scholarly journals Perlukah menghitung ukuran sampel?

2019 ◽  
Vol 15 (1) ◽  
Author(s):  
Bhisma Murti
Keyword(s):  
Systematic Error ◽  
Sample Size ◽  
Random Error ◽  
Actual Sample ◽  
Statistical Aspect ◽  
Good Research ◽  
Larger Sample ◽  
Association Effect

Sample size is an issue worth-considering but not the most essential thing to fulfil for a good research. A much more crucial cause of concern to any research is the validity of inference a research is drawing, i.e. the extent to which the research is able to control systematic error that stems from bias and confounding. Sample size refers to random error; it does not address nor correct systematic error. The larger sample size, the less random error, the more precise estimates a research can yield about difference/ association/ effect of a variable(s). Most of the assignment of values in any sample size formula is arbitrary. As such, the product of estimating sample size, regardless of the formula being used,  cannot be viewed as an absolute end; the actual sample size can be larger or smaller than the estimated one. Beyond statistical aspect, several other important factors should be considered when estimating sample size, such as ethics, cost, and the amount oftime available for conducting the research.

Planning the Size of Clinical Trials with Allowance for Patient Noncompliance

1990 ◽  
Vol 29 (03) ◽  
pp. 243-246 ◽  
Author(s):  
M. A. A. Moussa
Keyword(s):  
Clinical Trial ◽  
Clinical Trials ◽  
Sample Size ◽  
Event Rate ◽  
Survival Functions ◽  
Time Intervals ◽  
Patient Noncompliance ◽  
Event Rates ◽  
Larger Sample

AbstractVarious approaches are considered for adjustment of clinical trial size for patient noncompliance. Such approaches either model the effect of noncompliance through comparison of two survival distributions or two simple proportions. Models that allow for variation of noncompliance and event rates between time intervals are also considered. The approach that models the noncompliance adjustment on the basis of survival functions is conservative and hence requires larger sample size. The model to be selected for noncompliance adjustment depends upon available estimates of noncompliance and event rate patterns.

Augmentation Strategies for Clozapine-Resistant Patients with Schizophrenia

2020 ◽  
Vol 26 (2) ◽  
pp. 218-227
Author(s):  
Yi-Hang Chiu ◽  
Chia-Yueh Hsu ◽  
Mong-Liang Lu ◽  
Chun-Hsin Chen
Keyword(s):  
Sample Size ◽  
Repetitive Transcranial Magnetic Stimulation ◽  
Mood Stabilizers ◽  
Treatment Resistant ◽  
Double Blind ◽  
Beneficial Effects ◽  
Augmentation Strategies ◽  
Pubmed Database ◽  
Augmentation Strategy ◽  
Larger Sample

Background: Clozapine has been used in treatment-resistant patients with schizophrenia. However, only 40% of patients with treatment-resistant schizophrenia have response to clozapine. Many augmentation strategies have been proposed to treat those clozapine-resistant patients, but the results are inconclusive. In this review, we intended to review papers dealing with the augmentation strategies in the treatment of clozapineresistant patients with schizophrenia. Method: We reviewed randomized, double-blind, placebo- or sham-controlled trials (RCT) for clozapine-resistant patients with schizophrenia in Embase, PsycINFO, Cochrane, and PubMed database from January 1990 to June 2019. Results: Antipsychotics, antidepressants, mood stabilizers, brain stimulation, such as electroconvulsive therapy (ECT) and repetitive transcranial magnetic stimulation, and other strategies, were used as an augmentation in clozapine-resistant patients with schizophrenia. Except for better evidence in memantine with 2 RCTs and cognitive behavior therapy in 2 studies to support its effectiveness, we found that all the other effective augmentations, including sulpiride, ziprasidone, duloxetine, mirtazapine, ECT, sodium benzoate, ginkgo biloba, and minocycline, had only one RCT with limited sample size. Conclusion: In this review, no definite effective augmentation strategy was found for clozapine-resistant patients. Some potential strategies with beneficial effects on psychopathology need further studies with a larger sample size to support their efficacy.

scholarly journals ‘Statistical Irreproducibility’ Does Not Improve with Larger Sample Size: How to Quantify and Address Disease Data Multimodality in Human and Animal Research

2021 ◽  
Vol 11 (3) ◽  
pp. 234
Author(s):  
Abigail R. Basson ◽  
Fabio Cominelli ◽  
Alexander Rodriguez-Palacios
Keyword(s):  
Sample Size ◽  
Data Visualization ◽  
Random Sampling ◽  
Intestinal Inflammation ◽  
Random Number Generation ◽  
Outcome Data ◽  
Multimodal Distributions ◽  
Disease Subtypes ◽  
Study Designs ◽  
Larger Sample

