Loading

JSM Arthritis

Long Term Outcomes of Total Hip Replacement in Patients with Ankylosing Spondylitis

Research Article | Open Access | Volume 1 | Issue 3

  • 1. Section of Rheumatology. Instituto de Rehabilitación Psicofísica, Argentina
+ Show More - Show Less
Corresponding Authors
Gustavo Citera, Section of Rheumatology, Instituto de Rehabilitación Psicofísica. Echeverría 955 (zipcode1428), Buenos Aires, Argentina Tel: 541147888841; Fax:541147885552
Abstract

Background: Total hip replacement (THR) is a reliable therapeutic intervention for patients with severe hip involvement. The aim of our study was to determine the long term outcome and associated risk factors of THR in patients with Ankylosing Spondylitis (AS).

Materials and Methods: A cross sectional study was performed. Patients ≥ 18 years diagnosed with Ankylosing Spondylitis (AS) according to modified NY criteria from the ESPAXIA (Estudio de Espondiloartritis Axial IREP Argentina) cohort were included. Demographic, clinical and data related to THR were recorded. Pain, patient global assessment (VAS), disease activity (BASDAI), functional capacity (BASFI), enthesitis (MASES), axial mobility (BASMI) and radiological damage (mSASSS) were assessed. Hips functional capacity was evaluated by the Merle d`Aubigné and Postel method and pelvis x rays were taken to determine: presence of periprosthesic osteolysis of the femoral and acetabular components, fracture, luxation and heterotopic ossification (HO).

Results: 190 patients were evaluated and 25 (14,53%) underwent THR. 16 patients were included in the analysis. Nine (56,2%) had bilateral THR with a median time of THR`s evolution of 12,5 years (IQR 8.7-16.7). 25 prosthesis were evaluated. 3 (12%) prosthesis had surgery complications, 3 (12%) had revision surgery. Pain and functional capacity significantly improved after surgery (median VAS for pain previous to surgery was 10 cm (IQR 9.7-10) vs 0 cm (IQR 0-1.2) after surgery). Twenty twopelvis x-rays were taken, 15 prosthetis had heterotopic ossification, 15 femoral osteolysis, 11 acetabularosteolysis, 3 subluxation and 1 peri-prosthesis fracture. Younger age at disease onset was the main variable associated to THR in multivariate analysis [OR 0,91 (95% CI 0,85-0,97) p=0,001].

Conclusion: A substantial relief in pain and improvement of functional capacity were seen inASpatients who underwent THR. Younger age at disease onset was the only predictor associated to THR.

Keywords
  • Ankylosing spondylitis
  • Total hip replacement (THR)
Citation

Lizarraga A, Zamora N, Betancur G, Cayetti A, Schneeberger EE, et al. (2016) Long Term Outcomes of Total Hip Replacement in Patients with Ankylosing Spondylitis. JSM Arthritis 1(3): 1014.

INTRODUCTION

Ankylosing Spondylitis (AS) is a chronic inflammatory systemic disease that mainly affects the sacroiliac joints and spine [1]. Hip involvement is commonly observed, with a reported prevalence from 19 to 36% and it is associated with functional disability decreased quality of life and employability [2-6]. Younger age at disease onset, axial involvement and enthesitis are associated with severe hip disease [3]. Total hip replacement (THR) surgery is a reliable therapeutic intervention for patients with severe hip involvement. However surgery outcomes have beensubject of concern due to the high probability of ankylosis recurrence, mechanical failure and poor function [7]. Furthermore there are reports of a higher frequency of heterotopic ossification after THR in patients with AS [8]. Several studies have demonstrated that short and long term outcomes after THR in patients with AS are good, with long term survival of the prosthesis and low rates of complications and need of revision surgeries[6,7,9,10].

The aim of our study was to determine the associated risk factors and long term outcomes of THR in patients with AS.

