Loading

JSM Clinical Case Reports

Pre-Emptive Deceased-Donor Kidney Transplantion: A Extended Matched Cohort Study

Case Report | Open Access | Volume 11 | Issue 1

  • 1. Department of Nephrology, General University Hospital of Alicantet, Spain
  • 2. Department of Pharmacology, General University Hospital of Alicantet, Spain
+ Show More - Show Less
Corresponding Authors
Antonio Franco, Department of Nephrology, General University Hospital of Alicantet, Pintor Baeza 1, 03010 Alicante, Spain; Tel: 34699438342
Abstract

Introduction: Kidney transplantation is the treatment of choice for patients with kidney disease who require replacement therapy. Dialysis is a step, but not mandatory prior to transplantation and pre-emptive transplant from deceased donors is possible.

Materials and methods: This is a retrospective, observational, matched cohort study. We compared 100 pre-emptive renal transplant recipients with 100 renal transplant recipients on dialysis both groups received a first renal graft, matched by age and gender of donors and recipients, time of transplant, immunological risk, immunosuppression and cold ischemia time.

Results: The percentage of recipients who presented early graft loss, delayed graft function and acute rejection was similar in both groups. No differences were observed in their renal function at 12 and 36 months after transplantation, as well as in the actuarial survival of patients (p = 0.730) and grafts (p = 0.693) in the studied period. The total calculated cost of the period on dialysis for the dialysis group was 12,172.565 Euros.

Conclusions: Pre-emptive transplantation can achieve comparable outcomes to those for post- dialysis kidney transplantation, and better quality of life with a reduced cost.

Keywords

• Pre-emptive renal transplantation; Deceased donor; Patient and graft survival; Dialysis; Psychological aspects

CITATION

Franco A, Más-Serrano P, González Y, de la Cruz1 E, Contreras1 FJP (2023) Pre-Emptive Deceased-Donor Kidney Transplantion: A Extended Matched Cohort Study. JSM Clin Case Rep 11(1): 1209.

INTRODUCTION

Chronic kidney disease (CKD) causes significant morbidity and mortality, especially cardiovascular [1]. CKD is divided into stages from least to most severe [2]; stage 5 is the situation to adopt a series of strategies of treatment including the start of renal replacement therapy which will not only keep the patients alive, but also, at least in part, will maintain their quality of life.

Usually, patients are initially included in a dialysis program, either hemodialysis or peritoneal dialysis [3]. Both treatments are effective to maintain the patient alive; but they require prior surgical procedures, either an arterio-venous fistula, insertion of a central venous or a peritoneal catheter [4,5]. Moreover, these replacement treatments are far from effective and we only achieve partial restoration of the lost renal functions [6].

At the present time, we have one effective and complete treatment for CKD. So kidney transplantation is the treatment of choice in most patients with end-stage CKD [7,8]. Renal transplantation restores the patient’s previous health condition, since the transplanted kidney fully replaces the functions lost by the native kidney; therefore the benefit/risk ratio is positive. However renal transplantation requires chronic pharmacological immunosuppression, which promotes opportunistic infections [9] and the incidence of cancer increases [10,11].

Usually, deceased-donor kidney transplantation is considered when the patient is already on renal replacement therapy. Dialysis is generally a necessary, but not a mandatory step before kidney transplantation in patients who are candidates for this procedure. It is possible to have kidney transplantation without prior dialysis. This procedure is known as a pre-emptive, or pre-dialysis kidney transplantation, a reality in recipients from living donors [12], although it remains controversial in the case of deceased donors due to the lack of organs [7,8,13]. In France, pre-emptive deceased-donor kidney transplantation has been incentivized in recent years, with an increase from 5.6% to 15.5% between 2007 and 2014, with good results [14].

In 2007, our center started a pre-emptive deceased-donor kidney transplant program. It should be noted that patients in a pre-dialysis situation only receive a graft if there is no candidate for transplant on renal replacement therapy. We reported the results of this program in 2020 [15].

The objective of this study is to evaluate the results of our experience in pre-emptive, deceased-donor kidney transplantation with more recipients enrolled and a longer follow-up period. 

