic hematuria, but the most common pathologies include urinary tract infection, benign prostatic enlargement, urolithiasis, urethral stricture disease, urologic malignancy, renal cystic disease, and renal disease (3,4,5). Male gender, age over 35 years, smoking history, analgesic abuse, and exposure to chemicals are the most common risk factors for urinary tract malignancy in patients with microscopic hematuria (5). Macroscopic hematuria can be described as a visible discoloration due to the presence of blood in the urine (2). In the diagnosis of macroscopic hematuria, the use of various medicines and foods that discolor urine should be investigated.

A detailed history should be taken in patients presenting with hematuria. Tobacco and anticoagulant drug use should be questioned. A physical examination involving the urogenital system should be performed. All patients are evaluated with whole blood count, renal function tests, urine analysis, and urine culture. Intravenous urography has been used to evaluate microscopic hematuria in the past, but now it is not preferred due to its low sensitivity (3). Ultrasonography (USG), computed tomographic urography and magnetic resonance imaging are more frequently preferred because they provide detailed images in the evaluation of microscopic hematuria (3,5). Upper urinary tract can be examined by radiological methods but cystoscopy should be done especially for lower urinary tract evaluation (1). Cystoscopy should be recommended to hematuria patients with risk factor for urinary system malignancy, such as male gender, age over 35 years, and tobacco use (3,6). Although cystoscopy is an invasive procedure, it continues to be a reference standard in the evaluation of patients with asymptomatic microscopic hematuria (7). USG is considered the imaging method of choice for hematuria and it has an indisputable role in the evaluation of hematuria. Since contrast media and radiation are not applied during USG, it is a less risky diagnostic method for hematuria patients (2).

Every day, many patients visit hospital due to hematuria. In some of these patients, malignancy can be detected during the evaluation of hematuria. USG and/or cystoscopy are performed in the initial evaluation and management. In this study, we compared USG and cystoscopy in the evaluation of microscopic or macroscopic hematuria.

Materials and Methods

Patient Selection

This study was approved by the Gülhane Training and Research Hospital Ethical Committee (approval number: 18/88, date: 5 April 2018) and followed the Institutional Review Board for Human Subjects Researches Guidelines.

This is a retrospective study. The sample size was calculated with the help of sample size calculator at www.calculator.net and examining >50 patients were found to be enough for this study. A total of 55 patients who presented to our clinic with the complaint of hematuria between July 2016 and October 2017 were enrolled in this study. The patients, who were included in the study, had no history of upper urinary tract or bladder malignancy. After obtaining informed consent, the patients were directed to urinary USG and cystoscopy for the evaluation of hematuria.

All patients underwent a complete physical examination especially for costovertebral tenderness. After physical examination, all patients were evaluated by urinalysis, urine culture, measurement of hemoglobin, serum urea and creatinine, and kidneys, ureters, and bladder (KUB) X-ray. Patients, who had positive urine cultures, were treated according to the reported antibiogram results until the urine cultures became sterile. All procedures were done when the urine cultures were sterile. A second urinalysis was taken for the presence of blood and to investigate white cell count in the urine after sterile urine culture was obtained. Firstly, urinary system USG was used for diagnosis. Then, cystoscopy was applied to investigate any mass in the bladder. Patients with negative urine cultures had a single-dose oral antibiotic with a first-generation cephalosporin or quinolone for cystoscopy procedures.

Statistical Analysis

Statistical analysis was done using Statistical Package for Social Sciences 20.0 software (SPSS 20.0 for MAC). Descriptive statistics of nominal samples were expressed with numbers and percentiles. Descriptive statistics of scale samples were expressed as mean ± standard deviation (minimum-maximum). The Shapiro-Wilk test and Kurtosis and Skewness test were used to assess normality of the variables. Cross-tabs were used to detect sensitivity and specificity. A chi-square test was used to compare the independent nominal parameters. The paired samples t-test was used to compare the independent scale parameters with normal distribution. A p value of less than 0.05 was considered statistically significant.

Results

Of 55 patients included in the study, 39 (70.9%) were female and 16 (29.1%) were male. The mean age of the patients was 62.43±14.79 (21-91) years. Nine patients (16.3%) had a history of tobacco smoking at the time of interview. None of the patients had costovertebral tenderness. The mean hemoglobin, urea, and creatinine levels were 12.9±1.5 (10.50-16.73) g/dL, 30.43±5.3 (17-48) mg/dL, and 1.07±0.2 (0.74-1.79) mg/dL, respectively. Thirty-two patients had urinary infection at first visit, and they were treated according to antibiogram results. None of our patients had active urinary tract infections, and urine samples and urine cultures were normal before USG and cystoscopy procedures. The mean blood and white cell count, when the urine culture, was sterile was 82.23±62 (0-1249) and 15.81±13.2 (0-364), respectively.

