Loading

Annals of Orthopedics and Rheumatology

Clinical Outcome of Minimally Invasive Repair of Pars Defect Using Percutaneous Pedicle Screws and Hook-Rod System in Adults with Lumbar Spondylolysis

Research Article | Open Access

  • 1. Department of Orthopedics, University of Tokushima, Japan
+ Show More - Show Less
Corresponding Authors
Koichi Sairyo, Department of Orthopedics,University of Tokushima, Tokushima, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan,
Abstract

Various techniques to directly repair a pars defect have been described. The aim of these procedures is to restore normal lumbar kinesiology, preserve a spinal motion segment and retain the associated spinal mobility. We have already reported a minimally invasive technique for the direct repair of a pars defect using a percutaneous pedicle screw system. This time, we report the clinical outcome obtained with this procedure. In all patients, both the Japanese Orthopedic Association score and pain assessed using a visual analogue scale improved postoperatively. Bony union was attained in 80% of the patients. Using this procedure, normalization of the lumbar kinesiology in terms of the instantaneous axis of rotation during lumbar extension/ flexion was attained. Also, it was possible to preserve the spinal motion segment and to retain lumbar spine mobility.

Keywords

Spondylolysis, Pedicle screw, Pars defect, Lumbar spine

Citation

Takata Y, Sakai T, Tezuka F, Goda Y, Higashino K, et al. (2014) Clinical Outcome of Minimally Invasive Repair of Pars Defect Using Percutaneous Pedicle Screws and Hook-Rod System in Adults with Lumbar Spondylolysis. Ann Orthop Rheumatol 2(2): 1013

INTRODUCTION

The incidence of lumbar spondylolysis (pars defect) has been estimated to be approximately 6% in the general population [1]. Regarding surgical treatment, various techniques to directly repair the pars defect have been described [2–10]. These techniques include bone grafting with the placement of wire, screws, or hook-screw constructs to stabilize the fractured pars. The aim of these procedures is to restore normal lumbar kinesiology, preserve a spinal motion segment and retain the associated spinal mobility. Most of them require large skin incisions and they injure par vertebral muscles (PVM) during the exposure. Recently, minimally invasive surgery (MIS) has been proposed as an alternative to these classical procedures. First, in order to resolve these problems, we developed an endoscopic direct repair of the pars using a modification of the classical Buck’s procedure [11]. Although the damage of PVM was reduced, the procedure had the following shortcomings: (1) it was not applicable in patients with a thin lamina, (2) screws themselves limited the size of the graft bone mass, (3) it took a long operation time due to the difficulty of the technique. Then, since 2006, we started to employ applied a pedicle screw-hookrod (PSHR) method using a percutaneous pedicle screw system to reduce the damage of PVM. The preliminary report on this technique has been published [12]. In this paper, we report the clinical outcome we obtained with this MIS-PSHR procedure.

MATERIALS AND METHODS

 

Patients

Ten patients (8 men, 2 women) with bilateral L5 spondylolysis were treated using our MIS-PSHR method (Table 1). Their mean age was 32.8 (range: 23-53) years. None of the patients had responded to conservative treatment for at least six months. Preoperatively all patients were confirmed the relief of their daily low back pain (LBP) after lido canine infiltration of the pars defects.

Surgical procedure

The details of the surgical procedure have been reported elsewhere [12]. After making a 3-4 cm midline incision, the par vertebral muscles are separated from the lamina. Then, the defect is confirmed, and the fibro cartilage mass is removed from the defect. In the cases with LBP as well as leg pain due to the ragged edge around the pars defect, the ragged edge is respected to decompress the L5 nerve root (Case 3-6,8,9). Next, pedicle screws are inserted through 2-cm longitudinal incisions on both sides, 5 cm laterally from the midline incision. Prior to screwing, chancellor’s bone is harvested through the same lateral incision using a bone harvester. As the iliac crest is located close to the point of pedicle screwing, we can use the same lateral incisions. After the 2 screws are inserted, hooks are inserted into the caudal lamina and rods are inserted into the hole of the pedicle screws. Finally, the bone grafts are packed onto the defects.

Clinical assessments

All patients were evaluated using the Japanese Orthopedic Association (JOA) score, visual analogue scale (VAS) for low back pain and leg pain, operation time, intra operative blood loss, and complications.

