Literature DB >> 29661251

Under diagnosis of intestinal schistosomiasis in a referral hospital, North Ethiopia.

Megbaru Alemu1, Eyob Zigta2, Awoke Derbie3.   

Abstract

OBJECTIVE: The present cross-sectional study was aimed at determining the magnitude of under diagnosis of intestinal schistosomiasis among patients requested for routine ova/parasite examination at Ayder referral hospital.
RESULTS: A total of 280 stool samples were collected and only 5% of the patients were positive for ova of Schistosoma mansoni in the routine direct wet mount microscopy. On the other hand, 12.5% of the patients were positive for ova Schistosoma mansoni when the stool samples were processed by either Kato Kat or formol ether concentration techniques. Moderate test agreement (κ = 0.48) was recorded for wet mount. Formol-ether concentration (κ = 0.89) and Kato-Katz (κ = 0.92) showed excellent agreements with the 'Gold' standard. Direct wet mount technique exhibited the poorest sensitivity (35%) of detection of ova of Schistosoma mansoni. Hence, the Kato-Katz technique should be implemented in parallel with the direct wet mount microscopy for Schistosoma mansoni presumptive patients.

Entities:  

Keywords:  Ethiopia; Formol ether concentration; Kato-Katz; Mekelle; Wet mount

Mesh:

Substances:

Year:  2018        PMID: 29661251      PMCID: PMC5902945          DOI: 10.1186/s13104-018-3355-0

Source DB:  PubMed          Journal:  BMC Res Notes        ISSN: 1756-0500


Introduction

Human bilharziasis is caused by the trematode species of Schistosoma mansoni, Schistosoma hematobium, Schistosoma japonicum, Schistosoma intercalatum and Schistosoma mekongi [1]. The disease is highly prevalent throughout Africa, South America and several Caribbean islands [2]. It is one of the most widespread of all human parasitic diseases, ranking second only to malaria in terms of its socioeconomic and public health importance in tropical and subtropical areas [3]. Estimates suggest that over 250 million people were infected and the disease caused 11,700 deaths and a global burden of 3.3 million disability-adjusted life years [4]. In Ethiopia, schistosomiasis is widely spread in the country where endemic areas are located in the altitudinal range of 1200–2000 m above sea level [5]. Rapid spread of the disease also appears to have been facilitated in areas which were originally non-endemic as a result of the initiation of water-based development schemes [6]. High infection rates of S. mansoni were reported in the hyper endemic areas of northwestern, northeastern and northern parts of the country [6-8]. Examination of stool is the primary method of diagnosing suspected Schistosoma mansoni infections. There are several diagnostic techniques such as Kato-Katz, wet-mount, and formol-ether concentration technique (FECT). Despite its low sensitivity, the direct wet mount is the only method employed for diagnostic purpose of intestinal parasites in general and schistosomiasis in particular in health institutions of Ethiopia while FECT and Kato-Katz are reserved for research purpose [9-12]. The Kato-Katz method is characteristically rapid, easy to perform and require minimal training. The formol-ether concentration technique on the other hand is time-consuming, and requires several materials. Schistosome species lay only few numbers of eggs and only two-third of the eggs are excreted intermittently with stool, making single wet mount microscopy prone for false negative results [13]. The reliable diagnosis of intestinal schistosomiasis therefore requires a more rapid, economical, easy, and sensitive method. Stool examination for intestinal parasitosis is performed solely by wet mount procedure at Ayder referral hospital. It has been a custom that clinicians sending stool specimens of patients with presumptive S. mansoni infection to Microbiology and parasitology research laboratory whose stool examination results turned negative in Ayder hospital laboratory. Consequently, ova of S. mansoni were isolated from most of the referred stool specimens in the research laboratory. Hence, we sought to assess performance of wet mount against the Kato-Katz and FECT in the diagnosis of intestinal schistosomiasis and to recommend the best technique in the hospital.

Main text

Methods

Study design and area

This cross-sectional study was conducted in Ayder referral hospital, North Ethiopia, from August to October 2016. The Hospital provides referral and non-referral services to more than 8 million populations in its catchment areas. It provides a broad range of medical services to both in and outpatients of all age groups. With the total capacity of about 500 inpatient beds in four major departments and other specialty units, the hospital is also used as a teaching hospital for the College of Health Sciences, Mekelle University. Stool examination for intestinal parasitic infections in general and intestinal schistosomiasis in particular is mainly based on direct wet mount microscopy.