MATERIAL AND METHODS

This is a retrospective and observational study with matched cohorts. Recipients who received a renal transplant from a brain dead donor at our Hospital between 2007 and 2016 were included. Two groups were defined: a pre-dialysis group (predialysis patients who received a pre-emptive, deceased- do transplant) and a control group (patients on renal replacement therapy who received a first transplant from a deceased donor).

In the pre-dialysis group, patients had a glomerular filtration rate under 15 ml/min (measured by CKD-EPI), an estimated time to start dialysis under 6 months, and more than one year of followup after transplantation. Each case in the pre-dialysis group was matched by age and sex of donor and recipient, percentage of donors over 60 years, cold ischemia time, the blood group of the recipients as well as by transplant date .So the time between the dates of the transplantation of the pre-emptive recipient and the control was less than 7 days.

The immunological status of the recipients was evaluated via donor-recipient compatibility and the preformed antibody level and was similar in both groups.

The general immunosuppressive regime at the time of the kidney transplantion consisted of tacrolimus (initial dose: Advagraf® 0.2 mg/kg per day; subsequent doses were adjusted to maintain a trough concentration of tacrolimus between 8 and 10 ng/mL during the first month and afterwards between 6 and 8 ng/mL), mycophenolate mofetil (500 mg/12 h orally), basiliximab or timoglobulin in high- risk patients and a tapered corticosteroids regimen.

The variables evaluated were incidence of early graft loss (before 48 h), acute rejection (sudden alteration in graft function or presence of delayed graft function, with specific histological changes), delayed graft function ( dialysis in the first week post-transplant), kidney function at 12 and 36 months (serum creatinine level), and graft and patient survivals at 1, 3 and 10 years.

The period of time in the transplant waiting list in each patient group was evaluated. Adherence to treatment was studied in both groups with the variation in the trough tacrolimus concentration (calculated as the mean of the coefficients of variation [CV] of the trough tacrolimus concentration for the individual patients obtained from month 3 through month 24 post-transplant, expressed as a percentage) along with a personal interview conducted at every visit.

CV (%) Standard deviation x 100

Mean

The theoretical cost resulting from the care of the patients on dialysis of the control group patients was quantified according to the study conducted by Arietta et al., [16]. The cost per patient on dialysis was calculated as the result of months on dialysis multiplied by monthly cost depending on the technique.

Statistical study

The continuous variables are expressed as the mean 95% confidence interval, or median and interquartile range (p25– p75), depending on the distribution type. The categorical variables are described as the number of percentage of patients by response category.

The continuous variables were compared between groups with Student’s T-test or Mann-Whitney’s U test depending on the type of variable distribution. Categorical variables were analyzed using Fischer’s test.

A survival analysis (Kaplan–Meier) was performed to analyze the percentage of patients and grafts lost during the follow-up period. Both groups were compared using the statistical test (logrank). The level of significance was 0.05. The statistical analysis was performed with the SPSS software, version 24.

RESULTS

One hundred (100) recipients were included in the predialysis group, matched with 100 patients in the control group, 75 of them on hemodialysis and 25 on continuous outpatient peritoneal dialysis. The less period of follow-up was 3 years post transplant. The median follow-up (months) in the pre- dialysis and control groups was 74.0 (p25–p75: 24.0–122.0) and 76 (p25–p75: 28.8–128.3), respectively. The time on the waiting list was similar in both groups (median in months: p25–p75; 4 [2–7] vs. 6 [2–11] months; p = 0.100).

No significant differences were observed between the groups in the age and sex of the donor and recipient, percentage of donors over 60 years, cold ischaemia time, and patients who received induction with thymoglobulin or basiliximab. No significant differences were also observed in the blood group of the recipients or their immunization status. The variability in the trough tacrolimus concentration was similar in both groups, with no lack of adherence detected during the interviews. Table 1 shows the similarity of the variables in both groups.

