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SM Journal of Nephrology and Kidney Diseases

Characteristics and Treatment Outcomes of Ketamine-Induced Uropathy in Wales in 2024: A Pilot Study

[ ISSN : 2576-5450 ]

Abstract Citation INTRODUCTION MATERIAL AND METHODS RESULTS DISCUSSION CONCLUSION ETHICS STATEMENT TRANSPARENCY STATEMENT CONSENT TO PUBLISH REFERENCES
Details

Received: 20-May-2026

Accepted: 30-Jun-2026

Published: 02-Jul-2026

Fares Alzubair Basheer Idrees*, Vaikuntam Srinivasan, and Haytham Araibi

Department of Urology, Glan Clwyd Hospital, United Kingdom

Corresponding Author:

Fares Alzubair Basheer Idrees, Department of Urology, Glan Clwyd Hospital, United Kingdom

Keywords

Ketamine; Uropathy; Urinary Symptoms

Abstract

Background: Ketamine use is increasingly associated with lower urinary tract symptoms, including ketamine-induced uropathy (KIU). Characterising affected patients and treatment outcomes is essential to guide management.

Method: A cross-sectional study included 20 patients diagnosed with KIU between January and June 2024 at our institution. Urinary symptoms were assessed at presentation and three months after treatment, including frequency, dysuria, urgency, nocturia, incontinence, incomplete emptying, weak stream, and straining. Symptom severity was measured using the International Prostate Symptom Score (IPSS). Statistical analysis was performed using SPSS version 26.0.

Results: Most patients were male (n=15; 75%) and aged 16–21 yr (n=11; 55%). Regular ketamine use was reported by 14 patients (70%), and 15 (75%) had used ketamine for over six years. At presentation, all patients reported urinary frequency and dysuria (100%), and 17 reported urgency (85%). After treatment, significant improvement was observed in dysuria (100% vs 75%; p=0.016), urgency (85% vs 40%; p=0.003), urinary incontinence (35% vs 10%; p=0.047), and incomplete emptying (30% vs 5%; p=0.037). IPSS scores shifted from severe to mild symptoms, although this change was not statistically significant (p=0.546).

Conclusions: KIU is associated with a high burden of urinary symptoms in young users. Recognition and targeted treatment can significantly improve key urinary outcomes. Patient summary: Young ketamine users frequently develop bladder symptoms. Symptoms improved following treatment, suggesting intervention may improve quality of life.

Keywords: Ketamine; Uropathy; Urinary Symptoms.

Highlights

• Ketamine-induced uropathy is associated with a significant burden of lower urinary tract symptoms in a predominantly young patient population.

• Urinary frequency, dysuria, and urgency were the most common presenting symptoms, with frequency and dysuria reported in all patients.

• Targeted treatment resulted in statistically significant improvement in dysuria, urgency, urinary incontinence, and incomplete bladder emptying at three months.

• Despite treatment, a proportion of patients continued to experience persistent symptoms, highlighting the chronic nature of the condition.

• These findings emphasise the importance of early recognition and structured management in patients with ketamine-induced uropathy.

Citation

Idrees FAB, Srinivasan V, Araibi H (2026) Characteristics and Treatment Outcomes of Ketamine-Induced Uropathy in Wales in 2024: A Pilot Study. J Nephrol Kidney Dis 7(1): 1042.

INTRODUCTION

I Ketamine is a dissociative anesthetic agent that acts as an N-methyl D-aspartate (NMDA) receptor antagonist. It is used clinically for analgesia and sedation, but has also gained popularity as a recreational drug due to its psychoactive effects. The recreational use of ketamine has increased significantly in recent years, particularly among young adults [1,2].

Ketamine has gained notoriety for its recreational use, particularly among younger populations in the UK. The drug’s increasing prevalence, particularly in Wales, has raised concerns regarding its associated health risks, notably ketamine-induced uropathy (KIU). Recent studies have highlighted a troubling rise in ketamine abuse among younger populations in the UK, with reported usage increasing from 1.9% in 2008/2009 to 2.9% in 2018/2019 among individuals aged 16-24 years [3].