Sample collection and parasitological examination

Patients were provided with stool cups to bring adequate stool samples. The routine direct wet mount microscopy performed in the hospital laboratory. The Kato-Katz and formol-ether concentration (FEC) methods, on the other hand, were performed in microbiology and parasitology research laboratory. The test procedures were carried out in accordance with standard protocols reported by World Health Organization (WHO) [14].

Kato-Katz method

An approximately 42 mg fecal sample was sieved through a 200 µm Kato nylon screen mesh. The stool was transferred into a 6 mm hole of a template on a microscopic slide and covered with glycerol soaked cellophane strip. The microscopic examination then proceeded to identify schistosome eggs and to calculate the number of eggs per gram (EPG) of feces [15]. Based on egg counts, cut-off values for classification of the intensity of infection were used. The intensity of S. mansoni was classified into: light infection (1–99 EPG), moderate (100–399 EPG) and heavy (≥ 400 EPG) [14].

Formol ether concentration technique (FEC)

Approximately 500 mg of feces was mixed with 10 ml of normal saline and the mixed stool was strained via gauze into a funnel. The strained contents were collected in a centrifuge tube. About 2.5 ml of 10% formaldehyde (Loba Chemie Pvt Ltd., 107, Wodehouse Road, Jehangir villa, Mumbai-40005, India) and 1 ml of diethyl ether (Blulux laboratories Pvt Ltd. 121005) was then added and centrifuged at 1000g for 3 min. The supernatant was removed and a drop of the sediment was covered with cover glass for a microscopic investigation [16].

Wet mount preparation

Fresh stool samples (approximately 2 mg of stool) were put on a slide with wooden applicator, emulsified with a drop of physiological saline (0.85%) covered with a cover slide and examined at 10× and 40× microscopic objectives [16].

Data entry and analysis

Data were entered and analyzed using SPSS version 20 statistical software. Estimation of the performance of the three diagnostic tests was made by taking the combined results of the wet mount, FEC and Kato-Katz tests as a “Gold” standard diagnostic test, because stool investigation for intestinal parasitosis lacks ‘Gold’ standard method [17]. Sensitivity, specificity, PPV (positive predictive value), NPV (negative predictive value) and Kappa value of wet mount, FEC and Kato-Katz techniques were computed against the ‘Gold’ standard. The kappa score was used to estimate the agreement between stool diagnostic tests and the ‘Gold’ standard.

Data quality control

Laboratory technicians in charge of microscopic investigations were blinded to the results of the wet mount, FECT, and Kato-Katz. A different laboratory technician was responsible for preparing and reading Kato-Katz and FEC. In addition, results of the wet mount, Kato-Katz, and FEC techniques were recorded on different sheets to ensure strict blinding.

Results

The overall prevalence of S. mansoni infection was 40 (14.3%) with a parasitic load ranging from 24 to 480 eggs per gram of stool. S. mansoni infections were predominantly light, 65% and moderate 35%. The peak prevalence of S. mansoni infection was recorded for the 10–14 years of age (17.6%) followed by those 15 and above years of age (14.5%). Mean intensity of infection was also higher in the age group 10–14 years (224 EPG). The overall prevalence of infection was 12.7% for females and 15.8% for male participants (P > 0.05). The mean intensity of infection was also higher for males (201 EPG) than females (169 EPG) (Table 1).
Table 1

Prevalence and intensity of S. mansoni with age and sex at Ayder referral hospital, 2016

S. mansoni infectionTotal n (%)
Positive n (%)Negative n (%)Mean intensity (EPG)
Gender
 Male23 (15.8)123 (84.2)201146 (100)
 Female17 (12.7)117 (87.3)169134 (100)
Age (years)
 5–94 (9.3%)39 (90.7%)20343 (100)
 10–149 (17.6)42 (82.4)22451 (100)
 ≥ 1527 (14.5)159 (85.5)168186 (100)
Prevalence and intensity of S. mansoni with age and sex at Ayder referral hospital, 2016 The prevalence of S. mansoni using wet mount, Kato-Katz and FEC was 5, 12.5 and 12.5%, respectively (Table 2). The detection rate when two techniques were used at a time was 13.2% for wet mount and Kato-Katz, 12.9% for wet mount and FEC and 13.6% for Kato-Katz and FEC. The detection rate was 14.3% when all the three tests were used together (Table 2). Kato-Katz detected 23 samples that were negative by wet mount. Similarly, 21 samples were detected by FEC that were negative by wet mount technique.
Table 2

Prevalence of S. mansoni identified in stool diagnostic tests at Ayder referral hospital, 2016

