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102
Elif Umay Altas* 0002 4877 5871
Ayhan Askin
Aliye Tosun *0003 2827 6255
1 M.D., Department of Physical Medicine and Reha-
bilitaon, Kap Celebi University Ataturk Educaon
and Research Hospital, Izmir, Turkey
Correspondence: Elif Umay Altas, MD.
Department of Physical Medicine and Rehabilitaon,
Kap Celebi University Ataturk Educaon and Rese-
arch Hospital, 35360, Izmir, Turkey
E-mail: elifumayaslan@hotmail.com
Abstract
Objecves: We aimed to assess the ecacy of hyper-
tonic dextrose injecon (prolotherapy; PT) in the tre-
atment of paents with plantar fasciis (PFs).
Material and methods: In this single-blind, randomi-
zed, controlled study, 30 PFs paents were randomly
assigned into 2 groups. Group 1 (PT group) received
3 injecons of 3 ml 15% dextrose into plantar fascia
at an interval of 3 weeks and PFs exercise treatment;
meanwhile Group 2 (control group) received 3 in-
jecons of 3 ml saline and PFs exercise treatment.
Clinical assessments included measurement of pain
intensity (VAS score), foot funcon index (FFI), Roles-
Moudsley Scoring, and American Orthopedic Foot
and Ankle Society (AOFAS) ankle-hindfoot scores. As-
sessments were performed before the rst and aer
the last injecons. All paents completed the study
without any complicaon.
Results: Signicant improvements were observed in
post-treatment VAS, FFI, AOFAS (pain, funcon, total)
and Roles-Moudsley scores in both groups, however
VAS, FFI and Roles-Moudsley score improvements
were greater in the PT group when compared with
the control group (p<0.001).
Conclusion: PT improved pain and funconal outco-
mes, and seems to be eecve in the treatment of
PFs. Further studies including larger number of pa-
ents and longer follow-up periods are needed to va-
lidate these results.
Keywords: Plantar fasciis, dextrose, prolotherapy,
saline
Öz
Amaç: Plantar fasiitli (PF) hastalarda hipertonik deks-
troz enjeksiyonunun (proloterapi; PT) etkinliğini de-
ğerlendirmeyi amaçladık.
Materyal Metod: Değerlendiricinin kör olduğu ran-
domize kontrollü olarak tasarlanan bu çalışmada
PFs tanılı 30 hasta 2 gruba ayrıldı. 1. Gruba (PT grup)
%15’lik dextroz PT ve egzersiz, 2.gruba(kontrol grup)
salin enjeksiyonu ve egzersiz verildi. Enjeksiyonlar
3’er haa arayla 3 kez yapıldı. Klinik değerlendirmede
ağrı yoğunluğu (VAS skoru), ayak fonksiyon indeksi
(FFI), Roles-Moudsley skorlaması, Amerikan orto-
pedik ayak ve ayak bileği topluluğu ayak bileği arka
ayak skoru (AOFAS) kullanıldı. Değerlendirmeler ilk
KLİNİK ÇALIŞMA / CLINICAL TRIAL
Is hypertonic dextrose injecon eecve in the tre-
atment of plantar fasciis: A clinical randomized
study
Plantar fasiit tedavisinde hipertonik dekstroz en-
jeksiyonu etkili midir: Klinik randomize çalışma
Geliş Tarihi: 01/08/2018
Kabul Tarihi: 27/09/2018
Ege Klin Tıp Derg 2018; 56 (3): 102-108
103
enjeksiyon öncesi ve son enjeksiyonlardan sonra ger-
çekleşrildi. Tüm hastalar herhangi bir komplikasyon
olmaksızın çalışmayı tamamladı.
Bulgular: Her iki grupta da tedavi sonrası VAS, FFI,
AOFAS (pain, funcon, total) ve Roles-Moudsley skor-
larında anlamlı düzelme oldu. Ancak kontrol grubuna
göre VAS, FFI ve Roles-Moudsley skorundaki iyileş-
meler PT grubunda daha fazlaydı (p <0.001).