Ketamine-induced uropathy (KIU) is an emerging clinical entity characterized by severe lower urinary tract symptoms, small bladder capacity, and pelvic pain in chronic ketamine users. The exact prevalence of KIU is unknown, but it appears to be increasing in recent years along with rising recreational ketamine use, especially among young adults in the UK. A systematic review and meta-analysis found the pooled prevalence of frequency, the most common symptom, to be 77.1% in patients with KIU. Other common manifestations include urgency (69.9%) and suprapubic pain (60.4%) [4].

The pathophysiology of KIU is complex and multifactorial. Ketamine’s metabolites exert toxic effects on the urinary tract, leading to inflammation, fibrosis, and ultimately, damage to both the bladder and kidneys. Clinical presentations can vary widely, with many patients experiencing lower urinary tract symptoms (LUTS) such as frequency, urgency, and dysuria, while others may present with hydronephrosis, a condition that can result from prolonged ketamine abuse. Reports suggest that a significant proportion of patients with a history of ketamine use exhibit upper urinary tract involvement, which can complicate management and increase the risk of renal failure [5,6].

The outcomes of ketamine-induced uropathy are concerning, particularly given the potential for irreversible damage to the urinary system. Studies have shown that a substantial number of patients may progress to severe complications, including hydronephrosis and impaired renal function. The recognition of KIU as a distinct clinical entity is crucial for timely diagnosis and intervention. Current management strategies emphasize the importance of cessation of ketamine use, alongside symptomatic treatment and monitoring of renal function. However, many patients may be reluctant to disclose their drug use, complicating diagnosis and treatment efforts [7,8].

Various medications have been used for symptomatic relief, including anticholinergics and pain medications. However, data on the efficacy of these treatments is limited. A large case series from a single UK center reported using oral medications in addition to intravesical therapies and surgery in 81 patients with KIU. However, the specific oral medications used and their outcomes were not detailed. Given the increasing prevalence of KIU and the paucity of data on treatment outcomes, further research is needed to characterize the oral pharmacological management of this condition. This thesis aims to evaluate the prevalence of KIU in a large cohort of chronic ketamine users and assess the efficacy of various oral medications used in its management [9].

Despite the growing body of evidence surrounding KIU, there remains a paucity of data specifically addressing the characteristics and treatment outcomes of patients in Wales. This gap underscores the need for comprehensive research to evaluate the prevalence of KIU and the effectiveness of various oral treatment strategies within this population. This study aims to provide a detailed examination of the characteristics and treatment outcomes of KIU in Wales, thereby contributing to the development of more effective management protocols and formal treatment guidelines for affected patients.

MATERIAL AND METHODS

A cross-sectional study included 20 patients diagnosed with KIU between January and June 2024 at our institution. Urinary symptoms were assessed at presentation and three months after treatment, including frequency, dysuria, urgency, nocturia, incontinence, incomplete emptying, weak stream, and straining. Symptom severity was measured using the International Prostate Symptom Score (IPSS). Statistical analysis was performed using SPSS version 26.0.

Study Design

This is a retrospective cross-sectional hospital-based study enrolled 20 KIU individuals in our institution, during the period from January to June 2024. The inclusion criteria include ketamine users aged 16 years old or above. Any with a history of significant urological conditions or prior surgeries affecting the urinary tract were excluded.

Data Collection Tools and Methods

Data at admission after 3 months of treatments were collected retrospectively from hospital’s computer data base by using a pre-designed structured questionnaire composed of demographic characteristics (age, gender, smoking), ketamine usage details (the person who guided you to use ketamine, duration of use, regularity of use, amount per day, other substances with ketamine), duration of treatment, urological evaluation by radiological modalities (ultrasound-US and computed tomography CT), renal evaluation by eGFR, and symptom assessment before and after the treatment.

All the patients were treated orally with Tamsulosin 400 µg and Solifenacin 5 mg once daily for one month in addition to Pentosan polyphosphate 100 mg three times a day for three months up to 6 months.