Poor study reproducibility is a concern in translational research. As a solution, it is recommended to increase sample size (N), i.e., add more subjects to experiments. The goal of this study was to examine/visualize data multimodality (data with >1 data peak/mode) as cause of study irreproducibility. To emulate the repetition of studies and random sampling of study subjects, we first used various simulation methods of random number generation based on preclinical published disease outcome data from human gut microbiota-transplantation rodent studies (e.g., intestinal inflammation and univariate/continuous). We first used unimodal distributions (one-mode, Gaussian, and binomial) to generate random numbers. We showed that increasing N does not reproducibly identify statistical differences when group comparisons are repeatedly simulated. We then used multimodal distributions (>1-modes and Markov chain Monte Carlo methods of random sampling) to simulate similar multimodal datasets A and B (t-test-p = 0.95; N = 100,000), and confirmed that increasing N does not improve the ‘reproducibility of statistical results or direction of the effects’. Data visualization with violin plots of categorical random data simulations with five-integer categories/five-groups illustrated how multimodality leads to irreproducibility. Re-analysis of data from a human clinical trial that used maltodextrin as dietary placebo illustrated multimodal responses between human groups, and after placebo consumption. In conclusion, increasing N does not necessarily ensure reproducible statistical findings across repeated simulations due to randomness and multimodality. Herein, we clarify how to quantify, visualize and address disease data multimodality in research. Data visualization could facilitate study designs focused on disease subtypes/modes to help understand person–person differences and personalized medicine.

scholarly journals Prevalence and Diversity of Avian Haematozoan Parasites in Wetlands of Bangladesh

2014 ◽  
Vol 2014 ◽  
pp. 1-12 ◽  
Author(s):  
Rubayet Elahi ◽  
Ausraful Islam ◽  
Mohammad Sharif Hossain ◽  
Khaja Mohiuddin ◽  
Andrea Mikolon ◽  
...  
Keyword(s):  
Sample Size ◽  
Disease Ecology ◽  
Infection Intensity ◽  
Wild Birds ◽  
Wetland Birds ◽  
Domestic Ducks ◽  
Wide Range ◽  
Unidentified Species ◽  
Larger Sample ◽  
Resident Bird

The parasites of generaHaemoproteus, Plasmodium,andLeucocytozoonare well-known avian haematozoa and can cause declined productivity and high mortality in wild birds. The objective of the study was to record the prevalence of haematozoan parasites in a wide range of wetland birds in Bangladesh. Six species ofHaemoproteus, seven species ofPlasmodium, one unidentified species ofLeucocytozoon, and one unidentified microfilaria of the genusParonchocercawere found. Data on the morphology, size, hosts, prevalence, and infection intensity of the parasites are provided. The overall prevalence among the birds was 29.5% (95 out of 322 birds). Of those, 13.2% (42 of 319) of birds were infected withHaemoproteusspp., 15.1% withPlasmodiumspp. (48 of 319) and 0.6% withLeucocytozoonspp. (2 of 319). Two birds were positive for bothHaemoproteussp. andPlasmodiumsp. A single resident bird,Ardeola grayii, was found positive for an unidentified microfilaria. Prevalence of infection varied significantly among different bird families. Wild birds of Bangladesh carry several types of haematozoan parasites. Further investigation with a larger sample size is necessary to estimate more accurately the prevalence of haematozoan parasites among wild birds as well as domestic ducks for better understanding of the disease ecology.

scholarly journals Comparison of space analysis performed on plaster vs. digital dental casts applying Tanaka and Johnston's equation

2013 ◽  
Vol 18 (1) ◽  
pp. 128-133 ◽  
Author(s):  
Júlia Olien Sanches ◽  
Lourdes Aparecida Martins dos Santos-Pinto ◽  
Ary dos Santos-Pinto ◽  
Betina Grehs ◽  
Fabiano Jeremias
Keyword(s):  
Systematic Error ◽  
Random Error ◽  
Regression Equation ◽  
Predictive Values ◽  
Error Bias ◽  
Digital Caliper ◽  
Plaster Casts ◽  
Paired T Test ◽  
Lower Incisors ◽  
Dental Casts