Sonuç: PFs tedavisinde PT, ağrı ve fonksiyonel so-
nuçlar üzerine etkili bir yöntem olmakla birlikte, bu
sonuçları doğrulamak için daha fazla sayıda hasta ve
uzun takip süreleri de dahil olmak üzere daha ileri ça-
lışmalara ihyaç vardır.
Anahtar Kelimeler: Plantar fasiit, dextroz, prolotera-
pi, salin
1. Introducon
Plantar fasciis (PFs) is a degenerave syndrome in
which repeang microtraumas cause tracon perios-
s on central band’s inseron point of plantar fascia
and microtears [1]. As a result, a sharp pain develops
just below the heel or on medial collateral tubercle
which increases by pressure. Some addional comp-
laints also include snging and intense pain that radi-
ates below the heel towards lower leg. This condion
might aect the mobility and movement capability of
the paent signicantly [2].
Since PFs is a self-liming clinical condion, most of
the paents show improvement with a conservave
treatment [3]. The paents who do not show impro-
vement with conservave measures such as stretc-
hing, orthoses, physical therapy, nighme splints
and immobilizaon might be treated with alternave
methods such as extracorporeal shock wave therapy
(ESWT), steroid injecons, prolotherapy, platelet-rich
plasma (PRP) injecons and in most severe cases,
surgery [4].
Hypertonic dextrose injecon (prolotherapy) is a
method in which an irritant soluon is injected to the
damaged ligament or tendon structures in order to
increase the new cell proliferaon on those structu-
res, therefore strengthening them [5, 6]. The main
goal of prolotherapy (PT) is to strengthen bro-osse-
ous inseron points of ligaments, tendons and joint
capsules by creang a ght and thick brous ssue
[7]. PT is thought to create a curave cascade by ca-
using a therapeuc trauma, characterized by increa-
sing cellular stress on the weakened ligament or ten-
don area and causing mild inammaon on injecon
site. This cascade includes granulaon ssue forma-
on, matrix formaon and remodeling of the ssue
[8, 9]. Macrophages clean out dead cells and fore-
ign materials by phagocytosis meanwhile broblasts
help new cell producon and development in addi-
on to collagen synthesis by increasing DNA synthe-
sis and protein by growth factor exposure. New cells
and matrix stack up with organizaon in the aected
area. Remodeling occurs weeks later. Contemporary
theory says that PT mimics the natural healing pro-
cess of the body [10-12].
PT was rst standardized by Hacke in 1950’s, and
hypertonic dextrose in addion to morrhuate sodium
is the most commonly used soluon today [13, 14].
Although its indicaon is usually reported as chronic
back pain, some studies reported successful results
when used in the treatment of thoracic and cervical
pain syndromes, whiplash injuries, lateral and medial
epicondylis, rotator cu or bicipital tendinosis, PFs,
coccygodynia and osteoarthris [15]. When all evi-
dence-based studies on PT were reviewed, evidence
level was classied as A in lateral epicondylis [13],
and B in Achilles’ tendinopathy [16], PFs [17] and os-
teoarthris [18].
To our knowledge, only two studies evaluated the ef-
cacy of PT in paents with PFs in English literature.
Ryan et al reported a good clinical response to dext-
rose injecons in 20 paents with PFs [17]. Kim et
al compared the ecacy of PT versus PRP on 20 PFs
paents, and reported that both treatments seemed
to be eecve, however PRP led to a beer inial
improvement in funcon [19]. In this study, our
main objecve is to assess the ecacy of PT treat-
ment on pain and funconal status in paents with
PFs.
2. Material and Methods
Our study design was designed as a prospecve,
single-blind, randomized, controlled study. All par-
cipants were informed about the study and their
informed consents were obtained. Ethical approval
was obtained from our hospital’s local ethics com-
miee.