International Prostate Symptom Score (IPSS) was used to assess LUTS. The IPSS questionnaire consists of 7 questions that evaluate the sensation of incomplete emptying, frequency of urinating at intervals of ≤2 hours, intermittency of the urinary stream, difficulty postponing urination characterized as urinary urgency, weakness of urinary stream (weak stream), the need to push or strain to urinate (straining), and the need to awaken at night to urinate (nocturia). The overall IPSS ranges from 0 to 35 and categorized as mild when score from 0 to 7, moderate 8-19 and severe from 20-35 [10].

Statistical analysis

Data analyzed by using statistical package for social sciences (SPSS; IBM, version 26.0). The results showed in tables and figures designed by Microsoft Excel 2010. The Chi-Square test was employed for significance testing, with a p-value of less than 0.05 considered statistically significant (two-sided).

RESULTS

Most patients were male (n=15; 75%) and aged 16–21 yr (n=11; 55%). Regular ketamine use was reported by 14 patients (70%), and 15 (75%) had used ketamine for over six years. At presentation, all patients reported urinary frequency and dysuria (100%), and 17 reported urgency (85%). After treatment, significant improvement was observed in dysuria (100% vs 75%; p=0.016), urgency (85% vs 40%; p=0.003), urinary incontinence (35% vs 10%; p=0.047), and incomplete emptying (30% vs 5%; p=0.037). IPSS scores shifted from severe to mild symptoms, although this change was not statistically significant (p=0.546).

A total of 20 participants were included in the study, with 15 males (75%) and 5 females (25%). The majority of participants 11(55%) were aged from 16-21 years. Most participants 14(70%) were regular ketamine users, with duration of use above 6 years in 15(75%) cases. The amount of ketamine used per day was mostly between 1-2 grams by 14(70%) cases. The majority of participants 16(80%) still using ketamine even after being diagnosed with uropathy, and 13(65%) received treatment for 1-3 months. Radiological imaging modalities used included CT in eight (40%) and US in six (30%) cases. The estimated glomerular filtration rate (eGFR) was greater than 90 ml/min in 16(80%) participants and between 80-90 ml/min in four (20%) cases. The baseline characteristics were detailed in Table 1.

Table 1: The baseline characteristics (N= 20)

 

N

%

Gender

 

 

  • Male

15

75.0

  • Female

5

25.0

Age (Years)

 

 

  • 16-21

11

55.0

  • 22-27

8

40.0

  • 27-32

1

5.0

Smoking (yes)

19

95.0

The person who guided you to use ketamine

 

 

  • Friends

9

45.0

  • School peer

6

30.0

  • Both

5

25.0

Duration of use (Years)

 

 

  • <1

1

5.0

  • 1-3

3

15.0

  • 4-6

1

5.0

  • >6

15

75.0

Regularity of use

 

 

  • Regular

14

70.0

  • Occasional

6

30.0

Amount per day (gm)

 

 

  • <1

2

10.0

  • 1-2

14

70.0

  • >2

2

10.0

  • Don’t know

2

10.0

Use other substances with ketamine

1

5.0

Still use ketamine after uropathy diagnosis

16

80.0

Duration of treatment (months)

 

 

  • <1

2

10.0

  • 1-3

13

65.0

  • >3

5

25.0

Radiological Imaging modalities

 

 

  • CT

8

40.0

  • US

6

30.0

  • None

6

30.0

eGFR (ml/min)

 

 

  • >90

16

80.0

  • 80-90

4

20.0

Pretreatment, the most common symptoms were urinary frequency (n=20; 100%), dysuria (n=20; 100%) and urgency (n=17; 85%). After three months of treatment, there was significant reduction in dysuria [at admission= 20(100%) vs post-treatment= 15(75%); P= 0.016], urgency [at admission= 17(85%), post-treatment= eight (40%); P= 0.003], urine incontinence [at admission= seven (35%), post-treatment= two (10%); P= 0.047] and incomplete emptying [at admission= six (30%), post treatment= one (5%); P= 0.037] as illustrated in Table 2.