Radiographic measurements

Bony union was confirmed by multi detector computed tomography (CT). From the lateral dynamic radiographs of the lumbar spine obtained pre- and post-operatively, inter vertebral motion of L5-S1, % slip of L5-S1, and instantaneous axis of rotation (IAR) were measured (Figure 1) [13].

RESULTS

The mean operation time was 278 (range, 205 to 326) minutes and the mean intra operative blood loss was 301 (range, 250 to 350) mL. There were no wound infections or neurologic complications. No hardware breakage or loosening was observed.

The results are summarized in Table 1. The mean postoperative follow-up was 16.1 (range: 12-25) months. Preoperative JOA score ranged from 4 to 20 (mean 15.8 points). Postoperative JOA scores of all patients ranged from 14 to 29 (mean, 26.4 points) were improved. The preoperative assessment of pain using a visual analogue scale (VAS) ranged from 50 to 100 (mean, 75.8 points) and greatly improved postoperatively (0 to 15; mean, 2.5 points). Multi-detector CT in eight patients except for Case 3 and Case 7 confirmed bony fusion.

Radiographic measurements were performed in eight patients except for Case 3 and Case 10 (Table 2). In Case 3, no postoperative lateral dynamic radiographs of the lumbar spine were obtained. Case 10 had lumbar scoliosis as well as spondylolysis, and a correct evaluation was impossible. After the direct repair, L5-S1 inters vertebral motions decreased in all patients except for Case 4. The L5-S1 slip at maximum lumbar flexion decreased in all patients except for Case 7. Location of the instantaneous axis of rotation of L5-S1 moved poster caudally in all patients except for Case 7.

Table 1: Clinical results after direct repair of a pars defect using our percutaneous pedicle screw and hook-rod system.

No. Sex Age Follow-up
(months)
Op. time 
(minutes)
Blood loss 
(mL)
VAS (LBP) 
Pre-op.
VAS (LBP) Post-op. VAS 
(leg pain) 
Pre-op.
VAS 
(leg pain) 
Post-op.
JOA score 
Pre-op.
JOA score 
Pre-op.
1 male 32 18 281 300 100 0 0 0 15 29
2 male 23 20 284 280 100 0 0 0 20 27
3 male 35 15 326 350 70 0 0 0 18 29
4 male 35 25 301 332 83 0 60 0 4 26
5 male 31 14 309 300 50 0 70 0 16 28
6 male 53 13 294 250 80 0 82 0 19 28
7 female 34 16 267 25 70 15 0 0 11 14
8 male 31 16 241 350 100 10 85 10 17 27
9 male 25 12 269 350 50 0 40 10 19 28
10 female 33 12 205 250 55 0 0 0 19 28

Table 2: Radiographic results of direct repair of a pars defect using our percutaneous pedicle screw and hook-rod system.

  L5-S1 intervertabral motion (degree) L5-S1% slip (%) location of IAR of L5-S1
No. Pre-op. Post-op. Pre-op. Post-op. Pre-op. Post-op.
1 15.6 6.3 14.2 6.3 AD PD
2 11.9 11.2 0 0 AR PR
3 NA NA NA NA NA NA
4 4.3 5 12.8 10.5 AR PC
5 11.8 5.1 6 4.2 AR PR
6 10.7 2.3 9.4 75 PR PD
7 9.8 2.1 14.1 16.3 AD PR
8 9.4 4.9 12.4 11.8 AR PD
9 13.5 5.9 17.7 16.1 PC PC
10 NA NA NA NA NA NA

 

REPRESENTATIVE CASE

A 33-year-old woman with a 2-year history of low back pain. She had no leg pain. Tenderness at the spinous process of L5 was apparent. The radio graphical examination revealed bilateral pars defects at L5, which was in the pseudoarthrosis stage. Additionally, grade 1 spondylolisthesis according to Meyer ding’s classification, and scoliosis were found (Figure 2). Her daily LBP was verified to be transiently relieved by local anesthetic injection into the bilateral pars defects. Her preoperative JOA score was 19/29 points, and her VAS of LBP was 55/100 points.