2.1.Parcipants
Paents with a clinical diagnosis of PFs (pain during
rst few minutes in the morning with walking and
with pain by pressure on calcaneal tubercle when
the foot was on passive dorsiexion) and with uni-
lateral symptoms ongoing for at least 2 months and
had minimal pain levels of 4 on VAS were included in
the study.
Paents were excluded if they used nonsteroidal an-
-inammatory drugs (NSAIDs) in the last 2 weeks,
received physical therapy for PFs in last 3 months, re-
ceived previous injecons, had history of foot, ankle
or heel surgical intervenons or haddetected anato-
mical anomalies such as pes planus or pes cavus on
x-rays. They were also excluded if theyhad infecons
on injecon site, coagulaon disorders / ancoagu-
Is hypertonic dextrose injecon eecve in the treatment of plantar fasciis: A
clinical randomized study
Plantar fasiit tedavisinde hipertonik dekstroz enjeksiyonu etkili midir: Klinik ran-
domize çalışma
104
lant treatments, pregnancy or nursing, peripheral ne-
uropathies or lower extremity paresis or paraplegia.
2.2.Intervenons
Paents were randomly divided into 2 groups by
a stascal soware. Group 1 received PT and PFs
exercise treatment; while Group 2 received saline in-
jecons and PFs exercise treatment.
Exercise programmes: Exercise programmes presc-
ribed to the paents included plantar fascial stretc-
hing, towel carrying using toes, rolling solid objects
with the sole, dorsiexion against resistance, resis-
tant plantar exion, inversion and eversion. Exercises
were iniated 72 hours following the inial injecons
and were demonstrated to the paents on their rst
sessions. Paents were instructed to connue to the
home-based exercise programmes for 3 months (one
session per day with a duraon of 10 minutes).
Prolotherapy injecons: Group 1 (PT group) received
3 injecons of 3 ml 15% dextrose into the plantar
fascia-bone inseron point at an interval of 3 weeks
under sterile condions. The applicaon was done
under asepc condions using a 22-gauge needle
with a single skin entry on the fascia ligament-bone
inseron point with peppering technique which con-
tained 5 penetraons.
Saline injecons: Group 2 (control group) received
3 injecons of 3 ml saline at an interval of 3 weeks
under asepc condions with the same peppering
technique.
Following injecons, the injecon area was exposed
to surface heat for 10 minutes and paents were as-
ked to remain in a sing posion for 30 minutes and
instructed to apply heat to the injecon surface 3 -
mes for 10 minutes for 3 days. Paents were warned
that their pain might worsen during that period and
were told not to take any NSAIDs during the treat-
ment, but can take acetaminophen for pain if neces-
sary. They were also adviced to avoid heavy loading
acvies and to begin exercises 72 hours aer the
injecons. None of the paents were given foot ort-
hoses.
2.3.Assessments
Clinical assessments were done prior to treatment
and on the 3rd month of the treatment by an asses-
sor who was blind to the treatments. Clinical assess-
ments included the measurement of pain intensity
(VAS score), foot funcon index (FFI), Roles-Mouds-
ley scores, and American Orthopedic Foot and Ankle
Society (AOFAS) ankle-hindfoot scores.
FFI is a funconal index that reviews the eect foot
pain has on the daily life of the paent. It is made of
23 quesons with pain, disability and acvity limita-
on subscales. Pain and disability subscales have 9
and acvity limitaon subscale has 5 quesons. The
paent scores each queson from 0 (no pain) to 10
(worst pain ever) [22].
Roles-Moudsley Scoring measures the relaonship
between pain in the extremity with acvity. It is gra-
ded as 1 point for asymptomac paent, 2 points
for paents with transient symptoms that respond
well to treatment, 3 points for paents with mild-
to-moderate pain following acvity and 4 points for
paents with no improvement in the symptoms [21].