Diagnostic methodsNo examinedPositive n (%)Negative n (%)
Wet mount28014 (5.0)266 (95)
Kato-Katz28035 (12.5)245 (87.5)
FEC28035 (12.5)245 (87.5)
Kato-Katz + wet mount28037 (13.2)243 (95)
FEC + wet mount28036 (12.9)244 (87.1)
Kato-Katz + FEC28038 (13.6)242 (86.4)
KK + FEC + WM28040 (14.3)240 (85.7)
Prevalence of S. mansoni identified in stool diagnostic tests at Ayder referral hospital, 2016 The sensitivity of wet mount, Kato-Katz and FEC in the detection of S. mansoni infection was 35 (95% CI 20.6–51.7), 87.5 (95% CI 73.2–95.8), 85 (95% CI 70.2–94.3), respectively. Similarly, NPV of 90.2 (95% CI 88–92.1), 98 (95% CI 95.5–99.1) and 97.6 (95% CI 95–98.8) were reported, respectively for the wet mount, FEC, and Kato-Katz. Moderate test agreement (κ = 0.48) was recorded for the wet mount. FEC (κ = 0.89) and Kato-Katz (κ = 0.92) on the other hand showed excellent agreements with the Gold standard (Table 3).
Table 3

The performance of stool diagnostic techniques for diagnosis of intestinal schistosomiasis at Ayder referral hospital, 2016

Diagnostic methodsGold standard
Sensitivity (95% CI)Specificity (95% CI)PPV (95% CI)NPV (95% CI)Kappa value
Wet mount35 (20.6–51.7)10010090.2 (88–92.1)0.48
Kato-Katz87.5 (73.2–95.8)100 (98.5–100)10098 (95.5–99.1)0.92
FEC85 (70.2–94.3)99.6 (97.7–99.9)97.1 (82.7–99.6)97.6 (95–98.8)0.89
The performance of stool diagnostic techniques for diagnosis of intestinal schistosomiasis at Ayder referral hospital, 2016

Discussion

The prevalence of S. mansoni infection in this study was 14.3%, which was higher than previous reports [18, 19]. This might be explained in part by the nature of the study participants, as symptomatic patients were recruited in our study. The prevalence and intensity of S. mansoni were found to be higher in males than females in the current study. This goes in agreement with other studies in Africa [20-22]. The existence of more outdoor activities and water exposure habits among males might have contributed to these findings. The peak prevalence of S. mansoni was recorded for the 10–14 age group which was consistent with similar other findings [18]. Diagnosis of intestinal parasitosis is based on detection of the eggs in stool samples examined through a variety of parasitologic methods, and no single technique is satisfactory. In Ethiopia, healthcare laboratories employ the direct wet mount as the preferred stool parasitological examination technique by virtue of its simplicity, low cost, and rapidity. Although the wet mount technique is the preferred method in resource-limited settings [23], reliance on it as the sole diagnostic tool in routine practice is very likely to cause misdiagnosis of infections. This, in turn, leads to grave clinical and public health consequences [24]. It is supported by our study in which wet mount technique detected only one-third (14/40) of the study participants infected by S. mansoni. The Kato-Katz method is characteristically rapid, easy to perform and require minimal training. Its high sensitivity (87.5%) and specificity (100%) for the diagnosis of S. mansoni compared to the wet mount is well noted in our study. It was also slightly sensitive than formol-ether concentration. Consistent results were reported by others [17, 25]. The technique is a useful tool for the quantification of egg counts to determine infection intensities. These qualities make the Kato-Katz the most frequently employed method in research works [14]. Time-consuming procedures, the requirement of trained personnel and several materials/equipment make the FEC technique the most expensive method to be considered as an alternative for routine laboratory diagnosis of intestinal schistosomiasis. However, our study revealed that the sensitivity and specificity of FEC are not much less than the Kato-Katz method for detecting eggs of S. mansoni. The prevalence of S. mansonia via wet mount, FEC, and Kato-Katz was 5, 12.5 and 12.5%, respectively. Our study revealed that the Kato-Katz and FEC techniques had about threefold increased in the detection rate of S. mansoni than the wet mount. Consistent findings were reported in previous studies [17, 25]. Our study revealed that Kato-Katz (87.5%) was slightly sensitive than FEC (85%) to detect S. mansoni. Similarly, Kato-Katz showed the highest agreement with the Gold standard (κ = 0.92) while wet mount showed the lowest agreement (κ = 0.48). This showed that the use of Kato-Katz can ultimately reduce misdiagnosis of intestinal schistosomiasis, and reduce morbidity and mortality due to schistosomiasis. This was supported by other findings in Ethiopia [17, 25].