USG reported 45 (81.8%) normal bladder, and 10 (18.2%) masses; and cystoscopy detected 39 (70.9%) normal bladder, and 16 (29.1%) masses in the bladder (p=0.001). USG was able to report only 8 (50%) of 16 masses detected by cystoscopy. Two (20%) of 10 masses reported by USG were not confirmed via cystoscopy (Table 1). The sensitivity and specificity of USG to detect and exclude masses in the bladder were calculated to be 50% and 94.9%, respectively. The positive and negative likelihood ratios of USG to detect masses in the bladder were 8.3 and 0.53, respectively. There was a statistically significant difference in examining the location of the lesions in the bladder between USG and cystoscopy (p=0.001). USG failed to detect lesions at the posterior, dome, and right side, and bladder neck (Table 2). The mean lesion diameter detected by USG and cystoscopy was 13.62±16.16 (0-47) mm, and 20±13.9 (5-50) mm, respectively (p=0.007).

Calculating the receiver operating characteristic curve using the blood cell count in urine sample, there was a 0.534 area under curve value. This meant that blood cell count in urine sample could be a moderately (not very useful) used parameter for the diagnosis of any lesion in the bladder (Figure 1). The cut-off value for blood cell count in urine to refer the patient to a cystoscopy procedure was detected to be 15 with 60% sensitivity and 50% specificity.

Discussion

Hematuria is a prevalent symptom and it may be an occult sign of genitourinary abnormality. This finding sometimes presents as a symptom but it can also be detected incidentally. It is necessary to find the underlying cause. Hematuria is described as the presence of RBCs that are visible in the urine (macroscopic hematuria) or directly detected by microscopy (microscopic hematuria) (8). Hematuria can be defined as ≥3 RBCs per (hpf2) and ≥5 RBCs/hpf3 in urine sample (3,8). Hematuria can be classified as nephrological (glomerular disease) or urological (tumors, urinary tract infection, stone disease, benign prostatic enlargement, urethral caruncle, meatal ulcers, trauma) in origin (3,4,5,8). Sometimes microscopic hematuria can also occur with an excessive exercise when there is no underlying cause (9). Based on biochemical and radiological studies, we decided that the case in our study was hematuria of urological origin. Since the risk of urinary system malignancy is relatively low in young people, the prevalence of an important underlying pathology for hematuria is low and it ranges between 0 and 7.2% (10). In this age group, hematuria related to nephrologic causes is more common than that of urological origin. Along with advancing age, the risks for important diseases also increase (8). Risk factors for significant diseases in patients with microscopic hematuria include male gender, age over 35 years, smoking history, analgesic abuse, exposure to chemicals (benzenes or aromatic amines), history of gross hematuria, history of urological disease, history of urinary tract infection, and history of pelvic irradiation (3,5,8). Macroscopic hematuria is more closely related to the underlying serious urological diseases (8). In our study, we performed cystoscopy for all patients with macroscopic hematuria. On the other hand, we performed cystoscopy by questioning of the risk factors for microscopic hematuria. All these patients had risk factors for microscopic hematuria.

Different radiological diagnostic methods are used to detect this abnormality such as KUB X-ray, intravenous pyelography, USG, computed tomography, computed tomographic urography and magnetic resonance imaging (3,5). The important thing is to find the underlying cause of hematuria with some of these imaging methods, not all of them. Although cystoscopy is an invasive procedure, it is an endoscopic method that allows direct observation of the urethra, prostate, and the bladder (11). The procedure can be performed using rigid or flexible cystoscopy, but rigid cystoscopy is more traumatic (11). Tissue biopsy may be done during cystoscopy. Cystoscopy is recommended in patients with a risk of malignancy in the urinary system (6). Radiological methods should be accompanied by cystoscopy in the evaluation of hematuria because in most cases, it has been determined that the lower urinary tract pathologies were the cause of bleeding (12). There is no radiologic method which shows the cause of the hematuria in the lower urinary tract as good as cystoscopy (12). Therefore, cystoscopy was performed after sonographic evaluation in all patients who presented with hematuria in our study. In some patients, a mass in the bladder was detected only by cystoscopy. In a study published in 2008, it has been reported that the sensitivity and specifity of USG were 50% and 95%, respectively (13). In a study published in 2002, the sensitivity and specifity of of USG in detecting bladder masses in patients who were admitted with hematuria were reported to be 63% 99%, respectively (14). In our study, we found that the sensitivity and specificity of USG in detecting bladder cancer were 50% and 94.9%, respectively. These results are compatible with the literature data.

Anticoagulant medication use at the therapeutic doses does not cause hematuria, thus, urologic problems should be investigated for hematuria etiology in these patients (12,15). We questioned the use of anticoagulant medication before the diagnostic methods in patients who presented with hematuria. We found that the international normalized ratio was within the normal limits. We did not consider the use of anticoagulant medication as the cause of hematuria.

When the literature is examined, there is no study that examines the relationship between the number of RBCs in urinalysis and the requirement of cystoscopy procedure. It was determined that the number of RBCs in urinalysis was 15 RBCs/hpf2 for the requirement of cystoscopy.

Study Limitations

The small number of patients may be the main limitation of the study. Further studies with a larger sample size would provide more reliable results.

Conclusion

With low sensitivity, USG could not offer enough knowledge about bladder masses as sufficiently as cystoscopy.

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Comparison of Ultrasonography and Cystoscopy in the Evaluation of Hematuria