AOFAS is a scoring system developed for measuring
the pain, limitaon in acvity, walking distance and
disorders, foot mobility, stability and alignment of
the foot [22].
At the follow up of the paents 3 months aer the
rst injecons; clinical assessments were repeated
by the same invesgator.
2.4.Stascal Analysis
All stascal analyses were performed by using SPSS
22.0 (IBM Corporaon, Armonk, New York, United
States) and Medcalc 14 (Acacialaan 22, B-8400 Os-
tend, Belgium) soware. Normality assessment was
made with Shapiro-Wilk test. Comparison of two in-
dependent groups was performed with independent
samples t-test and Mann Whitney U (Exact) test.
Wilcoxon’s signed-rank test were performed to de-
termine dierences within groups. Comparison for
categorical variables was made with Pearson Chi-
Square test and Monte Carlo simulaon technique
was applied. Variables were analyzed at 95% con-
dence level, and a p-value of less than 0.05 was ac-
cepted as signicant.
3. Results
Thirthy PFs paents were included in the study. No
signicant dierence was seen in baseline demog-
raphical and clinical values between the groups. The
demographical and clinical properes of the paents
were shown on Table 1.
Table 1. Demographic and clinical characteris-
cs of the paents in both groups.
Altas ve ark. Altas et al.
105
A signicant dierence was seen between Group 1
and 2 on VAS scores prior to treatment, with higher
VAS scores in Group 1 (p = 0.007). Similarly, acvity
limitaon (subscale of FFI) was signicantly dierent,
with higher values on Group 1 (p = 0.039). When
pre- and post-treatment results were compared,
signicant improvements were seen in both groups
on VAS, AOFAS (pain, funcon, total), FFI (pain, di-
sability, acvity limitaon, total) and Roles-Maudsley
scores. In addion, there was a signicantly higher
improvement in Group 1 compared to Group 2 in
terms of VAS, AOFAS (pain, funcon, total), FFI (pain,
disability, acvity limitaon, total) and Roles-Mauds-
ley scores in post-treatment results. Intergroup and
intragroup pre- and post-treatment improvement re-
sults were summarized on Table 2.
Table 2. Baseline / posntervenon comparisons in
outcome measures within and between the groups.
In intergroup improvement dierences, Group 1 had
signicantly beer outcomes except AOFAS (Align-
ment) parameter compared to Group 2. The die-
rences in improvement measures were shown on
Table 3.
Table 3. Comparison of median dierences in outco-
me measuresfrom baseline.
4. Discussion
Our study results revealed that PT treatment is more
eecve in improving pain and funconal outcomes
when compared to saline injecons. No signicant
improvement was seen in AOFAS – Alignment sub-
score in both groups. When groups were compared
in terms of improvement in all other scores, paents
who received PT revealed signicant improvements
compared to saline injecons. To the best of our
knowledge, our study is the rst randomized, cont-
rolled study that compared PT ecacy with saline in
PFs treatment.
PFs is a common disease without a clear eology
which causes pain and tenderness of the foot soles
with a wide clinical spectrum that might even cause
disability in some paents [23]. The underlying pat-
hology is thought to be the degenerave ssue on
the area where plantar fascia originates on the me-
dial tuberosity of calcaneus [24]. Structural deformi-
es, excessive foot pronaon, forefoot varus defor-
mity and weakness of bialis posterior muscle are all
though to be parts of eology [25]. The most frequ-
ently used conservave measures include changing
daily acvies, using orthoses, stretching exercises
and treatment with NSAIDs [26]. In more severe ca-
ses, extracorporeal shockwave treatment (ESWT),
Is hypertonic dextrose injecon eecve in the treatment of plantar fasciis: A
clinical randomized study
Plantar fasiit tedavisinde hipertonik dekstroz enjeksiyonu etkili midir: Klinik ran-
domize çalışma
106
laser therapy, acupuncture, dry needling and ion-
tophoresis can also be used [27, 29]. As those treat-
ments are thought to be eecve in almost 90% of all
cases, some authors argue that PFs is a self-liming
condion and that there is not enough evidence for
treatment ecacy, about 10% of more severe cases
might need more aggressive treatment intervenons
such as surgery [17, 29].