MATERIAL AND METHODS

Patients equal or greater than 18 years old, belonging to the ESPAXIA (Estudio de Espondiloartritis Axial IREP Argentina) cohort with Ankylosing Spondylitis (AS) diagnosis according to modified New York `84 criteria were included in this cross sectional study. ESPAXIA is an observational prospective cohort of patients with axial spondyloarthritis from the Instituto de Rehabilitación Psicofísica in Buenos Aires. This ongoing cohort started in August 2008 and includes patients over 16 years of age fulfilling, New York `84 or ASAS axSpa criteria. At the time of this study the cohort included information of 190 patients who had annual schedule visits. Demographic data, disease duration, articular and extra articular manifestations, comorbidities and current treatment (usage of Non-steroidal anti-inflamatory drugs, analgesics, disease modifying antirheumatic drugs, anti-TNF therapy) were collected. Pain, patient global assessment by visual analog scale (VAS), enthesitis (MASES), functional capacity by Bath Ankylosing Spondylitis Functional Index (BASFI), disease activity by Bath Ankylosing Spondylitis Disease Index (BASDAI), axial mobility by Bath Ankylosing Spondylitis Metrology Index (BASMI), quality of life by Ankylosing Spondylitis Quality of Life (AsQoL) were assessed [11-14]. Radiological damage was evaluated using the modified Stoke Ankylosing Spondylitis Spine Score (mSASSS) by a single reader, who had previously shown an excellent intraobserver correlation (Kappa=0.86) [15].

Patients with AS and THR were identified and the following data were recorded: date of each total hip arthroplasty (right, left), type of prosthesis (cemented, cementless or hybrid), surgery complications, cause and number of revision surgeries. Actual hip pain by VAS and Steimbroker functional classes (Functional Class (FC) I: complete ability to carry out all usual duties without handicaps, FCII: adequate for normal activities despite handicap of discomfort or limited motion of one of the joints, FCIII: limited to little or none of the duties of usual occupation or selfcare and FCIV: incapacitated, largely or wholly bed ridden or confined to a wheelchair with little or no self care) were evaluated. As all the surgeries had already been performed, patients were asked to recall and rate the pain previous to the surgery by VAS (0-10 cm). Hips functional capacity was evaluated by Merle d´Aubigné and Postel method modified by Charnley [16]. This instrument evaluates pain, gait and mobility on a Likert scale from 1 to 6 for each item, where 1 indicates the worst and 6, the best state of the patient. The total score ranges from 3 to 18. In the modified version, the patients are also categorized by the alphabetical prefixes A: patient with one hip involved; B: patient with two hips involved and C: patient with systemic disease that interferes with normal gait.

Panoramic pelvic plain X-ray was performed on each patient, taking into account the following requirements: anteroposterior view with focus on the pubic area, and inclusion of both up to the distal part of the femoral shaft. We determine the presence of periprothesic osteolysis of the femoral and acetabular component. Acetabular osteolysis was defined as the appearance of a radiolucent zone in the pelvic area around the acetabulum and femoral osteolysis as the appearance of the same lesions in the femoral zone. The margins of each lesion had to be sufficiently clear as to be delineated with a pencil. In order to determine the location, the femoral component was divided into 7 zones (GruenZones) and the acetabular component into 3 according to De Lee and Charnley [17,18] (Figure 1)

 Radiologic osteolysis according to (A) Gruen zones and (B) De Lee  and Charnley zones

Figure 1 Radiologic osteolysis according to (A) Gruen zones and (B) De Lee and Charnley zones

. We also evaluated the presence of fracture, luxation and heterotopic ossification (HO) according to Brooker´s classification that categorized patients into 4 groups; group 1 when there are islands of bone within the soft tissue around the hip and group 4 when there is apparent bone ankylosis of the hip [19]. All radiographs were read by a single independent reader blinded to patient’s clinical data.