OBJECTIVE: The purpose of this study was to compare dental size measurements, their reproducibility and the application of Tanaka and Johnston regression equation in predicting the size of canines and premolars on plaster and digital dental casts. METHODS: Thirty plaster casts were scanned and digitized. Mesiodistal measurements of the teeth were then performed with a digital caliper on the plaster and digital casts using O3d software system (Widialabs©).The sum of the sizes of the lower incisors was used to obtain predictive values of the sizes of the premolars and canines using the regression equation, and these values were compared with the actual sizes of the teeth. The data were statistically analyzed by applying to the results Pearson's correlation test, Dahlberg's formula, paired t-test and analysis of variance (p<0.05). RESULTS: Excellent intraexaminer agreement was observed in the measurements performed on both dental casts. No random error was present in the measurements obtained with the caliper and systematic error (bias) was more frequent in the digital casts. Space prediction obtained by applying the regression equation was greater than the sum of the canines and premolars on the plaster and digital casts. CONCLUSIONS: Despite an adequate reproducibility of the measurements performed on both casts, most measurements on the digital casts were higher than those on the plaster casts. The predicted space was overestimated in both models and significantly higher in the digital casts.

scholarly journals Chloroquine and Hydroxychloroquine could be an Available Weapons to Treat COVID-19 Associated Pneumonia

2020 ◽  
pp. 52-60
Author(s):  
Nehad J. Ahmed
Keyword(s):  
Clinical Trials ◽  
Angiotensin Converting Enzyme ◽  
Sample Size ◽  
Small Sample Size ◽  
Small Sample ◽  
Google Scholar ◽  
Converting Enzyme ◽  
Larger Sample

Aims: This study aims to review the efficacy of chloroquine and hydroxychloroquine to treat coronavirus disease 2019 (COVID-19) associated pneumonia. Methodology: This review includes searching Google scholar for publications about the use of hydroxychloroquinein the treatment of COVID-19 using the words of (Covid-19) AND hydroxychloroquine. Results: Chloroquine and hydroxychloroquine have proven effective in treating coronavirus in China in vitro, but till now only few clinical trials are available and these trials were conducted on a small sample size of the patients. The efficacy of chloroquine and hydroxychloroquine is mainly due to its effect on angiotensin-converting enzyme II (ACE2). Conclusion: The use of chloroquine and hydroxychloroquine could be very promising but more trials are needed that include larger sample size and more data are required about the comparison between chloroquine and hydroxychloroquine with other antivirals.

Abstract W P20: A Model to Calculate the Expected Treatment Effect in Acute Endovascular Stroke Trials

Stroke ◽  
2014 ◽  
Vol 45 (suppl_1) ◽  
Author(s):  
Maarten G Lansberg ◽  
Robin Lemmens ◽  
Soren Christensen ◽  
Nishant K Mishra ◽  
Gregory W Albers
Keyword(s):  
Literature Review ◽  
Sample Size ◽  
Endovascular Therapy ◽  
Treatment Effect ◽  
Small Sample Size ◽  
Small Sample ◽  
Absolute Difference ◽  
Sample Size Calculations ◽  
And Control ◽  
Larger Sample

Background: Recent trials have shown no benefit of endovascular therapy. This may, in part, be explained by inaccurate estimates of the treatment effect used in the sample size calculations of these trials. A predictive model which includes variables that modify the expected treatment effect might yield more accurate estimates, and could be valuable in the design of future acute stroke trials. Methods: We conducted a literature review to obtain estimates of parameters that are associated with good functional outcome (GFO) following recanalization. We developed a model to estimate the treatment effect in endovascular stroke trials and applied this model to two recently published endovascular stroke trials. Results: We estimated a 40% absolute difference in the proportion of GFO (mRS 0-2 at 90 days) associated with reperfusion in patients with ICA or M1 occlusions who have a substantial ischemic penumbra at baseline. To estimate the effect size in trials, this value was multiplied by: 1) the proportion of patients undergoing endovascular therapy in the active treatment arm; 2) the proportion of patients with occlusions of the ICA or MCA-M1; 3) the proportion of patients with a substantial penumbra and a DWI lesion <50mL; and 4) the absolute difference in the proportion of patients with reperfusion, defined as TICI 2B-3, between the endovascular treatment and control arms. Based on literature review we assumed a reperfusion rate of 20% in the control arms of IMS III and MR Rescue, a 50% prevalence of patients with substantial penumbra and DWI lesions<50 mL in IMS III, and a 75% prevalence in the penumbral arms of MR Rescue. Based on these model inputs, a 2.2% increase in GFO with endovascular therapy was expected in IMS III, which closely matches the observed 2.1% increase. For MR Rescue, the model predicted a 1.5% increase in GFO with endovascular therapy. Considering the small sample size, this equates to 0.5 additional patients with GFO which closely matches the observed result of 3 fewer patients with GFO. Conclusion: A simple model shows promise for estimating the treatment effect of endovascular stroke trials. It may be useful for the design of future trials and could lead to different inclusion criteria or larger sample sizes compared to the recently conducted studies.