She underwent the direct repair using MIS-PSHR (Figure 3). We found synovial tissue (usually described as fibro cartilage mass in the literature) in the pars defect. The pathological examination showed synovial lining cells and a loose fibrous mass (Figure 4). Immediately after the operation, she experienced relief of LBP. About 2 months later, the postoperative JOA score had improved to 27 points, and VAS assessment of LBP had decreased to 10 points. Twelve months later her JOA score was 28 points, and VAS assessment of LBP indicated complete relief (VAS: 0/100 points).

DISCUSSION

Various techniques for repairing lumbar spondylolysis have been described, including bone grafting with the placement of wire, screws, or hook-screws across the pars [2–10] . Kimura was the first to describe a method for direct repair of the pars defect in Japanese literature; he used bone graft and postoperative plaster immobilization [14]. Thereafter, Buck introduced another method for direct repair that employed internal fixation [2]. His method was based on screwing to secure the floating lamina to the pedicle. Nicol and Scott proposed the use of a tension-band wire around the transverse process and spinous process to secure fixation and healing of the defects [7]. Morscher et al introduced a hook screw for the fixation of pars defects. [15] Taddonio et al first introduced segmental pedicle screw hook fixation. The biomechanical comparison of fixation techniques carried out by Deguchi et al demonstrated the pedicle screw hook device was one of the most rigid systems [16]. However, these procedures required bilateral exposure of the posterior structures down to the base of the transverse processes. They obviously caused more iatrogenic damage to the soft tissues. Thus, large soft tissue damage should be prevented using minimally invasive techniques. Therefore, we adapted minimally invasive surgical (MIS) techniques to these procedures. The principles of our procedure are similar to those reported by Tokuhashi and Kakiuchi [6,17]. However, the development of devices that allows percutaneous pedicle screwing, the setting method of the rod and hook, and bone harvester has enabled us to perform direct repair more easily than previously reported.

The aim of our procedures was to restore normal lumbar kinesiology, preserve the spinal motion segment and retain lumbar spine mobility. In the present study, the motion preservation of L5-S1 was achieved and L5-S1 slip was slightly reduced in all evaluated patients. Location of the IAR of L5- S1 moved postero-caudally in all patients except for Case 7. It correlated with the clinical result, because in Case 7 LBP did not alleviate completely (postoperative JOA score: 14/29, postoperative VAS, 15/100 points). The IAR of the lumbar spine has been reported to be located around the disc when the disc is normal Sakamaki et al [18–22] . reported that the IAR of the spondylolytic spine deviated cranially [13]. Actually, in the present study, in all but one patient, the IAR moved posteriorcaudally after the operation. These results suggested that the normal kinematics had been restored.

For this procedure to be successful, the pain source must be the pars defect itself. In all our patients we preoperatively verified that their pain disappeared after injection of an anesthetic into the defects. Bradford and Iza recommended anesthetic injection into the defect and disc to localize the pain source [23]. Such reported the value of pars infiltration as a prognostic test of surgical outcome [10] Wu et al. performed direct repair in 93 patients who had experienced pain relief after pars injection and whose bone scan was negative [24]. They achieved excellent or good results in 91% of the patients after 30 months on average. Kakiuchi operated on 16 patients who had temporary pain relief after local infiltration of an anesthetic [6]. The rate of excellent results after 25 months in his series was 88%. Therefore, we do not recommend the direct repair for patients whose pain does not alleviate after local injection of an anesthetic. In such case, other causes of low back pain should be searched.

The bony-healing rate varies among reports and procedures. It is difficult to correctly assess bony healing after direct repair from plain X-ray findings. A fissure-like pseudoarthrosis may remain undiscovered. In addition, metal implants obscure the vision. The findings previously reported in the literature regarding bony healing should be judged taking into consideration that they were obtained based only on plain X-ray films. Pai and Hodgson compared the status of bony union seen on plain X-ray films and on CT scans following Scott procedure and van Dam modification of the Scott procedure, their results showed a very different union rate (90% versus 50%) [25]. Our results assessed by multi-detector 3-dimensional CT showed a bony union rate of 80%. Recently, bone morphogenetic proteins (BMPs), which are a group of secreted growth factors that belong to the transforming growth factor-beta super family, were used to create a solid lumbar spinal fusion [26,27]. Recombinant BMP proteins, rhBMP-2 and rhBMP-7 (OP-1), have been successfully used in preclinical and clinical trials and are commercially available for clinical applications. These BMPs will probably be used in the future to improve the bony union rate of the pars defects.