Statistical analysis

Descriptive statistics were refered as median and interquartile range (IQR) frequencies and percentages. Continuous variables were compared usingT test and Mann Whitney U test, according to distribution and categorical variables by Chi2 and Fisher’s exact test. Wilcoxon Sing Rank test was used to compare pain intensity before and after surgery. Multiple logistic regression analysis was performed to explore risk factors associated to THR (odds ratio (OR) and 95% confidence intervals (95% CI) were calculated).

RESULTS

190 patients from the ESPAXIA cohort were evaluated, 172 had AS and 25 of them (14,53 %) underwent THR.Sixteen patients were included in the analysis because 2 died and 7 were lost to follow-up. Nine (56,25%) had bilateral THR. Fifteen (93,8%) were males, with a median age of 45 years (IQR 35-44), median disease duration 28,5 years (IQR 18-35,25). Eleven (68,8%) were HLA-B27positive. Two (12.5%) patients had psoriasis and two (12.5%) Juvenile AS. The median time since THR was 12, 5 years (IQR 8.75-16.75). Demographic and clinical data are presented in (Table 1).

Table 1: Demographic and clinical features of 16 patientes with AS.

Variables

N=16

Male n (%)

15 (93.8)

Age years m (IQR)

45 (35-54)

Age at symptoms onset years m (IQR)

24 (16-36)

Disease duration years m (IQR)

28.5 (18-35.25)

Time since THR years m (IQR)

12.75 (8.45-15)

JuvenilAxSpA n (%)

2 (12.5)

HLA-B27 n (%)

11/16 (68.8)

BASDAIm (IQR)

3.95 (1.41-6.33)

BASFIm (IQR)

4.5 (2.84-7.75)

ASQoLm (IQR)

4.5 (1-9)

Bilateral THR n (%)

9/16 (56.25)

Merle d`Aubigné and Postel method m(IQR)

15.21 (13.5-17)

THR (total hip replacement), BASDAI (Bath Ankylosing Spondylitis Disease Index), BASFI (Bath Ankylosing Spondylitis Functional Index), ASQoL (Ankylosing Spondylitis Quality of Life)

Twenty five prosthesis were evaluated (14 right y 11 left). 12 (48%) were cemented and 13 (54%) were noncemented. Three (12%) prosthesishad surgery complications (1 had loosening, 1 luxationand 1 fracture), 3 (12 %) had revision surgery (2 aseptic loosening and 1 luxation). A significant relief in pain was observed after THR surgery. Median pain (VAS) previous to surgery was 10 cm (IQR 9.75-10) vs 0 cm (IQR 0-1.25) after surgery (p=0.001). There was also animprovement after the surgery in functional class. Previous to the surgery 6 patients (24%) were in functional class II, 16 (64%) in class III and 3 (12%) in class IV, while in the last visit 15 (60%) were in class II and 10 (40%) in class III. Median score of Merle d`Aubigné and Postel assessing functional status was 15, 21 (IQR 13,5-17). We evaluated 22 THR x rays. Eleven, (50%) prosthesis had acetabular osteolysis, 3 (13, 63%) subluxacion, 1 peri-prosthesis fracture, 15/17 (88,2 %) femoral osteolysis, and fifteen heterotopic ossification (4 grade I, 4 II, 6 III y 1 IV) (Figure 2).

Figure 2 Heterotopic Ossification: Brooker´s classification n= 15/22

Figure 2 Heterotopic Ossification: Brooker´s classification n= 15/22

THR was associated with longer disease duration (27,1 ± 10,6 vs 19,6 ± 13,4 years, p= 0,03), younger age at disease onset (17,4 ± 7,6 vs 26,2 ± 11, 9 years, p= 0,0001), lower MASES score (0,6 ± 1,2 vs 1,6 ± 2,3 p= 0,007) and with a higher frequency of biologic treatment (50% vs 23,6%, p=0,03) in the univariate analysis (Table 2).