In placebo-controlled studies, corcosteroid (CS) tre-
atment was found to be eecve on the pain, but the
treatment eect is relavely short-lasng; between
4-12 weeks [30]. In addion, treatment complica-
ons such as fat pad atrophy, skin atrophy, plantar fas-
cia ruptures and osteomyelis in calcaneus limit the
usage of this treatment method [20]. PRP increases
rejuvenaon process by starng the inammatory
process which was interrupted by conservave treat-
ment of PFs by growth factors contained within [32].
PT is used for treang most of the musculoskeletal
paintypes including tendinopathies. PT works by cre-
ang a hypertonic environment which causes cell
rupture and up-regulang thrombocyte-rich growth
factor expression. Cellular shiing and increased
growth factors develop a healing cascade on the in-
jury. Fibroblasts’ exposure to growth factors increase
DNA synthesis and proteins, therefore causing new
cell growth and reproducon and collagen deposits
[33]. In the previous studies done on PT, Robago et
al, Distel and Best, Vara et al and Hauser et al all re-
ported successful results in majority of the cases,
however they did not have randomizaon or control
groups [18, 34]. In this perspecve, our study stands
out by its single-blind, prospecve randomized cont-
rolled study design. Rabago et al’s study done on 32
lateral epicondylis cases reported PT to be eecve
in improving pain and funcon in those paents [35].
Another study done on 61 paents with chondro-
malacia patella reported that PT caused a long-term
pain modicaon and could be a rst line of choice
in conservave treatment opons [36]. Yet another
randomized study done on 73 paents with chronic
shoulder pain caused by rotator cu tendinopathy
compared saline injecons with PT and reported PT
to be eecve on pain management [37]. A study
done on knee osteoarthris showed that PT caused
signicantly beer outcomes compared to saline
injecon and exercise; but warned that the results
showed heterogeneity and said that further studies
with wider paent series were necessary [38]. Again,
another study done on knee osteoarthris showed
that PT showed beer improvement compared to
local anesthec and CS injecons in 6-month term
and that there was no dierence in hand and knee
osteoarthris results [39]. A review done on lower
extremity tendinopathy and fasciopathy reported PT
to be benecial in Achilles’ tendinopathy, PFs and
Osgood-Schlaer disease, however more randomi-
zed controlled wider studies were necessary on this
subject [40]. Ryan et al’s study in which they made
3 PT injecons guided by USG with 6-week periods
reported that there was a signicant decrease in pain
severity during resng and acvity aer 18 months
[19]. There is only one randomized controlled study
done on PFs in the literature. Kim et al’s study with
20 PFs paents compared the ecacy of PRP and PT
by 2 injecons 2 weeks apart. The paents were fol-
lowed for 6 months and both methods were found to
be eecve. During inial period, PRP showed beer
outcomes in funconal improvement [19]. In accor-
dance with the previous results in the literature, we
also found out that PT treatment to be more eec-
ve in our study with 30 PFs paents. Our study’s main
advantages are the inclusion of larger number of pa-
ents, presence of control group and its randomized
and single-blind design. Therefore, we think that our
study, being a rst in this eld for the reasons stated
above, will make an extra contribuon to the litera-
ture on PFs.
No severe side-eects were reported on PT treat-
ments used on musculoskeletal system [29]. Dext-
rose is generally recognized as a safe proliferang
agent for injecon as it is a natural component of
blood biochemistry. The side eects which might
develop with the treatment are similar to other in-
jecon techniques and is mainly caused by injecon
technique rather than the agents injected [18]. No
adverse eects were seen in any of our paents du-
ring the study.