In the pre-dialysis group, the incidence of delayed graft function was similar to the control group (19.2 vs. 13.5%, respectively; p = 0.426). Similarly, no statistically significant differences were found between the two groups for the presence of acute rejection (pre-dialysis group: 10.1% vs. control group: 9.1%; p = 0.809) and early graft loss (pre-dialysis group: 5.2% vs. control group 7.1%; p = 0.800). Kidney function, evaluated by median serum creatinine, was similar in the pre-dialysis and control groups at one year (1.57 vs. 1.60 mg/dL, respectively; p = 0.428) and 3 years (1.74 vs. 1.62 mg/dL; p = 0.335) (Table 1)

Table 1 – Demographic data of the patients included in the pre-dialysis group and control group.

 

Pre-dialysis group

Control group

p

Donor age (years), mean (95% CI)

53.2 (50.4–56.0)

53.1 (50.9–56.0)

0.965

Recipient age (years), mean (95% CI)

52.6 (49.9–55.3)

53.1 (50.8–55.4)

0.791

Donor sex (%M/F)

62.1/39.9

54.1/45.9

0.384

Recipient sex (%M/F)

67.0/33.0

64.1/35.9

0.665

Donor >60 years (%)

28.8

28.8

1.000

Cold ischaemia time (hours), mean (95% CI)

17.4 (16.6–18.4)

17.2 (16.2–18.1)

0.813

Thymoglobulin (%)

56

60

0.567

Basiliximab (%)

12

16

0.415

Cp TAC Variability; CV (%), median (p25-p75)

24.1 (19.5–33.0)

26.1 (19.1–44.1)

0.602

Blood group

 

 

0.520

A

56.1

50

 

B

9.1

9.1

 

AB

10.6

6.1

 

O

24.2

34.8

 

HLA incompatibility

 

 

0.862

4–6

64.5

61.5

 

0–3

35.5

38.5

 

PRA >50%

0

4.5

0.244

Cp TAC: trough tacrolimus concentration; CV: coefficient of variation; HLA: histocompatibility antigens; 95% CI: 95% confidence interval; PRA: panel-reactive antibody; M/F: male/female.

Recipient survival at 1, 3 and 10 years was 94.1% 93.1% and 71.2% in the pre-dialysis group and 96.0% 89,7 and 74.1% in the control group, respectively (p = 0.730)

Similarly, graft survival in the pre- dialysis group was 90.4% at one year, 88.1% at 5 years and 62,8% at 10 years, and in the control group it was 92.3% at one year, 79.6% at 5 years and 61,7% at 10 years(p = 0.693).

The mean recipient survival time was not different in the pre-dialysis and control groups (126.8 [95% CI: 113.8–139.8] vs. 123.1 [95% CI: 109.7–135.5]) months, respectively; p = 0.730) Nor were significant differences in the graft survival time observed between the two groups (pre-dialysis group: 114.6 months [95% CI: 99.1–130.2] vs. control group: 109.3 months [95% CI: 93.7–124.8]; p = 0.693).

According to the total time on peritoneal dialysis (556 months) and hemodialysis (2697 months), the total cost of renal replacement therapy in our patients was 12,172.565 Euros.

DISCUSSION

The worldwide experience with pre-emptive, deceaseddonor kidney transplantation is hard to find and under debate [17] Some authors have reported that the time on dialysis before kidney transplantation has a negative impact on its outcome, therefore performing it pre-emptively would be associated with greater graft and recipient survivals as compared to patients who remained on dialysis for some time [3,6,8,17-19].Studies by Roake et al. [3] and Papalois et al. [19] have demonstrated superior survival in pre-dialysis recipients. These results were recently supported by a French multi-center studied by Prezelin–Reydit in which it was concluded that pre-emptive transplant is associated with a lower risk of graft failure. Nevertheless, this conclusion may be questionable, because the dialysis group was older, with more cardiovascular co-morbidity, with a higher percentage of patients with diabetes mellitus than the pre-emptive group, and the donors were also older [20]. Other authors such as Luo et al. recommend this type of transplant, since they improve the patient’s quality of life and reduce the economic cost, although they did not observe significant differences in terms of recipient or graft survivals. However, these authors did show evidence of a decreased rate of acute rejection [21].

In our study, as reported by Luo et al. [21], we did not find significant differences in recipient and graft survival rates. Foucher et al. reported the same conclusion in a recent study designed with a control group of more than 500 patients included in the waiting list for at least 6 months before their first dialysis session; in addition, they used an inverse probability score to make the groups more homogeneous. Nevertheless, the dialysis group had a significantly higher percentage of hyperimmunized patients that were treated with more immunosuppression, which could alter the results [22].