However, it should be noted that the non-union detected by CT did not affect the clinical results, indicating that bony fusion was not required to achieve good clinical results. Our patients experienced immediate LBP relief after the operation, which showed that there was little association between bony healing and clinical results.

There has been controversy concerning the relationship between pars defect and LBP. Eisenstein et al showed that there were neural elements in the spondylolytic tissue with the potential to act as nociceptors [28], and Hasegawa et al confirmed the presence of nociceptive free nerve endings [17]. Whereas, Miyauchi et al reported that the spondylolytict issue itself was not innervated [29]. We speculate that the pain of spondylolysis is due to synovitis in a pars defect communicated with the adjacent facet joint: the pain in terminal-stage spondylolysis may be caused by synovitis derived from the adjacent facet joint. In fact, all the patients reported in this study had communications with the adjacent facet joints, and synovial tissue was found in the pars defects. In addition, regardless of whether the bony union was obtained or not, all our patients experienced immediate pain relief after the operation. Shipley et al explained the origin of pain in a similar way as us [30]. They concluded that most patients of spondylolysis requiring surgical treatment present a synovial pseudoarthrosis in the pars interarticularis, which communicates with the adjacent superior facet. Additionally, they suggested that synovial fluid might prevent healing and lead to persistent synovial pseudoarthrosis. However, this theory is difficult to prove because it is almost impossile for us to obtain radio graphical and pathological findings from asymptomatic patients. Further research on this aspect will be required in the future.

CONCLUSION

All our adult patients operated on employing the minimally invasive technique for lumbar spondylolysis using a percutaneous pedicle screw and hook-rod system had clinically good results. The bony union rate was 80%. Normalization of the lumbar kinesiology, in terms of the instantaneous axis of rotation during the lumbar extension/flexion motion, was attained. Moreover, the spinal motion segment was preserved and lumbar spine mobility was retained.

REFERENCES

1. Sakai T, Sairyo K, Takao S, Nishitani H, Yasui N. Incidence of lumbar spondylolysis in the general population in Japan based on multidetector computed tomography scans from two thousand subjects. Spine (Phila Pa 1976). 2009; 34: 2346-2350.

2. Buck JE. Direct repair of the defect in spondylolisthesis. Preliminary report. J Bone Joint Surg Br. 1970; 52: 432-437.

3. Hefti F, Seelig W, Morscher E. Repair of lumbar spondylolysis with a hook-screw. Int. Orthop. 1992; 16: 81–85

4. Ivanic GM, Pink TP, Achatz W, Ward JC, Homann NC, May M, et al. Direct stabilization of lumbar spondylolysis with a hook screw: mean 11-year follow-up period for 113 patients. Spine (Phila Pa 1976). 2003; 28: 255-259.

5. Johnson GV, Thompson AG. The Scott wiring technique for direct repair of lumbar spondylolysis. J Bone Joint Surg Br. 1992; 74: 426- 430.

6. Kakiuchi M. Repair of the defect in spondylolysis. Durable fixation with pedicle screws and laminar hooks. J Bone Joint Surg Am. 1997; 79: 818-825.

7. Nico RO, Scott JH . Lytic spondylolysis. Repair by wiring. Spine (Phila Pa 1976). 1986; 11: 1027-1030. 

8. Pedersen AK, Hagen R. Spondylolysis and spondylolisthesis. Treatment by internal fixation and bone-grafting of the defect. J Bone Joint Surg Am. 1988; 70: 15-24.

9. JHS S. The Edinburgh repair of isthmic (group II) spondylolysis. J Bone Jt. Surg Br 1987; 69:491

10. Suh PB, Esses S, Kostuik JP. Repair of pars interarticularis defect. The prognostic value of pars infiltration. Spine (Phila Pa 1976). 1991; 16: S445-448.

11. Higashino K, Sairyo K, Katoh S, Sakai T, Kosaka H, Yasui N. Minimally invasive technique for direct repair of the pars defects in young adults using a spinal endoscope: a technical note. Minim Invasive Neurosurg. 2007; 50: 182-186.