The main limitaon of our study is the short follow-
up period. As this was designed as a pilot study, alt-
hough the period was kept short, PT’s ecacy on PFs
treatment was proven. However, we sll need furt-
her randomized single-blind studies with longer pa-
ent series and longer follow-up periods to support
our results.
5.Conclusions
Prolotheraphy improved pain and funconal outco-
mes, and seems to be eecve in the treatment of
paents with PFs. It may be considered as a new tre-
atment opon for PFs. Further studies including lar-
ger number of paents and longer follow-up periods
are needed to validate these results.
Abbreviaons
PFs: Plantar fasciis; VAS score: Clinical assessments
included measurement of pain intensity, FFI: foot
funcon index, AOFAS: American Orthopedic Foot
Altas ve ark. Altas et al.
107
and Ankle Society; ESWT: extracorporeal shock
wave therapy, PRP: steroid injecons, prolotherapy,
platelet-rich plasma; PT: prolotherapy; NSAIDs: nons-
teroidal an-inammatory drugs; CS: corcosteroid
Funding
No nancial support was received for this project.
Availability of data and materials
The datasets analyzed during the current study are
available from the corresponding author on reaso-
nable request.
Compeng interests
The authors declare they have no compeng inte-
rests.
Consent for publicaon
Not applicable.
Ethics approval and consent to parcipate
Ethics approval was granted for this study by the
instute’s Ethics Commiee of Izmir Kap Celebi Uni-
versity, School of Medicine (21 July 2016, No. 124).
Informed consent was provided by all parcipants.
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Altas ve ark. Altas et al.
Cilt / No: 56 Sayı/No: 3 Aralık/December 2018
İÇİNDEKİLER/CONTENTS
KLİNİKÇALIŞMALAR/CLINICALTRIALS
•DeneyselİrritablBağırsakSendromununİntesnalYüzeyEpitelindeBulunanDopaminerjikYolaklar
ÜzerindekiEtkisi
Fatma ŞİMŞEK ve Ark.
•Ishypertonicdextroseinjeconeecveinthetreatmentofplantarfasciis:Aclinicalrandomizedstudy
Elif Umay ALTAS ve Ark.
•FarklıHastaGruplarındakiTedaviSürecindeYaşamKalitesininDeğerlendirilmesi
Ayşe Gülsün AKSÜT ve Ark.
•EsansiyelTremorHastalarındaYüzDuyguTanıma
Yıldızhan ŞENGÜL ve Ark.
•AtrokVaginitTedavisindeUzunDönemDüşükDoz17-βEstradiol
VaginalTabletUygulamalarının;KlinikEtkinliğiİveEndometrialSonuçları
Dilek UYSAL ve Ark.
•PremenstrüelSendromluOlgulardaTiroidFonksiyonTestleri
Hakan ÇÖKMEZ ve Ark.
•AcilServisteAkutAortDiseksiyonuTanısıAlanHastalarınGeriyeDönükAnalizi
Erkan DOĞAN ve Ark.
OLGUSUNUMLARI/CASEREPORTS
•AmniyonSıvıEmbolisiNedenliBirÖlümOlgusu
Yasemin BALCI ve Ark.
•UlnarSinirPalsisininNadirBirNedeni:RadiusDistalUçKırığıSonucuUlnarSinirinDorsalDeplasmanı
Gürkan YILDIZ ve Ark.
•LaparoskopiSonrasıUmbilicalTrokarYeriHernisi
Eren AKBABA
•TheConcurrencethreedierentbeningnpathologiesinonenose
Ozan GÖKDOĞAN ve Ark.
DERLEME/REVIEW
•ÇocuklardaIgEAracılıOlmayanBesinAlerjileri
İrem TURGAY YAMUR ve Ark.