Conclusion

Direct wet mount technique exhibited the poorest sensitivity of detection of ova of Schistosoma mansoni. Most of the infections were predominantly light in the study area which requires implementation of concentration methods. Hence, the Kato-Katz technique should be implemented in parallel with the direct wet mount microscopy for Schistosoma mansoni presumptive patients.

Limitations of the study

In this study, we collected only a single stool sample and hence we were unable to describe the variation of egg counts as Schistosoma mansoni female worms undergo intermittent egg excretion. Future investigations should focus on the feasibility of the concentration techniques in terms of the turn-around-time (TAT) in health facilities that serve large number of outpatients.
  14 in total

1.  Epidemiology of schistosomiasis mansoni in three endemic communities in north-east Ethiopia: baseline characteristics before endod based intervention.

Authors:  H Birrie; F Abebe; S G Gundersen; G Medhin; N Berhe; T Gemetchu
Journal:  Ethiop Med J       Date:  1998-04

2.  Missed diagnosis of schistosomiasis leading to unnecessary surgical procedures in Jos University Teaching Hospital.

Authors:  Barnabas M Mandong; Aboi J K Madaki
Journal:  Trop Doct       Date:  2005-04       Impact factor: 0.731

3.  FLOTAC: a new sensitive technique for the diagnosis of hookworm infections in humans.

Authors:  Jürg Utzinger; Laura Rinaldi; Laurent K Lohourignon; Fabian Rohner; Michael B Zimmermann; Andres B Tschannen; Eliézer K N'goran; Giuseppe Cringoli
Journal:  Trans R Soc Trop Med Hyg       Date:  2007-10-29       Impact factor: 2.184

Review 4.  Human schistosomiasis.

Authors:  Bruno Gryseels; Katja Polman; Jan Clerinx; Luc Kestens
Journal:  Lancet       Date:  2006-09-23       Impact factor: 79.321

5.  Estimating the sensitivity and specificity of Kato-Katz stool examination technique for detection of hookworms, Ascaris lumbricoides and Trichuris trichiura infections in humans in the absence of a 'gold standard'.

Authors:  M R Tarafder; H Carabin; L Joseph; E Balolong; R Olveda; S T McGarvey
Journal:  Int J Parasitol       Date:  2009-09-20       Impact factor: 3.981

6.  The status of Schistosoma mansoni and snail hosts in Tigray and northern Wello regions, northern Ethiopia.

Authors:  H Birrie; T Woldemichael; A Redda; T Chane
Journal:  Ethiop Med J       Date:  1994-10

7.  A single FLOTAC is more sensitive than triplicate Kato-Katz for the diagnosis of low-intensity soil-transmitted helminth infections.

Authors:  Stefanie Knopp; Laura Rinaldi; I Simba Khamis; J Russell Stothard; David Rollinson; Maria P Maurelli; Peter Steinmann; Hanspeter Marti; Giuseppe Cringoli; Jürg Utzinger
Journal:  Trans R Soc Trop Med Hyg       Date:  2009-01-24       Impact factor: 2.184

8.  Disability-adjusted life years (DALYs) for 291 diseases and injuries in 21 regions, 1990-2010: a systematic analysis for the Global Burden of Disease Study 2010.