12. Sairyo K, Sakai T, Yasui N. Minimally invasive technique for direct repair of pars interarticularis defects in adults using a percutaneous pedicle screw and hook-rod system. J Neurosurg Spine. 2009; 10: 492- 495.

13. Sakamaki T, Katoh S, Sairyo K. Normal and spondylolytic pediatric spine movements with reference to instantaneous axis of rotation. Spine (Phila Pa 1976). 2002; 27: 141-145.

14. Kimura M. [My method of filing the lesion with spongy bone in spondylolysis and spondylolistesis]. Seikei Geka. 1968; 19: 285-296.

15. Morscher E, Gerber B, Fasel J. Surgical treatment of spondylolisthesis by bone grafting and direct stabilization of spondylolysis by means of a hook screw. Arch Orthop Trauma Surg. 1984; 103: 175-178.

16. Deguchi M, Rapoff AJ, Zdeblick TA. Biomechanical comparison of spondylolysis fixation techniques. Spine (Phila Pa 1976). 1999; 24: 328-333. .

17. Tokuhashi Y, Matsuzaki H. Repair of defects in spondylolysis by segmental pedicular screw hook fixation. A preliminary report. Spine (Phila Pa 1976). 1996; 21: 2041-2045.

18.Gertzbein SD, Seligman J, Holtby R, Chan KH, Kapasouri A, Tile M, et al. Centrode patterns and segmental instability in degenerative disc disease. Spine (Phila Pa 1976). 1985; 10: 257-261.

19. Pearcy MJ, Bogduk N. Instantaneous axes of rotation of the lumbar intervertebral joints. Spine (Phila Pa 1976). 1988; 13: 1033-1041.

20. Pennal GF, Conn GS, McDonald G, Dale G, Garside H. Motion studies of the lumbar spine: a preliminary report. J Bone Joint Surg Br. 1972; 54: 442-452.

21. Penning L, Blickman JR. Instability in lumbar spondylolisthesis: a radiologic study of several concepts. AJR Am J Roentgenol. 1980; 134: 293-301.

22. Yoshioka T, Tsuji H, Hirano N, Sainoh S. Motion characteristic of the normal lumbar spine in young adults: instantaneous axis of rotation and vertebral center motion analyses. J Spinal Disord. 1990; 3: 103- 113.

23. Bradford DS, Iza J. Repair of the defect in spondylolysis or minimal degrees of spondylolisthesis by segmental wire fixation and bone grafting. Spine (Phila Pa 1976). 1985; 10: 673-679.

24. Wu SS, Lee CH, Chen PQ. Operative repair of symptomatic spondylolysis following a positive response to diagnostic pars injection. J Spinal Disord. 1999; 12: 10-16.

25. Pai VS, Hodgson B. ssessment of bony union following surgical stabilisation for lumbar spondylolysis: a comparative study between radiography and computed tomography. J Orthop Surg (Hong Kong). 2006; 14: 17-20.

26. Boden SD, Kang J, Sandhu H, Heller JG. Use of recombinant human bone morphogenetic protein-2 to achieve posterolateral lumbar spine fusion in humans: a prospective, randomized clinical pilot trial: 2002 Volvo Award in clinical studies. Spine (Phila Pa 1976). 2002; 27: 2662- 2673.

27. Rihn JA, Gates C, Glassman SD, Phillips FM, Schwender JD, Albert TJ. The use of bone morphogenetic protein in lumbar spine surgery. Instr Course Lect. 2009; 58: 677-688.

28. Eisenstein SM, Ashton IK, Roberts S, Darby AJ, Kanse P, Menage J, et al. Innervation of the spondylolysis “ligament”. Spine (Phila Pa 1976). 1994; 19: 912-916.

29. Miyauchi A, Baba I, Sumida T, Manabe H, Hayashi Y, Ochi M. Relationship between the histological findings of spondylolytic tissue, instability of the loose lamina, and low back pain. Spine (Phila Pa 1976). 2008; 33: 687-693.

30. Shipley JA, Beukes CA. The nature of the spondylolytic defect. Demonstration of a communicating synovial pseudarthrosis in the pars interarticularis. J Bone Joint Surg Br. 1998; 80: 662-664

Received : 05 Mar 2014
Accepted : 01 May 2014
Published : 05 May 2014
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
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