Table 2: The symptoms before and after ketamine induced uropathy (KIU) treatment (N= 20)

 

pretreatment; n(%)

3 months posttreatment; n(%)

P. value

Urinary frequency

20(100%)

18(90%)

0.147a

Dysuria

20(100%)

15(75%)

0.016a*

Urinary urgency

17(85%)

8(40%)

0.003a*

Nocturia

7(35%)

6(30%)

0.735a

Urinary incontinence

7(35%)

2(10%)

0.047a*

Incomplete emptying

6(30%)

1(5%)

0.037a*

Weak stream

3(15%)

1(5%)

0.291a

intermittency

2(10%)

2(10%)

0.999a

Straining

2(10%)

1(5%)

0.548a

The International Prostate Symptom Score (IPSS) showed a slight shift from severe symptoms to mild symptoms after treatment, but this change was not statistically significant (P=0.546) as demonstrated in Figure 1.

Figure 1: Bar chart showing Patient distribution according to the severity of IPSS (N=20)

DISCUSSION

In this study ketamine was markedly used by males 15(75%), which supported by previous study of Merikangas et al., who is indicating a male predominance in substance use disorders [11]. The age distribution showed that 55% of participants were aged 16-21 years, and 40% were aged 22-27 years. This finding is consistent with Andrew et al., study where the younger adults are more likely to engage in recreational drug use, including ketamine [12].

A striking 70% (n= 14) of participants were regular ketamine users, with 75% (n= 15) having used the drug for over six years. Corresponding, Mak S et al., reported symptoms related KIU were significantly higher for ketamine use for more than 24 months [13]. This indicating that KIU is duration-dependent condition. A Taiwanese study of 106 ketamine users found that the prevalence of lower urinary tract symptoms (LUTS) was 84%, with symptoms beginning at a mean of 24 months after starting daily use. The study shat that all symptom severity scores (overactive bladder symptom score, international prostate symptom score, interstitial cystitis symptom / pain index) correlated with the duration of ketamine abuse [14].

Among our cohorts, the daily consumption of ketamine was 1-2 grams by 14(70%) participants also reflects a pattern seen in other research, which suggests that high doses are common among KIU patients. A review by Tsai and Kuo discussed the relationship between ketamine usage patterns and the development of ketamine-induced cystitis. The authors noted that higher doses and prolonged use are associated with increased risk of urinary symptoms, including frequency and urgency. They suggested that the toxic effects of ketamine and its metabolites on the bladder epithelium contribute to these symptoms.

Before treatment, the most common symptoms reported were frequency, dysuria and urgency. These findings are consistent with previous literature that identifies these symptoms as prevalent among individuals with uropathy related to ketamine use [4].

After three months of treatment, the prevalence of frequency, dysuria and urgency decreased to 90% (n= 18), 75% (n= 15), and 40% (n= 8), respectively. Also, notable improvement was observed in incontinence, which decreased from 35% (n= 7) to 10% (n= 2), with a statistically significant P. value of 0.037. Similarly, incomplete emptying decreased from 30% (n= 6) to 5% (n= 1), with a P. value of 0.047. These results support findings from the comprehensive review of Li et al and systematic review of Zhou et al those reported non-invasive therapies, including the use of oral anti-inflammatories and anticholinergics, can also lead to improvements in urinary symptoms. These treatments, combined with ketamine cessation, contribute to symptom relief and improved bladder function.

The IPSS results indicated a shift from severe symptoms to mild symptoms three months post-treatment, but this change was not statistically significant (P=0.546). This finding agreed with studies that have shown that while treatment can lead to symptom improvement. In the work of Li et al., who surveyed ketamine users in Taiwan and compared IPSS-S scores between treated and non-treated groups. They found that the non-treated group had lower IPSS-S scores compared to the treated group (5.14 ± 4.36 vs. 7.31 ± 6.71, p=0.0055), suggesting that treatment may have led to a slight improvement in storage symptoms (14). Chu et al., conducted a systematic review and meta-analysis on ketamine associated uropathy. They found that the pooled prevalence of storage symptoms, as measured by the IPSS storage subscore (IPSS-S), was 69.9% (95% CI=48.8%-87.3%). However, the review did not specifically report on changes in IPSS scores after treatment [4].