The percentage of recipients who experienced acute rejection was similar in both groups (Table 2), which contrasts with the previously mentioned study by Luo et al. and other studies reported in the literature, which show that a longer time on dialysis increases the risk of rejection [21].

Table 2 – Efficacy and safety variables in the pre-dialysis group and control group (p25–p75: 25th and 75th percentile of the median).

 

Pre-dialysis group

Control group

p

Delayed graft function (%)

19.2

13.5

0.426

Acute rejection (%)

10.1

9.1

0.809

Early graft loss (%)

5.2

7.1

0.800

Serum creatinine at 12 months, median (p25–p75) mg/dL

1.5 (1.4–1.6)

1.6 (1.4–1.7)

0.428

Serum creatinine at 36 months, median (p25–p75) mg/dL

1.7 (1.5–1.9)

1.6 (1.5–1.7)

0.335

The study by Cacciarelli, with 325 kidney transplants, concluded that the incidence of acute rejection was lower in patients who remained on dialysis for a period less than 6 months [18]. In contrast, it has been proposed that patients who have not experienced the symptoms of CKD or the morbidity associated with dialysis may be less compliant with the immunosuppressant treatment [23], which would lead to a higher incidence of rejection. There was no evidence of any compliance in our group of recipients with pre-emptive transplant such as the results obtained by Papalois, who did not find a higher rate of non-adherence to treatment in patients who received pre-emptive kidney transplant [19].

Kidney function at 12 and 36 months after the transplantation was similar in both groups. However, in other studies, a higher rate of delayed kidney function in patients who were already on dialysis has been reported [17]. The hypothesis proposed is a higher inflammatory status, as well as an inadequate clearance of certain metabolites in these patients [24].

Foucher et al., exhaustively reviewed the ethical justification for transplanting patients in a pre-dialysis situation, which could lead to a longer time on the waiting list for patients on dialysis. In this study, the recipients from the dialysis group were on the waiting list for a mean time of 38 months, significantly longer (p < 0.0001) than the pre-dialysis group, with a mean time of 14 months [22]. Our experience is different, since the time on the waiting list in our patients is much shorter and it was not significantly different between the pre-dialysis and dialysis group: 4 and 6 months, respectively; therefore it was consider that, in our case, performing a pre-emptive; deceased-donor transplantion does not constitute an ethical dilemma.

As for the economic cost, it is worth to mention that renal replacement therapy (hemodialysis, peritoneal dialysis, and kidney transplantation) spends a 2.5% of the National Health System’s budget and more the 4% of that for Specialised Care. The mean cost of hemodialysis, peritoneal dialysis, and kidney transplantion first year is 46,660, 32,432, and 47,136 Euros per patient per year, respectively. However, in subsequent years, the cost of the kidney transplantation decreases considerably: 6477 Euros per patient per year; renal transplantation is the technique with the best cost-effectiveness ratio [16], therefore we can affirm that it not only prolongs life, but that as far as the economic cost it is also a more advantageous option as compared with longterm dialysis [25]. Thus, the time on dialysis for the recipients in the control group entailed a cost which could have been reduced in the case of pre-emptive transplant. This is an objective data which should be added to the subjective benefit for the patient by avoiding dialysis and, prior to this, the proceedings needed before starting dyalisis.21 However, it is necessary to point out the limited grafts available from deceased donors [3,8,17], a fact which would significantly limit the implementation of the proposed strategy.

The strong point of our study is in the analysis of the variables studied. So matching were made between pairs of recipients (pre-dialysis situation vs recipients already on dialysis) who were transplanted with a narrow time margin (under 7 days); whereas in the other referenced series [3,17-19], the group of recipients in a pre- dialysis situation constituted a sub-group of their transplant populations, without matching in terms of transplant time.

The weak point of this study is the limited number of enrolled patients and the follow up period could be longer.

CONCLUSION

In Conclusion, deceased-donor kidney transplantation offers patients in a pre- dialysis situation outcomes which are at least comparable to those of recipients on dialysis and prevents the morbidity, mortality and psychological impact derived from dialysis, in addition to be economically advantageous.