90
95
İÇİNDEKİLER / CONTENTS
KLİNİK ÇALIŞMALAR/ CLINICAL TRIALS
Deneysel İrritabl Bağırsak Sendromunun İntesnal Yüzey Epitelinde
Bulunan Dopaminerjik Yolaklar Üzerindeki Etkisi
The Eects of Experimental Irritable Bowel Syndrome on Dopaminergic Pathways in Intesnal Surface Epithelium
Fatma ŞİMŞEK, Selen BAHÇECİ
Is hypertonic dextrose injecon eecve in the treatment of plantar fasciis:
A clinical randomized study
Plantar fasiit tedavisinde hipertonik dekstroz enjeksiyonu etkili midir: Klinik randomize çalışma
Elif Umay ALTAS, Ayhan ASKIN, Aliye TOSUN
Farklı Hasta Gruplarındaki Tedavi Sürecinde Yaşam Kalitesinin Değerlendirilmesi
Evaluaon of Quality of Life in The Treatment Process in Dierent Paent Groups
Ayşe Gülsün AKSÜT, Nazlı SOYSAL, Umut Gök BALCI, Kurtuluş ÖNGEL
Esansiyel Tremor Hastalarında Yüz Duygu Tanıma
Facial Emoon Recognion in the Paents With Essenal
Yıldızhan ŞENGÜL, Abdulkadir TUNÇ, Onur YILMAZ, Ahmet ÖZTÜRK
Atrok Vaginit Tedavisinde Uzun Dönem Düşük Doz 17-β Estradiol
Vaginal Tablet Uygulamalarının; Klinik Etkinliğiİ ve Endometrial Sonuçları
The Clinical Ecacy and Endometrial Outcome of Long-term Low-dose
17-β Estradiol Vaginal Tablet Applicaons in the Treatment of Atrophic Vaginis
Dilek UYSAL, Ali BALOĞLU
Premenstrüel Sendromlu Olgularda Tiroid Fonksiyon Testleri
Thyroid Funcon Tests in Cases With Premenstrual Ssyndrome
Hakan ÇÖKMEZ, Ayşegül GÜLBAHAR
Acil Serviste Akut Aort Diseksiyonu Tanısı Alan Hastaların Geriye Dönük Analizi
Retrospecve Analysis of Paents Diagnosed as Acute Aorc Dissecon in Emergency Department
Erkan DOĞAN, Akkan AVCI, Müge GÜLEN, Ertan CÖMERTPAY, Begüm Şeyda AVCİ, Salim SATAR
OLGU SUNUMLARI/ CASE REPORTS
Amniyon Sıvı Embolisi Nedenli Bir Ölüm Olgusu
Amnioc Fluid Embolism as a Cause of Death: A Case Report
Yasemin BALCI, Ümit Ünüvar GÖÇEOĞLU
Ulnar Sinir Palsisinin Nadir Bir Nedeni: Radius Distal Uç Kırığı Sonucu Ulnar Sinirin Dorsal Deplasmanı
A Very Rare Cause Of Ulnar Nerve Palsy: Dorsal Shi of the Ulnar Nerve Aer Distal Radius Fracture
Gürkan YILDIZ, Mesut TAHTA, Eyüp Çağatay ZENGİN, Ahmet SAVRAN
Laparoskopi Sonrası Umbilical Trokar Yeri Hernisi
Umbilical Port Hernia Following Laparoscopic Surgery
Eren AKBABA
The Concurrence three dierent beningn pathologies in one nose
Bir burunda 3 farklı iyi huylu patolojinin es zamanlı bulunması
Ozan GÖKDOĞAN, Harun ÜÇÜNCÜ
DERLEME/ REVIEW
Çocuklarda IgE Aracılı Olmayan Besin Alerjileri
Non IgE Mediated Food Allergies in Children
İrem TURGAY YAMUR, Özge YILMAZ TOPAL, Emine DİBEK MISIRLIOĞLU
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.....143
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89