While this study provides valuable insights, several limitations should be acknowledged; firstly, the study comprises a relatively small sample size of participants, which may limit the generalizability of the findings to the broader population. Secondly, the cross-sectional nature of the study restricts the ability to establish causal relationships between variables. Longitudinal studies are needed to understand the progression of KIU and its impacts over time. Thirdly, the reliance on self-reported data may introduce bias, as participants may underreport or overreport their symptoms and experiences.

While this study provides valuable insights, several limitations should be acknowledged; firstly, the study comprises a relatively small sample size of participants, which may limit the generalizability of the findings to the broader population. Secondly, the cross-sectional nature of the study restricts the ability to establish causal relationships between variables. Longitudinal studies are needed to understand the progression of KIU and its impacts over time. Thirdly, the reliance on self-reported data may introduce bias, as participants may underreport or overreport their symptoms and experiences.

CONCLUSION

In conclusion, this study provides valuable insights into the demographic and clinical characteristics of ketamine users with uropathy. While significant improvements were noted in certain symptoms, particularly dysuria, urgency, incontinence and incomplete emptying, the overall changes in symptomatology were not uniformly statistically significant. Future research should focus on larger sample sizes and longer follow-up periods to better understand the long-term effects of treatment on uropathy symptoms in this population.

ETHICS STATEMENT

Ethical approval was obtained from center’s ethical committee. Both verbal and written consents to publish this information were gained from the patients.

TRANSPARENCY STATEMENT

Fares Alzubair Basheer Idrees, the lead author, declares that this manuscript is an honest, accurate, and transparent. He also clarifies that significant aspects of this study were not excluded and any discrepancies from the planned study have been explicitly explained.

CONSENT TO PUBLISH

All authors gave their approval for publication.

Availability of Data and Materials, Ethical Approval, Informed Consent, Author Contributions, Declaration of Interests, and Funding.

REFERENCES

1. Peltoniemi MA, Hagelberg NM, Olkkola KT, Saari TI. Ketamine: A Review of Clinical Pharmacokinetics and Pharmacodynamics in Anesthesia and Pain Therapy. Clin Pharmacokinet. 2016; 55: 1059-1077.

2. Belal M, Downey A, Doherty R, Ali A, Hashim H, Kozan A, et al. British Association of Urological Surgeons Consensus statements on the management of ketamine uropathy. BJU Int. 2024; 134: 148-154.

3. Lamers G, Van Dyck J, Schapmans S, De Coster K, Mortier D, Zabegalina N. Ketamine-induced uropathy: A diagnostic pitfall in an increasing healthcare issue in youngsters. Urol Case Rep. 2022; 42: 102019.

4. Chan EOT, Chan VWS, Tang TST, Cheung V, Wong MCS, Yee CH, et al. Systematic review and meta-analysis of ketamine-associated uropathy. Hong Kong Med J. 2022; 28: 466-474.

5. Leaver R. Ketamine bladders: what community nurses should know.J Community Nursing. 2019; 33.

6. Chu PS, Ma WK, Wong SC, Chu RW, Cheng CH, Wong S, et al. The destruction of the lower urinary tract by ketamine abuse: a new syndrome? BJU Int. 2008; 102: 1616-1622.

7. Yee CH, Teoh JY, Lai PT, Leung VY, Chu WC, Lee WM, et al. The Risk of Upper Urinary Tract Involvement in Patients With Ketamine-Associated Uropathy. Int Neurourol J. 2017; 21: 128-132.

8. Tsai TH, Cha TL, Lin CM, Tsao CW, Tang SH, Chuang FP, et al. Ketamine-associated bladder dysfunction. Int J Urol. 2009; 16: 826-829.

9. Sturgess G, Beckley I, Shepherd R, Downey A. Ketamine uropathy: Clinical experience in a high prevalence center. Neurourol Urodyn. 2023; 42: 1555-1562.