REFERENCES
  1. Lees JS, Mark PB, Jardine AG. Cardiovascular complications of chronic kidney disease. Medicine (Baltimore). Elsevier. 2015; 43: 469–73.
  2. KDIGO Clinical Practice Guideline for Acute Kidney Injury. Kidney Int. 2012; 2(Suplemento 1).
  3. Roake JA, Cahill AP, Gray CM, Gray DWR, Morris PJ. Preemptive cadaveric renal transplantation--clinical outcome. Transplantation. 1996; 62: 1411–6.
  4. Rodriguez Hernandez J, López Pedret J, Piera L. El acceso vascular en España: análisis de su distribución, morbilidad y sistemas de monitorización. Nefrología. 2001; 21: 45–51.
  5. Peppelenbosch A, Van Kuijk WHM, Bouvy ND, Van Der Sande FM, Tordoir JHM. Peritoneal dialysis catheter placement technique and complications. NDT Plus. 2008; 1: iv23-iv28.
  6. Meier-Kriesche HU, Kaplan B. Waiting time on dialysis as the strongest modifiable risk factor for renal transplant outcomes: a paired donor kidney analysis. Transplantation. 2002; 74: 1377–81.
  7. Morales Ruiz E. Transplante renal anticipado. Nefrología. 2008; 28: 123–8.
  8. Asderakis A, Augustine T, Dyer P, Short C, Campbell B, Parrott NR, et al. Pre-emptive kidney transplantation: the attractive alternative. Nephrol Dial Transplant. 1998; 13: 1799–803.
  9. Karuthu S, Blumberg EA. Common infections in kidney transplant recipients. Clin J Am Soc Nephrol. 2012; 7: 2058–70.
  10. Gutiérrez-Dalmau A, Revuelta I, Campistol J. Renal Transplantation and Cancer: Focus on Immunosuppressive therapy. Trends Transpl. 2007; 1: 3–14.
  11. Campistol J, Cuervas-Mons V, Manito N, Almenar L, Arias M, Casafont F, et al. New concepts and best practices for management of pre- and post-transplantation cancer. Transplant Rev (Orlando). 2012; 26: 261-79.
  12. Innocenti GR, Wadei HM, Prieto M, Dean PG, Ramos EJ, Textor S, et al. Preemptive living donor kidney transplantation: do the benefits extend to all recipients? Transplantation. 2007; 83: 144-9.
  13. Goldfarb-Rumyantzev A, Hurdle JF, Scandling J, Wang Z, Baird B, Barenbaum L, et al. Duration of end-stage renal disease and kidney transplant outcome. Nephrol Dial Transplant. 2005; 20: 167-75.
  14. Vigneau C, Kolko A, Stengel B, Jacquelinet C, Landais P, Rieu P, et al. Ten-years trends in renal replacement therapy for end-stage renal disease in mainland France: Lessons from the French Renal Epidemiology and Information Network (REIN) registry. Nephrol Ther. 2017; 13: 228-35.
  15. Franco A, Más-Serrano P, González Y, Balibrea N, Rodríguez D, López MI, et al. Pre-emptive deceased-donor kidney transplant: A matched cohort study. Nefrologia. 2020; 40: 32-7.
  16. Arrieta J. Evaluación económica del tratamiento sustitutivorenal (hemodiálisis, diálisis peritoneal y trasplante) en España. Nefrologia. 2010; 1: 37-47.
  17. Kessler M, Ladriere M, Giral M, Soulillou JP, Legendre C, Martinez F, et al. Does pre-emptive kidney transplantation with a deceased donor improve outcomes? Results from a French transplant network. Transpl Int. 2011; 24: 266-75.
  18. Cacciarelli T, Sumrani N, Di Benedetto A, Hong J, Sommer B. Influence of length of time on dialysis before transplantation on long-term renal allograft outcome. Transplant Proc. 1993; 25: 2474-6.
  19. Papalois VE, Moss A, Gillingham KJ, Sutherland DER, Matas AJ, Humar A. Pre-emptive transplants for patients with renal failure: an argument against waiting until dialysis. Transplantation. 2000; 70: 625-31.
  20. Prezelin-Reydit M, Combe C, Harambat J, Jacquelinet C, Merville P, Couzi L, et al. Prolonged dialysis duration is associated with graft failure and mortality after kidney transplantation: results from theFrench transplant database. Nephrol Dial Transplant. 2019; 34: 538-45.
  21. Luo M, Qiu F, Wang Y, Zhou Z. Preemptive deceased-donor renal transplant in adults: single-center experience and outcome. Exp Clin Transplant. 2012; 10: 101-4.
  22. Foucher Y, Le Borgne F, Legendre C, Morelon E, Buron F, Girerd S, et al. Lack of impact of pre-emptive deceased-donor kidney transplantation on graft outcomes: a propensity score-based study. Nephrol Dial Transplant. 2019; 34: 886-91.
  23. Girndt M, Sester M, Sester U, Kaul H, Köhler H. Molecular aspects of T- and B-cell function in uremia. Kidney Int Suppl. 2001; 78: S206-11.
  24. Zimmermann J, Herrlinger S, Pruy A, Metzger T, Wanner C. Inflammation enhances cardiovascular risk and mortality in hemodialysis patients. Kidney Int. 1999; 55: 648-58.
  25. Schnitzler MA, Lentine KL, Burroughs TE. The cost effectiveness of deceased organ donation. Transplantation. 2005; 80: 1636-7.