Partition Chromatographic-Gravimetric Assay of Opium

1972 ◽  
Vol 55 (1) ◽  
pp. 173-176
Author(s):  
Edward Smith ◽  
Eric B Sheixix ◽  
Joseph Levixe
Keyword(s):  
Sample Size ◽  
Chromatographic System ◽  
Gravimetric Measurement ◽  
Spectrophotometric Measurement ◽  
Partition System ◽  
Aoac Method ◽  
Larger Sample ◽  
Gravimetric Procedure

Abstract The current AOAC method for the determination of morphine in opium, 36.031–36.035, utilizes a 3-column partition chromatographic system for the isolation of morphine, with spectrophotometric measurement of the product. The same partition system has been modified to accommodate a larger sample size to permit a gravimetric measurement of the isolated morphine as its dinitrophenyl ether. The gravimetric procedure yields values comparable to those obtained by the much shorter and simpler UV method.

scholarly journals Outcome assessment by central adjudicators in randomised stroke trials: Simulation of differential and non-differential misclassification

2020 ◽  
Vol 5 (2) ◽  
pp. 174-183 ◽  
Author(s):  
Peter J Godolphin ◽  
Philip M Bath ◽  
Christopher Partlett ◽  
Eivind Berge ◽  
Martin M Brown ◽  
...  
Keyword(s):  
Sample Size ◽  
Outcome Assessment ◽  
Treatment Effect ◽  
Primary Outcome ◽  
Event Rate ◽  
Considerable Proportion ◽  
Binary Outcome ◽  
Primary Trial ◽  
Differential Misclassification ◽  
Larger Sample

Introduction Adjudication of the primary outcome in randomised trials is thought to control misclassification. We investigated the amount of misclassification needed before adjudication changed the primary trial results. Patients (or materials) and methods: We included data from five randomised stroke trials. Differential misclassification was introduced for each primary outcome until the estimated treatment effect was altered. This was simulated 1000 times. We calculated the between-simulation mean proportion of participants that needed to be differentially misclassified to alter the treatment effect. In addition, we simulated hypothetical trials with a binary outcome and varying sample size (1000–10,000), overall event rate (10%–50%) and treatment effect (0.67–0.90). We introduced non-differential misclassification until the treatment effect was non-significant at 5% level. Results For the five trials, the range of unweighted kappa values were reduced from 0.89–0.97 to 0.65–0.85 before the treatment effect was altered. This corresponded to 2.1%–6% of participants misclassified differentially for trials with a binary outcome. For the hypothetical trials, those with a larger sample size, stronger treatment effect and overall event rate closer to 50% needed a higher proportion of events non-differentially misclassified before the treatment effect became non-significant. Discussion: We found that only a small amount of differential misclassification was required before adjudication altered the primary trial results, whereas a considerable proportion of participants needed to be misclassified non-differentially before adjudication changed trial conclusions. Given that differential misclassification should not occur in trials with sufficient blinding, these results suggest that central adjudication is of most use in studies with unblinded outcome assessment. Conclusion: For trials without adequate blinding, central adjudication is vital to control for differential misclassification. However, for large blinded trials, adjudication is of less importance and may not be necessary.

scholarly journals Sexual Size Dimorphism and Positive Assortative Mating in Alpine Choughs (Pyrrhocorax graculus)

The Auk ◽  
2001 ◽  
Vol 118 (2) ◽  
pp. 553-556 ◽  
Author(s):  
Anne Delestrade
Keyword(s):  
Sample Size ◽  
Assortative Mating ◽  
Body Condition ◽  
Sexual Size Dimorphism ◽  
Morphological Characters ◽  
Positive Trend ◽  
Tarsus Length ◽  
Size Dimorphism ◽  
Positive Assortative Mating ◽  
Larger Sample

Abstract The degree of sexual size dimorphism in a number of different morphological characters was examined in a social corvid, the Alpine Chough, using measurements taken on 178 males and 144 females. A small amount of size dimorphism appeared in all morphological characters, and weight was the most dimorphic character. To identify if Alpine Choughs mate assortatively, measurements of mates were compared in 76 pairs. A positive assortative mating was found on tarsus length, and a small positive trend is suggested between body condition of partners, but that needs to be confirmed with a larger sample size.

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