Authors:  Christopher J L Murray; Theo Vos; Rafael Lozano; Mohsen Naghavi; Abraham D Flaxman; Catherine Michaud; Majid Ezzati; Kenji Shibuya; Joshua A Salomon; Safa Abdalla; Victor Aboyans; Jerry Abraham; Ilana Ackerman; Rakesh Aggarwal; Stephanie Y Ahn; Mohammed K Ali; Miriam Alvarado; H Ross Anderson; Laurie M Anderson; Kathryn G Andrews; Charles Atkinson; Larry M Baddour; Adil N Bahalim; Suzanne Barker-Collo; Lope H Barrero; David H Bartels; Maria-Gloria Basáñez; Amanda Baxter; Michelle L Bell; Emelia J Benjamin; Derrick Bennett; Eduardo Bernabé; Kavi Bhalla; Bishal Bhandari; Boris Bikbov; Aref Bin Abdulhak; Gretchen Birbeck; James A Black; Hannah Blencowe; Jed D Blore; Fiona Blyth; Ian Bolliger; Audrey Bonaventure; Soufiane Boufous; Rupert Bourne; Michel Boussinesq; Tasanee Braithwaite; Carol Brayne; Lisa Bridgett; Simon Brooker; Peter Brooks; Traolach S Brugha; Claire Bryan-Hancock; Chiara Bucello; Rachelle Buchbinder; Geoffrey Buckle; Christine M Budke; Michael Burch; Peter Burney; Roy Burstein; Bianca Calabria; Benjamin Campbell; Charles E Canter; Hélène Carabin; Jonathan Carapetis; Loreto Carmona; Claudia Cella; Fiona Charlson; Honglei Chen; Andrew Tai-Ann Cheng; David Chou; Sumeet S Chugh; Luc E Coffeng; Steven D Colan; Samantha Colquhoun; K Ellicott Colson; John Condon; Myles D Connor; Leslie T Cooper; Matthew Corriere; Monica Cortinovis; Karen Courville de Vaccaro; William Couser; Benjamin C Cowie; Michael H Criqui; Marita Cross; Kaustubh C Dabhadkar; Manu Dahiya; Nabila Dahodwala; James Damsere-Derry; Goodarz Danaei; Adrian Davis; Diego De Leo; Louisa Degenhardt; Robert Dellavalle; Allyne Delossantos; Julie Denenberg; Sarah Derrett; Don C Des Jarlais; Samath D Dharmaratne; Mukesh Dherani; Cesar Diaz-Torne; Helen Dolk; E Ray Dorsey; Tim Driscoll; Herbert Duber; Beth Ebel; Karen Edmond; Alexis Elbaz; Suad Eltahir Ali; Holly Erskine; Patricia J Erwin; Patricia Espindola; Stalin E Ewoigbokhan; Farshad Farzadfar; Valery Feigin; David T Felson; Alize Ferrari; Cleusa P Ferri; Eric M Fèvre; Mariel M Finucane; Seth Flaxman; Louise Flood; Kyle Foreman; Mohammad H Forouzanfar; Francis Gerry R Fowkes; Marlene Fransen; Michael K Freeman; Belinda J Gabbe; Sherine E Gabriel; Emmanuela Gakidou; Hammad A Ganatra; Bianca Garcia; Flavio Gaspari; Richard F Gillum; Gerhard Gmel; Diego Gonzalez-Medina; Richard Gosselin; Rebecca Grainger; Bridget Grant; Justina Groeger; Francis Guillemin; David Gunnell; Ramyani Gupta; Juanita Haagsma; Holly Hagan; Yara A Halasa; Wayne Hall; Diana Haring; Josep Maria Haro; James E Harrison; Rasmus Havmoeller; Roderick J Hay; Hideki Higashi; Catherine Hill; Bruno Hoen; Howard Hoffman; Peter J Hotez; Damian Hoy; John J Huang; Sydney E Ibeanusi; Kathryn H Jacobsen; Spencer L James; Deborah Jarvis; Rashmi Jasrasaria; Sudha Jayaraman; Nicole Johns; Jost B Jonas; Ganesan Karthikeyan; Nicholas Kassebaum; Norito Kawakami; Andre Keren; Jon-Paul Khoo; Charles H King; Lisa Marie Knowlton; Olive Kobusingye; Adofo Koranteng; Rita Krishnamurthi; Francine Laden; Ratilal Lalloo; Laura L Laslett; Tim Lathlean; Janet L Leasher; Yong Yi Lee; James Leigh; Daphna Levinson; Stephen S Lim; Elizabeth Limb; John Kent Lin; Michael Lipnick; Steven E Lipshultz; Wei Liu; Maria Loane; Summer Lockett Ohno; Ronan Lyons; Jacqueline Mabweijano; Michael F MacIntyre; Reza Malekzadeh; Leslie Mallinger; Sivabalan Manivannan; Wagner Marcenes; Lyn March; David J Margolis; Guy B Marks; Robin Marks; Akira Matsumori; Richard Matzopoulos; Bongani M Mayosi; John H McAnulty; Mary M McDermott; Neil McGill; John McGrath; Maria Elena Medina-Mora; Michele Meltzer; George A