 

Franco A, Más-Serrano P, González Y, de la Cruz1 E, Contreras1 FJP (2023) Pre-Emptive Deceased-Donor Kidney Transplantion: A Extended Matched Cohort Study. JSM Clin Case Rep 11(1): 1209.

Received : 16 Jan 2023
Accepted : 25 Feb 2023
Published : 27 Feb 2023
Journals
Annals of Otolaryngology and Rhinology
ISSN : 2379-948X
Launched : 2014
JSM Schizophrenia
Launched : 2016
Journal of Nausea
Launched : 2020
JSM Internal Medicine
Launched : 2016
JSM Hepatitis
Launched : 2016
JSM Oro Facial Surgeries
ISSN : 2578-3211
Launched : 2016
Journal of Human Nutrition and Food Science
ISSN : 2333-6706
Launched : 2013
JSM Regenerative Medicine and Bioengineering
ISSN : 2379-0490
Launched : 2013
JSM Spine
ISSN : 2578-3181
Launched : 2016
Archives of Palliative Care
ISSN : 2573-1165
Launched : 2016
JSM Nutritional Disorders
ISSN : 2578-3203
Launched : 2017
Annals of Neurodegenerative Disorders
ISSN : 2476-2032
Launched : 2016
Journal of Fever
ISSN : 2641-7782
Launched : 2017
JSM Bone Marrow Research
ISSN : 2578-3351
Launched : 2016
JSM Mathematics and Statistics
ISSN : 2578-3173
Launched : 2014
Journal of Autoimmunity and Research
ISSN : 2573-1173
Launched : 2014
JSM Arthritis
ISSN : 2475-9155
Launched : 2016
JSM Head and Neck Cancer-Cases and Reviews
ISSN : 2573-1610
Launched : 2016
JSM General Surgery Cases and Images
ISSN : 2573-1564
Launched : 2016
JSM Anatomy and Physiology
ISSN : 2573-1262
Launched : 2016
JSM Dental Surgery
ISSN : 2573-1548
Launched : 2016
Annals of Emergency Surgery
ISSN : 2573-1017
Launched : 2016
Annals of Mens Health and Wellness
ISSN : 2641-7707
Launched : 2017
Journal of Preventive Medicine and Health Care
ISSN : 2576-0084
Launched : 2018
Journal of Chronic Diseases and Management
ISSN : 2573-1300
Launched : 2016
Annals of Vaccines and Immunization
ISSN : 2378-9379
Launched : 2014
JSM Heart Surgery Cases and Images
ISSN : 2578-3157
Launched : 2016
Annals of Reproductive Medicine and Treatment
ISSN : 2573-1092
Launched : 2016
JSM Brain Science
ISSN : 2573-1289
Launched : 2016
JSM Biomarkers
ISSN : 2578-3815
Launched : 2014
JSM Biology
ISSN : 2475-9392
Launched : 2016
Archives of Stem Cell and Research
ISSN : 2578-3580
Launched : 2014
Annals of Clinical and Medical Microbiology
ISSN : 2578-3629
Launched : 2014
JSM Pediatric Surgery
ISSN : 2578-3149
Launched : 2017
Journal of Memory Disorder and Rehabilitation
ISSN : 2578-319X
Launched : 2016
JSM Tropical Medicine and Research
ISSN : 2578-3165
Launched : 2016
JSM Head and Face Medicine
ISSN : 2578-3793
Launched : 2016
JSM Cardiothoracic Surgery
ISSN : 2573-1297
Launched : 2016
JSM Bone and Joint Diseases
ISSN : 2578-3351
Launched : 2017
JSM Bioavailability and Bioequivalence
ISSN : 2641-7812
Launched : 2017
JSM Atherosclerosis
ISSN : 2573-1270
Launched : 2016
Journal of Genitourinary Disorders
ISSN : 2641-7790