10. Gewanter RM, Sandhu JS, Tin AL, Gross JP, Mazzarella K, Urban J, et al. Assessment of Patients With Prostate Cancer and Their Understanding of the International Prostate Symptom Score Questionnaire. Adv Radiat Oncol. 2023; 8: 101200.

11. Merikangas KR, McClair VL. Epidemiology of substance use disorders. Hum Genet. 2012; 131: 779-789.

12. Ni A, Lee Cantrell F, Clark RF. Ketamine exposure demographics and outcomes over 16 years as reported to US poison centers. Am J Emerg Med. 2018; 36: 1459-1462.

13. Mak SK, Chan MT, Bower WF, Yip SK, Hou SS, Wu BB, et al. Lower urinary tract changes in young adults using ketamine. J Urol. 2011; 186: 610-614.

14. Li CC, Wu ST, Cha TL, Sun GH, Yu DS, Meng E. A survey for ketamine abuse and its relation to the lower urinary tract symptoms in Taiwan. Sci Rep. 2019; 9: 7240.

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Background: India is “diabetes capital of the world”. Diabetes Atlas 2006 published by International Diabetes Federation, India currently around 40.9 million is expected to rise to 69.9 million by 2025 unless urgent preventive steps are taken. Over the past 30 yr, the status of diabetes has changed from being considered as a mild disorder to major causes of morbidity and mortality.

Methods: Rats treated with Alloxan (150 mg/kg) i.p. results diabetic rats given ethanol extract of Senna auriculata leaf, Syzygium cumini (L.) Skeels seeds and Syzygium cumini (L.) Skeels seeds (150 mg/kg) p.o., respectively for 42 days. Biochemical parameters of diabetic neuropathy, nephropathy and cardiomyopathy and histopathology of sciatic nerve, kidney and heart was done at the end of study.

Results: In Diabetic Group found Blood Glucose Level (BGL) (84.42±6.384 to 369.36±7.784mg/dl); Muscle Grip Strength (MGS) (59.32±1.052 to 13.52±0.883seconds); Thermal Pain Response (TPR) (5.55±0.621 to 13.67±1.164seconds). blood protein (7.48±0.051 to 25.18±0.046mg/dl); urine protein (0.692±0.061 to 2.68±0.056mg/dl); blood albumin (1.94±0.043 to 0.248±0.007mg/dl); urine albumin (0.082±0.009 to 2.68±0.056mg/dl); blood myoglobin (0.042±0.00274 to 0.056±0.00207ng/dl); urine myoglobin (0.0048±0.00142 to 0.0098±0.00107mg/dl); Blood Urea Nitrogen (BUN) (23.04±1.093 to 124.81±1.238 mg/dl); Serum Creatinine (84.06±6.723 to 218.56±7.586 (µMol/dl). Etholic extract of Senna auriculata leaf, Phyllanthus emblica.L. fruits and Syzygium cumini (L.) Skeels seeds & combination treated groups found BGL124.42±7.042, 112.07±6.942, 126.25±7.051 & 98.83±6.932mg/dl; MGS 49.06±0.962, 52.05±1.247, 54.06±1.268 & 56.79±1.125 seconds; TPR 6.54±0.841, 7.38±0.802, 6.45±1.062 & 6.14±0.837 seconds; blood protein 7.98±0.039, 8.02±0.053, 8.06±0.039 & 7.48±0.045mg/dl; urine protein 1.22±0.058, 0.94±0.049, 0.96±0.056 & 0.82±0.062mg/dl; blood albumin 1.64±0.033, 1.82±0.036, 1.87±0.044 & 1.96±0.039mg/dl; urine albumin 0.122±0.008, 0.098±0.007, 0.132±0.009 & 0.108±0.011mg/dl; blood myoglobin 0.045±0.00189, 0.036±0.00177, 0.041±0.00223 & 0.043±0.00175ng/dl; urine myoglobin 0.0042±0.00129, 0.0052±0.00119, 0.0064±0.00126 & 0.0036±0.00125mg/dl; BUN 35.81±1.186, 36.06±1.123, 34.53±1.177 & 29.03±1.229mg/dl; Serum Creatinine 98.42±5.526, 99.73±6.064, 101.97±6.052 & 94.83±6.678µMol/dl.