Table 2: Comparison of sociodemographic and clinical variables between patients with and without THR.

Variable

Without THR n=174

With THR n=16

P

Disease duration years X (SD)

19.6 (13.4)

27.1 (10.6)

0.03

Age at symptoms onset X (SD)

26.2 (11.9)

17.4 (7.6)

0.021

MASES X (SD)

1.6 (2,3)

0.6 (1.2)

0.007

Biologic treatment n (%)

41 (23.6)

8 (50)

0.03

BASDAI X (SD)

4.3 (2.6)

3.9 (2.1)

0.07

BASFI X (SD)

3.8 ()2.8

4.6 (2.1)

0.085

ASQoL X (SD)

6.8 (4.9)

4.9 (4.2)

0.31

MASES (Maastricht Ankylosing Spondylitis Enthesitis Score), BASDAI (Bath Ankylosing Spondylitis Disease Index), BASFI (Bath Ankylosing Spondylitis Functional Index), ASQoL (Ankylosing Spondylitis Quality of Life)

In the multivariate analysis, the only variable independently associated with THR was younger age at disease onset. [OR 0,91 (95% CI: 0,85-0,97) p=0,001] (Table 3).

Table 3: Variables associated with THR.

Variable

β

Standard Error

P

OR

95 % CI

Inferior                  Superior

Positive Family History

0.292

0.585

0.617

1.339

0.426

4.213

Type of AxSpA

0.451

0.262

0.086

1.569

0.939

2.623

HLA-B27

-0.549

0.594

0.355

0.577

0.180

1.850

Enthesitis

-0.165

0.619

0.790

0.848

0.252

2.853

Age at symptoms onset

-0.091

0.033

0.006

0.913

0.856

0.974

AxSpA (Axial Spondyloarthritis)

 

DISCUSSION

In the present study 25 (14, 53%) of 172 patients with AS underwent THR and 56% of the patients included had bilateral hip replacement. The prevalence of THR in our cohort is slightly superior of that observed in the study of Vander Cruyssen et al., that included patients with AS from several countries (Belgium, Spain, Chile, Argentina, Venezuela, Costa Rica, Mexico, Peru, Ecuador and Uruguay). In this study 5 to 8% of the patients had THR and approximately half of the patients had both hips replaced [3]. This data shows the high probability of having a bilateral hip involvement in patients with AS.

We found a substantial relief in pain after the surgery and this is consistent with previous studies [6,7,9,10,20,21]. The functional capacity of the hip was evaluated according to the Merle d`Aubigné and Postel method. Although we were not able to use this instrument previous to the surgery to compare the later results, the median value observed in our patients indicate a good functional status after THR. Joshi et al., evaluated 180 patients that underwent hip replacement, 96% of them did not have pain, 65% had good to excellent function and 67% had excellent to good mobility [21]. Sweeney et al., also demonstrated that out of 340 patients with AS that underwent THR, 83% reported none/ mild pain, 52% good/very good movement and 58% high/very high success [6]. In another study, from 24 hips replaced, all improved function and flexion deformity was corrected [20].

Even thoughTHR surgery is a challenging procedure because patients with AS often have ankylosis of the spine and involvement of other joints and systems such as the pulmonary and cardiovascular, the rates of postoperative complications in our study was low. Other studies had reported complications in 19/181 hips replaced (10.5%) [21] and in 5/24 hips (20.8%), and the number of hips that had to be revised was only 3 (12 %), similar to previous studies [6,9,20,21]. Three prosthesis had surgical complications and revision was required only in the one that had loosening.

Active lifestyle and spinal stiffness of young patients with AS may be risk factors for increasing stress on the prostheses and thus resulting in early aseptic loosening, the main reason for a revision surgery in this patients [5]. In our study we found a high frequency of periprosthesic osteolysis, 50% had acetabular osteolysis (11/22 hips) and 88% (15/17 hips) femoral osteolysis. This values are higher than those published in the study of Sochart et al. [7]. This difference may be explained by a more strict criteria of periprosthetic osteolysis used in their study. In a previous study done in our hospital evaluating the prevalence of periprosthetic osteolysis after THR in patients with rheumatic diseases we found that 11 out of 17 hips of patients with AS, had periprosthetic osteolysis [22].