Launched : 2017
Journal of Fractures and Sprains
ISSN : 2578-3831
Launched : 2016
Journal of Autism and Epilepsy
ISSN : 2641-7774
Launched : 2016
Annals of Marine Biology and Research
ISSN : 2573-105X
Launched : 2014
JSM Health Education & Primary Health Care
ISSN : 2578-3777
Launched : 2016
JSM Communication Disorders
ISSN : 2578-3807
Launched : 2016
Annals of Musculoskeletal Disorders
ISSN : 2578-3599
Launched : 2016
Annals of Virology and Research
ISSN : 2573-1122
Launched : 2014
JSM Renal Medicine
ISSN : 2573-1637
Launched : 2016
Journal of Muscle Health
ISSN : 2578-3823
Launched : 2016
JSM Genetics and Genomics
ISSN : 2334-1823
Launched : 2013
JSM Anxiety and Depression
ISSN : 2475-9139
Launched : 2016
Clinical Journal of Heart Diseases
ISSN : 2641-7766
Launched : 2016
Annals of Medicinal Chemistry and Research
ISSN : 2378-9336
Launched : 2014
JSM Pain and Management
ISSN : 2578-3378
Launched : 2016
JSM Women's Health
ISSN : 2578-3696
Launched : 2016
Clinical Research in HIV or AIDS
ISSN : 2374-0094
Launched : 2013
Journal of Endocrinology, Diabetes and Obesity
ISSN : 2333-6692
Launched : 2013
Journal of Substance Abuse and Alcoholism
ISSN : 2373-9363
Launched : 2013
JSM Neurosurgery and Spine
ISSN : 2373-9479
Launched : 2013
Journal of Liver and Clinical Research
ISSN : 2379-0830
Launched : 2014
Journal of Drug Design and Research
ISSN : 2379-089X
Launched : 2014
JSM Clinical Oncology and Research
ISSN : 2373-938X
Launched : 2013
JSM Bioinformatics, Genomics and Proteomics
ISSN : 2576-1102
Launched : 2014
JSM Chemistry
ISSN : 2334-1831
Launched : 2013
Journal of Trauma and Care
ISSN : 2573-1246
Launched : 2014
JSM Surgical Oncology and Research
ISSN : 2578-3688
Launched : 2016
Annals of Food Processing and Preservation
ISSN : 2573-1033
Launched : 2016
Journal of Radiology and Radiation Therapy
ISSN : 2333-7095
Launched : 2013
JSM Physical Medicine and Rehabilitation
ISSN : 2578-3572
Launched : 2016
Annals of Clinical Pathology
ISSN : 2373-9282
Launched : 2013
Annals of Cardiovascular Diseases
ISSN : 2641-7731
Launched : 2016
Journal of Behavior
ISSN : 2576-0076
Launched : 2016
Annals of Clinical and Experimental Metabolism
ISSN : 2572-2492
Launched : 2016
Clinical Research in Infectious Diseases
ISSN : 2379-0636
Launched : 2013
JSM Microbiology
ISSN : 2333-6455
Launched : 2013
Journal of Urology and Research
ISSN : 2379-951X
Launched : 2014
Journal of Family Medicine and Community Health
ISSN : 2379-0547
Launched : 2013
Annals of Pregnancy and Care
ISSN : 2578-336X
Launched : 2017
JSM Cell and Developmental Biology
ISSN : 2379-061X
Launched : 2013
Annals of Aquaculture and Research
ISSN : 2379-0881
Launched : 2014
Clinical Research in Pulmonology
ISSN : 2333-6625
Launched : 2013
Journal of Immunology and Clinical Research
ISSN : 2333-6714
Launched : 2013