Mensah; Tony R Merriman; Ana-Claire Meyer; Valeria Miglioli; Matthew Miller; Ted R Miller; Philip B Mitchell; Charles Mock; Ana Olga Mocumbi; Terrie E Moffitt; Ali A Mokdad; Lorenzo Monasta; Marcella Montico; Maziar Moradi-Lakeh; Andrew Moran; Lidia Morawska; Rintaro Mori; Michele E Murdoch; Michael K Mwaniki; Kovin Naidoo; M Nathan Nair; Luigi Naldi; K M Venkat Narayan; Paul K Nelson; Robert G Nelson; Michael C Nevitt; Charles R Newton; Sandra Nolte; Paul Norman; Rosana Norman; Martin O'Donnell; Simon O'Hanlon; Casey Olives; Saad B Omer; Katrina Ortblad; Richard Osborne; Doruk Ozgediz; Andrew Page; Bishnu Pahari; Jeyaraj Durai Pandian; Andrea Panozo Rivero; Scott B Patten; Neil Pearce; Rogelio Perez Padilla; Fernando Perez-Ruiz; Norberto Perico; Konrad Pesudovs; David Phillips; Michael R Phillips; Kelsey Pierce; Sébastien Pion; Guilherme V Polanczyk; Suzanne Polinder; C Arden Pope; Svetlana Popova; Esteban Porrini; Farshad Pourmalek; Martin Prince; Rachel L Pullan; Kapa D Ramaiah; Dharani Ranganathan; Homie Razavi; Mathilda Regan; Jürgen T Rehm; David B Rein; Guiseppe Remuzzi; Kathryn Richardson; Frederick P Rivara; Thomas Roberts; Carolyn Robinson; Felipe Rodriguez De Leòn; Luca Ronfani; Robin Room; Lisa C Rosenfeld; Lesley Rushton; Ralph L Sacco; Sukanta Saha; Uchechukwu Sampson; Lidia Sanchez-Riera; Ella Sanman; David C Schwebel; James Graham Scott; Maria Segui-Gomez; Saeid Shahraz; Donald S Shepard; Hwashin Shin; Rupak Shivakoti; David Singh; Gitanjali M Singh; Jasvinder A Singh; Jessica Singleton; David A Sleet; Karen Sliwa; Emma Smith; Jennifer L Smith; Nicolas J C Stapelberg; Andrew Steer; Timothy Steiner; Wilma A Stolk; Lars Jacob Stovner; Christopher Sudfeld; Sana Syed; Giorgio Tamburlini; Mohammad Tavakkoli; Hugh R Taylor; Jennifer A Taylor; William J Taylor; Bernadette Thomas; W Murray Thomson; George D Thurston; Imad M Tleyjeh; Marcello Tonelli; Jeffrey A Towbin; Thomas Truelsen; Miltiadis K Tsilimbaris; Clotilde Ubeda; Eduardo A Undurraga; Marieke J van der Werf; Jim van Os; Monica S Vavilala; N Venketasubramanian; Mengru Wang; Wenzhi Wang; Kerrianne Watt; David J Weatherall; Martin A Weinstock; Robert Weintraub; Marc G Weisskopf; Myrna M Weissman; Richard A White; Harvey Whiteford; Natasha Wiebe; Steven T Wiersma; James D Wilkinson; Hywel C Williams; Sean R M Williams; Emma Witt; Frederick Wolfe; Anthony D Woolf; Sarah Wulf; Pon-Hsiu Yeh; Anita K M Zaidi; Zhi-Jie Zheng; David Zonies; Alan D Lopez; Mohammad A AlMazroa; Ziad A Memish
Journal:  Lancet       Date:  2012-12-15       Impact factor: 79.321

9.  Evaluation performance of diagnostic methods of intestinal parasitosis in school age children in Ethiopia.

Authors:  Mulat Yimer; Tadesse Hailu; Wondemagegn Mulu; Bayeh Abera
Journal:  BMC Res Notes       Date:  2015-12-26

10.  Comparison of the Kato-Katz, Wet Mount, and Formol-Ether Concentration Diagnostic Techniques for Intestinal Helminth Infections in Ethiopia.

Authors:  Mengistu Endris; Zinaye Tekeste; Wossenseged Lemma; Afework Kassu
Journal:  ISRN Parasitol       Date:  2012-10-22
View more
  2 in total

1.  Evaluation of Wet Mount and Concentration Techniques of Stool Examination for Intestinal Parasites Identification at Debre Markos Comprehensive Specialized Hospital, Ethiopia.

Authors:  Gebreselassie Demeke; Abebe Fenta; Tebelay Dilnessa
Journal:  Infect Drug Resist       Date:  2021-04-09       Impact factor: 4.003

Review 2.  Schistosomiasis: Life Cycle, Diagnosis, and Control.

Authors:  Martin L Nelwan
Journal:  Curr Ther Res Clin Exp       Date:  2019-06-22
  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.