Patients with ankylosing spondylitis have an increased prevalence of heterotopic ossification (HO) compared with the general population [8], possible leading to increase pain, reduce mobility and function of the hip replaced [6,9]. In the study of Sochart et al., in patients with AS and THR, they found 6 hips (14%) with heterotopic ossification grade I or II [7]. Goodman et al, reported in 3 of 17 radiographs the presence of bone formation after THR in patients with AS, being two of them grade IV of the Brooker classification [10]. In our study, we found a high frequency of HO, in 15 of 22 hips evaluatedalthough it should be noted that the functional capacity of the hips remained good in most of the patients. We were not able to recall if the patients had additional risk factors for HO like multiple operations of the hips, the surgical approach used or if prophylaxis for HO with non steroidal anti inflammatory drugs or perioperative radiation therapy was given.

Early onset of disease, axial and enthesal involvement are associated with hip replacement surgery in AS [3]. In our study younger age at disease onset was the only predictor associated to THR. This may be explained because juvenile AS cases are more prone to have peripheral joint involvement, both at presentation and during the disease course, while adult AS onset cases are more likely to present with axial disease [23].

Limitations of our study were that ESPAXIA is not an inception cohort, therefore most of the data collected were retrospective, not being able to analyse specific recall data previous to the surgery. A recall bias of pain before the surgery must also be contemplated. Radiographs were evaluated by a single observer, and we had missing radiographs of some patients to assess the mSASSS. Besides, it is also important to remark a probably selection bias in our study because 36% of patients with THR from our cohort were lost follow up.

In conclusion, a substantial relief in pain and improvement of functional capacity were seen inASpatients who underwent THR. Younger age at disease onset was the only predictor associated to THR.

REFERENCES

1. Maldonado Cocco J, Citera G. Reumatologia Segunda Edición. Ediciones Azzurras. Capítulo 32. 2012. 440-459.

2. Vander Cruyssen B, Vastesaeger N, Collantes-Estéves E. Hip disease in ankylosing spondylitis. Curr Opin Rheumatol. 2013; 25: 448-54.

3. Vander Cruyssen B, Muñoz Gomariz E, Font P, Mulero J, de Vlam K, Boonen A, et al. Hip involvement in ankylosing spondylitis: epidemiology and risk factors associated with hip replacement surgery. Rheumatology. 2010; 49: 73-81.

4. Zhao J, Zheng W, Zhang C, Li J, Liu D, Xu W. Radiographic hip involvement in ankylosing spondylitis: factors associated with severe hip diseases. J Rheumatol. 2015; 42: 106-10.

5. Guan M, Wang J, Zhao L, Xiao J, Li Z, Shi Z. Management of hip involvement in ankylosing spondylitis. Clin Rheumatol. 2013; 32: 1115-20.

6. Sweeney S, Gupta R, Taylor G, Calin A. Total hip arthroplasty in ankylosing spondylitis: outcome in 340 patients. J Rheumatol. 2001; 28: 1862-6.

7. Sochart DH, Porter ML. Long-term results of total hip replacement in young patients who had ankylosing spondylitis. Eighteen to thirty-year results with survivorship analysis. J Bone Joint Surg Am. 1997; 79:1181-1190.

8. Iorio R, Healy WL. Heterotopic ossification after hip and knee arthroplasty: risk factors, prevention, and treatment. J Am Acad Orthop Surg. 2002; 10: 409-16.

9. Calin A, Elswood J. The outcome of 138 total hip replacements and 12 revisions in ankylosing spondylitis: high success rate after a mean followup of 7.5 years. J Rheumatol. 1989; 16: 955-8.