Annals of Forensic Research and Analysis
ISSN : 2378-9476
Launched : 2014
JSM Biochemistry and Molecular Biology
ISSN : 2333-7109
Launched : 2013
Annals of Breast Cancer Research
ISSN : 2641-7685
Launched : 2016
Annals of Gerontology and Geriatric Research
ISSN : 2378-9409
Launched : 2014
Journal of Sleep Medicine and Disorders
ISSN : 2379-0822
Launched : 2014
JSM Burns and Trauma
ISSN : 2475-9406
Launched : 2016
Chemical Engineering and Process Techniques
ISSN : 2333-6633
Launched : 2013
Annals of Clinical Cytology and Pathology
ISSN : 2475-9430
Launched : 2014
JSM Allergy and Asthma
ISSN : 2573-1254
Launched : 2016
Journal of Neurological Disorders and Stroke
ISSN : 2334-2307
Launched : 2013
Annals of Sports Medicine and Research
ISSN : 2379-0571
Launched : 2014
JSM Sexual Medicine
ISSN : 2578-3718
Launched : 2016
Annals of Vascular Medicine and Research
ISSN : 2378-9344
Launched : 2014
JSM Biotechnology and Biomedical Engineering
ISSN : 2333-7117
Launched : 2013
Journal of Hematology and Transfusion
ISSN : 2333-6684
Launched : 2013
JSM Environmental Science and Ecology
ISSN : 2333-7141
Launched : 2013
Journal of Cardiology and Clinical Research
ISSN : 2333-6676
Launched : 2013
JSM Nanotechnology and Nanomedicine
ISSN : 2334-1815
Launched : 2013
Journal of Ear, Nose and Throat Disorders
ISSN : 2475-9473
Launched : 2016
JSM Ophthalmology
ISSN : 2333-6447
Launched : 2013
Journal of Pharmacology and Clinical Toxicology
ISSN : 2333-7079
Launched : 2013
Annals of Psychiatry and Mental Health
ISSN : 2374-0124
Launched : 2013
Medical Journal of Obstetrics and Gynecology
ISSN : 2333-6439
Launched : 2013
Annals of Pediatrics and Child Health
ISSN : 2373-9312
Launched : 2013
JSM Clinical Pharmaceutics
ISSN : 2379-9498
Launched : 2014
JSM Foot and Ankle
ISSN : 2475-9112
Launched : 2016
JSM Alzheimer's Disease and Related Dementia
ISSN : 2378-9565
Launched : 2014
Journal of Addiction Medicine and Therapy
ISSN : 2333-665X
Launched : 2013
Journal of Veterinary Medicine and Research
ISSN : 2378-931X
Launched : 2013
Annals of Public Health and Research
ISSN : 2378-9328
Launched : 2014
Annals of Orthopedics and Rheumatology
ISSN : 2373-9290
Launched : 2013
Journal of Clinical Nephrology and Research
ISSN : 2379-0652
Launched : 2014
Annals of Community Medicine and Practice
ISSN : 2475-9465
Launched : 2014
Annals of Biometrics and Biostatistics
ISSN : 2374-0116
Launched : 2013
Journal of Cancer Biology and Research
ISSN : 2373-9436
Launched : 2013
Journal of Surgery and Transplantation Science
ISSN : 2379-0911
Launched : 2013
Journal of Dermatology and Clinical Research
ISSN : 2373-9371
Launched : 2013
JSM Gastroenterology and Hepatology
ISSN : 2373-9487
Launched : 2013
Annals of Nursing and Practice
ISSN : 2379-9501
Launched : 2014
JSM Dentistry
ISSN : 2333-7133
Launched : 2013
Author Information X