Conclusion: Ethanol extract of Senna auriculata leaf, Phyllanthus emblica L. fruit and Syzygium cumini (L.) Skeels seeds (150mg/kg) and its combination normalizes biochemical parameters & Morphological changes in sciatic nerve, myocardium & kidney and improvement of the general behavioral parameters. Combination was found to be more effective in these diabetic complications.

Syed Ahmed Hussain and Ashish Kumar Sharma*


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Uric Acid, Metabolic Risk Factors, and Chronic Kidney Disease: Clinical Investigation in a Female Elderly Occupational Population in Taipei, Taiwan

Purpose: To explore the prevalence and associated factors for Chronic Kidney Disease (CKD) among female elderly fishing and agricultural population in Taipei, Taiwan.

Methods: Females (n=1,606) aged 65 years and over voluntarily admitted to a teaching hospital for a physical check-up were collected in 2010.

Results: The prevalence of CKD was 8.2%. Age, hyperuricemia, and hyperglycemia were statistical significantly related to CKD. The sensitivity and specificity of serum uric acid and fasting blood glucose concentration as a marker of CKD were estimated 76.5%, 70.9% and 51.5%, 53.5%, respectively.

Conclusion: Hyperuricemia and hyperglycemia independently affect the prevalent CKD in this sub-population.

Ya-Ting Liang¹, Hsi-Che Shen²˒³˒⁴, Yi-Chun Hu²˒³˒⁵, Yu-Fen Chen⁶˒⁷˒⁸ and Tao-Hsin Tung⁹˒¹⁰˒¹¹*


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Pseudohypercreatininemia after Sustanon Injection

The drugs used in the treatment of certain diseases may give impression of impaired renal function. These drugs cause a false high serum creatinine level. Laboratory findings other than serum creatinine and hypertriglyceridemia were normal. We presented a 28-year-old male with a high serum creatinine level, who was referred for consideration of urgent renal replacement therapy. The results of the investigations revealed that the result was the falsely-elevated serum creatinine due to the sustenance injection.

Can Hüzmeli¹, Mustafa Sağlam¹, Bariş Döner¹, Serkan Çağlar² and Özkan Güngör³


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Peripheral Arterial Disease Holding Central Stage in Chronic Kidney Disease (Kdoqi Stage 3-5): Prevalence and Related Risk Factors - Experience from Kashmir Valley Tertiary Care Centre

Patients with CKD are highly predisposed for developing accelerated atherosclerosis. These patients have non-traditional risk factors such inflammation, malnutrition and increased oxidative stress that enhance and accelerate atherosclerosis in addition to traditional risk factors. Although relation between cardiovascular and cerebrovascular diseases with CKD is well established, studies are suggesting about association of Peripheral Arterial Disease (PAD) with CKD. PAD is associated with increased morbidity and mortality in patients of CKD.

This study is rendezvous to look for PAD and related risk factors in patients of CKD having eGFR less than 60 ml/ min/ 1.73 m2 (MDRDS) and not on RRT.

Two hundred ten subjects with CKD attending department of nephrology at tertiary care institute in valley were included in study. Out of 210 subjects selected, 30 were having PAD that constituted 14% of study population. IC was seen in 25 (11.9%) of 210 subjects. Out of PAD patients 16 (53.3%) were having history of IC and 14 (46.7%) were asymptomatic. As reported in literature, prevalence of peripheral arterial disease in CKD patients not on dialysis ranged from 7% to 32% in previous cases. This study will sensitize us to plan more effective screening, preventive and management strategies. This will go long way to decrease morbidity and mortality in patients.

Mohamad Muzzafer Mir*, Mohamad Saleem Najar, Bipin Kumar Sharma, Mangit Singh, Ursilla Taranum Mir and Majid Khalil Rather