10. Goodman SM, Zhu R, Figgie MP, Huang WT, Mandl LA. Short-term total hip replacement outcomes in ankylosing spondylitis. J Clin Rheumatol. 2014; 20: 363-8.

11. Calin A, Garrett S, Whitelock H, Kennedy LG, O´Hea J, Mallorie P, et al. A new approach to defining functional ability in ankylosing spondylitis: the development of the Bath Ankylosing Spondylitis Functional Index. J Rheumatol. 1994; 21: 2281-2285.

12. Garret S, Jenkinson T, Kennedy LG, Whitelock H, Gaisford P, Calin A. A new approach to defining disease status in ankylosing spondylitis: The Bath Ankylosing Spondylitis Disease Activity Index. J Rheumatol. 1994; 21: 2286-2291.

13. Jenkinson TR, Mallorie PA, Whitelock HC, Kennedy LG, Garrett SL, Calin A. Defining spinal mobility in ankylosing spondylitis (AS). The Bath AS Metrology Index. J Rheumatol. 1994; 21: 1694-8.

14. Doward LC, Spoorenberg A, Cook SA, Whalley D, Helliwell PS, Kay LJ, et al. Development of the ASQoL: a quality of life instrument specific to ankylosing spondylitis. Ann Rheum Dis. 2003; 62: 20-26.

15. Creemers MC, Franssen MJ, van’t Hof MA, Gribnau FW, van de Putte LB, van Riel PL. Assessment of outcome in ankylosing spondylitis: an extended radiographic scoring system. Ann Rheum Dis. 2005; 64: 127-129.

16. Ugino FK, Righetti CM, Alves DP, Guimaraes RP, Honda EK, Ono NK. Evaluation of the reliability of the modified Merle d´Aubigné and Postel Method. Acta Ortop Bras. 2012; 20: 213-7.

17. Gruen TA, McNeice GM, Amstutz HC. “Modes of failure” of cemented stem-type femoral components: a radiographic analysis of loosening. Clin Orthop Relat Res. 1979; 17-27.

18. DeLee JG, Charnley J. Radiological demarcation of cemented sockets in total hip replacement. Clin Orthop Relat Res. 1976; 20-32.

19. Brooker AF, Bowerman JW, Robinson RA, Riley LH Jr. Ectopic ossification following total hip replacement. Incidence and a method of classification. J Bone Joint Surg Am. 1973; 55: 1629-1632.

20. Bangjian H, Peijian T, Ju L. Bilateral synchronous total hip arthroplasty for ankylosed hips. Int Orthop. 2012; 36: 697-701.

21. Joshi AB, Markovic L, Hardinge K, Murphy JC. Total hip arthroplasty in ankylosing spondylitis: an analysis of 181 hips. J Arthroplasty. 2002; 17: 427-33.

22. Pérez Alamino R, Casellini C, Baños A, Schneeberger EE, Gagliardi SA, Maldonado Cocco JA, et al. Prevalence of periprosthetic osteolysis after total hip replacement in patients with rheumatic diseases. Open Access Rheumatology: Research and Reviews. 2012; 4:1-6.

23. Jadon DR, Shaddick G, Jobling A, Ramanan AV, Sengupta R. Clinical outcomes and progression to orthopedic surgery in juvenile- versus adult-onset ankylosing spondylitis. Arthritis Care Res (Hoboken). 2015; 651-657.

Lizarraga A, Zamora N, Betancur G, Cayetti A, Schneeberger EE, et al. (2016) Long Term Outcomes of Total Hip Replacement in Patients with Ankylosing Spondylitis. JSM Arthritis 1(3): 1014.

Received : 27 Jun 2016
Accepted : 05 Sep 2016
Published : 07 Sep 2016
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 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
JSM Clinical Case Reports
ISSN : 2373-9819
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